Cited by 462Neurogenesis and neuroplasticity mechanismsNeonatal and fetal brain pathologyFetal and Pediatric Neurological Disorders

The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.

The development of the subplate and thalamocortical connections in the human foetal brain

Kostović, Ivica, Judaš, Miloš·2010·Acta Paediatrica

DOI 10.1111/j.1651-2227.2010.01811.x

Open this paper in CoChat — free account

Abstract

The aim of this review is to present clinically relevant data on prenatal development of thalamocortical connections in the human brain. The analysis is based on extensive Zagreb Neuroembryological Collection, including more than 500 prenatal human brains stained with various classical neurohistological, as well as modern histochemical and immunohistochemical methods. The connection of thalamocortical axons during the ‘waiting’ period with transient cortical subplate zone and subsequent synaptic engagement in the cortical plate is the main connectivity event in the late foetus and preterm infant. This connectivity is the structural substrate for the endogeneous subplate and sensory‐driven circuitry generating transient electrical phenomena and may represent a transient network in the developmental history of consciousness. Conclusion: Findings presented in this review should be considered in the management of pain in preterm infants, in searching for the vulnerability of the subplate zone in diagnostic procedures using the in vivo MRI and in revealing the developmental origin of cognitive and mental disorders.

Integrity signals

Registry

Crossref · 10.1111/j.1651-2227.2010.01811.x

Cites

75 of 75 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Untitled work
(1909) · Cited by 2,575
Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances
Volpe, J. J. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70294-1 · Cited by 2,501
Pain and Its Effects in the Human Neonate and Fetus
Anand, K. J. S., & Hickey, P. R. (1987) · New England Journal of Medicine · doi:10.1056/nejm198711193172105 · Cited by 1,715
Normal development of brain circuits
Tau, G. Z., & Peterson, B. S. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.115 · Cited by 1,391
Fiber Pathways of the Brain
Schmahmann, J. D., & Pandya, D. N. (2006) · doi:10.1093/acprof:oso/9780195104233.001.0001 · Cited by 1,157
Developmental history of the transient subplate zone in the visual and somatosensory cortex of the macaque monkey and human brain
Kostović, I., & RAKIC, P. T. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902970309 · Cited by 912
Self-citation
The development of nociceptive circuits
Fitzgerald, M. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1701 · Cited by 778
Prenatal development of the visual system in rhesus monkey
RAKIC, P. T., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0040 · Cited by 739
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
The Subplate, A Transient Neocortical Structure: Its Role in the Development of Connections between Thalamus and Cortex
Allendoerfer, K. L., & Shatz, C. J. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001153 · Cited by 653

Show all 75 references

Research works printed but not linked: 1

Kostović I, 1974, A new interpretation of the laminar development of cerebral cortex: synaptogenesis in different layers of neopallium in the human fetus, Anat Rec, 178, 395

Sorted by citations

Items 201–300 of 460

Early metabolic development of posteromedial cortex and thalamus in humans analyzed via in vivo quantitative magnetic resonance spectroscopy
Degnan, A. J., Ceschin, R. C., Lee, V., Schmithorst, V. J., Blüml, S., & Panigrahy, A. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23634 · Cited by 22
Mental development is associated with cortical connectivity of the ventral and nonspecific thalamus of preterm newborns
András, J., Natalucci, G., Koller, B. M., Tuura, R., Rüegger, C. M., & Hagmann, C. F. (2020) · Brain and Behavior · doi:10.1002/brb3.1786 · Cited by 22
Clinical signs and electroencephalographic patterns of emergence from sevoflurane anaesthesia in children
Cornelissen, L., Donado, C., Lee, J. M., Liang, N. E., Mills, I., Tou, A. M., Bilge, A., & Berde, C. B. (2017) · European Journal of Anaesthesiology · doi:10.1097/eja.0000000000000739 · Cited by 22
Subcortico-Cortical Functional Connectivity in the Fetal Brain: A Cognitive Development Blueprint
Canini, M., Cavoretto, P. I., Scifo, P., Pozzoni, M., Petrini, A., Iadanza, A., Pontesilli, S., Scotti, R., Candiani, M., Falini, A., et al. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa008 · Cited by 22
Overview of the Development of the Human Brain and Spinal Cord
ten Donkelaar, H. J., Yamada, S., Shiota, K., & van der Vliet, T. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_1 · Cited by 22
Process of cortical network formation and impact of early brain damage
Kiss, J. Z., Vasung, L., & Petrenko, V. (2014) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000068 · Cited by 22
Music impacts brain cortical microstructural maturation in very preterm infants: A longitudinal diffusion MR imaging study
de Almeida, J. S., Baud, O., Fau, S., Munoz, F. B., Courvoisier, S., Lordier, L., Lazeyras, F., & Hüppi, P. S. (2023) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2023.101254 · Cited by 24
The Newborn's Reaction to Light as the Determinant of the Brain's Activation at Human Birth
Polese, D., Riccio, M. L., Fagioli, M., Mazzetta, A., Fagioli, F., Parisi, P., & Fagioli, M. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.933426 · Cited by 22
Dendritic Spines: Synaptogenesis and Synaptic Pruning for the Developmental Organization of Brain Circuits
Petanjek, Z., Banovac, I., Sedmak, D., & Hladnik, A. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_4 · Cited by 34
A brain-age model for preterm infants based on functional connectivity
Lavanga, M., Wel, O. D., Caicedo, A., Jansen, K., Dereymaeker, A., Naulaers, G., & Huffel, S. V. (2018) · Physiological Measurement · doi:10.1088/1361-6579/aabac4 · Cited by 21
Basal ganglia and thalamic tract connectivity in very preterm and full-term children; associations with 7-year neurodevelopment
Thompson, D. K., Loh, W. Y., Connelly, A., Cheong, J. L. Y., Spittle, A. J., Chen, J., Kelly, C. E., Inder, T. E., Doyle, L. W., & Anderson, P. J. (2019) · Pediatric Research · doi:10.1038/s41390-019-0546-x · Cited by 21
IS FOUR-DIMENSIONAL (4D) ULTRASOUND ENTERING A NEW FIELD OF FETAL PSYCHIATRY?
Kurjak, A., Stanojević, M., Salihagič-Kadić, A., Barišić, L. S., & Jakovljević, M. (2019) · Psychiatria Danubina · doi:10.24869/psyd.2019.133 · Cited by 21
Developmental synergy between thalamic structure and interhemispheric connectivity in the visual system of preterm infants
Ceschin, R. C., Wisnowski, J. L., Paquette, L. B., Nelson, M. D., Blüml, S., & Panigrahy, A. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.05.014 · Cited by 20
Brain Development in Preterm Infants Assessed Using Advanced MRI Techniques
Tusor, N., Arichi, T., Counsell, S. J., & Edwards, A. D. (2013) · Clinics in Perinatology · doi:10.1016/j.clp.2013.10.001 · Cited by 20
High Resolution MRI Reveals Detailed Layer Structures in Early Human Fetal Stages: In Vitro Study with Histologic Correlation
Wang, R., Dai, G., & Takahashi, E. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00150 · Cited by 20
Cortical responses to tactile stimuli in preterm infants
Leikos, S., Tokariev, A., Koolen, N., Nevalainen, P., & Vanhatalo, S. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14613 · Cited by 19
Impaired structural connectivity between dorsal attention network and pulvinar mediates the impact of premature birth on adult visual–spatial abilities
Berndt, M. T., Bäuml, J., Menegaux, A., Meng, C., Daamen, M., Baumann, N., Zimmer, C., Boecker, H., Bartmann, P., Dieter Wolke, C., et al. (2019) · Human Brain Mapping · doi:10.1002/hbm.24685 · Cited by 20
A neural window on the emergence of cognition
Cusack, R., Ball, G., Smyser, C. D., & Dehaene‐Lambertz, G. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13036 · Cited by 23
Structural and functional brain connectivity in moderate–late preterm infants with low-grade intraventricular hemorrhage
Argyropoulou, M. I., Xydis, V. G., Drougia, A. A., Giantsouli, A., Giapros, V. I., & Astrakas, L. G. (2021) · Neuroradiology · doi:10.1007/s00234-021-02770-3 · Cited by 18
Functional thalamocortical connectivity development and alterations in preterm infants during the neonatal period
Cai, Y., Wu, X., Su, Z., Shi, Y., & Gao, J. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.011 · Cited by 19
Assessment of Comfort during Less Invasive Surfactant Administration in Very Preterm Infants: A Multicenter Study
Pichler, K., Kuehne, B., Dekker, J., Stummer, S., Giordano, V., Berger, A., Kribs, A., & Klebermaß-Schrehof, K. (2023) · Neonatology · doi:10.1159/000530333 · Cited by 17
Neuronal Coupling Modes Show Differential Development in the Early Cortical Activity Networks of Human Newborns
Yrjölä, P., Vanhatalo, S., & Tokariev, A. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1012-23.2024 · Cited by 19
Are We Ready to investigate Cognitive Function of Fetal Brain? The Role of Advanced Four-dimensional Sonography
Kadić, A. S., & Barišić, L. S. (2016) · Donald School Journal of Ultrasound in Obstetrics & Gynecology · doi:10.5005/jp-journals-10009-1453 · Cited by 17
Frequency of Spontaneous BOLD Signal Differences between Moderate and Late Preterm Newborns and Term Newborns
Wu, X., Wei, L., Wang, N., Hu, Z., Wang, L., Ma, J., Feng, S., Cai, Y., Song, X., & Shi, Y. (2016) · Neurotoxicity Research · doi:10.1007/s12640-016-9642-4 · Cited by 21
Reduced thalamic volume in preterm infants is associated with abnormal white matter metabolism independent of injury
Wisnowski, J. L., Ceschin, R. C., Choi, S., Schmithorst, V. J., Painter, M. J., Nelson, M. D., Blüml, S., & Panigrahy, A. (2015) · Neuroradiology · doi:10.1007/s00234-015-1495-7 · Cited by 17
Development of the Ontogenetic Self-Regulation Clock
Ferber, S. G., Weller, A., Ben‐Shachar, M., Klinger, G., & Geva, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020993 · Cited by 17
The suppression curve as a quantitative approach for measuring brain maturation in preterm infants
Dereymaeker, A., Koolen, N., Jansen, K., Vervisch, J., Ortibus, E., Vos, M. D., Huffel, S. V., & Naulaers, G. (2016) · Clinical Neurophysiology · doi:10.1016/j.clinph.2016.05.362 · Cited by 16
Amplitude-integrated EEG and range-EEG modulation associated with pneumatic orocutaneous stimulation in preterm infants
Barlow, S. M., Jegatheesan, P., Weiss, S., Govindaswami, B., Wang, J., Lee, J., Oder, A. L., & Song, D. (2013) · Journal of Perinatology · doi:10.1038/jp.2013.150 · Cited by 16
Gut Microbiota and Neurodevelopment in Preterm Infants: Mechanistic Insights and Prospects for Clinical Translation
Dai, K., Ding, L., Yang, X., Wang, S., & Rong, Z. (2025) · Microorganisms · doi:10.3390/microorganisms13092213 · Cited by 17
Abnormal Development of Thalamic Microstructure in Premature Neonates with Congenital Heart Disease
Paquette, L. B., Votava‐Smith, J. K., Ceschin, R. C., Nagasunder, A., Jackson, H. A., Blüml, S., Wisnowski, J. L., & Panigrahy, A. (2015) · Pediatric Cardiology · doi:10.1007/s00246-015-1106-8 · Cited by 15
Advances in functional and diffusion neuroimaging research into the long-term consequences of very preterm birth
Kanel, D., Counsell, S., & Nosarti, C. (2020) · Journal of Perinatology · doi:10.1038/s41372-020-00865-y · Cited by 14
MRI assessment of neonatal brain maturation
Girard, N. J., Dory‐Lautrec, P., Koob, M., & Dediu, M. (2012) · Imaging in Medicine · doi:10.2217/iim.12.59 · Cited by 15
Changing subplate circuits: Early activity dependent circuit plasticity
Mukherjee, D., & Kanold, P. O. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1067365 · Cited by 19
Paradigm shift in consciousness research: the child′s self‐awareness and abnormalities in autism, ADHD and schizophrenia
Lou, H. C. (2011) · Acta Paediatrica · doi:10.1111/j.1651-2227.2011.02456.x · Cited by 14
Prenatal Development of the Human Fetal Telencephalon
Judáš, M. (2010) · Medical radiology · doi:10.1007/174_2010_119 · Cited by 14
Infant Emotion Development and Temperament
Aktar, E., & Pérez‐Edgar, K. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.026 · Cited by 17
Brain Maturation, Early Sensory Processing, and Infant Colic
Leuchter, R. H., Darqué, A., & Hüppi, P. S. (2013) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/01.mpg.0000441929.05684.78 · Cited by 13
The role of self-touch experience in the formation of the selfPreprint
Hoffmann, M. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1712.07843 · Cited by 14
Fetal neuroimaging applications for diagnosis and counseling of brain anomalies: Current practice and future diagnostic strategies
Tarui, T., Gimovsky, A. C., & Madan, N. (2024) · Seminars in Fetal and Neonatal Medicine · doi:10.1016/j.siny.2024.101525 · Cited by 13
The Subplate Layers: The Superficial and Deep Subplate Can be Discriminated on 3 Tesla Human Fetal Postmortem MRI
Pogledić, I., Schwartz, E., Mitter, C., Baltzer, P., Milos, R., Gruber, G. M., Brugger, P. C., Hainfellner, J. A., Bettelheim, D., Langs, G., et al. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa099 · Cited by 13
Atypical brain structure mediates reduced IQ in young adults born preterm with very low birth weight
Rimol, L. M., Rise, H. H., Evensen, K. A. I., Yendiki, A., Løhaugen, G. C. C., Indredavik, M. S., Brubakk, A., Bjuland, K. J., Eikenes, L., Weider, S., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119816 · Cited by 14
On the origins of autism: The Quantitative Threshold Exposure hypothesis
Crawford, S. (2015) · Medical Hypotheses · doi:10.1016/j.mehy.2015.10.006 · Cited by 13
Effect of antenatal growth and prematurity on brain white matter: diffusion tensor study
PIPARI study group, Lepomäki, V., Paavilainen, T., Matomäki, J., Hurme, S. A. M., Haataja, L. M., Lapinleimu, H., Lehtonen, L., Komu, M. E. S., & Parkkola, R. K. (2012) · Pediatric Radiology · doi:10.1007/s00247-012-2352-z · Cited by 13
The Awakening of the Newborn Human Infant and the Emergence of Consciousness
Lagercrantz, H. (2025) · Acta Paediatrica · doi:10.1111/apa.70031 · Cited by 12
Development of the human fetal brain and the influence of prenatal damaging factors on the main stages of neurogenesis
Sidorova, I. S., Nikitina, N. A., Unanyan, A. L., & Борисович, А. М. (2022) · Russian Bulletin of Obstetrician-Gynecologist · doi:10.17116/rosakush20222201135 · Cited by 12
Altered development of structural MRI connectome hubs at near-term age in very and moderately preterm infants
Jang, Y. H., Kim, H., Lee, J. Y., Ahn, J., Chung, A. W., & Lee, H. J. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac438 · Cited by 11
Preterm Modulation of Connectivity by Endogenous Generators: The Theta Temporal Activities in Coalescence with Slow Waves
Adebimpe, A., Routier, L., & Wallois, F. (2019) · Brain Topography · doi:10.1007/s10548-019-00713-z · Cited by 12
Evaluating Complexity of Fetal MEG Signals: A Comparison of Different Metrics and Their Applicability
Moser, J., Bensaid, S., Kroupi, E., Schleger, F., Wendling, F., Ruffini, G., & Preissl, H. T. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00023 · Cited by 15
Fetal Pain: The Science Behind Why It Is the Medical Standard of Care
Pierucci, R. (2020) · The Linacre Quarterly · doi:10.1177/0024363920924877 · Cited by 12
Home-based early stimulation program targeting visual and motor functions for preterm infants with delayed tracking: Feasibility of a Randomized Clinical Trial
Rodovanski, G. P., Réus, B. A. B., Damiani, A. V. C., Mattos, K. F., Moreira, R. S., & dos Santos, A. N. (2021) · Research in Developmental Disabilities · doi:10.1016/j.ridd.2021.104037 · Cited by 12
Long-term effects of pain in children
GRUNAU, R. E. (2013) · Oxford University Press eBooks · doi:10.1093/med/9780199642656.003.0004 · Cited by 12
Monitoring Effective Connectivity in the Preterm Brain: A Graph Approach to Study Maturation
Lavanga, M., Wel, O. D., Caicedo, A., Jansen, K., Dereymaeker, A., Naulaers, G., & Huffel, S. V. (2017) · Complexity · doi:10.1155/2017/9078541 · Cited by 12
Cross-Cultural Perspectives on Parent–Infant Interactions
Bornstein, M. H., & Esposito, G. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.029 · Cited by 12
Fatty Acids: A Safe Tool for Improving Neurodevelopmental Alterations in Down Syndrome?
Martínez‐Cué, C., & Bartesaghi, R. (2022) · Nutrients · doi:10.3390/nu14142880 · Cited by 10
Early and late anti nociceptive effects of sucrose on neonatal inflammatory pain in rats: Comparison to a non-steroidal anti-inflammatory drug
Nuseir, K. Q., Altarifi, A., Tasslaq, A., Alhusban, A. Y., & Alzoubi, K. H. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.03.014 · Cited by 11
Pre- and Postnatal Damage to the Retro-Geniculate Visual Pathways Cause Retinal Degeneration Predictive for Visual Function
Lennartsson, F., Öhnell, H. M., Jacobson, L. K., & Nilsson, M. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.734193 · Cited by 11
Somatosensory evoked potentials in children with autism
Azouz, H. G., Khalil, M., Ghani, H. M. A. E., & Hamed, H. M. (2013) · Alexandria Journal of Medicine · doi:10.1016/j.ajme.2013.07.002 · Cited by 11
Fetal functional imaging portrays heterogeneous development of emerging human brain networks
Jakab, A., Schwartz, E., Kasprian, G., Gruber, G. M., Prayer, D., SchÃ¶pf, V., & Langs, G. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00852 · Cited by 10
From sensory motor and perceptual development to primary consciousness in the fetus: converging neural, behavioral, and imaging correlates of cognition-mediated emergent transitions
Leisman, G., Alfasi, R., & D’Angiulli, A. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101455 · Cited by 12
An intrinsic hierarchical, retinotopic organization of visual pulvinar connectivity in the human neonate
Ayzenberg, V., Song, C., & Arcaro, M. J. (2024) · Current Biology · doi:10.1016/j.cub.2024.11.042 · Cited by 13
Development of the basic architecture of neocortical circuitry in the human fetus as revealed by the coupling spatiotemporal pattern of synaptogenesis along with microstructure and macroscale in vivo MR imaging
Kostović, I. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02838-9 · Cited by 12
Self-citation
Multimodal assessment shows misalignment of structural and functional thalamocortical connectivity in children and adolescents born very preterm
Wehrle, F. M., Lustenberger, C., Buchmann, A., Latal, B., Hagmann, C. F., Tuura, R., & Huber, R. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116779 · Cited by 10
Evolution of cross-frequency coupling between endogenous oscillations over the temporal cortex in very premature neonates
Saadatmehr, B., Edalati, M., Routier, L., Mahmoudzadeh, M., Safaie, J., Kongolo, G., Ghostine, G., Wallois, F., & Moghimi, S. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac067 · Cited by 10
FACILITATED TUCKING EFFECTIVE TO PAIN RELIEF ON THE PRETERM INFANTS IN PERINATAL UNIT IN JAKARTA
Oktaviani, E., Rustina, Y., & Efendi, D. (2018) · Jurnal Keperawatan Indonesia · doi:10.7454/jki.v21i1.539 · Cited by 9
Development and Developmental Disorders of the Cerebral Cortex
ten Donkelaar, H. J., Lammens, M. M. Y., Aronica, E., van Bokhoven, H., Ulzen, K. K.-V., & Hori, A. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_10 · Cited by 9
Auditory structural connectivity in preterm and healthy term infants during the first postnatal year
Zubiaurre‐Elorza, L., Linke, A. C., Herzmann, C., Wild, C. J., Duffy, H., Lee, D. S. C., Han, V. K. M., & Cusack, R. (2018) · Developmental Psychobiology · doi:10.1002/dev.21610 · Cited by 9
Brain Development in Infants
Richards, J. E., & Conte, S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.004 · Cited by 12
When the Mind Comes to Live Inside the Body: The Ontogeny of the Perceptual Control Clock
Ferber, S. G., Geva, R., & Weller, A. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220411095508 · Cited by 9
Thalamus–cortex interactions drive cell type–specific cortical development in human pluripotent stem cell–derived assembloids
Nishimura, M., Adachi, S., Kodera, T., Sato, A., Takeuchi, R. F., & Osakada, F. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2506573122 · Cited by 10
Sensory event-related potential morphology predicts age in premature infants
Zandvoort, C. S., van der Vaart, M., Robinson, S., Usman, F., Mellado, G. S., Fry, R. E., Worley, A., Adams, E., Slater, R., Baxter, L., et al. (2023) · Clinical Neurophysiology · doi:10.1016/j.clinph.2023.11.007 · Cited by 8
At First Sight: Fetal Eye Movements Reveal a Preference for Face‐Like Configurations From 26 Weeks of Gestation
Ronga, I., Poles, K., Pace, C., Fantoni, M., Luppino, J., Gaglioti, P., Todros, T., & Garbarini, F. (2025) · Developmental Science · doi:10.1111/desc.13597 · Cited by 11
Neural Transcription Correlates of Multimodal Cortical Phenotypes during Development
Pecheva, D., Lee, A., Poh, J. S., Chong, Y. S., Shek, L. P., Gluckman, P. D., Meaney, M. J., Fortier, M. V., & Qiu, A. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz271 · Cited by 8
Brain tissue volumes at term‐equivalent age are associated with early motor behavior in very preterm infants
Katušić, A., Raguž, M., & Išasegi, I. Ž. (2020) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10039 · Cited by 8
Action in Development
Rachwani, J., Hoch, J. E., & Adolph, K. E. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.017 · Cited by 9
Multi-scale structural rich-club organization of the brain in full-term newborns: a combined DWI and fMRI study
Fouladivanda, M., Kazemi, K., Makki, M., Khalilian, M., Danyali, H., Gervain, J., & Aarabi, A. (2021) · Journal of Neural Engineering · doi:10.1088/1741-2552/abfd46 · Cited by 9
Consistently lower volumes across thalamus nuclei in very premature-born adults
Thalhammer, M., Nimpal, M., Schulz, J., Meedt, V., Menegaux, A., Schmitz‐Koep, B., Daamen, M., Boecker, H., Zimmer, C., Priller, J., et al. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120732 · Cited by 7
The cumulative impact of clinical risk on brain networks and associations with executive function impairments in adolescents with congenital heart disease
Ehrler, M., Speckert, A., Kretschmar, O., Tuura, R., Latal, B., & András, J. (2024) · Human Brain Mapping · doi:10.1002/hbm.70028 · Cited by 9
Longitudinal Measurement of the Developing Thalamus in the Preterm Brain Using Multi-modal MRI
Eaton-Rosen, Z., Melbourne, A., Orasanu, E., Marc Modat, A., Cardoso, M. J., Bainbridge, A. P., Kendall, G. S., Robertson, N. J., Marlow, N., & Sebastien Ourselin, A. (2014) · Lecture notes in computer science · doi:10.1007/978-3-319-10470-6_35 · Cited by 8
Modulation of EEG spectral edge frequency during patterned pneumatic oral stimulation in preterm infants
Song, D., Jegatheesan, P., Pooley, S., Govindaswami, B., Wang, J., Lee, J., Oder, A. L., & Barlow, S. M. (2013) · Pediatric Research · doi:10.1038/pr.2013.179 · Cited by 8
Interhemispheric connectivity estimated from EEG time-correlation analysis in preterm infants with normal follow-up at age of five
Meijer, E. J., Niemarkt, H. J., Raaijmakers, I. I., Mulder, A., van Pul, C., Wijn, P. F. F., & Andriessen, P. (2016) · Physiological Measurement · doi:10.1088/1361-6579/37/12/2286 · Cited by 9
Infant Object Manipulation and Play
Tamis‐LeMonda, C. S., & Lockman, J. J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.019 · Cited by 8
Organizational Events
Kinney, H. C., & Volpe, J. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-323-42876-7.00007-7 · Cited by 8
Perinatal development of structural thalamocortical connectivity
Oldham, S., Sina Mansour, L., & Ball, G. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00418 · Cited by 7
Linking histology and neurological development of the fetal and infant brain
Kostović, I., Katušić, A., & Srzentić, M. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817986-4.00019-5 · Cited by 8
Self-citation
The effect of preterm birth on thalamic development based on shape and structural covariance analysis
Li, H., Liu, M., Zhang, J., Liu, S., Fang, Z., Pan, M., Sui, X., Rang, W., Xiao, H., Jiang, Y., et al. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120708 · Cited by 7
Neural oscillations suggest periodicity encoding during auditory beat processing in the premature brain
Edalati, M., Wallois, F., Ghostine, G., Kongolo, G., Trainor, L. J., & Moghimi, S. (2024) · Developmental Science · doi:10.1111/desc.13550 · Cited by 11
The developing Human Connectome Project fetal functional MRI release: Methods and data structures
Karolis, V. R., Cordero‐Grande, L., Price, A. N., Hughes, E., Fitzgibbon, S. P., Kyriakopoulou, V., Uus, A. U., Harper, N., Prokopenko, D. A., Bridglal, D., et al. (2025) · Imaging Neuroscience · doi:10.1162/imag_a_00512 · Cited by 11
Overview of the Development of the Human Brain and Spinal Cord
ten Donkelaar, H. J., Takakuwa, T., Vasung, L., Yamada, S., Shiota, K., & van der Vliet, T. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_1 · Cited by 8
The maternal-fetal neurodevelopmental groundings of preterm birth risk
Miglioli, C., Canini, M., Vignotto, E., Pecco, N., Pozzoni, M., Victoria‐Feser, M., Guerrier, S., Candiani, M., Falini, A., Baldoli, C., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e28825 · Cited by 7
A perinatal stress calculator for the neonatal intensive care unit: an unobtrusive approach
Lavanga, M., Smets, L., Bollen, B., Jansen, K., Ortibus, E., Huffel, S. V., Naulaers, G., & Caicedo, A. (2020) · Physiological Measurement · doi:10.1088/1361-6579/ab9b66 · Cited by 7
Infant Vocal Learning and Speech Production
Warlaumont, A. S. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.022 · Cited by 10
The Development of Infant Feeding
Mennella, J. A., Forestell, C. A., Ventura, A. K., & Fisher, J. O. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.010 · Cited by 7
How to grow a self: development of self-representation in the Bayesian brain
Wozniak, M. M. (2024) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2024.1441931 · Cited by 15
Developmental anatomy of the thalamus, perinatal lesions, and neurological development
Govaert, P. P., Arena, R., Dudink, J., Steggerda, S. J., Agut, T., Marissens, G., Hoebeek, F. E., & EurUS.Brain group (2024) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.15992 · Cited by 7
Infant Attachment (to Mother and Father) and Its Place in Human Development
Dagan, O., & Sagi‐Schwartz, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108351959.025 · Cited by 6
Differential maturation of the brain networks required for the sensory, emotional, and cognitive aspects of pain in human newborns
Jones, L., Batallé, D., Meek, J. H., Edwards, A. D., Fitzgerald, M., Arichi, T., & Lorenzo Fabrizi, D. (2025) · Pain · doi:10.1097/j.pain.0000000000003619 · Cited by 6
Fetal neurobehavior and consciousness: a systematic review of 4D ultrasound evidence and ethical challenges
Pramono, M. B. A., Andonotopo, W., Bachnas, M. A., Dewantiningrum, J., Sanjaya, I. N. H., Sulistyowati, S., Stanojević, M., & Kurjak, A. (2025) · Journal of Perinatal Medicine · doi:10.1515/jpm-2025-0281 · Cited by 5
Abnormal thalamocortical connectivity of preterm infants with elevated thyroid stimulating hormone identified with diffusion tensor imaging
Jang, Y. H., Kim, J., Kim, S., Lee, K., Na, J. Y., Ahn, J., Kim, H., Kim, B.-N., & Lee, H. J. (2022) · Scientific Reports · doi:10.1038/s41598-022-12864-4 · Cited by 5
Oxidative Stress Biomarkers and Early Brain Activity in Extremely Preterm Infants: A Prospective Cohort Study
Coviello, C., Perrone, S., Buonocore, G., Negro, S., Longini, M., Groenendaal, F., Vijlbrief, D. C., Dani, C., Benders, M. J. N. L., & Tataranno, M. L. (2022) · Children · doi:10.3390/children9091376 · Cited by 5
Language performance and brain volumes, asymmetry, and cortical thickness in children born extremely preterm
Kvanta, H., Bolk, J., Broström, L., Nosko, D., de Gamarra‐Oca, L. F., Padilla, N., & Ådén, U. (2023) · Pediatric Research · doi:10.1038/s41390-023-02871-0 · Cited by 5

Authors: Kostović, I., & Judaš, M.
Affiliations: University of Zagreb (HR)
ORCID: Kostović, Ivica
Venue: Acta Paediatrica
Publisher: Wiley
Published: 2010-07
Volume: 99
Issue: 8
Pages: 1119-1127
ISSN: 0365-1436 (ISSN-L)
0803-5253
1651-2227
DOI: 10.1111/j.1651-2227.2010.01811.x
OpenAlex: W1755908671
Cited by: 462
References: 75
Citations by year: 2026: 22 · 2025: 26 · 2024: 28 · 2023: 24 · 2022: 26 · 2021: 19 · 2020: 68 · 2019: 30 · 2018: 24 · 2017: 25 · 2016: 31 · 2015: 33 · 2014: 36 · 2013: 29 · 2012: 15
FWCI: 1.78
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Acta Paediatrica (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and fetal brain pathology
Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
Keywords: subplate, thalamocortical connections, fetal brain development, cortical plate, preterm infants, pain management, consciousness development
MeSH terms: Afferent Pathways, Axons, Cerebral Cortex, Humans, Infant, Newborn, Infant, Premature, Neural Pathways, Staining and Labeling, Thalamus, Fetal Development

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

The development of the subplate and thalamocortical connections in the human foetal brain

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks