Imaging structural and functional brain development in early childhood
Open accessAbstract
In humans, the period from term birth to ∼2 years of age is characterized by rapid and dynamic brain development and plays an important role in cognitive development and risk of disorders such as autism and schizophrenia. Recent imaging studies have begun to delineate the growth trajectories of brain structure and function in the first years after birth and their relationship to cognition and risk of neuropsychiatric disorders. This Review discusses the development of grey and white matter and structural and functional networks, as well as genetic and environmental influences on early-childhood brain development. We also discuss initial evidence regarding the usefulness of early imaging biomarkers for predicting cognitive outcomes and risk of neuropsychiatric disorders.
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- Premisecitation
Cortical and subcortical grey matter undergoes robust growth in the first year of life.
“Cortical and subcortical grey matter also undergoes robust growth in the first year of life10, although cortical grey-matter networks seem to mature much later in childhood, perhaps driven by coordinated activity across the cortex from functional networks that arise much earlier in development.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Gilmore, J. H. et al. Longitudinal development of cortical and subcortical gray matter from birth to 2 years. Cereb. Cortex 22, 2478–2485 (2012). source
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- Premisecitation
Some neurogenesis occurs after birth: neurons continue to arise and migrate from the subventricular zone of the anterior lateral ventricles to the olfactory bulb and ventromedial prefrontal cortex during the first 18 months of postnatal life.
“one study showed that neurons continue to arise and migrate from the subventricular zone of the anterior lateral ventricles to the olfactory bulb and ventromedial prefrontal cortex in the first 18 months of postnatal life205.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [205] Sanai, N. et al. Corridors of migrating neurons in the human brain and their decline during infancy. Nature 478, 382–386 (2011). source
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- Premisecitation
Changing contrast challenges determination of cortical thickness, which depends on a clear boundary between cortical grey matter and underlying white matter.
“This changing contrast also presents challenges for determining cortical thickness, which depends on a clear boundary between cortical grey matter and underlying white matter.28”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [28] Walhovd, K. B., Fjell, A. M., Giedd, J., Dale, A. M. & Brown, T. T. Through thick and thin: a need to reconcile contradictory results on trajectories in human cortical development. Cereb. Cortex 27, 1472–1481 (2017).
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- Interpretationreasoning
After age two, brain development mainly involves reorganization, fine-tuning, plasticity and remodelling of already established circuits and networks.
“Brain development after age 2 years is characterized mainly by reorganization, ‘fine-tuning’, plasticity and remodelling of the major circuits and networks that are already established.”
Quote in the paperSubstantial claim - Premisecitation
The basic structural and functional framework of the human brain is in place by the second year of life and perhaps earlier.
“These studies, along with more recent postmortem histological and gene-expression studies7, 8 (Box 1), suggest that the basic structural and functional framework of the human brain is in place by the second year of life and perhaps even earlier.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [7] Petanjek, Z. et al. Extraordinary neoteny of synaptic spines in the human prefrontal cortex. Proc. Natl Acad. Sci. USA 108, 13281–13286 (2011). source
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- cites [8] Pletikos, M. et al. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron 81, 321–332 (2014). source
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Motion in the scanner can significantly influence measures of cortical thickness and surface area, DTI parameters, and resting-state networks.
“It is increasingly recognized that motion in the scanner can significantly influence measures of cortical thickness and surface area27, 218, as well as DTI parameters (Box 2)219 and resting-state networks (Box 3)220,219.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [27] Ducharme, S. et al. Trajectories of cortical thickness maturation in normal brain development — the importance of quality control procedures. Neuroimage 125, 267–279 (2016). source
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- cites [218] Alexander-Bloch, A. et al. Subtle in-scanner motion biases automated measurement of brain anatomy from in vivo MRI. Hum. Brain Mapp. 37, 2385–2397 (2016). source
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- cites [219] Sairanen, V., Kuusela, L., Sipila, O., Savolainen, S. & Vanhatalo, S. A novel measure of reliability in diffusion tensor imaging after data rejections due to subject motion. Neuroimage 147, 57–65 (2017). source
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- Premisecitation
Widespread migration of new neurons, mainly inhibitory interneurons, to the cingulate cortex and superior frontal gyrus occurs in the first five months after birth.
“Another study found widespread migration of new neurons, mainly inhibitory interneurons, to the cingulate cortex and superior frontal gyrus in the first 5 months after birth206.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [206] Paredes, M. F. et al. Extensive migration of young neurons into the infant human frontal lobe. Science 354, aaf7073 (2016). source
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- Interpretationreasoning
Neurogenesis in early childhood contributes to grey-matter expansion in at least some frontal lobe areas.
“These studies suggest that neurogenesis in early childhood contributes to grey-matter expansion in at least some areas of the frontal lobe.”
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Sensorimotor regions mature before higher-order association areas.
“consistent with imaging findings that sensorimotor regions mature before higher-order association areas10.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Gilmore, J. H. et al. Longitudinal development of cortical and subcortical gray matter from birth to 2 years. Cereb. Cortex 22, 2478–2485 (2012). source
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Recent imaging studies in early childhood have begun to reveal the very rapid pace of postnatal structural and functional brain development.
“Recently, however, imaging studies in early childhood have begun to illuminate the extremely rapid pace of postnatal structural and functional brain development3–6.”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [3] Knickmeyer, R. C. et al. A structural MRI study of human brain development from birth to 2 years. J. Neurosci. 28, 12176–12182 (2008). This is a comprehensive study of structural brain development in the first 2 years of life demonstrating the rapid growth of cortical grey matter in the first year of life. source
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- cites [4] Lyall, A. E. et al. Dynamic development of regional cortical thickness and surface area in early childhood. Cereb. Cortex 25, 2204–2212 (2015). source
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- cites [5] Dubois, J. et al. The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants. Neuroscience 276, 48–71 (2014). This is a comprehensive review of the use of imaging to study white matter in early brain development. source
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- cites [6] Gao, W. et al. Evidence on the emergence of the brain's default network from 2-week-old to 2-year-old healthy pediatric subjects. Proc. Natl Acad. Sci. USA 106, 6790–6795 (2009). source
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Most neurons in the human brain are generated before birth.
“The bulk of neurons in the human brain are generated prenatally204.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [204] Bhardwaj, R. D. et al. Neocortical neurogenesis in humans is restricted to development. Proc. Natl Acad. Sci. USA 103, 12564–12568 (2006). source
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The overall complexity of cortical neurons increases quickly after birth and peaks at two to four years.
“Conel’s classic survey of cortical neuron development in children found that the overall complexity of cortical neurons increases quickly after birth, peaking at 2–4 years207”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [207] Conel, J. L. The Cortex of the Four-Year Child (Harvard Univ. Press, Cambridge, Massachusetts, 1963). source
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The gyrification index increases in the first two years of life in parallel with overall brain growth.
“The gyrification index (the amount of cortex within a sulcal fold), increases in the first 2 years of life in parallel with overall brain growth23.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [23] Li, G. et al. Mapping region-specific longitudinal cortical surface expansion from birth to 2 years of age. Cereb. Cortex 23, 2724–2733 (2013). source
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Diffusion properties of white-matter tracts are highly correlated at birth, but this correlation decreases with development as tracts mature and differentiate.
“The diffusion properties of white-matter tracts are highly correlated with each other at birth, but this correlation decreases with development as tracts mature and differentiate38.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [38] Lee, S. J. et al. Common and heritable components of white matter microstructure predict cognitive function at 1 and 2 y. Proc. Natl Acad. Sci. USA 114, 148–153 (2017). source
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Diffusion-weighted imaging has many limitations and sources of error at each step of the analysis pipeline.
“Moreover, diffusion-weighted imaging has many limitations and sources of error at each step of the analysis pipeline that must be considered when interpreting results236, 237.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [236] Jones, D. K. & Cercignani, M. Twenty-five pitfalls in the analysis of diffusion MRI data. NMR Biomed. 23, 803–820 (2010). source
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- cites [237] Jones, D. K., Knosche, T. R. & Turner, R. White matter integrity, fiber count, and other fallacies: the do's and don'ts of diffusion MRI. Neuroimage 73, 239–254 (2013). source
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Postnatal growth of global tissue volume and subcortical structures is most rapid in the first three months after birth.
“Postnatal growth of global tissue volume and subcortical structures is most rapid in the first 3 months after birth16.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [16] Holland, D. et al. Structural growth trajectories and rates of change in the first 3 months of infant brain development. JAMA Neurol. 71, 1266–1274 (2014). source
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White-matter networks at birth, and even in premature infants at 30 weeks gestational age, have a rich club property similar to that in adults.
“White-matter networks at birth, and even in premature infants at 30 weeks gestational age50, have a rich club property similar to that in adults.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [50] Ball, G. et al. Rich-club organization of the newborn human brain. Proc. Natl Acad. Sci. USA 111, 7456–7461 (2014). This paper presents an early study of the white-matter connectome in preterm and term infants, demonstrating that major hubs are already present at 30 weeks gestational age. source
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- Premisecitation
Grey and white matter have different growth trajectories soon after birth, with rapid grey-matter volume development compared with a more gradual increase in white-matter volume.
“Grey and white matter have different growth trajectories soon after birth, with rapid development of grey-matter volume compared to white-matter volume, which increases much more gradually15,3.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [15] Matsuzawa, J. et al. Age-related volumetric changes of brain gray and white matter in healthy infants and children. Cereb. Cortex 11, 335–342 (2001). source
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- cites [3] Knickmeyer, R. C. et al. A structural MRI study of human brain development from birth to 2 years. J. Neurosci. 28, 12176–12182 (2008). This is a comprehensive study of structural brain development in the first 2 years of life demonstrating the rapid growth of cortical grey matter in the first year of life. source
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The hippocampus grows somewhat more slowly, about 84%, than other subcortical structures in the first year.
“The hippocampus grows somewhat slower (about 84%) than other subcortical structures in year one10.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Gilmore, J. H. et al. Longitudinal development of cortical and subcortical gray matter from birth to 2 years. Cereb. Cortex 22, 2478–2485 (2012). source
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Myelination increases more gradually after the second year.
“similarly, myelination increases more gradually after the second year36,37.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [36] Dean, D. C. et al. Modeling healthy male white matter and myelin development: 3 through 60 months of age. Neuroimage 84, 742–752 (2014). source
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- cites [37] Dean, D. C. et al. Characterizing longitudinal white matter development during early childhood. Brain Struct. Funct. 220, 1921–1933 (2015). source
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Cortical thickness might gradually decrease even between ages one and six years.
“Indeed, a recent study reported that cortical thickness might gradually decrease even between ages 1 and 6 years22.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [22] Remer, J. et al. Quantifying cortical development in typically developing toddlers and young children, 1–6 years of age. Neuroimage 153, 246–261 (2017). source
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The medial temporal cortex and rolandic operculum are larger in male neonates.
“the medial temporal cortex and rolandic operculum are larger in males”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [123] Tanaka, C., Matsui, M., Uematsu, A., Noguchi, K. & Miyawaki, T. Developmental trajectories of the fronto-temporal lobes from infancy to early adulthood in healthy individuals. Dev. Neurosci. 34, 477–487 (2012). source
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Female neonates have greater grey-matter volumes around the temporal-parietal junction.
“female neonates have greater grey-matter volumes around the temporal-parietal junction, a crucial brain region for social cognition124.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [124] Li, G. et al. Mapping longitudinal development of local cortical gyrification in infants from birth to 2 years of age. J. Neurosci. 34, 4228–4238 (2014). source
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The brain's functional organization is hierarchical.
“The hierarchical nature of the brain’s functional organization has long been recognized113, 114”
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The dorsolateral prefrontal, motor, and visual cortices are larger in female neonates.
“the dorsolateral prefrontal, motor, and visual cortices are larger in females123.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [123] Tanaka, C., Matsui, M., Uematsu, A., Noguchi, K. & Miyawaki, T. Developmental trajectories of the fronto-temporal lobes from infancy to early adulthood in healthy individuals. Dev. Neurosci. 34, 477–487 (2012). source
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Males on average have a higher number of neocortical neurons than females.
“On average, males exhibit a higher number of neocortical neurons than females”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [125] Liu, Y. et al. Gender differences in language and motor-related fibers in a population of healthy preterm neonates at term-equivalent age: a diffusion tensor and probabilistic tractography study. AJNR Am. J. Neuroradiol. 32, 2011–2016 (2011). source
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The newborn brain already has small-world functional network properties.
“the newborn brain already demonstrates ‘small-world’ functional network properties93, 118”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [93] Thomason, M. E. et al. Cross-hemispheric functional connectivity in the human fetal brain. Sci. Transl Med. 5, 173ra24 (2013). source
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- cites [118] Ruigrok, A. N. et al. A meta-analysis of sex differences in human brain structure. Neurosci. Biobehav. Rev. 39, 34–50 (2014). source
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- Interpretationcitation
Interactions between experience-dependent processes and gene expression further modify or refine primary functional circuits for more efficient signal processing and action generation.
“Transitioning from the later part of gestation to postnatal development, interactions between the experience-dependent processes120 and gene expression further modify or refine the primary functional circuits for more efficient signal processing and action generation.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [120] Knickmeyer, R. C. et al. Impact of sex and gonadal steroids on neonatal brain structure. Cereb. Cortex 24, 2721–2731 (2014). source
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An inverse correlation between the dorsal attention network and the default-mode network emerges during the first year of life.
“Moreover, the inverse correlation between the dorsal attention network and the default-mode network, interpreted by most as a sign of ‘competition’ between the processing of external and internal events in the mature brain106, also emerges during the first year of life112.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [106] Rothbart, M. K., Sheese, B. E., Rueda, M. R. & Posner, M. I. Developing mechanisms of self-regulation in early life. Emot. Rev. 3, 207–213 (2011). source
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- cites [112] Sepulcre, J., Sabuncu, M. R., Yeo, T. B., Liu, H. & Johnson, K. A. Stepwise connectivity of the modal cortex reveals the multimodal organization of the human brain. J. Neurosci. 32, 10649–10661 (2012). source
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Many sex differences in brain structure and function are present at birth.
“Studies focused on infancy and early childhood are more limited, but indicate that many of these sex differences are present at birth.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [121] Knickmeyer, R. C. et al. Impact of demographic and obstetric factors on infant brain volumes: a population neuroscience study. Cereb. Cortex 27, 5616–5625 (2016).
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- cites [122] Pakkenberg, B. & Gundersen, H. J. Neocortical neuron number in humans: effect of sex and age. J. Comp. Neurol. 384, 312–320 (1997). source
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- Premisecitation
Sensorimotor-auditory integration via convergent connectivity in the sylvian-parietal-temporal area has been observed in neonates.
“preliminary manifestations of sensorimotor-auditory integration through convergent connectivity within the sylvian-parietal-temporal area110, 111 has been observed in neonates.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [110] Damasio, A. R. Time-locked multiregional retroactivation: a systems-level proposal for the neural substrates of recall and recognition. Cognition 33, 25–62 (1989). source
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- cites [111] Mesulam, M. M. From sensation to cognition. Brain 121, 1013–1052 (1998). source
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Male neonate brains are about 6% larger than female brains at birth.
“Male neonate brains are about 6% larger than female brains at birth”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [123] Tanaka, C., Matsui, M., Uematsu, A., Noguchi, K. & Miyawaki, T. Developmental trajectories of the fronto-temporal lobes from infancy to early adulthood in healthy individuals. Dev. Neurosci. 34, 477–487 (2012). source
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- Interpretationreasoning
The brain's functional hierarchy emerges during infancy.
“suggesting that the brain’s functional hierarchy also emerges during infancy.”
Quote in the paperSubstantial claim - Interpretationreasoning
Primary functional networks are formed before birth through activity-dependent but largely experience-independent development.
“Through activity-dependent but largely experience-independent development, primary functional networks are formed before birth.”
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Functional network development across the brain is coordinated.
“the study of inter-network relationships reveals that functional network development is coordinated109.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [109] Andersen, R. A. Multimodal integration for the representation of space in the posterior parietal cortex. Phil. Trans. R. Soc. Lond. B Biol Sci. 352, 1421–1428 (1997). source
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- Premisecitation
Whole-brain efficiency continues to improve during postnatal development.
“although whole-brain efficiency continues to improve during postnatal development118, 119.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [118] Ruigrok, A. N. et al. A meta-analysis of sex differences in human brain structure. Neurosci. Biobehav. Rev. 39, 34–50 (2014). source
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- cites [119] Sacher, J., Neumann, J., Okon-Singer, H., Gotowiec, S. & Villringer, A. Sexual dimorphism in the human brain: evidence from neuroimaging. Magn. Reson. Imag. 31, 366–375 (2013). source
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- Premisecitation
Genetically determined early synaptic connections enable the first appearance of synchronized oscillatory electrical activity in the prenatal brain.
“Genetically determined early synaptic connections enable the first appearance of synchronized oscillatory electrical activity in the prenatal brain62, 63.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [62] Khazipov, R. & Luhmann, H. J. Early patterns of electrical activity in the developing cerebral cortex of humans and rodents. Trends Neurosci. 29, 414–418 (2006). source
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- cites [63] Dehaene-Lambertz, G. & Spelke, E. S. The infancy of the human brain. Neuron 88, 93–109 (2015). source
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- Interpretationreasoning
New social, cognitive, and emotional experiences parallel the emergence, growth and fine tuning of corresponding higher-order functional circuits.
“Enabled by and rooted in these primary functions, new social, cognitive, and emotional experiences parallel the emergence, growth and fine tuning of corresponding higher-order functional circuits.”
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A larger-sample study replicated increased medial temporal cortex in male neonates.
“A more recent study with a larger sample size and more stringent statistical thresholds replicated the finding of increased medial temporal cortex in males”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [124] Li, G. et al. Mapping longitudinal development of local cortical gyrification in infants from birth to 2 years of age. J. Neurosci. 34, 4228–4238 (2014). source
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- Premisecitation
Several brain areas already show local sexual dimorphism at birth.
“and even at this stage there are already several areas that evidence local sexual dimorphism123.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [123] Tanaka, C., Matsui, M., Uematsu, A., Noguchi, K. & Miyawaki, T. Developmental trajectories of the fronto-temporal lobes from infancy to early adulthood in healthy individuals. Dev. Neurosci. 34, 477–487 (2012). source
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- Premisecitation
Structural covariance networks of grey-matter volume and cortical thickness exhibit small-world properties and modular organization at birth and at three years.
“SCNs of grey-matter volume and cortical thickness exhibit small-world properties and modular organization at birth58 and 3 years59.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [58] Fan, Y. et al. Brain anatomical networks in early human brain development. Neuroimage 54, 1862–1871 (2011). source
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- cites [59] Nie, J., Li, G. & Shen, D. Development of cortical anatomical properties from early childhood to early adulthood. Neuroimage 76, 216–224 (2013). source
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- Premisecitation
Step-wise analysis of functional connectivity is a novel technique that could probe the brain's functional hierarchy.
“step-wise analysis [G] of functional connectivity emerges as a novel technique that could probe this hierarchy115.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [115] Gao, W. et al. Temporal and spatial evolution of brain network topology during the first two years of life. PLoS ONE 6, e25278 (2011). source
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- Premisecitation
Genetic factors account for 56% of variance in neonatal global grey-matter volume.
“56% variance in neonatal global grey-matter volume146.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [146] Geng, X. et al. White matter heritability using diffusion tensor imaging in neonatal brains. Twin Res. Hum. Genet. 15, 336–350 (2012). source
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- Premisecitation
Infancy and early childhood are characterized by relatively minimal differences in gene expression across cortical areas, as general neuronal and glial differentiation transcription programmes are initiated.
“infancy and early childhood are characterized by relatively minimal differences in gene expression across cortical areas, as more ‘general’ neuronal and glial differentiation transcription programmes are initiated8.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] Pletikos, M. et al. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron 81, 321–332 (2014). source
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- Premisecitation
Postnatally, brain volume increases more rapidly in male infants than in female infants, widening the separation in brain sizes.
“Postnatally, brain volume increases more rapidly in male infants than in female infants, leading to a widening separation in brain sizes16, 126.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [16] Holland, D. et al. Structural growth trajectories and rates of change in the first 3 months of infant brain development. JAMA Neurol. 71, 1266–1274 (2014). source
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- cites [126] Ratnarajah, N. et al. Structural connectivity asymmetry in the neonatal brain. Neuroimage 75, 187–194 (2013). source
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- Premisecitation
In adults, females show stronger positive amygdala connectivity with areas for face monitoring and discrimination, sensory processing, and emotional processing.
“females showing stronger positive connectivity between the amygdala and areas associated with face monitoring and discrimination (middle temporal gyrus and inferior frontal gyrus), sensory processing (postcentral gyrus), and emotional processing (hippocampus)”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [139] Jansen, A. G., Mous, S. E., White, T., Posthuma, D. & Polderman, T. J. What twin studies tell us about the heritability of brain development, morphology, and function: a review. Neuropsychol. Rev. 25, 27–46 (2015). source
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- cites [140] Blokland, G. A., de Zubicaray, G. I., McMahon, K. L. & Wright, M. J. Genetic and environmental influences on neuroimaging phenotypes: a meta-analytical perspective on twin imaging studies. Twin Res. Hum. Genet. 15, 351–371 (2012). source
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- Premisecitation
These developmental programmes are mediated by transcription factors binding specific genomic sequences, transcriptional cofactors, chromatin regulators, epigenetic modifications, RNA-binding proteins, and non-coding RNAs.
“These developmental programmes are mediated by transcription factors that bind to specific genomic sequences (such as cis-regulatory elements), as well as transcriptional cofactors, chromatin regulators, epigenetic modifications, RNA-binding proteins and non-coding RNAs157.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [157] Knickmeyer, R. C. et al. Common variants in psychiatric risk genes predict brain structure at birth. Cereb. Cortex 24, 1230–1246 (2014). source
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- Premisecitation
Prenatal cortical development is characterized by robust regional differences in gene expression that are probably crucial for establishing area-specific subcortical-cortical and cortico-cortical projections.
“prenatal cortical development is characterized by robust regional differences in gene expression that are probably crucial for establishing area-specific subcortical-cortical and cortico-cortical projections8.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] Pletikos, M. et al. Temporal specification and bilaterality of human neocortical topographic gene expression. Neuron 81, 321–332 (2014). source
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- Premisecitation
The morphometry and functional organization of the infant brain arises in part through precise spatiotemporal regulation of gene expression.
“The morphometry and functional organization of the infant brain arises, in part, through the precise spatiotemporal regulation of gene expression156.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [156] Poretti, A., Boltshauser, E. & Huisman, T. A. Congenital brain abnormalities: an update on malformations of cortical development and infratentorial malformations. Semin. Neurol. 34, 239–248 (2014). source
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- Interpretationcitation
Genetic influences on resting-state networks are present as networks are established in the first years after birth.
“suggesting that genetic influences on resting-state networks are present as networks are established in the first years after birth.”
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Genetic factors account for 85% of variance in neonatal global white-matter volume.
“genetic factors account for 85% variance in neonatal global white-matter volume”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [146] Geng, X. et al. White matter heritability using diffusion tensor imaging in neonatal brains. Twin Res. Hum. Genet. 15, 336–350 (2012). source
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- Premisecitation
Local or regional gyrification index is similar between males and females at each age.
“local or regional gyrification index is similar between males and females at each age127.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [127] Deoni, S. C., Dean, D. C. III, O'Muircheartaigh, J., Dirks, H. & Jerskey, B. A. Investigating white matter development in infancy and early childhood using myelin water faction and relaxation time mapping. Neuroimage 63, 1038–1053 (2012). source
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- Interpretationreasoning
The heritability of grey-matter volume seems to increase during rapid grey-matter growth from birth to later childhood.
“the heritability of grey-matter volume seems to increase during the period of rapid grey-matter growth from birth to later childhood.”
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There is no global gyrification difference between males and females at 0 or 1 year of age.
“but not at 0 or 1 year of age”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [127] Deoni, S. C., Dean, D. C. III, O'Muircheartaigh, J., Dirks, H. & Jerskey, B. A. Investigating white matter development in infancy and early childhood using myelin water faction and relaxation time mapping. Neuroimage 63, 1038–1053 (2012). source
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- Premisecitation
The heritability of default resting-state network connectivity is 42%.
“the heritability of default resting-state network connectivity is 42%153.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [153] Gao, W. et al. Intersubject variability of and genetic effects on the brain's functional connectivity during infancy. J. Neurosci. 34, 11288–11296 (2014). source
Not checked in the free run.
- Premisecitation
Males show increased global gyrification at 2 years of age compared with females after adjusting for total brain volume.
“Males also show increased global gyrification at 2 years of age compared with females (adjusting for total brain volume)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [127] Deoni, S. C., Dean, D. C. III, O'Muircheartaigh, J., Dirks, H. & Jerskey, B. A. Investigating white matter development in infancy and early childhood using myelin water faction and relaxation time mapping. Neuroimage 63, 1038–1053 (2012). source
Not checked in the free run.
- Interpretationreasoning
The heritability of white-matter microstructure increases over the course of childhood.
“suggesting that the heritability of white-matter microstructure increases over the course of childhood”
Quote in the paperSubstantial claim - Premisecitation
In adults, males show greater amygdala connectivity with areas involved in acquisition of conditioned fear, extinction learning, and extinction memory.
“males showing greater connectivity between the amygdala and areas involved in the acquisition of conditioned fear, extinction learning and extinction memory 139, 140”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [139] Jansen, A. G., Mous, S. E., White, T., Posthuma, D. & Polderman, T. J. What twin studies tell us about the heritability of brain development, morphology, and function: a review. Neuropsychol. Rev. 25, 27–46 (2015). source
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- cites [140] Blokland, G. A., de Zubicaray, G. I., McMahon, K. L. & Wright, M. J. Genetic and environmental influences on neuroimaging phenotypes: a meta-analytical perspective on twin imaging studies. Twin Res. Hum. Genet. 15, 351–371 (2012). source
Not checked in the free run.
- Premisecitation
Between 3 and 60 months, females have a higher rate of myelination than males in the genu of the corpus callosum, left frontal and left temporal white matter, and right optic radiation.
“between 3 and 60 months, females exhibit a higher rate of myelination compared with males in the genu of the corpus callosum, in left frontal and left temporal white matter, and in the right optic radiation130.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [130] Rametti, G. et al. White matter microstructure in female to male transsexuals before cross-sex hormonal treatment. A diffusion tensor imaging study. J. Psychiatr. Res. 45, 199–204 (2011). source
Not checked in the free run.
- Interpretationreasoning
If sex differences in intracranial volume reflect differences in neocortical neuron number, their origin may be in the second trimester when neurogenesis peaks and male fetal testosterone is high.
“If sex differences in ICV reflect differences in neocortical neuron number, this suggests an origin in the second trimester, when neurogenesis is at its peak and male fetal testosterone levels are high.”
Quote in the paperNot a substantial claim - Interpretationreasoning
The heritability of white-matter volume is stable over postnatal brain development.
“these results suggest that the heritability of white-matter volume is stable over the course of postnatal brain development”
Quote in the paperSubstantial claim - Premisecitation
Twin studies in adults and older children find high genetic contribution to variance of global brain-tissue volumes, with heritability estimates typically greater than 80% for global grey and white matter.
“Twin studies in adults and older children find that the genetic contribution to variance of global brain-tissue volumes is high, with heritability [G] estimates typically greater than 80% for global grey and white matter142, 143.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [142] Chen, C. H. et al. Genetic topography of brain morphology. Proc. Natl Acad. Sci. USA 110, 17089–17094 (2013). source
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- cites [143] Gilmore, J. H. et al. Genetic and environmental contributions to neonatal brain structure: a twin study. Hum. Brain Mapp. 31, 1174–1182 (2010). source
Not checked in the free run.
- Interpretationcitation
The higher neocortical neuron number in males is a likely contributor to their larger intracranial volume.
“this difference is a likely contributor to the larger intracranial volume observed in males125”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [125] Liu, Y. et al. Gender differences in language and motor-related fibers in a population of healthy preterm neonates at term-equivalent age: a diffusion tensor and probabilistic tractography study. AJNR Am. J. Neuroradiol. 32, 2011–2016 (2011). source
Not checked in the free run.
- Premisecitation
In 12-year-olds, the path length of resting-state networks has a heritability of 42%.
“In 12-year-olds, the path length of resting-state networks has a heritability of 42%155.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [155] Shibata, M., Gulden, F. O. & Sestan, N. From trans to cis: transcriptional regulatory networks in neocortical development. Trends Genet. 31, 77–87 (2015). source
Not checked in the free run.
- Interpretationreasoning
Early exposure to stress may have an impact on early structural and functional brain development.
“Thus, early exposure to stress may have an impact on early structural and functional brain development”
Quote in the paperSubstantial claim - Premisecitation
BDNF genotype may regulate the sensitivity of the methylome to maternal anxiety, with differential effects on amygdala and hippocampal volume.
“BDNF genotype may also regulate the sensitivity of the methylome [G] to maternal anxiety, with differential effects on amygdala and hippocampal volume160.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [160] Chen, L. et al. Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism influences the association of the methylome with maternal anxiety and neonatal brain volumes. Dev. Psychopathol 27, 137–150 (2015). source
Not checked in the free run.
- Interpretationreasoning
Risk genes may influence the earliest stages of human brain development.
“these studies indicate that risk genes may influence the earliest stages of human brain development”
Quote in the paperSubstantial claim - Premisecitation
Genetic mutations are associated with various brain abnormalities evident on MRI.
“Genetic mutations are associated with various brain abnormalities that are evident on MRI (see REF. 158 for review).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [158] Dean, D. C. et al. Brain differences in infants at differential genetic risk for late-onset Alzheimer disease: a cross-sectional imaging study. JAMA Neurol. 71, 11–22 (2014). source
Not checked in the free run.
- Premisecitation
This locus is within 100 kb of REST, a master negative regulator of neurogenesis.
“this locus is within 100kb of REST, a master negative regulator of neurogenesis163.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [163] Johnson, D. S., Mortazavi, A., Myers, R. M. & Wold, B. Genome-wide mapping of in vivo protein-DNA interactions. Science 316, 1497–1502 (2007). source
Not checked in the free run.
- Premisecitation
White-matter volume does not seem to be affected by socio-economic status.
“white-matter volume does not seem to be affected by SES169, 171”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [169] Mackey, A. P. et al. Neuroanatomical correlates of the income-achievement gap. Psychol. Sci. 26, 925–933 (2015). source
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- cites [171] Hanson, J. L. et al. Family poverty affects the rate of human infant brain growth. PLoS ONE 8, e80954 (2013). source
Not checked in the free run.
- Premisecitation
White-matter microstructure can be affected by socio-economic status.
“white-matter microstructure can be172.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [172] Ursache, A. & Noble, K. G. Socioeconomic status, white matter, and executive function in children. Brain Behav. 6, e00531 (2016). source
Not checked in the free run.
- Interpretationcitation
Infant genotype may moderate the impact of environmental variables on brain development.
“Infant genotype may also moderate the impact of environmental variables on brain development.”
Quote in the paperSubstantial claim - Premisecitation
Studies of premature infants have generally found that abnormalities of grey-matter and white-matter volume and white-matter diffusivity are associated with poor neurodevelopmental outcomes.
“studies of premature infants have generally found that abnormalities of grey-matter and white-matter volume and of white-matter diffusivity are associated with poor neurodevelopmental outcomes 11, 186.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [11] Anderson, P. J., Cheong, J. L. & Thompson, D. K. The predictive validity of neonatal MRI for neurodevelopmental outcome in very preterm children. Semin. Perinatol. 39, 147–158 (2015). source
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- cites [186] Keunen, K. et al. Brain volumes at term-equivalent age in preterm infants: imaging biomarkers for neurodevelopmental outcome through early school age. J. Pediatr. 172, 88–95 (2016). source
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- Premisecitation
The influence of socio-economic status on brain structure seems to become greater with age in early childhood.
“The influence of SES on brain structure seems to become greater with age in early childhood171”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [171] Hanson, J. L. et al. Family poverty affects the rate of human infant brain growth. PLoS ONE 8, e80954 (2013). source
Not checked in the free run.
- Premisecitation
Neonates carrying the ε4 allele of APOE have reduced volumes in temporal cortex, similar to those reported in the elderly.
“neonates carrying the ε4 allele of APOE (which encodes apolipoprotein E), a major susceptibility allele for late-onset Alzheimer disease, have reduced volumes in temporal cortex, highly similar to those reported in the elderly.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [171] Hanson, J. L. et al. Family poverty affects the rate of human infant brain growth. PLoS ONE 8, e80954 (2013). source
Not checked in the free run.
- Premisecitation
Maternal depression during pregnancy is associated with reduced cortical thickness and white-matter diffusivity in children aged 2.5-5 years.
“Maternal depression during pregnancy is associated with reduced cortical thickness and white-matter diffusivity in children aged 2.5–5 years174”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [174] Lebel, C. et al. Prepartum and postpartum maternal depressive symptoms are related to children's brain structure in preschool. Biol. Psychiatry 80, 859–868 (2016). source
Not checked in the free run.
- Premisecitation
Prenatal exposure to alcohol or other drugs of abuse has important effects on developing brain structure.
“Prenatal exposure to alcohol or other drugs of abuse also have important effects on developing brain structure”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [180] Derauf, C., Kekatpure, M., Neyzi, N., Lester, B. & Kosofsky, B. Neuroimaging of children following prenatal drug exposure. Semin. Cell Dev. Biol. 20, 441–454 (2009). source
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- cites [181] Donald, K. A. et al. Neuroimaging effects of prenatal alcohol exposure on the developing human brain: a magnetic resonance imaging review. Acta Neuropsychiatr. 27, 251–269 (2015). source
Not checked in the free run.
- Premisecitation
Common variants in psychiatric risk genes are associated with individual differences in brain tissue volumes in neonates.
“Common variants in psychiatric risk genes are associated with individual differences in brain tissue volumes in neonates171.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [171] Hanson, J. L. et al. Family poverty affects the rate of human infant brain growth. PLoS ONE 8, e80954 (2013). source
Not checked in the free run.
- Premisecitation
Maternal anxiety is associated with slower hippocampal growth between birth and 6 months of age.
“Maternal anxiety is associated with slower hippocampal growth between birth and 6 months of age178”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [178] Qiu, A. et al. Maternal anxiety and infants' hippocampal development: timing matters. Transl Psychiatry 3, e306 (2013). source
Not checked in the free run.
- Premisecitation
Neonates homozygous for the rs821616 serine allele of DISC1 exhibit numerous large areas of reduced grey matter in the frontal lobes.
“neonates homozygous for the rs821616 serine allele of DISC1 (which encodes disrupted-in schizophrenia 1) exhibit numerous large areas of reduced grey matter in the frontal lobes.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [171] Hanson, J. L. et al. Family poverty affects the rate of human infant brain growth. PLoS ONE 8, e80954 (2013). source
Not checked in the free run.
- Premisecitation
High maternal cortisol levels during pregnancy are associated with greater amygdala volumes in female 7-year-olds.
“high maternal cortisol levels during pregnancy are associated with greater amygdala volumes in female 7-year-olds173.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [173] Buss, C. et al. Maternal cortisol over the course of pregnancy and subsequent child amygdala and hippocampus volumes and affective problems. Proc. Natl Acad. Sci. USA 109, E1312–E1319 (2012). source
Not checked in the free run.
- Interpretationreasoning
Alzheimer disease could be, in part, a developmental disorder.
“support the idea that Alzheimer disease could be, in part, a developmental disorder.”
Quote in the paperSubstantial claim - Premisecitation
Socio-economic status can influence the structure of the developing brain.
“Recent studies indicate that socio-economic status (SES) can influence the structure of the developing brain166, 167.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [166] Brito, N. H. & Noble, K. G. Socioeconomic status and structural brain development. Front. Neurosci. 8, 276 (2014). source
Not checked in the free run.
- cites [167] Farah, M. J. The neuroscience of socioeconomic status: correlates, causes, and consequences. Neuron 96, 56–71 (2017). source
Not checked in the free run.
- Premisecitation
An intronic SNP in WWOX (rs10514437) fell just short of genome-wide significance for white matter.
“An intronic SNP in WWOX (rs10514437) fell just short of genome-wide significance for white matter.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [162] Xia, K. et al. Genome-wide association analysis identifies common variants influencing infant brain volumes. Transl Psychiatry 7, e1188 (2017). source
Not checked in the free run.
- Interpretationreasoning
The prenatal period is important for future psychiatric and neurological risk.
“highlight the important role of the prenatal period for future psychiatric and neurological risk”
Quote in the paperSubstantial claim - Premisecitation
An intronic SNP in IGFBP7 (rs114518130) is significantly associated with grey-matter volume, with volume increasing with increasing dose of the G allele.
“an intronic single-nucleotide polymorphism (SNP) in IGFBP7 (rs114518130) was found to be significantly associated with grey-matter volume (volume increases with increasing dose of the G allele).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [162] Xia, K. et al. Genome-wide association analysis identifies common variants influencing infant brain volumes. Transl Psychiatry 7, e1188 (2017). source
Not checked in the free run.
- Premisecitation
There are only marginal associations between parental education and brain volumes at birth.
“only marginal associations between parental education and brain volumes at birth124.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [124] Li, G. et al. Mapping longitudinal development of local cortical gyrification in infants from birth to 2 years of age. J. Neurosci. 34, 4228–4238 (2014). source
Not checked in the free run.
- Study design and conductcitation
That PPAR study is best considered a proof-of-concept study because of its very small sample size.
“this study might best be considered a proof-of-concept study, given its very small sample size.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [165] Krishnan, M. L. et al. Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. Brain Behav. 6, e00434 (2016). source
Not checked in the free run.
- Premisecitation
Neonates homozygous for the rs4680 valine allele of COMT exhibit reduced grey matter in the temporal cortex and hippocampus, mirroring adult findings.
“neonates homozygous for the rs4680 valine allele of COMT (which encodes catechol-O-methyltransferase) exhibit reduced grey matter in the temporal cortex and hippocampus, mirroring findings in adults.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [171] Hanson, J. L. et al. Family poverty affects the rate of human infant brain growth. PLoS ONE 8, e80954 (2013). source
Not checked in the free run.
- Premisecitation
Recent studies have revealed substantial alterations of resting-state networks due to prenatal drug exposure.
“Recent studies have revealed substantial alterations of resting-state networks due to prenatal drug exposure182, 183”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [182] Salzwedel, A. P., Grewen, K. M., Goldman, B. D. & Gao, W. Thalamocortical functional connectivity and behavioral disruptions in neonates with prenatal cocaine exposure. Neurotoxicol. Teratol. 56, 16–25 (2016). source
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- cites [183] Salzwedel, A. P. et al. Prenatal drug exposure affects neonatal brain functional connectivity. J. Neurosci. 35, 5860–5869 (2015). source
Not checked in the free run.
- Premisecitation
In that study, interaction effects between maternal anxiety and infant genotype were observed in several regions, including the right ventromedial prefrontal cortex.
“interaction effects between maternal anxiety and infant genotype were observed in several regions, including the right ventromedial prefrontal cortex, an area involved in the regulation of anxiety and mood.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [159] Qiu, A. et al. COMT haplotypes modulate associations of antenatal maternal anxiety and neonatal cortical morphology. Am. J. Psychiatry 172, 163–172 (2015). source
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- Premisecitation
Common variants associated with neonatal brain structure have been identified using a genome-wide association study.
“common variants associated with neonatal brain structure have been identified using a genome-wide association study (GWAS) approach162.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [162] Xia, K. et al. Genome-wide association analysis identifies common variants influencing infant brain volumes. Transl Psychiatry 7, e1188 (2017). source
Not checked in the free run.
- Premisecitation
Maternal depression during pregnancy is associated with altered microstructure and functional connectivity of the amygdala in 6-month-olds.
“altered microstructure and functional connectivity of the amygdala in 6-month-olds175, 176.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [175] Rifkin-Graboi, A. et al. Prenatal maternal depression associates with microstructure of right amygdala in neonates at birth. Biol. Psychiatry 74, 837–844 (2013). source
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- cites [176] Qiu, A. et al. Prenatal maternal depression alters amygdala functional connectivity in 6-month-old infants. Transl Psychiatry 5, e508 (2015). source
Not checked in the free run.
- Premisecitation
Prenatal marijuana exposure is associated with altered striatal and insular functional connectivity.
“prenatal marijuana exposure is associated with altered striatal and insular functional connectivity184.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [184] Grewen, K., Salzwedel, A. P. & Gao, W. Functional connectivity disruption in neonates with prenatal marijuana exposure. Front. Hum. Neurosci. 9, 601 (2015). source
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- Premisecitation
Maternal depression and selective serotonin-uptake inhibitor use during pregnancy are associated with reduced FA across many white-matter tracts in neonates.
“Maternal depression and use of selective serotonin-uptake inhibitors during pregnancy is associated with reduced FA across many white-matter tracts in neonates177.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [177] Jha, S. C. et al. Antenatal depression, treatment with selective serotonin reuptake inhibitors, and neonatal brain structure: a propensity-matched cohort study. Psychiatry Res. 253, 43–53 (2016). source
Not checked in the free run.
- Premisecitation
The common variant rs17203281 in DLG4 is associated with significant differences in white-matter microstructure as indexed by FA in preterm infants.
“the common variant rs17203281 in DLG4 (also known as PSD95, which encodes postsynaptic density protein 95) is associated with significant differences white-matter microstructure (as indexed by FA) in preterm infants.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [161] Krishnan, M. L. et al. Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants. Nat. Commun. 8, 428 (2017). source
Not checked in the free run.
- Premisecitation
A separate study indicated a possible role for PPAR signaling in white matter development in preterm infants.
“The results indicated a possible role for peroxisome proliferator-activated receptor (PPAR) signaling in white matter development in preterm infants”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [165] Krishnan, M. L. et al. Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. Brain Behav. 6, e00434 (2016). source
Not checked in the free run.
- Premisecitation
Myelin water fraction studies found small but statistically significant associations between myelination trajectories in bilateral frontal and temporal cortex and language development from 3 months to 4 years.
“Studies using myelin water fraction have found small but statistically significant associations between myelination trajectories in several regions including bilateral frontal and temporal cortex and language development from 3 months to 4 years199”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [199] O'Muircheartaigh, J. et al. White matter development and early cognition in babies and toddlers. Hum. Brain Mapp. 35, 4475–4487 (2014). source
Not checked in the free run.
- Interpretationcitation
This neonatal amygdala connectivity pattern may be a precursor of later anxiety disorders.
“which may be a precursor of later anxiety disorders.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [190] Graham, A. M. et al. Implications of newborn amygdala connectivity for fear and cognitive development at 6-months-of-age. Dev. Cogn. Neurosci. 18, 12–25 (2016). source
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- Premisecitation
Stronger amygdala functional connectivity to the anterior insula and ventral striatum in neonates is associated with higher levels of fear in 6-month-olds.
“Stronger amygdala functional connectivity to the anterior insula and ventral striatum in neonates is associated with higher levels of fear in 6-month-olds190”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [190] Graham, A. M. et al. Implications of newborn amygdala connectivity for fear and cognitive development at 6-months-of-age. Dev. Cogn. Neurosci. 18, 12–25 (2016). source
Not checked in the free run.
- Premisecitation
White-matter microstructure properties measured using DTI are moderately associated with working memory performance in 1-year-olds.
“white-matter microstructure properties measured using DTI are moderately associated with working memory performance in 1-year-olds198.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [198] Short, S. J. et al. Associations between white matter microstructure and infants' working memory. Neuroimage 64, 156–166 (2013). source
Not checked in the free run.
- Interpretationnone given
Early studies find only modest relationships between structural and functional biomarkers and cognition and behaviour.
“Early studies find only modest relationships between structural and functional biomarkers and cognition and behaviour.”
Quote in the paperNot a substantial claim - Premisecitation
Male neonates with high genetic risk for schizophrenia have increased grey-matter volumes compared with controls.
“male neonates with high genetic risk for schizophrenia have increased grey-matter volumes compared with controls187.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [187] Gilmore, J. H. et al. Prenatal and neonatal brain structure and white matter maturation in children at high risk for schizophrenia. Am. J. Psychiatry 167, 1083–1091 (2010). source
Not checked in the free run.
- Premisecitation
Myelin water fraction studies found age-dependent relationships between myelination and general cognitive ability from 3 months to 5 years.
“age-dependent relationships between myelination and general cognitive ability from 3 months to 5 years200.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [200] Deoni, S. C. et al. White matter maturation profiles through early childhood predict general cognitive ability. Brain Struct. Funct. 221, 1189–1203 (2016). source
Not checked in the free run.
- Interpretationreasoning
The associations between imaging markers and outcomes are generally not strong.
“although the associations between imaging markers and outcomes are generally not strong.”
Quote in the paperSubstantial claim - Premisecitation
A smaller corpus callosum length at 6 weeks is related to parental reports of executive function at age 4 years.
“a smaller corpus callosum length is related to parental reports of childrens’ executive function at age 4 years191”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [191] Ghassabian, A. et al. Infant brain structures, executive function, and attention deficit/hyperactivity problems at preschool age. A prospective study. J. Child Psychol. Psychiatry 54, 96–104 (2013). source
Not checked in the free run.
- Interpretationcitation
Thalamus-salience network connectivity might have potential as a candidate biomarker for differences in cognitive performance.
“Thus, thalamus–salience network connectivity might have potential as a candidate biomarker for differences in cognitive performance”
Quote in the paperSubstantial claim - Premisecitation
Factors describing common variation of FA, AD, or RD across groups of white matter tracts are weakly related to cognitive development in an age-specific way.
“Factors that describe common variation of FA, AD or RD across groups of white matter tracts are weakly related to cognitive development in an age-specific way”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [38] Lee, S. J. et al. Common and heritable components of white matter microstructure predict cognitive function at 1 and 2 y. Proc. Natl Acad. Sci. USA 114, 148–153 (2017). source
Not checked in the free run.
- Premisecitation
Smaller subcortical volumes are associated with higher internalizing behaviour scores at 18 and 36 months.
“smaller subcortical volumes are associated with higher internalizing behaviour [G] scores at 18 and 36 months192.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [192] Herba, C. M. et al. Infant brain development and vulnerability to later internalizing difficulties: the Generation R study. J. Am. Acad. Child Adolesc. Psychiatry 49, 1053–1063 (2010). source
Not checked in the free run.
- Premisecitation
Lower connectivity between the thalamus and the salience network in 1-year-olds is associated with poorer working memory performance and lower cognitive development at 2 years of age.
“lower connectivity between the thalamus and the salience network in 1-year-olds is associated with poorer working memory performance and lower cognitive development at 2 years of age97.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [97] Ball, G. et al. Thalamocortical connectivity predicts cognition in children born preterm. Cereb. Cortex 25, 4310–4318 (2015). source
Not checked in the free run.
- Premisecitation
Machine-learning based prediction frameworks are beginning to be applied to infant imaging.
“Machine-learning based prediction frameworks are beginning to be applied to infant imaging201–203”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [201] Emerson, R. W. et al. Functional neuroimaging of high-risk 6-month-old infants predicts a diagnosis of autism at 24 months of age. Sci. Transl Med. 9 eaag2882 (2017). source
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- cites [202] Smyser, C. D. et al. Prediction of brain maturity in infants using machine-learning algorithms. Neuroimage 136, 1–9 (2016). source
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- cites [203] Ball, G. et al. Machine-learning to characterise neonatal functional connectivity in the preterm brain. Neuroimage 124, 267–275 (2016). source
Not checked in the free run.
- Premisecitation
Structure-cognitive function relationships in early childhood are age dependent.
“with a general theme that structure–cognitive function relationships in early childhood are age dependent196.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [196] Fjell, A. M. et al. Multimodal imaging of the self-regulating developing brain. Proc. Natl Acad. Sci. USA 109, 19620–19625 (2012). source
Not checked in the free run.
- Interpretationreasoning
It is unlikely that a single or even a few imaging parameters will have sufficient power for accurate prediction.
“It is unlikely that a single or even a few imaging parameters will have sufficient power for accurate prediction.”
Quote in the paperNot a substantial claim- Rests on an assumption: Imaging, genetic and environmental variables each contribute only a small percentage of variance to developmental outcomes.
- Interpretationreasoning
Early imaging biomarkers for risk for later behavioral abnormalities may exist.
“These studies suggest that early imaging biomarkers for risk for later behavioral abnormalities may exist”
Quote in the paperSubstantial claim - Premisecitation
The search for imaging biomarkers for brain disorders is fraught with difficulty related to the complexity and distribution of cognitive processing, generalization from heterogeneous clinical samples, and small effect sizes with limited clinical utility.
“The search for imaging biomarkers for brain disorders is fraught with difficulty related to the complexity and distribution of cognitive processing in the brain, the generalization of findings from heterogeneous clinical samples, and small effect sizes that have limited clinical utility194, 195.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [194] Woo, C. W., Chang, L. J., Lindquist, M. A. & Wager, T. D. Building better biomarkers: brain models in translational neuroimaging. Nat. Neurosci. 20, 365–377 (2017). source
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- cites [195] Reddan, M. C., Lindquist, M. A. & Wager, T. D. Effect size estimation in neuroimaging. JAMA Psychiatry 74, 207–208 (2017). source
Not checked in the free run.
- Premisecitation
White-matter networks at birth may be predictive of internalizing and externalizing behaviour at 2 and 4 years of age.
“white-matter networks at birth may be predictive of internalizing and externalizing behaviour [G] at 2 and 4 years of age193.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [193] Wee, C. Y. et al. Neonatal neural networks predict children behavioral profiles later in life. Hum. Brain Mapp. 38, 1362–1373 (2017). source
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- Premisecitation
Children at risk of autism exhibit hyper-expansion of cortical surface area between 6 and 12 months.
“they also exhibit a hyper-expansion of cortical surface area between 6 and 12 months189.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [189] Hazlett, H. C. et al. Early brain development in infants at high risk for autism spectrum disorder. Nature 542, 348–351 (2017). This study is an important example of how early imaging can be used to predict the development of autism. source
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- Premisecitation
A common factor of AD across 12 white matter tracts at birth is associated with cognitive development at age 1 year.
“a common factor of AD across 12 white matter tracts at birth is associated with cognitive development at age 1 year.38.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [38] Lee, S. J. et al. Common and heritable components of white matter microstructure predict cognitive function at 1 and 2 y. Proc. Natl Acad. Sci. USA 114, 148–153 (2017). source
Not checked in the free run.
- Classified as probably not a substantial claim. 11
- May combine two claims. 76
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PremisecitationIn the human hippocampus, myelination begins at 20 weeks gestational age; by age two many regions reach adult levels, although some areas continue to myelinate into adulthood.
“In the human hippocampus, myelination begins at 20 weeks gestational age, and by age 2 years, many regions have attained adult levels of myelination — although some areas, such as the hilus of the dentate, continue to myelinate throughout childhood into adulthood212–214.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [212] Abraham, H. et al. Myelination in the human hippocampal formation from midgestation to adulthood. Int. J. Dev. Neurosci. 28, 401–410 (2010). source
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- cites [213] Arnold, S. E. & Trojanowski, J. Q. Human fetal hippocampal development: I. Cytoarchitecture, myeloarchitecture, and neuronal morphologic features. J. Comp. Neurol. 367, 274–292 (1996). source
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- cites [214] Benes, F. M., Turtle, M., Khan, Y. & Farol, P. Myelination of a key relay zone in the hippocampal formation occurs in the human brain during childhood, adolescence, and adulthood. Arch. Gen. Psychiatry 51, 477–484 (1994). source
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PremisecitationThe complexity of cortical neurons increases rapidly in the first years after birth, mirroring imaging findings of rapid cortical thickness growth and surface area expansion.
“The complexity of cortical neurons increases rapidly in the first years after birth, mirroring imaging findings of rapid cortical thickness growth and surface area expansion.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [207] Conel, J. L. The Cortex of the Four-Year Child (Harvard Univ. Press, Cambridge, Massachusetts, 1963). source
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PremisecitationMyelination begins prenatally and is present in many regions at birth, especially primary sensory and motor pathways including the optic radiations and internal capsule.
“Postmortem studies of white-matter myelination in the human brain find that myelination begins prenatally and is present in many regions at the time of birth, especially primary sensory and motor pathways, including the optic radiations and internal capsule210, 211.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [210] Hasegawa, M. et al. Development of myelination in the human fetal and infant cerebrum: a myelin basic protein immunohistochemical study. Brain Dev. 14, 1–6 (1992). source
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- cites [211] Kinney, H. C., Brody, B. A., Kloman, A. S. & Gilles, F. H. Sequence of central nervous system myelination in human infancy II. Patterns of myelination in autopsied infants. J. Neuropathol. Exp. Neurol. 47, 217–234 (1988). source
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PremisecitationIn the corpus callosum, oligodendrocyte numbers increase until age five and are stable thereafter, with little turnover after age five.
“In the corpus callosum, oligodendrocyte numbers increase until age 5 years and are stable thereafter; a study of nuclear bomb test-derived 14C suggest that there is little turnover of oligodendrocytes after age 5 years217.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [217] Yeung, M. S. et al. Dynamics of oligodendrocyte generation and myelination in the human brain. Cell 159, 766–774 (2014). source
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PremisecitationThe relative intensities of grey and white matter in T1- and T2-weighted imaging change significantly over the first year and are typically very similar between four and eight months, making grey-white distinction difficult.
“the relative intensities of grey and white matter in T1- and T2-weighted imaging change significantly over the first year of life and are typically very similar between 4 to 8 months of age; this makes distinguishing grey and white matter difficult.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [28] Walhovd, K. B., Fjell, A. M., Giedd, J., Dale, A. M. & Brown, T. T. Through thick and thin: a need to reconcile contradictory results on trajectories in human cortical development. Cereb. Cortex 27, 1472–1481 (2017).
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PremisecitationThe number of oligodendrocytes in cerebral white matter increases rapidly and linearly after birth, from about seven billion at birth to 28 billion at age three, a rate of 600 million per month.
“the number of oligodendrocytes in cerebral white matter increases rapidly and linearly after birth, from approximately 7 billion at birth to 28 billion at age 3 years — a rate of 600 million per month216.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [216] Sigaard, R. K., Kjaer, M. & Pakkenberg, B. Development of the cell population in the brain white matter of young children. Cereb. Cortex 26, 89–95 (2016). source
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PremisecitationThe period from term birth to about two years of age is important for establishing lifelong cognitive abilities and behaviours and for risk of neuropsychiatric disorders such as autism and schizophrenia.
“Early childhood — especially the period between term birth and about ~2 years of age — is increasingly recognized as being very important for establishing cognitive abilities and behaviours that last a lifetime1, as well as for risk for neuropsychiatric disorders such as autism and schizophrenia2.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [1] Nelson, C. A. et al. Cognitive recovery in socially deprived young children: the Bucharest Early Intervention Project. Science 318, 1937–1940 (2007). source
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- cites [2] National Advisory Mental Health Council's Workgroup.Transformative Neurodevelopmental Research in Mental Illness (US National Institute of Mental Health, 2008).
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PremisecitationAfter birth, myelination generally proceeds in sensory before motor regions, projection before association areas, and posterior before anterior regions.
“Postnatally, myelination follows a general pattern of sensory before motor regions, projection areas before associative areas, and posterior before anterior regions211.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [211] Kinney, H. C., Brody, B. A., Kloman, A. S. & Gilles, F. H. Sequence of central nervous system myelination in human infancy II. Patterns of myelination in autopsied infants. J. Neuropathol. Exp. Neurol. 47, 217–234 (1988). source
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PremisecitationSynaptic spine density in prefrontal cortex peaks by two to five years and falls in adolescence.
“Synaptic spine density in prefrontal cortex also peaks by 2–5 years and falls in adolescence7.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] Petanjek, Z. et al. Extraordinary neoteny of synaptic spines in the human prefrontal cortex. Proc. Natl Acad. Sci. USA 108, 13281–13286 (2011). source
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PremisecitationAt birth, layer V neurons have more complex basal dendritic trees than layer IIIC neurons; layer V neurons reach maximum complexity at 16 to 30 months, before layer IIIC neurons.
“at birth layer V neurons have more complex basal dendritic trees which integrate synaptic inputs compared to layer IIIC neurons; layer V neurons reach maximum complexity at 16 to 30 months after birth, before layer IIIC209”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [209] Petanjek, Z., Judas, M., Kostovic, I. & Uylings, H. B. Lifespan alterations of basal dendritic trees of pyramidal neurons in the human prefrontal cortex: a layer-specific pattern. Cereb. Cortex 18, 915–929 (2008). source
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InterpretationreasoningCortical grey-matter networks mature much later in childhood, perhaps driven by coordinated activity from functional networks that arise earlier.
“Cortical and subcortical grey matter also undergoes robust growth in the first year of life10, although cortical grey-matter networks seem to mature much later in childhood, perhaps driven by coordinated activity across the cortex from functional networks that arise much earlier in development.”
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PremisecitationIn the neocortex, mature myelination patterns are attained only in adulthood, reflecting protracted maturation in humans compared with non-human primates.
“In the neocortex, mature myelination patterns are attained only in adulthood, reflecting a protracted maturation of this brain region in humans compared with that in non-human primates215.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [215] Miller, D. J. et al. Prolonged myelination in human neocortical evolution. Proc. Natl Acad. Sci. USA 109, 16480–16485 (2012). source
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InterpretationcitationWhite-matter tracts and networks are largely in place at birth, while resting-state functional networks develop rapidly after birth along with myelination and maturation of existing white-matter connections.
“They suggest a model in which white-matter tracts and networks are largely in place at birth, and resting-state functional networks develop rapidly after birth, along with rapid myelination and maturation of existing white-matter connections.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [9] Geng, X. et al. Structural and maturational covariance in early childhood brain development. Cereb. Cortex 27, 1795–1807 (2017).
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PremisecitationSynapse numbers increase rapidly after birth and decrease in adolescence, peaking in auditory and visual sensory areas before the prefrontal cortex.
“Synapse numbers increase rapidly after birth and decrease in adolescence, with synapse numbers peaking in the auditory and visual sensory areas before those in the prefrontal cortex208”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [208] Huttenlocher, P. R. & Dabholkar, A. S. Regional differences in synaptogenesis in human cerebral cortex. J. Comp. Neurol. 387, 167–178 (1997). source
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PremisecitationWith postnatal development, axial and radial diffusivity decrease while fractional anisotropy increases, thought to reflect increasing organization of already established white matter tracts, including myelination.
“With postnatal development, measures of white-matter microstructure and maturation, including axial diffusivity [G] (AD) and radial diffusivity [G] (RD), decrease, whereas fractional anisotropy [G] (FA) increases, thought to reflect the increasing organization of the already established white matter tracts, including myelination5,32.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [5] Dubois, J. et al. The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants. Neuroscience 276, 48–71 (2014). This is a comprehensive review of the use of imaging to study white matter in early brain development. source
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- cites [32] Geng, X. et al. Quantitative tract-based white matter development from birth to age 2 years. Neuroimage 61, 542–557 (2012). source
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PremisecitationLateral ventricle volume increases by over 100% in the first year and then decreases by 7-24% in the second year.
“Lateral ventricle volume increases by over 100% in year 1, but subsequently decreases by 7–24% in the second year of life3, 10, 19.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [3] Knickmeyer, R. C. et al. A structural MRI study of human brain development from birth to 2 years. J. Neurosci. 28, 12176–12182 (2008). This is a comprehensive study of structural brain development in the first 2 years of life demonstrating the rapid growth of cortical grey matter in the first year of life. source
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- cites [10] Gilmore, J. H. et al. Longitudinal development of cortical and subcortical gray matter from birth to 2 years. Cereb. Cortex 22, 2478–2485 (2012). source
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- cites [19] Bompard, L. et al. Multivariate longitudinal shape analysis of human lateral ventricles during the first twenty-four months of life. PLoS ONE 9, e108306 (2014). source
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PremisecitationMajor white matter tracts such as the corpus callosum, superior and inferior longitudinal fasciculus, arcuate and cingulum are present at birth, indicating that most brain wiring is established prenatally.
“Diffusion imaging studies find that major white matter tracts such as the corpus callosum, superior and inferior longitudinal fasciculus, arcuate, and cingulum are present at the time of birth, indicating that most of the ‘wiring’ of the brain is established during prenatal brain development31 (Fig. 1).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [31] Qiu, A., Mori, S. & Miller, M. I. Diffusion tensor imaging for understanding brain development in early life. Annu. Rev. Psychol. 66, 853–876 (2015). source
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PremisecitationmcDESPOT determines the myelin water fraction and assesses white-matter myelination more directly than traditional diffusion-weighted imaging, but depends on acquisition protocol and modelling assumptions.
“This method assesses white-matter myelination more directly than does traditional diffusion-weighted imaging, but is dependent on acquisition protocol and modelling assumptions5,233,5, 234.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [5] Dubois, J. et al. The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants. Neuroscience 276, 48–71 (2014). This is a comprehensive review of the use of imaging to study white matter in early brain development. source
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- cites [233] Lankford, C. L. & Does, M. D. On the inherent precision of mcDESPOT. Magn. Reson. Med. 69, 127–136 (2013). source
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- cites [234] Teixeira, R. P., Malik, S. J. & Hajnal, J. V. Joint system relaxometry (JSR) and Cramer-Rao lower bound optimization of sequence parameters: a framework for enhanced precision of DESPOT T1 and T2 estimation. Magn. Reson. Med. 79, 234–245 (2018). source
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PremisecitationGrowth rates of subcortical grey-matter structures are similar to cortical grey-matter growth rates, with the amygdala, thalamus, caudate, putamen and pallidum growing about 105% in the first year and roughly 15% in the second.
“The growth rates of subcortical grey-matter structures are similar to cortical grey-matter growth rates, with the amygdala, thalamus, caudate, putamen, and pallidum growing about 105% in the first year and roughly 15% in the second.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Gilmore, J. H. et al. Longitudinal development of cortical and subcortical gray matter from birth to 2 years. Cereb. Cortex 22, 2478–2485 (2012). source
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PremisecitationMaturation of white-matter regions and tracts measured by DTI is similar to that of grey matter regions, with rapid change in the first year and more gradual increase thereafter.
“the maturation of white-matter regions and tracts has been revealed by quantitative diffusion tensor imaging (DTI) studies to be similar to that observed for grey matter regions, with rapid rates of change in the first year of life, and a more gradual increase thereafter (Box 3; reviewed elsewhere5).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [5] Dubois, J. et al. The early development of brain white matter: a review of imaging studies in fetuses, newborns and infants. Neuroscience 276, 48–71 (2014). This is a comprehensive review of the use of imaging to study white matter in early brain development. source
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Premisenone givenThe patterns of white-matter maturation described by diffusion tensor imaging and myelin water fraction studies are consistent with each other and with previous postmortem studies of myelination.
“The patterns of white-matter maturation described by diffusion tensor imaging and myelin water fraction studies are consistent with one another and with previous postmortem studies of myelination (Box 1).”
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PremisecitationThe white-matter connectome at birth is highly organized and includes hub regions and connections similar to those observed in adults.
“Overall, the white-matter connectome at birth is highly organized and includes hub regions and connections that are similar to those observed in adults48,49.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [48] Yap, P. T. et al. Development trends of white matter connectivity in the first years of life. PLoS ONE 6, e24678 (2011). source
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- cites [49] van den Heuvel, M. P. et al. The neonatal connectome during preterm brain development. Cereb. Cortex 25, 3000–3013 (2015). source
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Premisenone givenWhite-matter volume growth is slower and more protracted than grey matter volume growth.
“As noted above, white-matter volume growth is more slow and protracted compared to grey matter volume (Figs 1, 2).”
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PremisecitationCortical surface area expands by 76% from birth in the first year and another 22% in the second year; by age two the mean surface area is about 69% of adult values.
“Cortical surface area expands by 76% from birth in year 1 and another 22% in year 2; by age 2 years, the mean surface area is about 69% of adult values4,23.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [4] Lyall, A. E. et al. Dynamic development of regional cortical thickness and surface area in early childhood. Cereb. Cortex 25, 2204–2212 (2015). source
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- cites [23] Li, G. et al. Mapping region-specific longitudinal cortical surface expansion from birth to 2 years of age. Cereb. Cortex 23, 2724–2733 (2013). source
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PremisecitationRegional heterogeneity of cortical thickness seen in adults is established at birth and persists through age two into adulthood.
“Regional heterogeneity of cortical thickness observed in adults is well established at birth and persists through age 2 years into adulthood4,26.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [4] Lyall, A. E. et al. Dynamic development of regional cortical thickness and surface area in early childhood. Cereb. Cortex 25, 2204–2212 (2015). source
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- cites [26] Li, G., Lin, W., Gilmore, J. H. & Shen, D. Spatial patterns, longitudinal development, and hemispheric asymmetries of cortical thickness in infants from birth to 2 years of age. J. Neurosci. 35, 9150–9162 (2015). source
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PremisecitationCortical thickness probably peaks at one to two years and declines thereafter, while surface area continues to expand well into late childhood or early adolescence.
“Imaging studies of infants and older childen21, 20, 22 have revealed that cortical thickness probably peaks in the range of 1–2 years and declines thereafter, whereas surface area continues to expand well into late childhood or early adolescence.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [21] Shaw, P. et al. Neurodevelopmental trajectories of the human cerebral cortex. J. Neurosci. 28, 3586–3594 (2008). source
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- cites [20] Raznahan, A. et al. How does your cortex grow? J. Neurosci. 31, 7174–7177 (2011). source
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- cites [22] Remer, J. et al. Quantifying cortical development in typically developing toddlers and young children, 1–6 years of age. Neuroimage 153, 246–261 (2017). source
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PremisecitationBrain volume is about 35% of adult volume two to three weeks after birth, doubles from term size in the first year, and increases an additional 15% in the second year to about 80% of adult size.
“Brain volume is about 35% of adult volume 2–3 weeks after birth after birth13, doubles from term size in the first year of life and increases an additional 15% in the second to about 80% of adult size3.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [13] Gilmore, J. H. et al. Regional gray matter growth, sexual dimorphism, and cerebral asymmetry in the neonatal brain. J. Neurosci. 27, 1255–1260 (2007). source
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- cites [3] Knickmeyer, R. C. et al. A structural MRI study of human brain development from birth to 2 years. J. Neurosci. 28, 12176–12182 (2008). This is a comprehensive study of structural brain development in the first 2 years of life demonstrating the rapid growth of cortical grey matter in the first year of life. source
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PremisecitationAverage cortical thickness increases by 31% in the first year and an additional 4.3% in the second year; by age two mean cortical thickness is about 97% of adult values.
“Average cortical thickness increases by an average of 31% in year 1 and an additional 4.3% in the second year; by age 2, the mean cortical thickness is about 97% of the values observed in adults4.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [4] Lyall, A. E. et al. Dynamic development of regional cortical thickness and surface area in early childhood. Cereb. Cortex 25, 2204–2212 (2015). source
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PremisecitationMotion tends to reduce estimates of grey-matter volume and cortical thickness and can influence observed trajectories of cortical thickness maturation.
“Motion tends to reduce estimates of grey-matter volume and cortical thickness221 and can influence observed trajectories of cortical thickness maturation as well27.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [221] Reuter, M. et al. Head motion during MRI acquisition reduces gray matter volume and thickness estimates. Neuroimage 107, 107–115 (2015). source
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- cites [27] Ducharme, S. et al. Trajectories of cortical thickness maturation in normal brain development — the importance of quality control procedures. Neuroimage 125, 267–279 (2016). source
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Premisenone givenSurface area expansion is regionally heterogeneous: lateral frontal, lateral parietal and occipital cortices grow relatively rapidly, while orbital frontal, insula and occipital regions grow more slowly.
“Surface area expansion is also regionally heterogeneous across the brain: the lateral frontal, lateral parietal and occipital cortices grow relatively rapidly, whereas regions in the orbital frontal, insula and occipital cortices tend to grow more slowly (Fig. 1).”
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PremisecitationFrom birth to age one, cortical grey-matter volume increases by 108-149% while white matter increases by about 11%; from age one to two, grey matter increases by 14-19% while white matter increases by 19%.
“From birth to age 1, cortical grey-matter volume increases 108–149%, whereas white matter increases by about 11%; from age 1 to age 2 years, grey matter increases 14–19%, whereas white matter increases by 19%3.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [3] Knickmeyer, R. C. et al. A structural MRI study of human brain development from birth to 2 years. J. Neurosci. 28, 12176–12182 (2008). This is a comprehensive study of structural brain development in the first 2 years of life demonstrating the rapid growth of cortical grey matter in the first year of life. source
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PremisecitationNetwork maturation in the first two years after birth generally consists of increased network efficiency and integration, decreased segregation, and some changes in modularity, with most major hubs and modules in place by age two.
“Network maturation in the first 2 years after birth generally consists of increased network efficiency and network integration [G], decreased network segregation [G], and some changes in the modularity48, 51, with most major hubs and modules in place by age 2 years52.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [48] Yap, P. T. et al. Development trends of white matter connectivity in the first years of life. PLoS ONE 6, e24678 (2011). source
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- cites [51] Huang, H. et al. Development of human brain structural networks through infancy and childhood. Cereb. Cortex 25, 1389–1404 (2015). source
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- cites [52] Hagmann, P. et al. White matter maturation reshapes structural connectivity in the late developing human brain. Proc. Natl Acad. Sci. USA 107, 19067–19072 (2010). source
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PremisecitationImaging measures are indirect measures of brain structure and function and are subject to confounds such as hydration, blood lipid levels and cortisol levels.
“It is also important to recognize that imaging measures are indirect measures of brain structure and function and are subject to the effect of many potential confounds, such as hydration, blood lipid levels and cortisol levels224.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [224] Weinberger, D. R. & Radulescu, E. Finding the elusive psychiatric “lesion” with 21st-century neuroanatomy: a note of caution. Am. J. Psychiatry 173, 27–33 (2016). source
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PremisecitationUsing multicomponent relaxometry, myelination in the first year begins in the cerebellum, pons and internal capsule and proceeds back-to-front: splenium and optic radiations at three to four months, occipital and parietal lobes at four to six months, and frontal and temporal lobes at six to eight months.
“myelination in the first year of life was shown to begin in the cerebellum, pons and internal capsule, and to proceed in a ‘back-to-front’ pattern, from the splenium of the corpus callosum and optic radiations (3–4 months), to the occipital and parietal lobes (4–6 months), and anteriorly to the frontal and temporal lobes ( 6–8 months)33.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [33] Deoni, S. C. et al. Mapping infant brain myelination with magnetic resonance imaging. J. Neurosci. 31, 784–791 (2011). This paper presents the initial imaging study of myelin development in the human infant using the myelin water fraction approach, a more direct assessment of myelin than standard diffusion-weighted imaging. source
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PremisecitationAfter age two, total grey-matter volume shows minimal absolute increases through childhood and decreases in adolescence, while white-matter volumes steadily increase through early adulthood, peaking around age 30.
“After age 2, total grey-matter volume shows minimal absolute increases through childhood and decreases in adolescence, whereas white-matter volumes steadily increase through early adulthood, peaking around age 30.17,18.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [17] Groeschel, S., Vollmer, B., King, M. D. & Connelly, A. Developmental changes in cerebral grey and white matter volume from infancy to adulthood. Int. J. Dev. Neurosci. 28, 481–489 (2010). source
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- cites [18] Mills, K. L. et al. Structural brain development between childhood and adulthood: convergence across four longitudinal samples. Neuroimage 141, 273–281 (2016). source
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PremisecitationDiffusion values change more gradually through later childhood and adolescence, with axial and radial diffusivity decreasing and fractional anisotropy increasing.
“Diffusion values change much more gradually through later childhood and adolescence, with AD and RD decreasing and FA increasing. 34,35”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [34] Faria, A. V. et al. Atlas-based analysis of neurodevelopment from infancy to adulthood using diffusion tensor imaging and applications for automated abnormality detection. Neuroimage 52, 415–428 (2010). source
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- cites [35] Krogsrud, S. K. et al. Changes in white matter microstructure in the developing brain — a longitudinal diffusion tensor imaging study of children from 4 to 11 years of age. Neuroimage 124, 473–486 (2016). source
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Premisenone givenRegions of faster cortical thickness growth after birth include speech and language regions, the insula and cingulate cortex, and some higher association areas, while primary and secondary sensory cortices grow more slowly.
“Regions of faster growth of cortical thickness after birth include speech and language regions [Heschel’s gyrus, Rolandic operulum], the insula and cingulate cortex as well as some higher association areas. The primary and secondary sensory cortices tend to grow more slowly.”
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PremisecitationMost studies find cortical thickness decreases linearly after age four to five years, although some studies suggest an increase from age six to ten and thinning after ten to twelve.
“Whereas some studies have suggested that cortical thickness increases from age 6 to 10 years and begins to thin after 10–12 years21,20, most studies find that cortical thickness decreases linearly after age 4–5 years25,27,28.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [21] Shaw, P. et al. Neurodevelopmental trajectories of the human cerebral cortex. J. Neurosci. 28, 3586–3594 (2008). source
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- cites [20] Raznahan, A. et al. How does your cortex grow? J. Neurosci. 31, 7174–7177 (2011). source
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- cites [25] Brown, T. T. et al. Neuroanatomical assessment of biological maturity. Curr. Biol. 22, 1693–1698 (2012). source
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PremisecitationFractional anisotropy increases by 9-44% in the first year, with most tracts increasing by more than 25%; in the second year it increases by 5-9% over age-one levels.
“For example, FA increases 9–44% in the first year, with most tracts increasing by more than 25%; in the second year, FA increases 5–9% over levels at age 1 year.”
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PremisecitationPrimary sensorimotor structural covariance networks are well developed by birth, while higher-order association networks mature and become increasingly distributed, involving more regions from age five to eighteen.
“Primary sensorimotor SCNs are well developed by birth, and higher-order association SCNs mature and became increasingly distributed, involving more regions from age 5 to 18 years. 60.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [60] Zielinski, B. A., Gennatas, E. D., Zhou, J. & Seeley, W. W. Network-level structural covariance in the developing brain. Proc. Natl Acad. Sci. USA 107, 18191–18196 (2010). source
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PremisecitationTopographic thalamic connections with each primary cortical network have been documented in premature babies at term age and in full-term newborns, and undergo postnatal refinement and expansion.
“topographic thalamic connections with each of the primary cortical networks has been documented in premature babies at term age96 and in full-term newborns97, and undergo postnatal refinement and expansion97.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [96] Alcauter, S. et al. Development of thalamocortical connectivity during infancy and its cognitive correlations. J. Neurosci. 34, 9067–9075 (2014). source
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- cites [97] Ball, G. et al. Thalamocortical connectivity predicts cognition in children born preterm. Cereb. Cortex 25, 4310–4318 (2015). source
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PremisecitationThe adult language network is lateralized and includes the inferior frontal gyrus and superior temporal gyrus; these regions begin to show asymmetry in functional connectivity with the contralateral homotopic region at about age two.
“The language network, in adults is lateralized and encompasses the inferior frontal gyrus (IFG) and the superior temporal gyrus (STG); these regions begin to exhibit asymmetry in functional connectivity with the homotopic region on the contralateral hemisphere at about age 2 years 102.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [102] Calhoun, V. D., Adali, T., Pearlson, G. D. & Pekar, J. J. A method for making group inferences from functional MRI data using independent component analysis. Hum. Brain Mapp. 14, 140–151 (2001). source
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PremisecitationProgressive maturation of primary functional networks has been shown in human fetuses and in premature infants before term age.
“Progressive maturation of these primary networks has been shown in human fetuses94 and in premature infants before term age88, 89,89”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [94] Jones, E. G. The Thalamus (Springer Science & Business Media, 2012).
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- cites [88] Smyser, C. D. et al. Longitudinal analysis of neural network development in preterm infants. Cereb. Cortex 20, 2852–2862 (2010). source
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- cites [89] Gao, W., Alcauter, S., Smith, J. K., Gilmore, J. H. & Lin, W. Development of human brain cortical network architecture during infancy. Brain Struct. Funct. 220, 1173–1186 (2015). source
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PremisecitationWhen defined by seed-based or independent component analysis, the default-mode, dorsal attention and salience networks establish distributed network-like topologies by age two, earlier than executive control networks, consistent with protracted development of executive functions.
“the default-mode network99, 104, the dorsal attention network [G] 105, 106 and the salience network [G] 107 establish distributed network-like topologies by 2 years of age90, 91 earlier than the executive control networks 91, 97, 107, consistent with the protracted development of executive functions108.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [90] Gao, W. et al. Functional network development during the first year: relative sequence and socioeconomic correlations. Cereb. Cortex 25, 2919–2928 (2015). This paper delineates the developmental sequence of nine major resting-state networks during the first year of life in a cohort of full-term infants. source
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- cites [91] Doria, V. et al. Emergence of resting state networks in the preterm human brain. Proc. Natl Acad. Sci. USA 107, 20015–20020 (2010). source
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- cites [105] Seeley, W. W. et al. Dissociable intrinsic connectivity networks for salience processing and executive control. J. Neurosci. 27, 2349–2356 (2007). source
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PremisecitationIn the first two years of life, structural covariance networks and maturational networks are not clearly related, suggesting that fine tuning of cortical structural covariance networks, especially high-order ones, occurs later in childhood.
“By contrast, in the first 2 years of life, SCNs and maturational networks [G] are not clearly related, suggesting that the fine tuning of cortical SCNs, especially high-order SCNs, occurs later in childhood61.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [61] Khundrakpam, B. S. et al. Developmental changes in organization of structural brain networks. Cereb. Cortex 23, 2072–2085 (2013). source
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PremisecitationBoth structural and functional thalamocortical connectivity predict later general cognition and working memory.
“both structural and functional thalamocortical connectivity have been shown to predict later general cognition and working memory 97, 98.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [97] Ball, G. et al. Thalamocortical connectivity predicts cognition in children born preterm. Cereb. Cortex 25, 4310–4318 (2015). source
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- cites [98] Raichle, M. E. et al. A default mode of brain function. Proc. Natl Acad. Sci. USA 98, 676–682 (2001). source
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PremisecitationInfants develop the functional hierarchy in a region- and step-dependent manner, with many top-hierarchy regions present at 1 year of age.
“Infants gradually develop this hierarchy in a region- and step-dependent manner, displaying many of the same regions in the top hierarchy (i.e., lateral frontoparietal, limbic and basal ganglia regions) at 1 year of age111”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [111] Mesulam, M. M. From sensation to cognition. Brain 121, 1013–1052 (1998). source
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PremisecitationThe default-mode network shows the earliest synchronization of its constituent regions and achieves an adult-like core structure by around six months, consistent with the emergence of self-awareness thought to depend on this network at that age.
“the default-mode network99, 100 shows the earliest synchronization of its constituent regions and achieves an adult-like core structure [G] by around 6 months of age91, consistent with the emergence of self-awareness, which is thought to depend on the default-mode network, at this age101.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [91] Doria, V. et al. Emergence of resting state networks in the preterm human brain. Proc. Natl Acad. Sci. USA 107, 20015–20020 (2010). source
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- cites [101] Emerson, R. W., Gao, W. & Lin, W. Longitudinal study of the emerging functional connectivity asymmetry of primary language regions during infancy. J. Neurosci. 36, 10883–10892 (2016). source
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PremisecitationPrimary functional networks, including sensorimotor, visual and auditory networks, develop first and show adult-like topologies in premature babies at term age and in full-term newborns.
“Specifically, primary functional networks, including the sensorimotor, visual, and auditory networks, develop first and show adult-like topologies in premature babies at term age86, 89, 92, 93 and in full-term newborns6, 90, 91.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [86] Lin, W. et al. Functional connectivity MR imaging reveals cortical functional connectivity in the developing brain. AJNR Am. J. Neuroradiol. 29, 1883–1889 (2008). source
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- cites [89] Gao, W., Alcauter, S., Smith, J. K., Gilmore, J. H. & Lin, W. Development of human brain cortical network architecture during infancy. Brain Struct. Funct. 220, 1173–1186 (2015). source
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- cites [92] Fransson, P., Aden, U., Blennow, M. & Lagercrantz, H. The functional architecture of the infant brain as revealed by resting-state fMRI. Cereb. Cortex 21, 145–154 (2011). source
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PremisecitationSensory networks exchange information through two-step inter-regional functional connectivity to the default-mode network and lateral frontoparietal, limbic and basal ganglia regions in subsequent steps, mimicking the hierarchy proposed by predictive encoding.
“sensory networks have been demonstrated to exchange information through two-step inter-regional functional connectivity to the default-mode network and lateral frontoparietal, limbic and basal ganglia regions in subsequent steps111, 115, mimicking the hierarchy proposed by the theory of predictive encoding [G]116, 117.”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [111] Mesulam, M. M. From sensation to cognition. Brain 121, 1013–1052 (1998). source
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- cites [115] Gao, W. et al. Temporal and spatial evolution of brain network topology during the first two years of life. PLoS ONE 6, e25278 (2011). source
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- cites [116] Supekar, K., Musen, M. & Menon, V. Development of large-scale functional brain networks in children. PLoS Biol. 7, e1000157 (2009). source
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- cites [117] Feldman, D. E. & Brecht, M. Map plasticity in somatosensory cortex. Science 310, 810–815 (2005). source
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PremisecitationIn children aged 5-18 years, 60% of the genetic variability of cortical thickness is shared across different cortical regions, with shared genetic variance in fronto-parietal and occipital regions.
“One twin study in children aged 5–18 years 154 found that 60% of the genetic variability of cortical thickness was shared across different regions of the cortex, with SCNs of shared genetic variance in fronto-parietal and occipital regions.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [154] Silbereis, J. C., Pochareddy, S., Zhu, Y., Li, M. & Sestan, N. The cellular and molecular landscapes of the developing human central nervous system. Neuron 89, 248–268 (2016). source
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PremisecitationSome studies show more focal sex differences in the thalamus, corpus callosum, cingulum, and superior cerebellar peduncles, and some show regions of increased FA in adult females, including the corpus callosum and fronto-occipital fasciculus.
“some studies have shown more focal differences in the thalamus, corpus callosum, cingulum, and superior cerebellar peduncles 136, 137, and some studies also show regions of increased FA in adult females compared with males, including the corpus callosum and fronto-occipital fasciculus137, 138.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [136] Kogler, L. et al. Sex differences in the functional connectivity of the amygdalae in association with cortisol. Neuroimage 134, 410–423 (2016). source
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- cites [137] Engman, J., Linnman, C., Van Dijk, K. R. & Milad, M. R. Amygdala subnuclei resting-state functional connectivity sex and estrogen differences. Psychoneuroendocrinology 63, 34–42 (2016). source
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- cites [138] Alarcon, G., Cservenka, A., Rudolph, M. D., Fair, D. A. & Nagel, B. J. Developmental sex differences in resting state functional connectivity of amygdala sub-regions. Neuroimage 115, 235–244 (2015). source
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Interpretationnone givenSexual differentiation of the brain during prenatal, perinatal and early postnatal periods probably reflects a dynamic interplay of biological and experiential mechanisms.
“Sexual differentiation of the brain during the prenatal, perinatal and early postnatal period probably reflects a dynamic interplay of many mechanisms”
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PremisecitationThe heritability of tract-based FA is relatively low in neonates and in 9- and 12-year-olds.
“the heritability of tract-based FA in neonates149, 150 and in 9- and 12-year-olds151 is relatively low”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [149] Bohlken, M. M. et al. Genes contributing to subcortical volumes and intellectual ability implicate the thalamus. Hum. Brain Mapp. 35, 2632–2642 (2014). source
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- cites [150] Glahn, D. C. et al. Genetic control over the resting brain. Proc. Natl Acad. Sci. USA 107, 1223–1228 (2010). source
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- cites [151] Schmitt, J. E. et al. The dynamic role of genetics on cortical patterning during childhood and adolescence. Proc. Natl Acad. Sci. USA 111, 6774–6779 (2014). source
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PremisecitationWhite-matter microstructure as represented by FA is generally highly heritable in adults, with variability across tracts.
“white-matter microstructure, as represented by FA, is generally highly heritable in adults, with variability across different white-matter tracts147, 148.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [147] Lee, S. J. et al. Quantitative tract-based white matter heritability in twin neonates. Neuroimage 111, 123–135 (2015). source
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- cites [148] Brouwer, R. M. et al. White matter development in early puberty: a longitudinal volumetric and diffusion tensor imaging twin study. PLoS ONE 7, e32316 (2012). source
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PremisecitationDevelopmental patterns of resting-state functional connectivity are remarkably similar between males and females, except that interconnectivity between the two lateralized fronto-parietal networks increases at a greater rate in males.
“Developmental patterns of resting-state functional connectivity are remarkably similar between males and females, with the exception that interconnectivity between the two lateralized fronto-parietal networks increases at a greater rate in males90.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [90] Gao, W. et al. Functional network development during the first year: relative sequence and socioeconomic correlations. Cereb. Cortex 25, 2919–2928 (2015). This paper delineates the developmental sequence of nine major resting-state networks during the first year of life in a cohort of full-term infants. source
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PremisecitationDTI studies find minimal sex differences in neonates and in the maturation pattern of major white-matter fibre bundles over time.
“DTI studies find minimal sex differences in neonates128, 129 and in the maturation pattern of major white-matter fibre bundles with time32.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [128] Inano, S., Takao, H., Hayashi, N., Abe, O. & Ohtomo, K. Effects of age and gender on white matter integrity. AJNR Am. J. Neuroradiol 32, 2103–2109 (2011). source
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- cites [129] van Hemmen, J. et al. Sex differences in white matter microstructure in the human brain predominantly reflect differences in sex hormone exposure. Cereb. Cortex 27, 2994–3001 (2017).
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- cites [32] Geng, X. et al. Quantitative tract-based white matter development from birth to age 2 years. Neuroimage 61, 542–557 (2012). source
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InterpretationcitationThe postnatal sex difference in brain volume is probably driven by differences in surface area expansion, because global and regional cortical thickness trajectories are highly similar in males and females.
“These differences are probably driven by differences in surface area expansion, as the maturational trajectories of global and regional cortical thickness are highly similar in males and females4, 20, 27.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [4] Lyall, A. E. et al. Dynamic development of regional cortical thickness and surface area in early childhood. Cereb. Cortex 25, 2204–2212 (2015). source
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- cites [20] Raznahan, A. et al. How does your cortex grow? J. Neurosci. 31, 7174–7177 (2011). source
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- cites [27] Ducharme, S. et al. Trajectories of cortical thickness maturation in normal brain development — the importance of quality control procedures. Neuroimage 125, 267–279 (2016). source
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PremisecitationThe path length and clustering coefficients of adult white-matter networks have heritabilities of 57% and 68%, respectively.
“the path length [G] and clustering coefficients [G] of adult white-matter networks have heritabilities of 57% and 68% respectively152”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [152] van den Heuvel, M. P. et al. Genetic control of functional brain network efficiency in children. Eur. Neuropsychopharmacol. 23, 19–23 (2013). source
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PremisecitationCortical thickness and surface area have considerable genetic influences that vary by cortical region but share little genetic variance, indicating regulation by different sets of genetic influences.
“Cortical thickness and surface area also have considerable genetic influences that vary by cortical region, but interestingly share little shared genetic variance between them, indicating that these two aspects of cortical volume are regulated by different sets of genetic influences 144, 145.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [144] Kochunov, P. et al. Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data. Neuroimage 111, 300–311 (2015). source
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- cites [145] Vuoksimaa, E. et al. Heritability of white matter microstructure in late middle age: a twin study of tract-based fractional anisotropy and absolute diffusivity indices. Hum. Brain Mapp. 38, 2026–2036 (2017). source
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PremisecitationStructural networks of white matter and resting-state functional networks each have considerable genetic components in adults.
“structural networks of white matter and resting-state functional networks each have considerable genetic components43.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [43] Richmond, S., Johnson, K. A., Seal, M. L., Allen, N. B. & Whittle, S. Development of brain networks and relevance of environmental and genetic factors: a systematic review. Neurosci. Biobehav. Rev. 71, 215–239 (2016). source
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InterpretationreasoningThese adult sex differences may emerge in adolescence, when FA increases more rapidly in males than females, driven by a reduction in RD.
“These sex differences may therefore emerge in adolescence, as FA increases more rapidly in males than females across this time period, driven by reduction in RD.”
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PremisecitationAdult studies suggest males have higher FA, higher AD, and lower RD in widespread white-matter regions.
“studies in adults suggest that males have higher FA, higher AD, and lower RD in widespread white-matter regions131–135.”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [131] den Braber, A. et al. Sex differences in gray and white matter structure in age-matched unrelated males and females and opposite-sex siblings. Int. J. Psychol. Res. 6, 7–21 (2013). source
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- cites [132] Takao, H., Hayashi, N. & Ohtomo, K. Sex dimorphism in the white matter: fractional anisotropy and brain size. J. Magn. Reson. Imag. 39, 917–923 (2014). source
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- cites [133] Menzler, K. et al. Men and women are different: diffusion tensor imaging reveals sexual dimorphism in the microstructure of the thalamus, corpus callosum and cingulum. Neuroimage 54, 2557–2562 (2011). source
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- cites [134] Kanaan, R. A. et al. Gender influence on white matter microstructure: a tract-based spatial statistics analysis. PLoS ONE 9, e91109 (2014). source
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- cites [135] Chou, K. H., Cheng, Y., Chen, I. Y., Lin, C. P. & Chu, W. C. Sex-linked white matter microstructure of the social and analytic brain. Neuroimage 54, 725–733 (2011). source
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PremisecitationRegions of significant heritability of functional connectivity are evident at birth and expand by age 2 years.
“Regions of significant heritability of functional connectivity are evident at birth and expand by age 2 years109”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [109] Andersen, R. A. Multimodal integration for the representation of space in the posterior parietal cortex. Phil. Trans. R. Soc. Lond. B Biol Sci. 352, 1421–1428 (1997). source
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PremisecitationIn older children and adolescents, lower family income and lower parental education are associated with reduced volumes of cortical grey matter, hippocampus, and amygdala, as well as reduced cortical surface area and cortical thickness.
“In older children and adolescents, lower family income and lower parental education have been associated with reduced volumes of cortical grey matter, the hippocampus, and the amygdala168 as well as reduced cortical surface area and cortical thickness169, 170.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [168] Luby, J. et al. The effects of poverty on childhood brain development: the mediating effect of caregiving and stressful life events. JAMA Pediatr. 167, 1135–1142 (2013). source
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- cites [169] Mackey, A. P. et al. Neuroanatomical correlates of the income-achievement gap. Psychol. Sci. 26, 925–933 (2015). source
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- cites [170] Noble, K. G. et al. Family income, parental education and brain structure in children and adolescents. Nat. Neurosci. 18, 773–778 (2015). source
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PremisecitationPrenatal cocaine exposure is associated with aberrant functional connectivity between the amygdala and medial prefrontal cortex and between the thalamus and frontal cortex.
“prenatal cocaine exposure is associated with aberrant functional connectivity between the amygdala and the medial prefrontal cortex183 and between the thalamus and frontal cortex182”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [183] Salzwedel, A. P. et al. Prenatal drug exposure affects neonatal brain functional connectivity. J. Neurosci. 35, 5860–5869 (2015). source
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- cites [182] Salzwedel, A. P., Grewen, K. M., Goldman, B. D. & Gao, W. Thalamocortical functional connectivity and behavioral disruptions in neonates with prenatal cocaine exposure. Neurotoxicol. Teratol. 56, 16–25 (2016). source
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InterpretationreasoningGenomic variants influencing these processes are expected to have an important role in generating individual differences in brain structure and function.
“Genomic variants that influence these processes are expected to have an important role in generating individual differences in brain structure and function.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationMutations in WWOX are associated with autosomal recessive spinocerebellar ataxia 12, mental retardation, microcephaly, and hypomyelination, among other neurological phenotypes.
“Mutations in WWOX are associated with autosomal recessive spinocerebellar ataxia 12, mental retardation, microcephaly and hypomyelination164, among other neurological phenotypes.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [164] Tabarki, B. et al. Severe CNS involvement in WWOX mutations: description of five new cases. Am. J. Med. Genet. A 167A, 3209–3213 (2015). source
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PremisecitationIn 6- to 12-month-olds, interparental conflict is associated with stronger resting-state connectivity among hubs of the default network, posterior cingulate cortex, and anterior medial prefrontal cortex, and between posterior cingulate cortex and amygdala.
“in 6- to 12-month-olds, interparental conflict is associated with stronger resting-state connectivity among hubs of the default network, posterior cingulate cortex and anterior medical prefrontal cortex, as well as between the posterior cingulate cortex and the amygdala179.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [179] Graham, A. M., Pfeifer, J. H., Fisher, P. A., Carpenter, S. & Fair, D. A. Early life stress is associated with default system integrity and emotionality during infancy. J. Child Psychol. Psychiatry 56, 1212–1222 (2015). source
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PremisecitationIn 2- to 25-month-old infants, ε4 carriers show lower myelin water fraction in precuneus, posterior and middle cingulate, lateral temporal cortex, and medial occipitotemporal regions, and greater myelin water fraction in extensive frontal regions compared with noncarriers.
“2- to 25-month-old infants who were ε4 carriers showed lower myelin water fraction in the precuneus, the posterior and middle cingulate, the lateral temporal cortex and medial occipitotemporal regions — areas preferentially affected by Alzheimer disease — and greater myelin water fraction in extensive frontal regions compared with noncarriers172.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [172] Ursache, A. & Noble, K. G. Socioeconomic status, white matter, and executive function in children. Brain Behav. 6, e00531 (2016). source
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PremisecitationIn a study of antenatal maternal anxiety and infant COMT genotypes, neither maternal anxiety nor infant COMT genotype was individually related to regional cortical thickness.
“Neither maternal anxiety nor infant COMT genotype were related to regional cortical thickness individually”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [159] Qiu, A. et al. COMT haplotypes modulate associations of antenatal maternal anxiety and neonatal cortical morphology. Am. J. Psychiatry 172, 163–172 (2015). source
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Classified as probably not a substantial claim.
Study design and conductreasoningThe first GWAS of neonatal brain structure requires independent replication, particularly for the imputed low-frequency IGFBP7 SNP absent from the largest racial/ethnic group.
“This is the first study of its kind162 and independent replication is crucial, especially for the IGFBP7 intronic SNP, which was imputed, has a low minor allele frequency, and was not present in the largest racial/ethnic group in the study.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [162] Xia, K. et al. Genome-wide association analysis identifies common variants influencing infant brain volumes. Transl Psychiatry 7, e1188 (2017). source
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PremisecitationHousehold income and maternal education are each correlated with within-network connectivity of the default resting-state network at 6 months of age.
“Household income and the level of maternal education are each correlated with within-network connectivity of the default resting-state network at 6 months of age91.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [91] Doria, V. et al. Emergence of resting state networks in the preterm human brain. Proc. Natl Acad. Sci. USA 107, 20015–20020 (2010). source
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PremisecitationIn the interaction, maternal anxiety decreased cortical thickness in neonates with two Met COMT alleles but increased cortical thickness in neonates with two Val alleles.
“maternal anxiety decreased cortical thickness in neonates with two copies of the Met COMT allele but increased cortical thickness in neonates with two copies of the Val allele.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [159] Qiu, A. et al. COMT haplotypes modulate associations of antenatal maternal anxiety and neonatal cortical morphology. Am. J. Psychiatry 172, 163–172 (2015). source
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PremisecitationCortical surface morphology, as determined by deformation of cortical surfaces, is associated with cognitive development in the first 2 years of life, and this association varies with age.
“Cortical surface morphology, as determined by deformation of cortical surfaces (a measure of grey-matter density), is associated with cognitive development in the first 2 years of life, and this association varies with age197.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [197] Spann, M. N., Bansal, R., Rosen, T. S. & Peterson, B. S. Morphological features of the neonatal brain support development of subsequent cognitive, language, and motor abilities. Hum. Brain Mapp. 35, 4459–4474 (2014). source
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Interpretationnone givenImaging studies in early childhood offer the promise of understanding the early origins of, and genetic and environmental influences affecting, individual differences in cognition, behaviour and risk for neuropsychiatric disease, and these studies are beginning to fulfil these aims.
“Imaging studies in early childhood offer the promise of understanding the early origins of, and genetic and environmental influences affecting, individual differences in cognition, behaviour and risk for neuropsychiatric disease, and these studies are beginning to fulfil these aims.”
Quote in the paperNot a substantial claim- Rests on an assumption: Early childhood is an understudied period.
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Interpretationnone givenBy birth, major white-matter tracts are in place and white-matter structural networks and sensorimotor resting-state functional networks are well developed.
“by birth, major white-matter tracts are in place and white-matter structural networks and sensorimotor resting-state functional networks are well developed.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationChildren at risk of autism have higher FA values at 6 months and a slower increase of FA after 6 months, resulting in lower FA values at 24 months.
“Children who are at risk of autism have higher FA values at 6 months and a slower increase of FA after 6 months, resulting in lower FA values at 24 months188”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [188] Wolff, J. J. et al. Differences in white matter fiber tract development present from 6 to 24 months in infants with autism. Am. J. Psychiatry 169, 589–600 (2012). source
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Interpretationnone givenThe first year of life is a period of robust grey-matter growth, rapid myelination and maturation of microstructure of existing white-matter tracts, and development of higher-order resting-state functional networks.
“The first year of life is a period of robust grey-matter growth, rapid myelination and maturation of microstructure of existing white-matter tracts, as well as development of higher-order resting-state functional networks.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningBy age 2 years, the fundamental structural and functional architecture of the brain seems to be in place, and later childhood brain maturation is much slower.
“By age 2 years, the fundamental structural and functional architecture of the brain seems to be in place, and the brain maturation that occurs in later childhood is much slower.”
Quote in the paperSubstantial claim
The paper relies on this without support.
Little is known about structural and functional brain development during early childhood, partly because of difficulties with image acquisition and analysis in very young children.
“In spite of its importance, little is known about structural and functional brain development during this critical period, in part owing to difficulties with image acquisition and image analysis in very young children.”
The paper relies on this without support.
Very few postmortem histologic studies of early childhood cortical development exist.
“There are very few postmortem histologic studies of early childhood cortical development; however, the studies that do exist are consistent with imaging studies and provide insights into the neurobiological process that underlie change observed in imaging studies.”
The paper relies on this without support.
Imaging studies cannot provide information at a cellular level.
“While imaging studies cannot provide information at a cellular level, they have significantly improved our understanding of early childhood structural brain development in humans and complement postmortem studies (Box 1).”
The paper relies on this without support.
Early childhood is an understudied period.
“this important but still understudied period”
The paper relies on this without support.
Imaging, genetic and environmental variables each contribute only a small percentage of variance to developmental outcomes.
“the imaging, genetic and environmental variables that contribute a small percentage of variance.”
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In the postnatal stage, in vivo tractography offers a superior tool to chart spatiotemporal maturation patterns of reconstructed tracts using quantitative dMRI metrics from infancy to adolescence.
“In the postnatal stage, in vivo tractography offers a superior tool to chart the spatiotemporal maturation patterns of the reconstructed tracts by employing quantitative dMRI metrics from the infancy period (Dubois et al., 2014; Gilmore et al., 2018; Lebel and Deoni, 2018; Qiu et al., 2015; Vasung et al., 2019) to the adolescent stage (Lebel et al., 2019; Tamnes et al., 2018).”
From Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review (2022) · cites this paper as Gilmore et al., 2018
The Introduction (White matter; page unavailable) says diffusion imaging visualizes major fibre tracts and measures their microstructure using AD, RD and FA. Structural development (White matter; page unavailable) describes how those measures change from infancy through later childhood and adolescence. The paper does not establish that in vivo tractography is a superior tool; the citing sentence assigns adolescence to other references. (LLM, conf=0.82)
Experimental — accuracy not yet measuredResearchers have implemented dMRI tractography investigations across broad brain developmental stages from middle fetal stage to adulthood.
“In the past decade, researchers have implemented dMRI tractography investigations across broad brain developmental stages ranging from the middle fetal stage to adulthood (Cao et al., 2017; Dubois et al., 2014; Gilmore et al., 2018; Huang, 2010; Lebel and Deoni, 2018; Lebel et al., 2019; Qiu et al., 2015; Zhao et al., 2019b).”
From Quantitative mapping of the brain’s structural connectivity using diffusion MRI tractography: A review (2022) · cites this paper as Gilmore et al., 2018
The White matter sections describe diffusion imaging of fibre tracts at birth and DTI studies of development through later childhood and adolescence; the References also list a DTI study spanning infancy to adulthood. Our copy does not document dMRI tractography investigations beginning in the middle fetal stage, so it does not support the full age range claimed. (LLM, conf=0.82)
Experimental — accuracy not yet measuredThe human brain undergoes considerable changes during the first years of life.
“The human brain undergoes considerable changes during the first years of life (Gilmore et al., 2018, Hadders-Algra, 2018)”
From Resting brain activity in early childhood predicts IQ at 18 years (2023) · cites this paper as Gilmore et al., 2018
Cites
Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881 · see citing works
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820 · see citing works
Complex network measures of brain connectivity: Uses and interpretations
Rubinov, M., & Sporns, O. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.003 · Cited by 11,522 · see citing works
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812 · see citing works
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553 · see citing works
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426 · see citing works
Correspondence of the brain's functional architecture during activation and rest
Smith, S. M., Fox, P. T., Miller, K. L., Glahn, D. C., Fox, P. M., Mackay, C. E., Filippini, N., Watkins, K. E., Toro, R., Laird, A. R., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905267106 · Cited by 5,150 · see citing works
Über das Elektrenkephalogramm des Menschen
Berger, H. (1929) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf01797193 · Cited by 4,266 · see citing works
Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.
Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212 · see citing works
Jöbsis, F. F. (1977) · Science · doi:10.1126/science.929199 · Cited by 3,899 · see citing works
Ogawa, S., Tank, D. W., Menon, R., Ellermann, J. M., Kim, S. G., Merkle, H., & Ugurbil, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5951 · Cited by 3,681 · see citing works
NODDI: Practical in vivo neurite orientation dispersion and density imaging of the human brain
Zhang, H., Schneider, T., Wheeler-Kingshott, C. A., & Alexander, D. C. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.072 · Cited by 3,288 · see citing works
The economy of brain network organization
Bullmore, E., & Sporns, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3214 · Cited by 3,284 · see citing works
Mesulam, M. (1998) · Brain · doi:10.1093/brain/121.6.1013 · Cited by 3,072 · see citing works
A method for making group inferences from functional MRI data using independent component analysis
Calhoun, V. D., Adali, T., Pearlson, G. D., & Pekar, J. J. (2001) · Human Brain Mapping · doi:10.1002/hbm.1048 · Cited by 2,994 · see citing works
Genome-Wide Mapping of in Vivo Protein-DNA Interactions
Johnson, D. S., Mortazavi, A., Myers, R. M., & Wold, B. (2007) · Science · doi:10.1126/science.1141319 · Cited by 2,927 · see citing works
White matter integrity, fiber count, and other fallacies: The do's and don'ts of diffusion MRI
Jones, D. K., Knösche, T. R., & Turner, R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.081 · Cited by 2,479 · see citing works
Canonical Microcircuits for Predictive Coding
Bastos, A. M., Usrey, W. M., Adams, R. A., Mangun, G. R., Fries, P., & Friston, K. J. (2012) · Neuron · doi:10.1016/j.neuron.2012.10.038 · Cited by 2,421 · see citing works
Common blood flow changes across visual tasks: II. Decreases in cerebral cortex
Shulman, G. L., Fiez, J. A., Corbetta, M., Buckner, R. L., Miezin, F. M., Raichle, M. E., & Petersen, S. E. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.5.648 · Cited by 1,890 · see citing works
Interoceptive predictions in the brain
Barrett, L. F., & Simmons, W. K. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3950 · Cited by 1,766 · see citing works
Neurodevelopmental Trajectories of the Human Cerebral Cortex
Shaw, P., Kabani, N. J., Lerch, J. P., Eckstrand, K., Lenroot, R., Gogtay, N., Greenstein, D., Clasen, L., Evans, A., Rapoport, J. L., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5309-07.2008 · Cited by 1,644 · see citing works
Damasio, A. R. (1989) · Cognition · doi:10.1016/0010-0277(89)90005-x · Cited by 1,538 · see citing works
Family income, parental education and brain structure in children and adolescents
Noble, K. G., Houston, S. M., Brito, N. H., Bartsch, H., Kan, E., Kuperman, J. M., Akshoomoff, N., Amaral, D. G., Bloss, C. S., Libiger, O., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.3983 · Cited by 1,423 · see citing works
Extraordinary neoteny of synaptic spines in the human prefrontal cortex
Petanjek, Z., Judaš, M., Šimić, G., Rašin, M. R., Uylings, H. B. M., Rakic, P., & Kostović, I. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105108108 · Cited by 1,411 · see citing works
Distinct Genetic Influences on Cortical Surface Area and Cortical Thickness
Panizzon, M. S., Fennema-Notestine, C., Eyler, L. T., Jernigan, T. L., Prom-Wormley, E., Neale, M., Jacobson, K., Lyons, M. J., Grant, M. D., Franz, C. E., et al. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp026 · Cited by 1,304 · see citing works
A meta-analysis of sex differences in human brain structure
Ruigrok, A. N. V., Salimi-Khorshidi, G., Lai, M.-C., Baron-Cohen, S., Lombardo, M. V., Tait, R. J., & Suckling, J. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.12.004 · Cited by 1,192 · see citing works
A Structural MRI Study of Human Brain Development from Birth to 2 Years
Knickmeyer, R. C., Gouttard, S., Kang, C., Evans, D., Wilber, K., Smith, J. K., Hamer, R. M., Lin, W., Gerig, G., & Gilmore, J. H. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3479-08.2008 · Cited by 1,151 · see citing works
Self-citationEarly brain development in infants at high risk for autism spectrum disorder
The IBIS Network, Hazlett, H. C., Gu, H., Munsell, B. C., Kim, S. H., Styner, M., Wolff, J. J., Elison, J. T., Swanson, M. R., Zhu, H., et al. (2017) · Nature · doi:10.1038/nature21369 · Cited by 1,128 · see citing works
Functional neuroimaging of speech perception in infants
Dehaene-Lambertz, G., Dehaene, S., & Hertz-Pannier, L. (2002) · Science · doi:10.1126/science.1077066 · Cited by 1,113 · see citing works
Imaging structural co-variance between human brain regions
Alexander-Bloch, A., Giedd, J. N., & Bullmore, E. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3465 · Cited by 1,064 · see citing works
Building better biomarkers: brain models in translational neuroimaging
Woo, C.-W., Chang, L. J., Lindquist, M. A., & Wager, T. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4478 · Cited by 1,056 · see citing works
Courchesne, E., Chisum, H. J., Townsend, J., Cowles, A., Covington, J., Egaas, B., Harwood, M., Hinds, S., & Press, G. A. (2000) · Radiology · doi:10.1148/radiology.216.3.r00au37672 · Cited by 1,049 · see citing works
Ciric, R., Wolf, D. H., Power, J. D., Roalf, D. R., Baum, G. L., Ruparel, K., Shinohara, R. T., Elliott, M. A., Eickhoff, S. B., Davatzikos, C., et al. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.03.020 · Cited by 1,042 · see citing works
Recent progress and outstanding issues in motion correction in resting state fMRI
Power, J. D., Schlaggar, B. L., & Petersen, S. E. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.044 · Cited by 957 · see citing works
Cognitive Recovery in Socially Deprived Young Children: The Bucharest Early Intervention Project
Nelson, C. A., Zeanah, C. H., Fox, N. A., Marshall, P. J., Smyke, A. T., & Guthrie, D. (2007) · Science · doi:10.1126/science.1143921 · Cited by 951 · see citing works
Kinney, H. C., Ann brody, B., Kloman, A. S., & Gilles, F. H. (1988) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-198805000-00003 · Cited by 888 · see citing works
Maturation of white matter in the human brain: A review of magnetic resonance studies.
Paus, T., Collins, D. L., Evans, A. C., Leonard, G., Pike, B., & Zijdenbos, A. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00434-2 · Cited by 863 · see citing works
Dubois, J., Dehaene-Lambertz, G., Kulikova, S., Poupon, C., Hüppi, P. S., & Hertz-Pannier, L. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.12.044 · Cited by 851 · see citing works
Corridors of migrating neurons in the human brain and their decline during infancy
Sanai, N., Nguyen, T., Ihrie, R. A., Mirzadeh, Z., Tsai, H.-H., Wong, M., Gupta, N., Berger, M. S., Huang, E., Garcia-Verdugo, J.-M., et al. (2011) · Nature · doi:10.1038/nature10487 · Cited by 849 · see citing works
Dehaene, S., Sergent, C., & Changeux, J.-P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1332574100 · Cited by 838 · see citing works
Twenty‐five pitfalls in the analysis of diffusion MRI data
Jones, D. K., & Cercignani, M. (2010) · NMR in Biomedicine · doi:10.1002/nbm.1543 · Cited by 827 · see citing works
The Cellular and Molecular Landscapes of the Developing Human Central Nervous System
Silbereis, J. C., Pochareddy, S., Zhu, Y., Li, M., & Sestan, N. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.008 · Cited by 818 · see citing works
Similar patterns of cortical expansion during human development and evolution
Hill, J., Inder, T., Neil, J., Dierker, D., Harwell, J., & Van Essen, D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001229107 · Cited by 811 · see citing works
Mirror self-image reactions before age two
Amsterdam, B. (1972) · Developmental Psychobiology · doi:10.1002/dev.420050403 · Cited by 811 · see citing works
Development of large-scale functional brain networks in children
Supekar, K., Musen, M., & Menon, V. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000157 · Cited by 807 · see citing works
Longitudinal Analysis of Neural Network Development in Preterm Infants
Smyser, C. D., Inder, T. E., Shimony, J. S., Hill, J. E., Degnan, A. J., Snyder, A. Z., & Neil, J. J. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq035 · Cited by 791 · see citing works
Cohen, D. (1972) · Science · doi:10.1126/science.175.4022.664 · Cited by 785 · see citing works
Benes, F. M. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950060041004 · Cited by 744 · see citing works
Luby, J., Belden, A., Botteron, K., Marrus, N., Harms, M. P., Babb, C., Nishino, T., & Barch, D. (2013) · JAMA Pediatrics · doi:10.1001/jamapediatrics.2013.3139 · Cited by 733 · see citing works
A universal scaling law between gray matter and white matter of cerebral cortex
Zhang, K., & Sejnowski, T. J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.090504197 · Cited by 723 · see citing works
Raznahan, A., Shaw, P., Lalonde, F., Stockman, M., Wallace, G. L., Greenstein, D., Clasen, L., Gogtay, N., & Giedd, J. N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0054-11.2011 · Cited by 712 · see citing works
White matter maturation reshapes structural connectivity in the late developing human brain
Hagmann, P., Sporns, O., Madan, N., Cammoun, L., Pienaar, R., Wedeen, V. J., Meuli, R., Thiran, J.-P., & Grant, P. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009073107 · Cited by 700 · see citing works
Prolonged myelination in human neocortical evolution
Miller, D. J., Duka, T., Stimpson, C. D., Schapiro, S. J., Baze, W. B., McArthur, M. J., Fobbs, A. J., Sousa, A. M. M., Šestan, N., Wildman, D. E., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117943109 · Cited by 699 · see citing works
Resting-state networks in the infant brain
Fransson, P., Skiöld, B., Horsch, S., Nordell, A., Blennow, M., Lagercrantz, H., & Åden, U. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704380104 · Cited by 696 · see citing works
Wolff, J. J., Gu, H., Gerig, G., Elison, J. T., Styner, M., Gouttard, S., Botteron, K. N., Dager, S. R., Dawson, G., Estes, A. M., et al. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.11091447 · Cited by 671 · see citing works
The neuroscience of socioeconomic status: Correlates, causes, and consequences
Farah, M. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.08.034 · Cited by 653 · see citing works
Buss, C., Davis, E. P., Shahbaba, B., Pruessner, J. C., Head, K., & Sandman, C. A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1201295109 · Cited by 652 · see citing works
Gao, W., Zhu, H., Giovanello, K. S., Smith, J. K., Shen, D., Gilmore, J. H., & Lin, W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811221106 · Cited by 601 · see citing works
Self-citationMills, K. L., Goddings, A.-L., Herting, M. M., Meuwese, R., Blakemore, S.-J., Crone, E. A., Dahl, R. E., Güroğlu, B., Raznahan, A., Sowell, E. R., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.07.044 · Cited by 600 · see citing works
Map Plasticity in Somatosensory Cortex
Feldman, D. E., & Brecht, M. (2005) · Science · doi:10.1126/science.1115807 · Cited by 587 · see citing works
Emergence of resting state networks in the preterm human brain
Doria, V., Beckmann, C. F., Arichi, T., Merchant, N., Groppo, M., Turkheimer, F. E., Counsell, S. J., Murgasova, M., Aljabar, P., Nunes, R. G., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007921107 · Cited by 574 · see citing works
The origin of spontaneous activity in the developing auditory system
Tritsch, N. X., Yi, E., Gale, J. E., Glowatzki, E., & Bergles, D. E. (2007) · Nature · doi:10.1038/nature06233 · Cited by 569 · see citing works
The functional architecture of the infant brain as revealed by resting-state fMRI
Fransson, P., Åden, U., Blennow, M., & Lagercrantz, H. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq071 · Cited by 542 · see citing works
Dynamics of Oligodendrocyte Generation and Myelination in the Human Brain
Yeung, M. S. Y., Zdunek, S., Bergmann, O., Bernard, S., Salehpour, M., Alkass, K., Perl, S., Tisdale, J., Possnert, G., Brundin, L., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.011 · Cited by 541 · see citing works
Developing Mechanisms of Self-Regulation in Early Life
Rothbart, M. K., Sheese, B. E., Rueda, M. R., & Posner, M. I. (2011) · Emotion Review · doi:10.1177/1754073910387943 · Cited by 538 · see citing works
Prediction as a Humanitarian and Pragmatic Contribution from Human Cognitive Neuroscience
Gabrieli, J. D. E., Ghosh, S., & Whitfield, S. (2015) · Neuron · doi:10.1016/j.neuron.2014.10.047 · Cited by 526 · see citing works
Socioeconomic status and structural brain development
Brito, N. H., & Noble, K. G. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00276 · Cited by 525 · see citing works
Retinal waves coordinate patterned activity throughout the developing visual system
Ackman, J. B., Burbridge, T. J., & Crair, M. C. (2012) · Nature · doi:10.1038/nature11529 · Cited by 525 · see citing works
Multimodal integration for the representation of space in the posterior parietal cortex
Andersen, R. A. (1997) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1997.0128 · Cited by 515 · see citing works
Diffusion Tensor MR Imaging and Fiber Tractography: Theoretic Underpinnings
Mukherjee, P., Berman, J., Chung, S. W., Hess, C. P., & Henry, R. G. (2008) · American Journal of Neuroradiology · doi:10.3174/ajnr.a1051 · Cited by 510 · see citing works
Mapping Infant Brain Myelination with Magnetic Resonance Imaging
Deoni, S. C. L., Mercure, E., Blasi, A., Gasston, D., Thomson, A., Johnson, M., Williams, S. C. R., & Murphy, D. G. M. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2106-10.2011 · Cited by 497 · see citing works
Early patterns of electrical activity in the developing cerebral cortex of humans and rodents
Khazipov, R., & Luhmann, H. J. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.05.007 · Cited by 482 · see citing works
Nir, Y., Mukamel, R., Dinstein, I., Privman, E., Harel, M., Fisch, L., Gelbard-Sagiv, H., Kipervasser, S., Andelman, F., Neufeld, M. Y., et al. (2008) · Nature Neuroscience · doi:10.1038/nn.2177 · Cited by 480 · see citing works
Gleaning multicomponent T 1 and T 2 information from steady‐state imaging data
Deoni, S., Rutt, B. K., Arun, T., Pierpaoli, C. M., & Jones, D. K. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21704 · Cited by 473 · see citing works
Regional Gray Matter Growth, Sexual Dimorphism, and Cerebral Asymmetry in the Neonatal Brain
Gilmore, J. H., Lin, W., Prastawa, M. W., Looney, C. B., Vetsa, Y. S. K., Knickmeyer, R. C., Evans, D. D., Smith, J. K., Hamer, R. M., Lieberman, J. A., et al. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3339-06.2007 · Cited by 465 · see citing works
Self-citationThe Convergence of Maturational Change and Structural Covariance in Human Cortical Networks
Alexander‐Bloch, A. F., Raznahan, A., Bullmore, E. T., & Giedd, J. N. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3554-12.2013 · Cited by 460 · see citing works
Head motion during MRI acquisition reduces gray matter volume and thickness estimates
Reuter, M., Tisdall, M. D., Qureshi, A., Buckner, R. L., van der Kouwe, A. J. W., & Fischl, B. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.12.006 · Cited by 457 · see citing works
Longitudinal Development of Cortical and Subcortical Gray Matter from Birth to 2 Years
Gilmore, J. H., Shi, F., Woolson, S. L., Knickmeyer, R. C., Short, S. J., Lin, W., Zhu, H., Hamer, R. M., Styner, M., & Shen, D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr327 · Cited by 456 · see citing works
Self-citationGenetic control over the resting brain
Glahn, D. C., Winkler, A. M., Kochunov, P., Almasy, L., Duggirala, R., Carless, M. A., Curran, J. C., Olvera, R. L., Laird, A. R., Smith, S. M., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909969107 · Cited by 450 · see citing works
Neocortical neurogenesis in humans is restricted to development
Bhardwaj, R. D., Curtis, M. A., Spalding, K. L., Buchholz, B. A., Fink, D., Björk-Eriksson, T., Nordborg, C., Gage, F. H., Druid, H., Eriksson, P. S., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605177103 · Cited by 448 · see citing works
Family Poverty Affects the Rate of Human Infant Brain Growth
Hanson, J. L., Hair, N., Shen, D. G., Shi, F., Gilmore, J. H., Wolfe, B. L., & Pollak, S. D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080954 · Cited by 430 · see citing works
Self-citationNetworks of anatomical covariance
Evans, A. C. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.054 · Cited by 429 · see citing works
Network-level structural covariance in the developing brain
Zielinski, B. A., Gennatas, E. D., Zhou, J., & Seeley, W. W. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003109107 · Cited by 405 · see citing works
Prefrontal white matter volume is disproportionately larger in humans than in other primates
Schoenemann, P. T., Sheehan, M. J., & Glotzer, L. D. (2005) · Nature Neuroscience · doi:10.1038/nn1394 · Cited by 405 · see citing works
Diffusion Tensor MR Imaging and Fiber Tractography: Technical Considerations
Mukherjee, P., Chung, S. W., Berman, J., Hess, C. P., & Henry, R. G. (2008) · American Journal of Neuroradiology · doi:10.3174/ajnr.a1052 · Cited by 391 · see citing works
Extensive migration of young neurons into the infant human frontal lobe
Paredes, M. F., James, D., Gil-Perotin, S., Kim, H., Cotter, J. A., Ng, C., Sandoval, K., Rowitch, D. H., Xu, D., McQuillen, P. S., et al. (2016) · Science · doi:10.1126/science.aaf7073 · Cited by 391 · see citing works
Deoni, S. C. L., Dean, D. C., O'Muircheartaigh, J., Dirks, H., & Jerskey, B. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.07.037 · Cited by 390 · see citing works
The Neonatal Connectome During Preterm Brain Development
van den Heuvel, M. P., Kersbergen, K. J., de Reus, M. A., Keunen, K., Kahn, R. S., Groenendaal, F., de Vries, L. S., & Benders, M. J. N. L. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu095 · Cited by 386 · see citing works
Gao, W., Alcauter, S., Elton, A., Hernandez-Castillo, C. R., Smith, J. K., Ramirez, J., & Lin, W. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu088 · Cited by 380 · see citing works
Self-citationDynamic Development of Regional Cortical Thickness and Surface Area in Early Childhood
Lyall, A. E., Shi, F., Geng, X., Woolson, S., Li, G., Wang, L., Hamer, R. M., Shen, D., & Gilmore, J. H. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu027 · Cited by 376 · see citing works
Self-citationFunctional Connectivity of the Infant Human Brain
Gao, W., Lin, W., Grewen, K., & Gilmore, J. H. (2016) · The Neuroscientist · doi:10.1177/1073858416635986 · Cited by 365 · see citing works
Self-citationRich-club organization of the newborn human brain
Ball, G., Aljabar, P., Zebari, S., Tusor, N., Arichi, T., Merchant, N., Robinson, E. C., Ogundipe, E., Rueckert, D., Edwards, A. D., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1324118111 · Cited by 360 · see citing works
Emerson, R. W., Adams, C., Nishino, T., Hazlett, H. C., Wolff, J. J., Zwaigenbaum, L., Constantino, J. N., Shen, M. D., Swanson, M. R., Elison, J. T., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aag2882 · Cited by 359 · see citing works
Development of human brain cortical network architecture during infancy
Gao, W., Alcauter, S., Smith, J. K., Gilmore, J. H., & Lin, W. (2015) · Brain Structure and Function · doi:10.1007/s00429-014-0710-3 · Cited by 356 · see citing works
Self-citationNetwork control principles predict neuron function in the Caenorhabditis elegans connectome
Yan, G. F., Vértes, P. E., Towlson, E. K., Chew, Y. L., Walker, D. S., Schafer, W. R., & Barabási, A.-Ĺ. (2017) · Nature · doi:10.1038/nature24056 · Cited by 349 · see citing works
Neuroanatomical Assessment of Biological Maturity
Brown, T. T., Kuperman, J. M., Chung, Y., Erhart, M., McCabe, C., Hagler, D. J., Venkatraman, V. K., Akshoomoff, N., Amaral, D. G., Bloss, C. S., et al. (2012) · Current Biology · doi:10.1016/j.cub.2012.07.002 · Cited by 332 · see citing works
Stepwise Connectivity of the Modal Cortex Reveals the Multimodal Organization of the Human Brain
Sepulcre, J., Sabuncu, M. R., Yeo, T. B., Liu, H., & Johnson, K. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0759-12.2012 · Cited by 323 · see citing works
Age-related Volumetric Changes of Brain Gray and White Matter in Healthy Infants and Children
Matsuzawa, J. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.4.335 · Cited by 315 · see citing works
Studying neuroanatomy using MRI
Lerch, J. P., van der Kouwe, A. J. W., Raznahan, A., Paus, T., Johansen‐Berg, H., Miller, K. L., Smith, S. M., Fischl, B. R., & Sotiropoulos, S. N. (2017) · Nature Neuroscience · doi:10.1038/nn.4501 · Cited by 313 · see citing works
Ducharme, S., Albaugh, M. D., Nguyen, T.-V., Hudziak, J. J., Mateos-Pérez, J. M., Labbe, A., Evans, A. C., & Karama, S. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.010 · Cited by 304 · see citing works
Gao, W., Lin, W., Chen, Y., Gerig, G., Smith, J. K., Jewells, V. L., & Gilmore, J. H. (2008) · American Journal of Neuroradiology · doi:10.3174/ajnr.a1363 · Cited by 299 · see citing works
Self-citationRetinal Waves Trigger Spindle Bursts in the Neonatal Rat Visual Cortex
Hanganu, I. L., Ben‐Ari, Y., & Khazipov, R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0752-06.2006 · Cited by 288 · see citing works
Regional Hemodynamic Responses to Visual Stimulation in Awake Infants
Meek, J. H., Firbank, M., Elwell, C. E., Atkinson, J., Braddick, O., & Wyatt, J. S. (1998) · Pediatric Research · doi:10.1203/00006450-199806000-00019 · Cited by 287 · see citing works
Developmental connectomics from infancy through early childhood
Cao, M., Huang, H., & He, Y. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.06.003 · Cited by 284 · see citing works
Prenatal maternal depression alters amygdala functional connectivity in 6-month-old infants
Qiu, A., Anh, T. T., Li, Y., Chen, H., Rifkin-Graboi, A., Broekman, B. F. P., Kwek, K., Saw, S.-M., Chong, Y.-S., Gluckman, P. D., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.3 · Cited by 282 · see citing works
Petanjek, Z., Judas, M., Kostovic, I., & Uylings, H. B. M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm124 · Cited by 273 · see citing works
Temporal and spatial evolution of brain network topology during the first two years of life
Gao, W., Gilmore, J. H., Giovanello, K. S., Smith, J. K., Shen, D., Zhu, H., & Lin, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025278 · Cited by 272 · see citing works
Self-citationThe Infancy of the Human Brain
Dehaene-Lambertz, G., & Spelke, E. S. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.026 · Cited by 264 · see citing works
Dean, D. C., Jerskey, B. A., Chen, K., Protas, H., Thiyyagura, P., Roontiva, A., O'Muircheartaigh, J., Dirks, H., Waskiewicz, N., Lehman, K., et al. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2013.4544 · Cited by 263 · see citing works
Prenatal maternal depression associates with microstructure of right amygdala in neonates at birth.
Rifkin-Graboi, A., Bai, J., Chen, H., Hameed, W. B., Sim, L. W., Tint, M. T., Leutscher-Broekman, B., Chong, Y.-S., Gluckman, P. D., Fortier, M. V., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.06.019 · Cited by 258 · see citing works
Socioeconomic status, white matter, and executive function in children
Ursache, A., Noble, K. G., & the Pediatric Imaging, N. A. G. S. (2016) · Brain and Behavior · doi:10.1002/brb3.531 · Cited by 256 · see citing works
Wozniak, J. R., & Lim, K. O. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.06.003 · Cited by 255 · see citing works
Li, G., Wang, L., Shi, F., Lyall, A. E., Lin, W., Gilmore, J. H., & Shen, D. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3976-13.2014 · Cited by 251 · see citing works
Self-citationStructural Growth Trajectories and Rates of Change in the First 3 Months of Infant Brain Development
Holland, D., Chang, L., Ernst, T. M., Curran, M., Buchthal, S. D., Alicata, D., Skranes, J., Johansen, H., Hernandez, A., Yamakawa, R., et al. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.1638 · Cited by 242 · see citing works
Diffusion tensor imaging for understanding brain development in early life
Qiu, A., Mori, S., & Miller, M. I. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015340 · Cited by 238 · see citing works
Menzler, K., Belke, M., Wehrmann, E., Krakow, K., Lengler, U., Jansen, A., Hamer, H. M., Oertel, W. H., Rosenow, F., & Knake, S. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.029 · Cited by 237 · see citing works
Lebel, C., Walton, M., Letourneau, N., Giesbrecht, G. F., Kaplan, B. J., & Dewey, D. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.12.004 · Cited by 237 · see citing works
Developmental Changes in Organization of Structural Brain Networks
Khundrakpam, B. S., Reid, A., Brauer, J., Carbonell, F., Lewis, J., Ameis, S., Karama, S., Lee, J., Chen, Z., Das, S., et al. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs187 · Cited by 234 · see citing works
Thalamocortical Connectivity Predicts Cognition in Children Born Preterm
Ball, G., Pazderova, L., Chew, A., Tusor, N., Merchant, N., Arichi, T., Allsop, J. M., Cowan, F. M., Edwards, A. D., & Counsell, S. J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu331 · Cited by 234 · see citing works
Walhovd, K. B., Fjell, A. M., Giedd, J. N., Dale, A. M., & Brown, T. T. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv301 · Cited by 233 · see citing works
Temporal Specification and Bilaterality of Human Neocortical Topographic Gene Expression
Pletikos, M., Sousa, A. M. M., Sedmak, G., Meyer, K. A., Zhu, Y., Cheng, F., Li, M., Kawasawa, Y. I., & Šestan, N. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.018 · Cited by 228 · see citing works
Development of Thalamocortical Connectivity during Infancy and Its Cognitive Correlations
Alcauter, S., Lin, W., Smith, J. K., Short, S. J., Goldman, B. D., Reznick, J. S., Gilmore, J. H., & Gao, W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0796-14.2014 · Cited by 228 · see citing works
Self-citationBrain anatomical networks in early human brain development
Fan, Y., Shi, F., Smith, J. K., Lin, W., Gilmore, J. H., & Shen, D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.025 · Cited by 225 · see citing works
Self-citationCross-hemispheric functional connectivity in the human fetal brain
Thomason, M. E., Dassanayake, M. T., Shen, S., Katkuri, Y., Alexis, M., Anderson, A. L., Yeo, L., Mody, S., Hernandez-Andrade, E., Hassan, S. S., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3004978 · Cited by 225 · see citing works
Motion correction in MRI of the brain
Godenschweger, F., Kägebein, U., Stucht, D., Yarach, U., Sciarra, A., Yakupov, R., Lüsebrink, F., Schulze, P., & Speck, O. (2016) · Physics in Medicine and Biology · doi:10.1088/0031-9155/61/5/r32 · Cited by 225 · see citing works
Development of Human Brain Structural Networks Through Infancy and Childhood
Huang, H., Shu, N., Mishra, V., Jeon, T., Chalak, L., Wang, Z. J., Rollins, N., Gong, G., Cheng, H., Peng, Y., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht335 · Cited by 223 · see citing works
Functional connectivity MR imaging reveals cortical functional connectivity in the developing brain
Lin, W., Zhu, Q., Gao, W., Chen, Y., Toh, C.-H., Styner, M., Gerig, G., Smith, J. K., Biswal, B., & Gilmore, J. H. (2008) · American Journal of Neuroradiology · doi:10.3174/ajnr.a1256 · Cited by 222 · see citing works
Self-citationBlokland, G. A. M., de Zubicaray, G. I., McMahon, K. L., & Wright, M. J. (2012) · Twin Research and Human Genetics · doi:10.1017/thg.2012.11 · Cited by 221 · see citing works
Sexual dimorphism in the human brain: evidence from neuroimaging
Sacher, J., Neumann, J., Okon-Singer, H., Gotowiec, S., & Villringer, A. (2013) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2012.06.007 · Cited by 221 · see citing works
Mapping Region-Specific Longitudinal Cortical Surface Expansion from Birth to 2 Years of Age
Li, G., Nie, J., Wang, L., Shi, F., Lin, W., Gilmore, J. H., & Shen, D. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs265 · Cited by 220 · see citing works
Self-citationGenetic topography of brain morphology
Chen, C.-H., Fiecas, M., Gutiérrez, E. D., Panizzon, M. S., Eyler, L. T., Vuoksimaa, E., Thompson, W. K., Fennema-Notestine, C., Hagler, D. J., Jernigan, T. L., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308091110 · Cited by 217 · see citing works
Kochunov, P., Jahanshad, N., Marcus, D., Winkler, A., Sprooten, E., Nichols, T. E., Wright, S. N., Hong, L. E., Patel, B., Behrens, T., et al. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.050 · Cited by 215 · see citing works
Maternal anxiety and infants’ hippocampal development: timing matters.
Qiu, A., Rifkin-Graboi, A., Chen, H., Chong, Y.-S., Kwek, K., Gluckman, P. D., Fortier, M. V., & Meaney, M. J. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.79 · Cited by 214 · see citing works
Effects of age and gender on white matter integrity
Inano, S., Takao, H., Hayashi, N., Abe, O., & Ohtomo, K. (2011) · American Journal of Neuroradiology · doi:10.3174/ajnr.a2785 · Cited by 213 · see citing works
Multimodal imaging of the self-regulating developing brain
Fjell, A. M., Walhovd, K. B., Brown, T. T., Kuperman, J. M., Chung, Y., Hagler, D. J., Venkatraman, V., Roddey, J. C., Erhart, M., McCabe, C., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208243109 · Cited by 212 · see citing works
Quantitative tract-based white matter development from birth to age 2 years
Geng, X., Gouttard, S., Sharma, A., Gu, H., Styner, M., Lin, W., Gerig, G., & Gilmore, J. H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.057 · Cited by 212 · see citing works
Self-citationCommon and distinct fusion proteins in axonal growth and transmitter release
Osen‐Sand, A., Staple, J. K., Naldi, E., Schiavo, G., Rossetto, O., Petitpierre, S., Malgaroli, A., Montecucco, C., & Catsicas, S. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960401)367:2 · Cited by 206 · see citing works
Jelescu, I. O., Veraart, J., Adisetiyo, V., Milla, S. S., Novikov, D. S., & Fieremans, E. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.12.009 · Cited by 202 · see citing works
Development of BOLD signal hemodynamic responses in the human brain
Arichi, T., Fagiolo, G., Varela, M., Melendez-Calderon, A., Allievi, A., Merchant, N. M., Tusor, N., Counsell, S. J., Burdet, E., Beckmann, C. F., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.054 · Cited by 202 · see citing works
Gao, W., Gilmore, J. H., Shen, D., Smith, J. K., Zhu, H., & Lin, W. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs043 · Cited by 194 · see citing works
Self-citationSchmitt, J. E., Lenroot, R., Wallace, G. L., Ordaz, S. J., Taylor, K. N., Kabani, N. J., GREENSTEIN, D. K., Lerch, J. P., Kendler, K. S., Neale, M. C., et al. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm211 · Cited by 193 · see citing works
Krogsrud, S. K., Fjell, A. M., Tamnes, C. K., Grydeland, H., Mork, L., Due-Tønnessen, P., Bjørnerud, A., Sampaio-Baptista, C., Andersson, J., Johansen-Berg, H., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.09.017 · Cited by 190 · see citing works
Development Trends of White Matter Connectivity in the First Years of Life
Yap, P.-T., Fan, Y., Chen, Y., Gilmore, J. H., Lin, W., & Shen, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024678 · Cited by 190 · see citing works
Self-citationRametti, G., Carrillo, B., Gómez-Gil, E., Junque, C., Segovia, S., Gomez, Á., & Guillamon, A. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.05.006 · Cited by 187 · see citing works
Donald, K. A., Eastman, E., Howells, F. M., Adnams, C., Riley, E. P., Woods, R. P., Narr, K. L., & Stein, D. J. (2015) · Acta Neuropsychiatrica · doi:10.1017/neu.2015.12 · Cited by 185 · see citing works
Jansen, A. G., Mous, S. E., White, T., Posthuma, D., & Polderman, T. J. C. (2015) · Neuropsychology Review · doi:10.1007/s11065-015-9278-9 · Cited by 184 · see citing works
White matter development and early cognition in babies and toddlers
O'Muircheartaigh, J., Dean, D. C., Ginestet, C. E., Walker, L., Waskiewicz, N., Lehman, K., Dirks, H., Piryatinsky, I., & Deoni, S. C. L. (2014) · Human Brain Mapping · doi:10.1002/hbm.22488 · Cited by 183 · see citing works
Faria, A. V., Zhang, J., Oishi, K., Li, X., Jiang, H., Akhter, K., Hermoye, L., Lee, S.-K., Hoon, A., & Stashinko, E. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.04.238 · Cited by 180 · see citing works
Alexander-Bloch, A., Clasen, L., Stockman, M., Ronan, L., Lalonde, F., Giedd, J., & Raznahan, A. (2016) · Human Brain Mapping · doi:10.1002/hbm.23180 · Cited by 178 · see citing works
Neuroanatomical Correlates of the Income-Achievement Gap
Mackey, A. P., Finn, A. S., Leonard, J. A., Jacoby-Senghor, D. S., West, M. R., Gabrieli, C. F. O., & Gabrieli, J. D. E. (2015) · Psychological Science · doi:10.1177/0956797615572233 · Cited by 176 · see citing works
Structural and Maturational Covariance in Early Childhood Brain Development
Geng, X., Li, G., Lu, Z., Gao, W., Wang, L., Shen, D., Zhu, H., & Gilmore, J. H. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw022 · Cited by 175 · see citing works
Self-citationCharacterizing longitudinal white matter development during early childhood
Dean, D. C., O’Muircheartaigh, J., Dirks, H., Waskiewicz, N., Walker, L., Doernberg, E., Piryatinsky, I., & Deoni, S. C. L. (2015) · Brain Structure and Function · doi:10.1007/s00429-014-0763-3 · Cited by 174 · see citing works
Finding the Elusive Psychiatric “Lesion” With 21st-Century Neuroanatomy: A Note of Caution
Weinberger, D. R., & Radulescu, E. (2016) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.15060753 · Cited by 173 · see citing works
Li, G., Lin, W., Gilmore, J. H., & Shen, D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4107-14.2015 · Cited by 164 · see citing works
Self-citationSpecialization and integration of functional thalamocortical connectivity in the human infant
Toulmin, H., Beckmann, C. F., O’Muircheartaigh, J., Ball, G., Nongena, P., Makropoulos, A., Ederies, A., Counsell, S. J., Kennea, N. L., Arichi, T., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422638112 · Cited by 164 · see citing works
Modeling healthy male white matter and myelin development: 3 through 60months of age
Dean, D. C., O'Muircheartaigh, J., Dirks, H., Waskiewicz, N., Lehman, K., Walker, L., Han, M., & Deoni, S. C. L. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.058 · Cited by 163 · see citing works
Kunz, N., Zhang, H. G., Vasung, L., O’Brien, K., Assaf, Y., Lazeyras, F., Alexander, D. C., & Hüppi, P. S. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.057 · Cited by 159 · see citing works
Remer, J., Croteau-Chonka, E., Dean, D. C., D’Arpino, S., Dirks, H., Whiley, D., & Deoni, S. C. L. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.04.010 · Cited by 152 · see citing works
Visual Activation in Infants and Young Children Studied by Functional Magnetic Resonance Imaging
Born, P., Leth, H., Miranda, M. J., Rostrup, E., Stensgaard, A., Peitersen, B., Larsson, H. B. W., & Lou, H. C. (1998) · Pediatric Research · doi:10.1203/00006450-199810000-00018 · Cited by 149 · see citing works
Common Variants in Psychiatric Risk Genes Predict Brain Structure at Birth
Knickmeyer, R. C., Wang, J., Zhu, H., Geng, X., Woolson, S., Hamer, R. M., Konneker, T., Lin, W., Styner, M., & Gilmore, J. H. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs401 · Cited by 149 · see citing works
Self-citationWhite matter maturation profiles through early childhood predict general cognitive ability
Deoni, S. C. L., O’Muircheartaigh, J., Elison, J. T., Walker, L., Doernberg, E., Waskiewicz, N., Dirks, H., Piryatinsky, I., Dean, D. C., & Jumbe, N. L. (2016) · Brain Structure and Function · doi:10.1007/s00429-014-0947-x · Cited by 147 · see citing works
Developmental changes in cerebral grey and white matter volume from infancy to adulthood
Groeschel, S., Vollmer, B., King, M. D., & Connelly, A. (2010) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2010.06.004 · Cited by 147 · see citing works
Toward Developmental Connectomics of the Human Brain
Cao, M., Huang, H., Peng, Y., Dong, Q., & Yong He, A. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00025 · Cited by 147 · see citing works
Prediction of brain maturity in infants using machine-learning algorithms
Smyser, C. D., Dosenbach, N. U. F., Smyser, T. A., Snyder, A. Z., Rogers, C. E., Inder, T. E., Schlaggar, B. L., & Neil, J. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.05.029 · Cited by 140 · see citing works
Hasegawa, M., Houdou, S., Mito, T., Takashima, S., Asanuma, K., & Ohno, T. (1992) · Brain and Development · doi:10.1016/s0387-7604(12)80271-3 · Cited by 137 · see citing works
Genetic and environmental contributions to neonatal brain structure: A twin study
Gilmore, J. H., Schmitt, J. E., Knickmeyer, R. C., Smith, J. K., Lin, W., Styner, M., Gerig, G., & Neale, M. C. (2010) · Human Brain Mapping · doi:10.1002/hbm.20926 · Cited by 136 · see citing works
Self-citationKeunen, K., Išgum, I., van Kooij, B. J. M., Anbeek, P., van Haastert, I. C., Koopman-Esseboom, C., Fieret-van Stam, P. C., Nievelstein, R. A. J., Viergever, M. A., de Vries, L. S., et al. (2016) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2015.12.023 · Cited by 132 · see citing works
Gao, W., Elton, A., Zhu, H., Alcauter, S., Smith, J. K., Gilmore, J. H., & Lin, W. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5072-13.2014 · Cited by 131 · see citing works
Self-citationGenetic control of functional brain network efficiency in children
van den Heuvel, M. P., van Soelen, I. L. C., Stam, C. J., Kahn, R. S., Boomsma, D. I., & Hulshoff Pol, H. E. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.06.007 · Cited by 127 · see citing works
The predictive validity of neonatal MRI for neurodevelopmental outcome in very preterm children
Anderson, P. J., Cheong, J. L. Y., & Thompson, D. K. (2015) · Seminars in Perinatology · doi:10.1053/j.semperi.2015.01.008 · Cited by 127 · see citing works
Structural connectivity asymmetry in the neonatal brain
Ratnarajah, N., Rifkin-Graboi, A., Fortier, M. V., Chong, Y. S., Kwek, K., Saw, S.-M., Godfrey, K. M., Gluckman, P. D., Meaney, M. J., & Qiu, A. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.02.052 · Cited by 124 · see citing works
Effect Size Estimation in Neuroimaging
Reddan, M. C., Lindquist, M. A., & Wager, T. D. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.3356 · Cited by 123 · see citing works
Implications of newborn amygdala connectivity for fear and cognitive development at 6-months-of-age
Graham, A. M., Buss, C., Rasmussen, J. M., Rudolph, M. D., Demeter, D. V., Gilmore, J. H., Styner, M., Entringer, S., Wadhwa, P. D., & Fair, D. A. (2016) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.09.006 · Cited by 122 · see citing works
Self-citationNeuroimaging of children following prenatal drug exposure
Derauf, C., Kekatpure, M., Neyzi, N., Lester, B., & Kosofsky, B. (2009) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2009.03.001 · Cited by 122 · see citing works
Prefrontal Cortical Involvement in Young Infants' Analysis of Novelty
Nakano, T., Watanabe, H., Homae, F., & Taga, G. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn096 · Cited by 116 · see citing works
Machine-learning to characterise neonatal functional connectivity in the preterm brain
Ball, G., Aljabar, P., Arichi, T., Tusor, N., Cox, D., Merchant, N., Nongena, P., Hajnal, J. V., Edwards, A. D., & Counsell, S. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.055 · Cited by 114 · see citing works
Selective prefrontal cortex responses to joint attention in early infancy
Großmann, T., & Johnson, M. H. (2010) · Biology Letters · doi:10.1098/rsbl.2009.1069 · Cited by 113 · see citing works
Emerson, R. W., Gao, W., & Lin, W. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.3980-15.2016 · Cited by 112 · see citing works
Self-citationFunctional connectivity of the sensorimotor area in naturally sleeping infants
Liu, W.-C., Flax, J. F., Guise, K. G., Sukul, V., & Benasich, A. A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.054 · Cited by 110 · see citing works
From trans to cis: transcriptional regulatory networks in neocortical development
Shibata, M., Gulden, F. O., & Sestan, N. (2015) · Trends in Genetics · doi:10.1016/j.tig.2014.12.004 · Cited by 109 · see citing works
Impact of Sex and Gonadal Steroids on Neonatal Brain Structure
Knickmeyer, R. C., Wang, J., Zhu, H., Geng, X., Woolson, S., Hamer, R. M., Konneker, T., Styner, M., & Gilmore, J. H. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht125 · Cited by 109 · see citing works
Self-citationBrouwer, R. M., Mandl, R. C. W., Schnack, H. G., van Soelen, I. L. C., van Baal, G. C., Peper, J. S., Kahn, R. S., Boomsma, D. I., & Pol, H. E. H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032316 · Cited by 107 · see citing works
Developmental sex differences in resting state functional connectivity of amygdala sub-regions
Alarcón, G., Cservenka, A., Rudolph, M. D., Fair, D. A., & Nagel, B. J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.04.013 · Cited by 105 · see citing works
Associations between white matter microstructure and infants' working memory
Short, S. J., Elison, J. T., Goldman, B. D., Styner, M., Gu, H., Connelly, M., Maltbie, E., Woolson, S., Lin, W., Gerig, G., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.09.021 · Cited by 105 · see citing works
Self-citationKrishnan, M. L., Van Steenwinckel, J., Schang, A.-L., Yan, J., Arnadottir, J., Le Charpentier, T., Csaba, Z., Dournaud, P., Cipriani, S., Auvynet, C., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00422-w · Cited by 105 · see citing works
The dynamic role of genetics on cortical patterning during childhood and adolescence
Schmitt, J. E., Neale, M. C., Fassassi, B., Perez, J., Lenroot, R. K., Wells, E. M., & Giedd, J. N. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311630111 · Cited by 103 · see citing works
The EEG of the early premature
Anderson, C. M., Torres, F., & Faoro, A. (1985) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(85)90015-x · Cited by 102 · see citing works
Tanaka, C., Matsui, M., Uematsu, A., Noguchi, K., & Miyawaki, T. (2012) · Developmental Neuroscience · doi:10.1159/000345152 · Cited by 101 · see citing works
COMT Haplotypes Modulate Associations of Antenatal Maternal Anxiety and Neonatal Cortical Morphology
Qiu, A., Tuan, T. A., Ong, M. L., Li, Y., Chen, H., Rifkin-Graboi, A., Broekman, B. F. P., Kwek, K., Saw, S.-M., Chong, Y.-S., et al. (2015) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2014.14030313 · Cited by 100 · see citing works
Maturation of Sensori-Motor Functional Responses in the Preterm Brain
Allievi, A., Arichi, T., Tusor, N., Kimpton, J., Arulkumaran, S., Counsell, S. J., Edwards, A. D., & Burdet, E. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv203 · Cited by 100 · see citing works
Gilmore, J. H., Kang, C., Evans, D. D., Wolfe, H. M., Smith, J. K., Lieberman, J. A., Lin, W., Hamer, R. M., Styner, M., & Gerig, G. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09101492 · Cited by 97 · see citing works
Self-citationNeurovascular coupling and energy metabolism in the developing brain
Kozberg, M. G., & Hillman, E. M. C. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.02.002 · Cited by 96 · see citing works
Myelination in the human hippocampal formation from midgestation to adulthood
Ábrahám, H., Vincze, A., Jewgenow, I., Veszprémi, B., Kravják, A., Gömöri, É., & Seress, L. (2010) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2010.03.004 · Cited by 94 · see citing works
Arichi, T., Whitehead, K., Barone, G., Pressler, R., Padormo, F., Edwards, A. D., & Lorenzo Fabrizi, D. (2017) · eLife · doi:10.7554/elife.27814 · Cited by 94 · see citing works
Prenatal Drug Exposure Affects Neonatal Brain Functional Connectivity
Salzwedel, A. P., Grewen, K. M., Vachet, C., Gerig, G., Lin, W., & Gao, W. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4333-14.2015 · Cited by 93 · see citing works
Self-citationTime‐efficient and flexible design of optimized multishell HARDI diffusion
Hutter, J. M., Tournier, J., Price, A. N., Cordero‐Grande, L., Hughes, E., Malik, S., Steinweg, J. K., Bastiani, M., Sotiropoulos, S. N., Jbabdi, S., et al. (2017) · Magnetic Resonance in Medicine · doi:10.1002/mrm.26765 · Cited by 93 · see citing works
Brain connectivity in normally developing children and adolescents
Khundrakpam, B. S., Lewis, J. D., Zhao, L., Chouinard-Decorte, F., & Evans, A. C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.062 · Cited by 91 · see citing works
Amygdala subnuclei resting-state functional connectivity sex and estrogen differences
Engman, J., Linnman, C., Van Dijk, K. R. A., & Milad, M. R. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.09.012 · Cited by 89 · see citing works
Early life stress is associated with default system integrity and emotionality during infancy
Graham, A. M., Pfeifer, J. H., Fisher, P. A., Carpenter, S., & Fair, D. A. (2015) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12409 · Cited by 84 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Jones, E. G. The Thalamus (Springer Science & Business Media, 2012).
Cited by
Sorted by citations
Brain charts for the human lifespan
Bethlehem, R. A. I., Seidlitz, J., White, S. R., Vogel, J. W., Anderson, K. M., Adamson, C., Adler, S., Alexopoulos, G. S., Anagnostou, E., Areces-Gonzalez, A., et al. (2022) · Nature · doi:10.1038/s41586-022-04554-y · Cited by 1,794 · see citing works
Self-citationSleep spindles: mechanisms and functions
Fernandez, L. M. J., & Lüthi, A. (2020) · Physiological Reviews · doi:10.1152/physrev.00042.2018 · Cited by 716 · see citing works
Environmental influences on the pace of brain development
Tooley, U. A., Bassett, D. S., & Mackey, A. P. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00457-5 · Cited by 488 · see citing works
Zhang, F., Daducci, A., He, Y., Schiavi, S., Seguin, C., Smith, R. E., Yeh, C.-H., Zhao, T., & O’Donnell, L. J. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2021.118870 · Cited by 302 · see citing works
“from the infancy period [124, 161, 253, 346, 469] to the adolescent stage [255, 443].”
BackgroundPregnancy as a period of risk, adaptation, and resilience for mothers and infants
Davis, E. P., & Narayan, A. J. (2020) · Development and Psychopathology · doi:10.1017/s0954579420001121 · Cited by 297 · see citing works
Adolescent Neurodevelopment and Vulnerability to Psychosis
Patel, P. K., Leathem, L. D., Currin, D. L., & Karlsgodt, K. H. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.06.028 · Cited by 152 · see citing works
Imaging transcriptomics of brain disorders
Arnatkeviciute, A., Fulcher, B. D., Bellgrove, M. A., & Fornito, A. (2022) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2021.10.002 · Cited by 113 · see citing works
Pujala, A., & Koyama, M. (2019) · eLife · doi:10.7554/elife.42135 · Cited by 80 · see citing works
Sun, Y.-J., Sahakian, B. J., Langley, C., Yang, A., Jiang, Y., Kang, J., Zhao, X., Li, C., Cheng, W., & Feng, J. (2024) · Psychological Medicine · doi:10.1017/s0033291723001381 · Cited by 68 · see citing works
“Then they expanded gradually until approximately ages 8 – 12, after which they declined progressively (Gilmore, Knickmeyer, & Gao, 2018; Sowell et al., 2003).”
BackgroundSpencer, R. M. C., & Riggins, T. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2123415119 · Cited by 41 · see citing works
CTNND2 moderates the pace of synaptic maturation and links human evolution to synaptic neoteny
Assendorp, N., Fossati, M., Libé-Philippot, B., Christopoulou, E., Depp, M., Rapone, R., Dingli, F., Loew, D., Vanderhaeghen, P., & Charrier, C. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114797 · Cited by 32 · see citing works
Robust sex differences in functional brain connectivity are present in utero
Cook, K. M., De Asis-Cruz, J., Lopez, C., Quistorff, J., Kapse, K., Andersen, N., Vezina, G., & Limperopoulos, C. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhac218 · Cited by 31 · see citing works
Resting brain activity in early childhood predicts IQ at 18 years
Tan, E., Tang, A., Debnath, R., Humphreys, K. L., Zeanah, C. H., Nelson, C. A., & Fox, N. A. (2023) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2023.101287 · Cited by 22 · see citing works
Hendrix, C. L., Srinivasan, H., Feliciano, I., Carré, J. M., & Thomason, M. E. (2022) · Life · doi:10.3390/life12070943 · Cited by 21 · see citing works
Maternal Nutrition during Pregnancy and Offspring Brain Development: Insights from Neuroimaging
Na, X., Mackean, P. P., Cape, G. A., Johnson, J. W., & Ou, X. (2024) · Nutrients · doi:10.3390/nu16193337 · Cited by 22 · see citing works
Literacy Promotion: An Essential Component of Primary Care Pediatric Practice: Technical Report
Klass, P., Mendelsohn, A. L., Hutton, J. S., Dunlap, M., Anderson, A. T., High, P. C., Navsaria, D., COUNCIL ON EARLY CHILDHOOD, Miller-Fitzwater, A., Roby, E., et al. (2024) · Pediatrics · doi:10.1542/peds.2024-069091 · Cited by 20 · see citing works
Kim, J.-H., De Asis-Cruz, J., Krishnamurthy, D., & Limperopoulos, C. (2023) · eLife · doi:10.7554/elife.80878 · Cited by 10 · see citing works
- Authors
- Gilmore, J. H., Knickmeyer, R. C., & Gao, W.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Cedars-Sinai Medical Center (US)
- Corresponding author
- Gilmore, John H.
- Venue
- Nature Reviews Neuroscience
- Published
- 2018-02-16
- Volume
- 19
- Issue
- 3
- Pages
- 123-137
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- PMC
- PMC5987539
- OpenAlex
- W2788755901
- Semantic Scholar
- 6e717ebb66b798e0412e68caf2fa9504239ca4c6
- Cited by
- 1,013
- References
- 250
- Citations by year
- 2026: 142 · 2025: 168 · 2024: 176 · 2023: 156 · 2022: 136 · 2021: 98 · 2020: 74 · 2019: 46 · 2018: 16
- FWCI
- 7.71
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (1r03da036645-01a1)
- National Institute of Mental Health (R21MH104330, R33MH104330, U01MH070890, R01MH092335, R01MH111944, R01MH070890)
- National Institute on Drug Abuse (R21DA043171, R03 DA036645)
- National Institute of Neurological Disorders and Stroke (R21NS088975)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD053000, U54HD079124)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Keywords
- early childhood brain development, structural brain development, white matter development, brain networks, cognitive development, autism risk, schizophrenia risk, neuropsychiatric disorders, environmental influences on brain development, imaging biomarkers, cognitive outcome prediction
- MeSH terms
- Mental Disorders, Brain, Child Development, Cognition, Humans, Infant, Infant, Newborn, Neural Pathways, Risk Factors, Biomarkers, Gene-Environment Interaction, Neuroimaging, White Matter, Gray Matter
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