Functional brain development in humans (original) (raw)

• Johnson, M. H. Into the minds of babes. Science 286, 247 (1999).
  Article CAS Google Scholar
• Finlay, B. L. & Darlington, R. B. Linked regularities in the development and evolution of mammalian brains. Science 268, 1578–1584 (1995).
  Article CAS Google Scholar
• Clancy, B., Darlington, R. B. & Finlay, B. L. The course of human events: predicting the timing of primate neural development. Dev. Sci. 3, 57–66 (2000).
  Article Google Scholar
• Born, P. et al. Change of visually induced cortical activation patterns during development. Lancet 347, 543 (1996).
  Article CAS Google Scholar
• Yamada, H. et al. A rapid brain metabolic change in infants detected by fMRI. Neuroreport 8, 3775–3778 (1997).
  Article CAS Google Scholar
• Yamada, H. et al. A milestone for normal development of the infantile brain detected by functional MRI. Neurology 55, 218–223 (2000).
  Article CAS Google Scholar
• Eriksson, P. S. et al. Neurogenesis in the adult human hippocampus. Nature Med. 4, 1313–1317 (1998).
  Article CAS Google Scholar
• Spreen, O., Risser, A. T. & Edgell, D. Developmental Neuropsychology (Oxford Univ. Press, New York, 1995).
  Google Scholar
• Huttenlocher, P. R. Morphometric study of human cerebral cortex development. Neuropsychologia 28, 517–527 (1990).
  Article CAS Google Scholar
• Huttenlocher, P. R. & Dabholkar, A. S. in Development of the Prefrontal Cortex: Evolution, Neurobiology, and Behavior (eds Krasnegor, N. A., Lyon, G. R. & Goldman-Rakic, P. S.) 69–84 (Paul. H. Brookes, Baltimore, 1997).
  Google Scholar
• Bourgeois, J. P. in Handbook of Developmental Cognitive Neuroscience (eds Nelson, C. A. & Luciana, M.) 23–34 (MIT Press, Boston, 2001).
  Google Scholar
• Chugani, H. T., Phelps, M. E. & Mazziotta, J. C. Positron emission tomography study of human brain functional development. Ann. Neurol. 22, 487–497 (1987).
  Article CAS Google Scholar
• Huttenlocher, P. R. et al. Synaptogenesis in human visual cortex: evidence for synapse elimination during normal development. Neurosci. Lett. 33, 247–252 (1982).
  CAS Google Scholar
• 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).
  Article CAS Google Scholar
• Paus, T. et al. Maturation of white matter in the human brain: a review of magnetic resonance studies. Brain Res. Bull. 54, 255–266 (2001).
  Article CAS Google Scholar
• Pfefferbaum, A. et al. A quantitative magnetic resonance imaging study of changes in brain morphology from infancy to late adulthood. Arch. Neurol. 51, 874–887 (1994).
  Article CAS Google Scholar
• Giedd, J. N. et al. Brain development during childhood and adolescence: a longitudinal MRI study. Nature Neurosci. 2, 861–863 (1999).
  Article CAS Google Scholar
• Haith, M. M. Who put the cog in infant cognition? Is the rich interpretation too costly? Infant Behav. Dev. 21, 167–180 (1998).
  Article Google Scholar
• Spelke, E. S. Nativism, empiricism and the origins of knowledge. Infant Behav. Dev. 21, 181–200 (1998).
  Article Google Scholar
• Spelke, E. S. et al. Origins of knowledge. Psychol. Rev. 99, 605–632 (1992).
  Article CAS Google Scholar
• Munakata, Y. et al. Rethinking infant knowledge: towards an adaptive process account of successes and failures in object permanence tasks. Pyschol. Rev. 104, 686–713 (1997).
  Article CAS Google Scholar
• Mareschal, D., Plunkett, K. & Harris, P. A computational and neuropsychological account of object-oriented behaviours in infancy. Dev. Sci. 2, 306–317 (1999).
  Article Google Scholar
• Johnson, S. C. & Aslin, R. N. Perception of object unity in young infants: the roles of motion, depth and orientation. Cogn. Dev. 11, 161–180 (1996).
  Article Google Scholar
• Slater, A. et al. The role of three-dimensional depth cues in infants' perception of partly occluded objects. Early Dev. Parenting 3, 187–191 (1995).
  Article Google Scholar
• Xu, F. & Carey, S. Infants' metaphysics: the case of numerical identity. Cogn. Psychol. 30, 111–153 (1996).
  Article CAS Google Scholar
• Wilcox, T. & Baillargeon, R. Object individuation in infancy: the use of featural information in reasoning about occlusion events. Cogn. Psychol. 37, 97–155 (1998).
  Article CAS Google Scholar
• Leslie, A. M. et al. Indexing and the object concept: developing 'what' and 'where' systems. Trends Cogn. Sci. 2, 10–18 (1997).
  Article Google Scholar
• Csibra, G. et al. Gamma oscillations and object processing in the infant brain. Science 290, 1582–1585 (2000).The first demonstration of task-related 'bursts' of neural oscillations in human infants of 8 months. These oscillatory bursts correspond to the ability of the brain to 'bind' spatially separate features into a new single object and provide a direct measure of infants' ability to process objects.
  Article CAS Google Scholar
• Brothers, L. & Ring, B. A neuroethological framework for the representation of minds. J. Cogn. Neurosci. 4, 107–118 (1992).
  CAS Google Scholar
• Baron-Cohen, S. How to build a baby that can read minds: cognitive mechanisms in mindreading. Curr. Psychol. Cogn. 13, 513–552 (1994).
  Google Scholar
• Duchaine, B., Cosmides, L. & Tooby, J. Evolutionary psychology and the brain. Curr. Opin. Neurobiol. 11, 225–230 (2001).
  Article CAS Google Scholar
• Johnson, M. H. et al. Newborns' preferential tracking of face-like stimuli and its subsequent decline. Cognition 40, 1–19 (1991).
  Article CAS Google Scholar
• Valenza, E. et al. Face preference at birth. J. Exp. Psychol. Hum. Percept. Perform. 22, 892–903 (1996).Confirms previous work, but with an improved methodology, showing that newborns will preferentially orient towards simple face-like patterns.
  Article CAS Google Scholar
• Mondloch, C. J. et al. Face perception during early infancy. Psychol. Sci. 10, 419–422 (1999).
  Article Google Scholar
• Morton, J. & Johnson, M. H. CONSPEC and CONLERN: a two-process theory of infant face recognition. Psychol. Rev. 98, 164–181 (1991).
  Article CAS Google Scholar
• Hood, B. M., Willen, J. D. & Driver, J. Adult's eyes trigger shifts of visual attention in human infants. Psychol. Sci. 9, 53–56 (1998).An important link between research on attentional cueing in young babies, and work on social cognition and joint attention. Shows that the attention of young infants can be cued to a target location by the direction of eye gaze of a realistic face.
  Article Google Scholar
• Farroni, T. et al. Infants' use of gaze direction to cue attention: the importance of perceived motion. Vis. Cogn. 7, 705–718 (2000).
  Article Google Scholar
• Johnson, S., Slaughter, V. & Carey, S. Whose gaze will infants follow? The elicitation of gaze-following in 12-month-olds. Dev. Sci. 1, 233–238 (1998).
  Article Google Scholar
• Gergely, G. et al. Taking the intentional stance at 12 months of age. Cognition 56, 165–193 (1995).
  Article CAS Google Scholar
• Meltzoff, A. N. What infant memory tells us about amnesia: long-term recall and deferred imitation. J. Exp. Child Psychol. 59, 497–515 (1995).A study using the imitation method to show that before 2 years of age, children encode the behaviour of other humans in terms of the intended goals of their actions.
  Article CAS Google Scholar
• Csibra, G. et al. Goal attribution without agency cues: the perception of 'pure reason' in infancy. Cognition 72, 237–267 (1999).
  Article CAS Google Scholar
• Atkinson, J. Human visual development over the first six months of life: a review and a hypothesis. Hum. Neurobiol. 3, 61–74 (1984).
  CAS Google Scholar
• Richards, J. E. Cortical indexes of saccade planning in infants. Infancy 2, 123–133 (2001).
  Article Google Scholar
• Johnson, M. H. Cortical maturation and the development of visual attention in early infancy. J. Cogn. Neurosci. 2, 81–95 (1990).
  Article CAS Google Scholar
• Hood, B. in Advances in Infancy Research (eds Rovee-Collier, C. & Lipsitt, L.) (Ablex, Norwood, New Jersey, 1995).
  Google Scholar
• Johnson, M. H. The inhibition of automatic saccades in early infancy. Dev. Psychobiol. 28, 163–216 (1995).
  Article Google Scholar
• Csibra, G., Tucker, L. A. & Johnson, M. H. Differential frontal cortex activation before anticipatory and reactive saccades in infants. Infancy 2, 159–174 (2001).
  Article Google Scholar
• Gilmore, R. O. & Johnson, M. H. Working memory in infancy: six-month-olds' performance on two versions of the oculomotor delayed response task. J. Exp. Child Psychol. 59, 397–418 (1995).
  Article CAS Google Scholar
• Piaget, J. The Construction of Reality in the Child (Basic Books, New York, 1954).
  Book Google Scholar
• Diamond, A. & Goldman-Rakic, P. S. Comparison of human infants and infant rhesus monkeys on Piaget's AB task: evidence for dependence on dorsolateral prefrontal cortex. Exp. Brain Res. 74, 24–40 (1989).
  Article CAS Google Scholar
• Diamond, A. in The Epigenesis of Mind: Essays on Biology and Cognition (eds Carey, S. & Gelman, R.) 67–110 (Lawrence Erlbaum Ass., Hillsdale, New Jersey, 1991).
  Google Scholar
• Bell, M. A. & Fox, N. A. The relations between frontal brain electrical activity and cognitive development during infancy. Child Dev. 63, 1142–1163 (1992).
  Article CAS Google Scholar
• Diamond, A. et al. Prefrontal cortex cognitive deficits in children treated early and continuously for PKU. Monogr. Soc. Res. Child Dev. 62, 1–208 (1997).
  Article Google Scholar
• Matthews, A., Ellis, A. E. & Nelson, C. A. Development of preterm and full-term infant ability on AB, recall memory, transparent barrier detour, and means-end tasks. Child Dev. 67, 2658–2676 (1996).
  Article CAS Google Scholar
• Johnson, M. H. Functional brain development in infants: elements of an interactive specialization framework. Child Dev. 71, 75–81 (2000).
  Article CAS Google Scholar
• Friston, K. J. & Price, C. J. Dynamic representations and generative models of brain function. Brain Res. Bull. 54, 275–285 (2001).
  Article CAS Google Scholar
• Neville, H. J., Mills, D. & Lawson, D. Fractionating language: different neural sub-systems with different sensitive periods. Cereb. Cortex 2, 244–258 (1992).
  Article CAS Google Scholar
• de Haan, M., Oliver, A. & Johnson, M. H. Electrophysiological correlates of face processing by adults and 6-month-old infants. J. Cogn. Neurosci. 10, 36 (1998).
  Google Scholar
• Filipek, P. A. Neuroimaging in the developmental disorders: the state of the science. J. Child Psychol. Psychiatr. 40, 113–128 (1999).
  Article CAS Google Scholar
• Filipek, P. A. et al. Morphometric analysis of the brain in develomental language disorders and autism. Ann. Neurol. 32, 475 (1992).
  Google Scholar
• Rumsey, J. M. & Ernst, M. Functional neuroimaging of autistic disorders. Ment. Retard. Dev. Disabil. Res. Rev. 6, 171–179 (2000).
  Article CAS Google Scholar
• Mills, D. L. et al. Electrophysiological studies of face processing in Williams syndrome. J. Cogn. Neurosci. 12, 47–64 (2000).
  Article Google Scholar
• Miller, E. K. The prefrontal cortex and cognitive control. Nature Rev. Neurosci. 1, 59–65 (2000).
  Article CAS Google Scholar
• Rushworth, M. F. et al. Ventral prefrontal cortex is not essential for working memory. J. Neurosci. 17, 4829–4838 (1997).
  Article CAS Google Scholar
• Shadmehr, R. & Holcomb, H. Neural correlates of motor memory consolidation. Science 277, 821–824 (1997).
  Article CAS Google Scholar
• Johnson, M. H. et al. Visual attention in infants with perinatal brain damage: evidence of the importance of left anterior lesions. Dev. Sci. 1, 53–58 (1998).
  Article Google Scholar
• Craft, S. & Schatz, J. The effects of bifrontal stroke during childhood on visual attention: evidence from children with sickle cell anemia. Dev. Neuropsychol. 10, 285–297 (1994).
  Article Google Scholar
• Gauthier, I. et al. Activation of the middle fusiform 'face area' increases with expertise in recognizing novel objects. Nature Neurosci. 2, 568–573 (1999).
  Article CAS Google Scholar
• Gauthier, I. & Nelson, C. A. The development of face expertise. Curr. Opin. Neurobiol. 11, 219–224 (2001).
  Article CAS Google Scholar
• Rossion, B. et al. The N170 occipito-temporal component is delayed and enhanced to inverted faces but not to inverted objects: an electrophysiological account of face-specific processes in the human brain. Neuroreport 11, 69–74 (2000).
  Article CAS Google Scholar
• Maurer, D. et al. Rapid improvement in the acuity of infants after visual input. Science 286, 108–110 (1999).A study with patients visually deprived over the first months or years of life owing to cataracts. The improvements in acuity following corrective surgery were surprisingly rapid, although some degree of deficit remained even after years of restored vision.
  Article CAS Google Scholar
• Le Grand, R. et al. Neuroperception: early visual experience and face processing. Nature 410, 890 (2001).
  Article CAS Google Scholar
• Karmiloff-Smith, A. Development itself is the key to understanding developmental disorders. Trends Cogn. Sci. 2, 389–398 (1998).
  Article CAS Google Scholar
• Paterson, S. J. et al. Cognitive modularity and genetic disorders. Science 286, 2355–2358 (1999).A study that investigated whether the profiles of cognitive abilities and disabilities observed in adults with developmental disorders are also observed during infancy. The results show that profiles of cognitive disability might change during development.
  Article CAS Google Scholar
• Kellman, P. and Spelke, E. S. Perception of partly occluded objects in infancy. Cogn. Psychol. 15, 483–524 (1983).
  Article CAS Google Scholar
• Baillargeon, R., Spelke, E. S. & Wasserman, S. Object permanence in five-month-old infants. Cognition 20, 191–208 (1985).
  Article CAS Google Scholar
• Sakai, K. et al. Transition of brain activation from frontal to parietal areas in visuo-motor sequence learning. J. Neurosci. 18, 1827–1840 (1998).
  Article CAS Google Scholar