Prenatal stress exposure and multimodal assessment of amygdala–medial prefrontal cortex connectivity in infants

The REDCap consortium: building an international community of software platform partners

Harris, P. A., Taylor, R., Minor, B. L., Elliott, V., Fernandez, M., O'Neal, L., McLeod, L., Delacqua, G., Delacqua, F., Kirby, J., et al. (2019) · Journal of Biomedical Informatics · doi:10.1016/j.jbi.2019.103208 · Cited by 24,013 · see citing works

Improved Optimization for the Robust and Accurate Linear Registration and Motion Correction of Brain Images

Jenkinson, M., Bannister, P., Brady, M., & Smith, S. (2002) · NeuroImage · doi:10.1006/nimg.2002.1132 · Cited by 11,888 · see citing works

Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion

Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.018 · Cited by 7,429 · see citing works

N4ITK: Improved N3 Bias Correction

Tustison, N. J., Avants, B., Cook, P. A., Zheng, Y., Egan, A., Yushkevich, P. A., & Gee, J. C. (2010) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2010.2046908 · Cited by 6,119 · see citing works

A component based noise correction method (CompCor) for BOLD and perfusion based fMRI

Behzadi, Y., Restom, K., Liau, J., & Liu, T. T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.04.042 · Cited by 4,502 · see citing works

The cognitive control of emotion

OCHSNER, K., & GROSS, J. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.03.010 · Cited by 4,495 · see citing works

How to correct susceptibility distortions in spin-echo echo-planar images: application to diffusion tensor imaging

Andersson, J. L. R., Skare, S., & Ashburner, J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00336-7 · Cited by 3,469 · see citing works

An integrated approach to correction for off-resonance effects and subject movement in diffusion MR imaging

Andersson, J., & Sotiropoulos, S. N. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.019 · Cited by 3,439 · see citing works

The origins of the developmental origins theory

Barker, D. J. P. (2007) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2007.01809.x · Cited by 2,955 · see citing works

The fetal and infant origins of adult disease.

Barker, D. J. (1990) · BMJ · doi:10.1136/bmj.301.6761.1111 · Cited by 2,768 · see citing works

The influence of head motion on intrinsic functional connectivity MRI

Van Dijk, K. R. A., Sabuncu, M. R., & Buckner, R. L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.044 · Cited by 2,344 · see citing works

Nipype: A Flexible, Lightweight and Extensible Neuroimaging Data Processing Framework in Python

Gorgolewski, K. J., Burns, C. D., Madison, C. M., Clark, D., Halchenko, Y. O., Waskom, M., & Ghosh, S. (2011) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2011.00013 · Cited by 2,206 · see citing works

The Adaptive Calibration Model of stress responsivity

Del Giudice, M., Ellis, B. J., & Shirtcliff, E. A. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.11.007 · Cited by 1,373 · see citing works

Precision Functional Mapping of Individual Human Brains

Gordon, E. M., Laumann, T. O., Gilmore, A. W., Newbold, D. J., Greene, D. J., Berg, J. J., Ortega, M., Hoyt-Drazen, C., Gratton, C., Sun, H., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.011 · Cited by 1,335 · see citing works

Amygdala–frontal connectivity during emotion regulation

Banks, S. J., Eddy, K. T., Angstadt, M., Nathan, P. J., & Phan, K. L. (2007) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsm029 · Cited by 1,187 · cited 1× · 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

Nonlinear Responses in fMRI: The Balloon Model, Volterra Kernels, and Other Hemodynamics

Friston, K. J., Mechelli, A., Turner, R., & Price, C. J. (2000) · NeuroImage · doi:10.1006/nimg.2000.0630 · Cited by 1,131 · see citing works

Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth

Satterthwaite, T. D., Wolf, D. H., Loughead, J., Ruparel, K., Elliott, M. A., Hakonarson, H., Gur, R. C., & Gur, R. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.063 · Cited by 1,125 · see citing works

Deterministic diffusion fiber tracking improved by quantitative anisotropy

Yeh, F.-C., Verstynen, T. D., Wang, Y., Fernández-Miranda, J. C., & Tseng, W.-Y. I. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080713 · Cited by 1,121 · see citing works

Antenatal maternal anxiety and stress and the neurobehavioural development of the fetus and child: links and possible mechanisms. A review

Van den Bergh, B. R. H., Mulder, E. J. H., Mennes, M., & Glover, V. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.10.007 · Cited by 1,104 · see citing works

Agreement Between Prospective and Retrospective Measures of Childhood Maltreatment: A Systematic Review and Meta-analysis

Baldwin, J. R., Reuben, A., Newbury, J. B., & Danese, A. (2019) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2019.0097 · Cited by 1,094 · see citing works

Towards a consensus regarding global signal regression for resting state functional connectivity MRI

Murphy, K., & Fox, M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.052 · Cited by 1,043 · see citing works

Generalized ${ q}$-Sampling Imaging

Yeh, F.-C. F., Wedeen, V. J., & Tseng, W. I. (2010) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2010.2045126 · Cited by 1,030 · see citing works

Developmental Origins of Health and Disease: Brief History of the Approach and Current Focus on Epigenetic Mechanisms

Wadhwa, P. D., Buß, C., Entringer, S., & Swanson, J. (2009) · Seminars in Reproductive Medicine · doi:10.1055/s-0029-1237424 · Cited by 986 · see citing works

Functional system and areal organization of a highly sampled individual human brain

Laumann, T. O., Gordon, E. M., Adeyemo, B., Snyder, A. Z., Joo, S. J., Chen, M.-Y., Gilmore, A. W., McDermott, K. B., Nelson, S. M., Dosenbach, N. U. F., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.037 · Cited by 911 · see citing works

The effect of scan length on the reliability of resting-state fMRI connectivity estimates

Birn, R. M., Molloy, E. K., Patriat, R., Parker, T., Meier, T. B., Kirk, G. R., Nair, V. A., Meyerand, M. E., & Prabhakaran, V. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.099 · Cited by 875 · see citing works

Early developmental emergence of human amygdala–prefrontal connectivity after maternal deprivation

Gee, D. G., Gabard-Durnam, L. J., Flannery, J., Goff, B., Humphreys, K. L., Telzer, E. H., Hare, T. A., Bookheimer, S. Y., & Tottenham, N. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1307893110 · Cited by 871 · see citing works

Child development in the context of adversity: Experiential canalization of brain and behavior.

Blair, C., & Raver, C. C. (2012) · American Psychologist · doi:10.1037/a0027493 · Cited by 799 · 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

The nuisance of nuisance regression: spectral misspecification in a common approach to resting-state fMRI preprocessing reintroduces noise and obscures functional connectivity

Hallquist, M. N., Hwang, K., & Luna, B. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.116 · Cited by 753 · see citing works

A Developmental Shift from Positive to Negative Connectivity in Human Amygdala–Prefrontal Circuitry

Gee, D. G., Humphreys, K. L., Flannery, J., Goff, B., Telzer, E. H., Shapiro, M., Hare, T. A., Bookheimer, S. Y., & Tottenham, N. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3446-12.2013 · Cited by 731 · see citing works

Prefrontal mechanisms in extinction of conditioned fear

Quirk, G. J., Garcia, R., & González-Lima, F. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.03.010 · Cited by 682 · see citing works

Sequence of Central Nervous System Myelination in Human Infancy. I. An Autopsy Study of Myelination

BRODY, B. A., KINNEY, H. C., KLOMAN, A. S., & GILLES, F. H. (1987) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-198705000-00005 · Cited by 682 · see citing works

Maternal cortisol over the course of pregnancy and subsequent child amygdala and hippocampus volumes and affective problems

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

Prefrontal control of fear: more than just extinction

Sotres-Bayon, F., & Quirk, G. J. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.02.005 · Cited by 625 · see citing works

The stress acceleration hypothesis: effects of early-life adversity on emotion circuits and behavior

Callaghan, B. L., & Tottenham, N. (2016) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2015.11.018 · Cited by 585 · 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

Developmental origins of adult health and disease

Barker, D. J. P. (2004) · Journal of Epidemiology & Community Health · doi:10.1136/jech.58.2.114 · Cited by 454 · see citing works

Biological aging in childhood and adolescence following experiences of threat and deprivation: a systematic review and meta-analysis

Colich, N. L., Rosen, M. L., Williams, E. S., & McLaughlin, K. A. (2020) · Psychological Bulletin · doi:10.1037/bul0000270 · Cited by 433 · see citing works

Biological Aging in Childhood and Adolescence Following Experiences of Threat and Deprivation: A Systematic Review and Meta-Analysis

Colich, N. L., Rosen, M. L., Williams, E. S., & McLaughlin, K. A. (2019) · doi:10.1101/642405 · Cited by 433 · see citing works

The UNC/UMN Baby Connectome Project (BCP): An overview of the study design and protocol development

Howell, B., Styner, M. A., Gao, W., Yap, P., Wang, L., Baluyot, K., Yacoub, E. S., Chen, G., Potts, T., Salzwedel, A., et al. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.03.049 · Cited by 431 · see citing works

Prenatal glucocorticoid programming of brain corticosteroid receptors and corticotrophin-releasing hormone: possible implications for behaviour

Welberg, L., Seckl, J. R., & Holmes, M. C. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00065-3 · Cited by 420 · see citing works

Maternal presence serves as a switch between learning fear and attraction in infancy

Moriceau, S., & Sullivan, R. M. (2006) · Nature Neuroscience · doi:10.1038/nn1733 · Cited by 386 · see citing works

Functional Network Development During the First Year: Relative Sequence and Socioeconomic Correlations

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

The role of physiological noise in resting-state functional connectivity

Birn, R. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.016 · Cited by 357 · see citing works

BET2 : MR-Based Estimation of Brain, Skull and Scalp Surfaces

Jenkinson, M. (2005) · Medical Entomology and Zoology · Cited by 348 · see citing works

Childhood Trauma Exposure Disrupts the Automatic Regulation of Emotional Processing

Marusak, H. A., Martin, K. R., Etkin, A., & Thomason, M. E. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.311 · Cited by 343 · see citing works

Prenatal stress, development, health and disease risk: A psychobiological perspective—2015 Curt Richter Award Paper

Entringer, S., Buss, C., & Wadhwa, P. D. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.08.019 · Cited by 324 · see citing works

Current Topics in Behavioral Neurosciences

Bowden, C. L. (2011) · Current topics in behavioral neurosciences · Cited by 318 · see citing works

Entrainment of Arteriole Vasomotor Fluctuations by Neural Activity Is a Basis of Blood-Oxygenation-Level-Dependent “Resting-State” Connectivity

Mateo, C., Knutsen, P. M., Tsai, P. S., Shih, A. Y., & Kleinfeld, D. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.012 · Cited by 303 · see citing works

The effects of prenatal maternal stress on children's cognitive development: Project Ice Storm

King, S., & Laplante, D. P. (2005) · Stress · doi:10.1080/10253890500108391 · Cited by 286 · 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

Maternal Systemic Interleukin-6 During Pregnancy Is Associated With Newborn Amygdala Phenotypes and Subsequent Behavior at 2 Years of Age

Graham, A. M., Rasmussen, J. M., Rudolph, M. D., Heim, C. M., Gilmore, J. H., Styner, M., Potkin, S. G., Entringer, S., Wadhwa, P. D., Fair, D. A., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.05.027 · Cited by 282 · see citing works

Serious life events and congenital malformations: a national study with complete follow-up

Hansen, D., Lou, H. C., & Olsen, J. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02676-3 · Cited by 260 · 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

Naturalistic rodent models of chronic early‐life stress

Molet, J., Maras, P. M., Avishai‐Eliner, S., & Baram, T. Z. (2014) · Developmental Psychobiology · doi:10.1002/dev.21230 · Cited by 258 · see citing works

Does Early-Life Exposure to Stress Shape or Impair Cognition?

Frankenhuis, W. E., & de Weerth, C. (2013) · Current Directions in Psychological Science · doi:10.1177/0963721413484324 · Cited by 256 · see citing works

vlPFC–vmPFC–amygdala interactions underlie age-related differences in cognitive regulation of emotion

Silvers, J. A., Insel, C., Powers, A., Franz, P., Helion, C., Martin, R. E., Weber, J., Mischel, W., Casey, B. J., & Ochsner, K. N. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw073 · Cited by 244 · see citing works

Differential functional connectivity within an emotion regulation neural network among individuals resilient and susceptible to the depressogenic effects of early life stress

Cisler, J. M., James, G. A., Tripathi, S., Mletzko, T., Heim, C., Hu, X. P., Mayberg, H. S., Nemeroff, C. B., & Kilts, C. D. (2013) · Psychological Medicine · doi:10.1017/s0033291712001390 · Cited by 236 · see citing works

Early cognitive and language skills are linked to resting frontal gamma power across the first 3 years

Benasich, A. A., Gou, Z., Choudhury, N., & Harris, K. D. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.08.049 · Cited by 230 · see citing works

Maternal Cortisol Concentrations During Pregnancy and Sex-Specific Associations With Neonatal Amygdala Connectivity and Emerging Internalizing Behaviors

Graham, A. M., Rasmussen, J. M., Entringer, S., Ben Ward, E., Rudolph, M. D., Gilmore, J. H., Styner, M., Wadhwa, P. D., Fair, D. A., & Buss, C. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.06.023 · Cited by 203 · see citing works

The Synchronization within and Interaction between the Default and Dorsal Attention Networks in Early Infancy

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

Alterations in amygdala–prefrontal circuits in infants exposed to prenatal maternal depression

Posner, J., Cha, J., Roy, A. K., Peterson, B. S., Bansal, R., Gustafsson, H. C., Raffanello, E., Gingrich, J., & Monk, C. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.146 · Cited by 184 · see citing works

In Vivo Imaging of Cerebral Microvascular Plasticity from Birth to Death

Harb, R., Whiteus, C., Freitas, C., & Grutzendler, J. (2012) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.152 · Cited by 182 · see citing works

Neurobiological Programming of Early Life Stress: Functional Development of Amygdala-Prefrontal Circuitry and Vulnerability for Stress-Related Psychopathology

VanTieghem, M., & Tottenham, N. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2016_42 · Cited by 170 · see citing works

Development of axonal pathways in the human fetal fronto-limbic brain: histochemical characterization and diffusion tensor imaging

Vasung, L., Huang, H., Jovanov‐Milošević, N., Pletikos, M., Mori, S., & Kostović, I. (2010) · Journal of Anatomy · doi:10.1111/j.1469-7580.2010.01260.x · Cited by 169 · see citing works

Maternal separation results in early emergence of adult-like fear and extinction learning in infant rats.

Callaghan, B. L., & Richardson, R. (2011) · Behavioral Neuroscience · doi:10.1037/a0022008 · Cited by 169 · see citing works

Estimation of fiber orientation and spin density distribution by diffusion deconvolution

Yeh, F.-C. F., Wedeen, V. J., & Tseng, W. I. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.087 · Cited by 167 · see citing works

Specialization 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

Does prenatal stress alter the developing connectome?

Scheinost, D., Sinha, R., Cross, S., Kwon, S. H., Sze, G. K., Constable, R. T., & Ment, L. R. (2016) · Pediatric Research · doi:10.1038/pr.2016.197 · Cited by 143 · see citing works

Antenatal Maternal Anxiety Predicts Variations in Neural Structures Implicated in Anxiety Disorders in Newborns

Rifkin-Graboi, A. E., Meaney, M. J., Chen, H., Bai, J., Hameed, W. B., Tint, M. T., Broekman, B. F. P., Chong, Y. S., Gluckman, P. D., Fortier, M. V., et al. (2015) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2015.01.013 · Cited by 140 · see citing works

Neonatal Amygdala Functional Connectivity at Rest in Healthy and Preterm Infants and Early Internalizing Symptoms

Rogers, C. E., Sylvester, C. M., Mintz, C. M., Kenley, J. K., Shimony, J. S., Barch, D. M., & Smyser, C. D. (2016) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2016.11.005 · Cited by 139 · see citing works

The Importance of Early Experiences for Neuro-Affective Development

Tottenham, N. (2013) · Current topics in behavioral neurosciences · doi:10.1007/7854_2013_254 · Cited by 133 · see citing works

Corticotropin releasing factor mRNA expression in the hypothalamic paraventricular nucleus and the central nucleus of the amygdala is modulated by repeated acute stress in the immature rat

Hatalski, C. G., Guirguis, C., & Baram, T. Z. (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00246.x · Cited by 132 · see citing works

Fetal Programming of Brain Development: Intrauterine Stress and Susceptibility to PsychopathologyA Presentation from the European Society for Paediatric Endocrinology (ESPE) New Inroads to Child Health (NICHe) Conference on Stress Response and Child Health in Heraklion, Crete, Greece, 18 to 20 May 2012.

Buß, C., Entringer, S., & Wadhwa, P. D. (2012) · Science Signaling · doi:10.1126/scisignal.2003406 · Cited by 131 · see citing works

Age-related changes in amygdala–frontal connectivity during emotional face processing from childhood into young adulthood

Wu, M., Kujawa, A., Lu, L. H., Fitzgerald, D. A., Klumpp, H., Fitzgerald, K. D., Monk, C. S., & Phan, K. L. (2016) · Human Brain Mapping · doi:10.1002/hbm.23129 · Cited by 130 · see citing works

The developing amygdala: a student of the world and a teacher of the cortex

Tottenham, N., & Gabard-Durnam, L. J. (2017) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2017.06.012 · Cited by 130 · see citing works

The Growth and Development of Microvasculature in Human Cerebral Cortex

Norman, M. G., & OʼKusky, J. R. (1986) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-198605000-00003 · Cited by 129 · see citing works

The Importance of Early Experiences for Neuro-Affective Development

Tottenham, N. (2013) · Current topics in behavioral neurosciences · doi:10.1007/978-3-662-45758-0_254 · Cited by 128 · see citing works

Glucocorticoid Prevents Brain-Derived Neurotrophic Factor-Mediated Maturation of Synaptic Function in Developing Hippocampal Neurons through Reduction in the Activity of Mitogen-Activated Protein Kinase

Kumamaru, E., Numakawa, T., Adachi, N., Yagasaki, Y., Izumi, A., Niyaz, M., Kudo, M., & Kunugi, H. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0264 · Cited by 116 · see citing works

The potential of infant fMRI research and the study of early life stress as a promising exemplar

Graham, A. M., Pfeifer, J. H., Fisher, P. A., Lin, W., Gao, W., & Fair, D. A. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2014.09.005 · Cited by 114 · see citing works

Ontogeny of hippocampal corticosteroid receptors: Effects of antenatal glucocorticoids in human and mouse

Noorlander, C. W., Graan, P. N. E. D., Middeldorp, J., van Beers, J. J. B. C., & Visser, G. H. A. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21162 · Cited by 98 · see citing works

Insensitive parenting may accelerate the development of the amygdala–medial prefrontal cortex circuit

Thijssen, S., Muetzel, R. L., Bakermans‐Kranenburg, M. J., Jaddoe, V. W. V., Tiemeier, H. W., Verhulst, F. C., White, T. J. H., & van IJzendoorn, M. H. (2017) · Development and Psychopathology · doi:10.1017/s0954579417000141 · Cited by 97 · see citing works

Aberrant development of intrinsic brain activity in a rat model of caregiver maltreatment of offspring

Yan, C., Rincón‐Cortés, M., Raineki, C., Sarro, E. C., Colcombe, S. J., Guilfoyle, D. N., Yang, Z., Gerum, S. V., Biswal, B. B., Milham, M. P., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2016.276 · Cited by 96 · see citing works

Cortical Functional Connectivity Evident After Birth and Behavioral Inhibition at Age 2

Sylvester, C. M., Smyser, C. D., Smyser, T. A., Kenley, J. K., Ackerman, J. J. H., Shimony, J. S., Petersen, S. E., & Rogers, C. E. (2017) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2017.17010018 · Cited by 96 · see citing works

Differential RET Signaling Pathways Drive Development of the Enteric Lymphoid and Nervous Systems

Patel, A. J., Harker, N., Moreira-Santos, L., Ferreira, M. M., Alden, K., Timmis, J., Foster, K., Garefalaki, A., Pachnis, P., Andrews, P. S., et al. (2012) · Science Signaling · doi:10.1126/scisignal.2002734 · Cited by 94 · see citing works

Altered corticolimbic connectivity reveals sex-specific adolescent outcomes in a rat model of early life adversity

Honeycutt, J. A., Demaestri, C., Peterzell, S., Silveri, M. M., Cai, X., Kulkarni, P. P., Cunningham, M. G., Ferris, C. F., & Brenhouse, H. C. (2020) · eLife · doi:10.7554/elife.52651 · Cited by 93 · see citing works

Repeated exposure to corticosterone, but not restraint, decreases the number of reelin-positive cells in the adult rat hippocampus

Lussier, A. L., Caruncho, H. J., & Kalynchuk, L. E. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.05.050 · Cited by 84 · see citing works

Amygdala–medial prefrontal cortex connectivity relates to stress and mental health in early childhood

Park, A. T., Leonard, J., Saxler, P. K., Cyr, A. B., Gabrieli, J. D. E., & Mackey, A. P. (2018) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsy017 · Cited by 81 · see citing works

Newborn amygdala connectivity and early emerging fear

Thomas, E., Buß, C., Rasmussen, J. M., Entringer, S., Ramirez, J. S. B., Marr, M. C., Rudolph, M. D., Gilmore, J. H., Styner, M. A., Wadhwa, P. D., et al. (2018) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2018.12.002 · Cited by 77 · see citing works

The association between early life stress and prefrontal cortex activation during implicit emotion regulation is moderated by sex in early adolescence

Colich, N. L., Williams, E., Ho, T. C., King, L. S., Humphreys, K. L., Price, A. N., Ordaz, S. J., & Gotlib, I. H. (2017) · Development and Psychopathology · doi:10.1017/s0954579417001444 · Cited by 72 · see citing works

Prenatal stress and limbic-prefrontal white matter microstructure in children aged 6–9 years: a preliminary diffusion tensor imaging study

Sarkar, S., Craig, M. C., Dell’Acqua, F., O’Connor, T. G., Catani, M., Deeley, Q., Glover, V., & Murphy, D. G. M. (2014) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2014.903336 · Cited by 70 · see citing works

Development of Amygdala Functional Connectivity During Infancy and Its Relationship With 4-Year Behavioral Outcomes

Salzwedel, A., Stephens, R. L., Goldman, B. D., Lin, W., Gilmore, J. H., & Gao, W. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.08.010 · Cited by 63 · see citing works

Altered Development of Amygdala-Anterior Cingulate Cortex Connectivity in Anxious Youth and Young Adults

Kujawa, A., Wu, M., Klumpp, H., Pine, D. S., Swain, J. E., Fitzgerald, K. D., Monk, C. S., & Phan, K. L. (2016) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.01.006 · Cited by 62 · see citing works

Paradoxical Prefrontal–Amygdala Recruitment to Angry and Happy Expressions in Pediatric Posttraumatic Stress Disorder

Keding, T. J., & Herringa, R. J. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.104 · Cited by 60 · see citing works

Characterization of developmental changes in EEG‐gamma band activity during childhood using the autoregressive model

Takano, T., & Ogawa, T. (1998) · Pediatrics International · doi:10.1111/j.1442-200x.1998.tb01966.x · Cited by 59 · see citing works

Human amygdala functional network development: A cross-sectional study from 3 months to 5 years of age

Gabard-Durnam, L. J., O’Muircheartaigh, J., Dirks, H., Dean, D., Tottenham, N., & Deoni, S. (2018) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2018.06.004 · Cited by 50 · see citing works

VALIDATION OF THE CRISIS IN FAMILY SYSTEMS-REVISED, A CONTEMPORARY MEASURE OF LIFE STRESSORS

Berry, C. A., Quinn, K., Shalowitz, M. U., & Wolf, R. L. (2001) · Psychological Reports · doi:10.2466/pr0.2001.88.3.713 · Cited by 49 · see citing works

Neuroendocrine and immune markers of maternal stress during pregnancy and infant cognitive development

Nazzari, S., Fearon, P. R. M., Rice, F. J., Ciceri, F., Molteni, M., & Frigerio, A. (2020) · Developmental Psychobiology · doi:10.1002/dev.21967 · Cited by 39 · see citing works

The relationship between biological and psychosocial risk factors and resting‐state functional connectivity in 2‐month‐old Bangladeshi infants: A feasibility and pilot study

Turesky, T. K., Jensen, S. K. G., Yu, X., Kumar, S., Wang, Y., Sliva, D. D., Gagoski, B. A., Sanfilippo, J. S., Zöllei, L., Boyd, E. C., et al. (2019) · Developmental Science · doi:10.1111/desc.12841 · Cited by 35 · see citing works

Glucocorticoids increase NPY gene expression in the arcuate nucleus by inhibiting mTOR signaling in rat hypothalamic organotypic cultures

Shimizu, H., Arima, H., Ozawa, Y., Watanabe, M., Banno, R., Sugimura, Y., Ozaki, N., Nagasaki, H., & Oiso, Y. (2009) · Peptides · doi:10.1016/j.peptides.2009.09.036 · Cited by 32 · see citing works

Quantitative validation of a nonlinear histology-MRI coregistration method using generalized Q-sampling imaging in complex human cortical white matter

Gangolli, M., Holleran, L., Kim, J. H., Stein, T. D., Alvarez, V. E., McKee, A. C., & Brody, D. L. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.03.059 · Cited by 30 · see citing works

Optimizing treatments for anxiety by age and genetics

Casey, B. J., & Lee, F. S. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12746 · Cited by 21 · see citing works

Cerebral blood flow in 5‐ to 8‐month‐olds: Regional tissue maturity is associated with infant affect

Camacho, M. C., King, L. S., Ojha, A., Garcia, C. M., Sisk, L. M., Cichocki, A. C., Humphreys, K. L., & Gotlib, I. H. (2019) · Developmental Science · doi:10.1111/desc.12928 · Cited by 18 · see citing works

Associations Between Prenatal Maternal Cortisol Levels and the Developing Human Brain

Lenniger, C. J., Espinoza‐Heredia, C., Trentacosta, C. J., & Thomason, M. E. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.02.340 · Cited by 5 · see citing works

Brain structural and functional outcomes in the offspring of women experiencing psychological distress during pregnancy

Wu, Y., De Asis-Cruz, J., & Limperopoulos, C. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02449-0 · Cited by 124 · see citing works

Maternal anxiety, depression and stress affects offspring gut microbiome diversity and bifidobacterial abundances

Galley, J. D., Mashburn‐Warren, L., Blalock, L. C., Lauber, C. L., Carroll, J., Ross, K. M., Hobel, C. J., Coussons‐Read, M. E., Schetter, C. D., & Gur, T. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.10.005 · Cited by 120 · see citing works

Early Social Adversity, Altered Brain Functional Connectivity, and Mental Health

Holz, N. E., Berhe, O., Sacu, S., Schwarz, E., Tesarz, J., Heim, C. C., & Tost, H. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.10.019 · Cited by 114 · see citing works

Mechanisms of neuroplasticity linking early adversity to depression: developmental considerations

Ho, T. C., & King, L. S. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01639-6 · Cited by 108 · see citing works

Prenatal Stress and the Developing Brain: Postnatal Environments Promoting Resilience

Nolvi, S., Merz, E. C., Kataja, E., & Parsons, C. E. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.11.023 · Cited by 108 · see citing works

Concurrent mapping of brain ontogeny and phylogeny within a common space: Standardized tractography and applications

Warrington, S., Thompson, E., Bastiani, M., Dubois, J., Baxter, L., Slater, R., Jbabdi, S., Mars, R. B., & Sotiropoulos, S. N. (2022) · Science Advances · doi:10.1126/sciadv.abq2022 · Cited by 56 · see citing works

Cortisol levels versus self-report stress measures during pregnancy as predictors of adverse infant outcomes: a systematic review

Caparrós-González, R. A., Lynn, F. A., Alderdice, F. A., & Peralta‐Ramírez, M. I. (2022) · Stress · doi:10.1080/10253890.2022.2059348 · Cited by 53 · see citing works

The Effects of Prenatal Exposure to Neighborhood Crime on Neonatal Functional Connectivity

Brady, R. G., Rogers, C. E., Prochaska, T., Kaplan, S., Lean, R. E., Smyser, T. A., Shimony, J. S., Slavich, G. M., Warner, B. B., Barch, D. M., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.01.020 · Cited by 50 · see citing works

Prefrontal cortex development and its implications in mental illness

Goodpaster, C. M., Christensen, C. R., Alturki, M.-B., & DeNardo, L. A. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02154-8 · Cited by 53 · see citing works

Dear reviewers: Responses to common reviewer critiques about infant neuroimaging studies

Korom, M., Camacho, M. C., Filippi, C. A., Licandro, R., Moore, L. A., Dufford, A. J., Zöllei, L., Graham, A. M., Spann, M. N., Howell, B., et al. (2021) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2021.101055 · Cited by 44 · see citing works

Prenatal stress and externalizing behaviors in childhood and adolescence: A systematic review and meta-analysis.

Tung, I., Hipwell, A. E., Grosse, P. J., Battaglia, L., Cannova, E., English, G. E., Quick, A. D., Llamas, B., Taylor, M., & Foust, J. E. (2023) · Psychological Bulletin · doi:10.1037/bul0000407 · Cited by 50 · see citing works

How prenatal exposures shape the infant brain: Insights from infant neuroimaging studies

Dufford, A. J., Spann, M. N., & Scheinost, D. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.09.017 · Cited by 41 · see citing works

A Comprehensive Overview of Stress, Resilience, and Neuroplasticity Mechanisms

Buenrostro-Jáuregui, M. H., Muñoz-Sánchez, S., Rojas-Hernández, J., Alonso-Orozco, A. I., Vega‐Flores, G., Tapia-de-Jesús, A., & Leal‐Galicia, P. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073028 · Cited by 46 · see citing works

Exposure to prenatal maternal distress and infant white matter neurodevelopment

Demers, C. H., Bagonis, M. M., Al‐Ali, K., Garcia, S. E., Styner, M. A., Gilmore, J. H., Hoffman, M. C., Hankin, B. L., & Davis, E. P. (2021) · Development and Psychopathology · doi:10.1017/s0954579421000742 · Cited by 36 · see citing works

The effect of prenatal maternal distress on offspring brain development: A systematic review

Mandl, S., Alexopoulos, J., Doering, S., Wildner, B., Seidl, R., & Bartha, L. (2024) · Early Human Development · doi:10.1016/j.earlhumdev.2024.106009 · Cited by 34 · see citing works

Depression Pathophysiology: Astrocyte Mitochondrial Melatonergic Pathway as Crucial Hub

Anderson, G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010350 · Cited by 29 · see citing works

Maternal Obesity during Pregnancy is Associated with Lower Cortical Thickness in the Neonate Brain

Na, X., Phelan, N. E., Tadros, M. R., Wu, Z., Andres, A., Badger, T. M., Glasier, C. M., Ramakrishnaiah, R. R., Rowell, A. C., Wang, L., et al. (2021) · American Journal of Neuroradiology · doi:10.3174/ajnr.a7316 · Cited by 27 · see citing works

The effects of experience of discrimination and acculturation during pregnancy on the developing offspring brain

Spann, M. N., Alleyne, K., Holland, C. M., Davids, A., Pierre-Louis, A., Bang, C., Oyeneye, V., Kiflom, R., Shea, E., Cheng, B., et al. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01765-3 · Cited by 22 · see citing works

A survey of protocols from 54 infant and toddler neuroimaging research labs

Hendrix, C. L., & Thomason, M. E. (2022) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2022.101060 · Cited by 19 · see citing works

The Translational Future of Stress Neurobiology and Psychosis Vulnerability: A Review of the Evidence

Cullen, A. E., Labad, J., Oliver, D., Al‐Diwani, A., Minichino, A., & Fusar‐Poli, P. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230322145049 · Cited by 22 · see citing works

Hypoconnectivity between anterior insula and amygdala associates with future vulnerabilities in social development in a neurodiverse sample of neonates

Scheinost, D., Chang, J. T., Lacadie, C., Brennan‐Wydra, E., Foster, R., Boxberger, A., Macari, S. L., Vernetti, A., Constable, R. T., Ment, L. R., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-20617-6 · Cited by 18 · see citing works

Multifactorial effects of probiotic Parasutterella excrementihominis on gestational inflammation, offspring behaviour and prenatal-stress induced disruptions in tryptophan metabolism

Galley, J. D., Rajasekera, T. A., Bennouna, D., Batabyal, A., Verosky, B. G., Woodke, S. T., Stokes, J., Brown, A. K., Murthy, S., Kopec, R. E., et al. (2024) · Beneficial Microbes · doi:10.1163/18762891-bja00047 · Cited by 17 · see citing works

Prenatal depressive symptoms are associated with altered structural brain networks in infants and moderated by infant sleep

Donnici, C., Tomfohr‐Madsen, L. M., Long, X., Manning, K. Y., Giesbrecht, G. F., & Lebel, C. A. (2023) · Journal of Affective Disorders · doi:10.1016/j.jad.2023.06.054 · Cited by 17 · see citing works

Advances in fetal and neonatal neuroimaging and everyday exposures

Lautarescu, A., Bonthrone, A., Bos, B., Barratt, B., & Counsell, S. (2024) · Pediatric Research · doi:10.1038/s41390-024-03294-1 · Cited by 16 · see citing works

Maternal trait anxiety symptoms, frontolimbic resting‐state functional connectivity, and cognitive development in infancy

Dufford, A. J., Salzwedel, A., Gilmore, J. H., Gao, W., & Kim, P. (2021) · Developmental Psychobiology · doi:10.1002/dev.22166 · Cited by 16 · see citing works

Prenatal Social Determinants of Health: Narrative review of maternal environments and neonatal brain development

Herzberg, M. P., & Smyser, C. D. (2024) · Pediatric Research · doi:10.1038/s41390-024-03345-7 · Cited by 18 · see citing works

Concurrent and prospective associations between infant frontoparietal and default mode network connectivity and negative affectivity

Ravi, S., Camacho, M. C., Fleming, B., Scudder, M. R., & Humphreys, K. L. (2023) · Biological Psychology · doi:10.1016/j.biopsycho.2023.108717 · Cited by 14 · see citing works

Validation of the Assessment of Parent and Child Adversity (APCA) in Mothers and Young Children

King, L. S., Humphreys, K. L., Shaw, G. M., Stevenson, D. K., & Gotlib, I. H. (2022) · Journal of Clinical Child & Adolescent Psychology · doi:10.1080/15374416.2022.2042696 · Cited by 12 · see citing works

Maternal anxiety during pregnancy is associated with weaker prefrontal functional connectivity in adult offspring

Turk, E., van den Heuvel, M. I., Sleurs, C., Billiet, T., Uyttebroeck, A., Sunaert, S. G., Mennes, M., & den Bergh, B. R. H. V. (2023) · Brain Imaging and Behavior · doi:10.1007/s11682-023-00787-1 · Cited by 12 · see citing works

Introduction to the special issue on childhood adversity and neurodevelopment

Sheridan, M. A., & McLaughlin, K. A. (2022) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2022.101082 · Cited by 12 · see citing works

Two-Hit Model of Behavioral Inhibition and Anxiety

Ostlund, B. D., & Pérez‐Edgar, K. E. (2023) · Annual Review of Developmental Psychology · doi:10.1146/annurev-devpsych-120621-043722 · Cited by 13 · see citing works

Examining the relationship between fetal cortical thickness, gestational age, and maternal psychological distress

Asis‐Cruz, J. D., Kim, J., Krishnamurthy, D., Lopez, C., Kapse, K. J., Andescavage, N. N., Vézina, G., & Limperopoulos, C. (2023) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2023.101282 · Cited by 11 · see citing works

Maternal anxiety‐driven modulation of fetal limbic connectivity designs a backbone linking neonatal brain functional topology to socio‐emotional development in early childhood

Canini, M., Pecco, N., Caglioni, M., Katušić, A., Išasegi, I. Ž., Oprandi, C., Scifo, P., Pozzoni, M., Lorioli, L., Garbetta, G., et al. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25207 · Cited by 10 · see citing works

The medial amygdala’s neural circuitry: Insights into social processing and sex differences

Ignacio, B., Baeza, J., Ruiz, B., Romero, J. P., Yáñez, P., Ramírez, C., Caprile, T., Farkas, C., & Recabal, A. (2025) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2025.101190 · Cited by 9 · see citing works

Prenatal Stress and Maternal Role in Neurodevelopment

Thomason, M. E., & Hendrix, C. L. (2024) · Annual Review of Developmental Psychology · doi:10.1146/annurev-devpsych-120321-011905 · Cited by 13 · see citing works

Neural Network Functional Interactions Mediate or Suppress White Matter–Emotional Behavior Relationships in Infants

Banihashemi, L., Schmithorst, V. J., Bertocci, M. A., Samolyk, A., Zhang, Y., Santos, J. P. L., Versace, A., Taylor, M., English, G. E., Northrup, J. B., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.03.004 · Cited by 9 · see citing works

Supporting Healthy Brain and Behavioral Development During Infancy

Scott, L. S., & Brito, N. H. (2022) · Policy Insights from the Behavioral and Brain Sciences · doi:10.1177/23727322211068172 · Cited by 8 · see citing works

Emotional dysregulation following prenatal stress is associated with altered prefrontal cortex responsiveness to an acute challenge in adolescence

Orso, R., Creutzberg, K. C., Begni, V., Petrillo, G., Cattaneo, A., & Riva, M. A. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111162 · Cited by 8 · see citing works

Atypical brain structure and function in young adults exposed to disaster‐related prenatal maternal stress: Project Ice Storm

Li, X., Qureshi, M. N. I., Laplante, D. P., Elgbeili, G., Jones, S. L., Long, X., Paquin, V., Bezgin, G., Lussier, F., King, S., et al. (2023) · Journal of Neuroscience Research · doi:10.1002/jnr.25246 · Cited by 7 · see citing works

The association between prenatal maternal anxiety, infant brain volumes, and temperament during the COVID-19 pandemic

Paolo, A.-L. D., Nichols, E. S., Tomfohr‐Madsen, L. M., Giesbrecht, G. F., Manning, K. Y., Lebel, C. A., & Duerden, E. G. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03527-9 · Cited by 6 · see citing works

Neural correlates of disaster-related prenatal maternal stress in young adults from Project Ice Storm: Focus on amygdala, hippocampus, and prefrontal cortex

Li, X., Qureshi, M. N. I., Laplante, D. P., Elgbeili, G., Jones, S. L., King, S., & Rosa‐Neto, P. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1094039 · Cited by 6 · see citing works

Circulating FGF21 vs. Stress Markers in Girls during Childhood and Adolescence, and in Their Caregivers: Intriguing Inter-Relations between Overweight/Obesity, Emotions, Behavior, and the Cared-Caregiver Relationship

Christaki, E. V., Pervanidou, P., Papassotiriou, I., Mantzou, A., Giannakakis, G. A., Boschiero, D., & Chrousos, G. P. (2022) · Children · doi:10.3390/children9060821 · Cited by 5 · see citing works

Decreased amygdala-sensorimotor connectivity mediates the association between prenatal stress and broad autism phenotype in young adults: Project Ice Storm

Li, X., Qureshi, M. N. I., Laplante, D. P., Elgbeili, G., Paquin, V., Jones, S. L., King, S., & Rosa‐Neto, P. (2023) · Stress · doi:10.1080/10253890.2023.2293698 · Cited by 4 · see citing works

The Regulation of Neuro-immune System by Pi (Parasympathetic) and SiGMA (Sympathetic Induction Governed by Meditation and Asana) Rhythmicity

Arora, R., Verma, H., Banumathy, N., & Sharma, M. (2024) · Springer eBooks · doi:10.1007/978-981-97-2851-0_2 · Cited by 4 · see citing works

Les stress pendant les 1 000 premiers jours de la vie quand tout commence

Verney, C., & Vitalis, T. (2023) · médecine/sciences · doi:10.1051/medsci/2023124 · Cited by 3 · see citing works

Prenatal stress and gestational epigenetic age: no evidence of associations based on a large prospective multi-cohort study

Murgatroyd, C., Salontaji, K., Smajlagić, D., Page, C. M., Sanders, F., Jugessur, A., Lyle, R., Tsotsi, S., Haftorn, K. L., Felix, J. F., et al. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-04405-8 · Cited by 3 · see citing works

Prenatal anticipatory stress: Baby preparation and worry scale-revised in the Dutch context

Bruinhof, N., Sehic, E., Hancock, G. R., Gartstein, M. A., & de Weerth, C. (2023) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2023.152437 · Cited by 3 · see citing works

Data representing expert ratings of emotional tone in adjectives used to describe infants and young children

Hill, K. E., Guyon‐Harris, K. L., & Humphreys, K. L. (2024) · Data in Brief · doi:10.1016/j.dib.2024.110745 · Cited by 3 · see citing works

Human amygdala-like telencephalic organoids model stress circuitry in assembloid systems

Yang, W. S., Choe, M. S., Lo, C., Liu, H.-W., Cho, Y. M., Kim, J., Kiral, F. R., Scandura, M., Lu, X., Kim, K.-Y., et al. (2026) · Cell stem cell · doi:10.1016/j.stem.2026.04.021 · Cited by 2 · see citing works

Through a teratological lens: A narrative review of exposure to stress and drugs of abuse during pregnancy on neurodevelopment

Willford, J. A., & Kaufman, J. M. (2024) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2024.107384 · Cited by 2 · see citing works

Prenatal Household Income Instability and Infant Subcortical Brain Volumes

Patterson, G., Dufford, A. J., Morrissey, T. W., Styner, M. A., Kim, S. H., & Kim, P. (2025) · Developmental Science · doi:10.1111/desc.70022 · Cited by 3 · see citing works

Maternal prenatal psychological distress and vitamin intake with children’s neurocognitive development

Ssewanyana, D., Knight, J. A., Matthews, S. G., Wong, J., Khani, N. A., Lye, J., Murphy, K. E., Foshay, K., Okeke, J. C., Lye, S. J., et al. (2022) · Pediatric Research · doi:10.1038/s41390-022-02003-0 · Cited by 2 · see citing works

The effects of ethnoracial-related stressors during pregnancy on the developing offspring brainPreprint

Spann, M. N., Alleyne, K., Holland, C. M., Davids, A., Pierre-Louis, A., Bang, C., Oyeneye, V., Kiflom, R., Shea, E., Cheng, B., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.08.503168 · Cited by 2 · see citing works

A two-hit model of behavioral inhibition and anxietyPreprint

Ostlund, B. D., & Pérez‐Edgar, K. E. (2023) · doi:10.31234/osf.io/ucdq4 · Cited by 2 · see citing works

Assessment of Prenatal Transportation Stress and Sex on Gene Expression Within the Amygdala of Brahman Calves

Baker, E. C., Riley, D. G., Cardoso, R. C., Hairgrove, T. B., Long, C. R., Randel, R. D., & Welsh, T. H. (2024) · Biology · doi:10.3390/biology13110915 · Cited by 1 · see citing works

Prenatal stress and cortical morphometric similarity network in offspring: Transcriptional signatures of associated genes

Zhang, J., Zhang, Y., Chen, Y., & Zhu, J. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.119519 · Cited by 1 · see citing works

Timing of Prenatal Stress Exposure Predicts Infant Sympathetic Nervous System and Affective Responses

Martinez‐Torteya, C., Nuttall, A. K., Bogat, G. A., Lonstein, J. S., Muzik, M., Grimm, K. J., Granger, D. A., & Levendosky, A. A. (2026) · Developmental Psychobiology · doi:10.1002/dev.70140 · Cited by 1 · see citing works

Hypoconnectivity between anterior insula and amygdala in neonates with familial history of autismPreprint

Scheinost, D., Chang, J., Lacadie, C., Brennan‐Wydra, E., Foster, R., Boxberger, A., Macari, S. L., Vernetti, A., Constable, R. T., Ment, L. R., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.24.481850

Mindfulness-Based Interventions during Pregnancy and Labour

Merchante, M. S., & Martinez-Hurtado, E. D. (2022) · Recent advances in anesthesiology · doi:10.2174/9789815051841122040022

Stress and Pain

Steck, B. (2023) · Springer eBooks · doi:10.1007/978-3-031-33038-4_3

The Impact of Early Life Experiences on Stress Neurobiology and the Development of Anxiety

Niu, Y., Camacho, M. C., Wu, S., & Humphreys, K. L. (2024) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_542

Neurodevelopmental Pathways from Temperamental Fear to Anxiety

Shin, E., & Pérez‐Edgar, K. E. (2025) · Current topics in behavioral neurosciences · doi:10.1007/7854_2024_571

Association of maternal antenatal distress with child amygdala-prefrontal cortex functional connectivity at 2–3 years in a South African birth cohort study

Miles, M., Wedderburn, C. J., Fairchild, G. F., Lake, M. T., Narr, K. L., Joshi, S. H., Lawrence, M., Hoffman, N., Groenewold, N. A., Barnett, W., et al. (2026) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2026.111836

Modulation of dendritic development by the neuronal hemoglobin: Role of beta-hemoglobin deficit in mediating prenatal stress-related affective disorders

Zhang, Y., Zhang, X., Liang, J., Huang, Y., Zhang, H., Feng, L., Wang, Z., Zhang, L., Yang, J., Yang, W., et al. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107426

Trauma in Attachment: Understanding the First Relationship Through Neurobiology and Psychodynamics

Chambers, J. E., & Sullivan, R. (2026) · Psychodynamic Psychiatry · doi:10.1521/pdps.2026.54.2.249

Prenatal Environmental Unpredictability: Effects on Neonatal Functional Connectivity and Socioemotional Functioning During Infancy

Chin, J. (2026) · doi:10.56902/etdcrp.2026.74

Trajectory of maternal perinatal negative psychological states and its association with early offspring neurodevelopment: A longitudinal cohort study

Du, Y., Cao, Y., Cheng, Z., Zhu, X., Chen, T., Liu, H., & Zhang, F. (2026) · Journal of Affective Disorders · doi:10.1016/j.jad.2026.122584

Prenatal stress alters amygdala functional connectivity in preterm neonates

Scheinost, D., Kwon, S. H., Lacadie, C., Sze, G., Sinha, R., Constable, R. T., & Ment, L. R. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.08.010 · Cited by 130 · see citing works

Amygdala-prefrontal functional connectivity mediates the effects of COVID-related prenatal stress on infant temperament

Li, X., Long, X., Manning, K. Y., Jaffer, A., Giesbrecht, G. F., Tomfohr‐Madsen, L. M., Donnici, C., Oberlander, T. F., & Lebel, C. A. (2025) · Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition · doi:10.58530/2025/3553

Amygdala–medial prefrontal cortex connectivity relates to stress and mental health in early childhood

Park, A. T., Leonard, J., Saxler, P. K., Cyr, A. B., Gabrieli, J. D. E., & Mackey, A. P. (2018) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsy017 · Cited by 81 · see citing works

Neural correlates of prenatal stress in young women

Favaro, A., Tenconi, E., Degortes, D., Manara, R., & Santonastaso, P. (2015) · Psychological Medicine · doi:10.1017/s003329171500046x · Cited by 51 · see citing works

3.20 The Trajectory of Maternal Prenatal Stress is Associated With Newborn Amygdala Functional Connectivity and Infant Negative Affect Development Over the First Two Years of Life

Marr, M. C., Graham, A. M., Feczko, E., Thomas, E., Sturgeon, D., Schifsky, E., Rasmussen, J. M., Gilmore, J. H., Styner, M. A., Potkin, S. G., et al. (2018) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2018.09.178 · Cited by 3 · see citing works