Abstract
The cerebral cortex can be divided into a large isocortex, a much smaller allocortex (the hippocampal formation and the olfactory cortex) and a transition zone (the mesocortex) in between. Although many individual variations exist in the sulcal pattern and in the extent of the various cortical areas, the remarkable conservation of the pattern of areal divisions within the human brain suggests the existence of a highly conserved and rather rigidly regulated regional specification programme that controls their development. Histogenesis of the cerebral cortex progresses through three major phases: cell production, cell migration, and cortical differentiation and maturation. Migrating cells from the ventricular zone to the cortical plate form ontogenetic radial cell columns. Recently, an important role in neurogenesis for the outer part of the subventricular zone became evident.
During the last decades, analysis of the genetic control of cortical development became possible. Mechanisms for induction and regionalization of the cerebral cortex are being unravelled and genes that are implicated in controlling regionalization, arealization and differentiation have been discovered in the mouse brain. This neurogenetic approach has given a great impetus to the study of neuronal migration disorders (NMDs). Advances in neurogenetics and the increasing application of MRI resulted in the distinction of a growing number of NMDs, of many of which the gene involved has been discovered. In this chapter, after a brief overview of the cerebral cortex (Sect. 10.2) and its main connections (Sect. 10.3), the development of the neocortex (Sect. 10.4), the hippocampus (Sect. 10.5) and their main fibre systems (Sect. 10.6) are discussed, followed by an overview of developmental disorders of the cerebral cortex. Malformations of cortical development (MCDs) include malformations due to abnormal cell production (Sect. 10.7.1), abnormal migration (Sect. 10.7.2), abnormal cortical organization (Sect. 10.7.3) and vascular disorders (Sect. 10.7.5). Many of these result in epilepsy (Sect. 10.7.4) and/or intellectual disability (Sect. 10.7.7). Finally, in Sect. 10.7.8 some neurobehavioural disorders are briefly reviwed. Throughout the chapter Clinical cases are presented illustrated with MRI and autopsy data.
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References
Abraham H, Pérez-García CG, Meyer G (2004) p73 and Reelin in Cajal-Retzius cells of the developing human hippocampal formation. Cereb Cortex 14:484–495
Abrahams BS, Geschwind DH (2008) Advances in autism genetics: on the threshold of a new neurobiology. Nat Rev Genet 9:341–355
Abrahams BS, Tentler D, Perederiy JV, Oldham MC, Coppola G, Geschwind DH (2007) Genome-wide analyses of human perisylvian cerebral cortical patterning. Proc Natl Acad Sci U S A 104:17849–17854
Abu-Khalil A, Fu L, Grove EA, Zecevic N, Geschwind DH (2004) Wnt genes define distinct boundaries in the developing human brain: implications for human forebrain patterning. J Comp Neurol 474:276–288
Adachi Y, Poduri A, Kawaguch A, Yoon G, Salih MA, Yamashita F et al (2011) Congenital microcephaly with a simplified gyral pattern: associated findings and their significance. AJNR Am J Neuroradiol 32:1123–1129
Aeby A, Liu Y, De Tiège X, Denolin V, David P, Balériaux D et al (2009) Maturation of thalamic radiations between 34 and 41 weeks’ gestation: a combined voxel-based study and probabilistic tractography with diffusion tensor imaging. AJNR Am J Neuroradiol 30:1780–1786
Aicardi J (1996) Aicardi syndrome. In: Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin BG, Pfanner P (eds) Dysplasias of cerebral cortex and epilepsy. Lippincott-Raven, Philadelphia, pp 211–216
Aicardi J (1998) Diseases of the nervous system in childhood, 2nd edn. Mac Keith, London
Aicardi J, Lefebvre J, Lerique-Koechlin A (1965) A new syndrome: spasms in flexion, callosal agenesis, ocular abnormalities. Electroencephalogr Clin Neurophysiol 19:609–610
Aicardi J, Chevrie JJ, Rousselie F (1969) Le syndrome spasmes en flexion, agénésie calleuse, anomalies choriorétiniennes. Arch Franc Pédiatr 26:1103–1120
Aicardi J, Chevrie J-J, Baraton J (1987) Agenesis of the corpus callosum. Handb Clin Neurol 50:149–173
Alcantara S, Ferrer I, Soriano E (1988) Postnatal development of parvalbumin and calbindin D28K immunoreactivities in the cerebral cortex of the rat. Anat Embryol (Berl) 188:63–73
Allendoerfer KL, Shatz CJ (1994) The subplate, a transient neocortical structure: its role in the development of connections between the thalamus and the cortex. Annu Rev Neurosci 17:185–218
Amaral DG (1987) Memory: anatomical organization of candidate brain regions. In: Plum F (ed) Handbook of physiology, sect 1: the nervous system, vol V, Higher functions of the nervous system. American Physiological Society, Bethesda, MD, pp 211–294
Amaral DG, Insausti R (1990) Hippocampal formation. In: Paxinos G (ed) The human nervous system. Academic, San Diego, CA, pp 711–755
Amaral DG, Scharfman HE, Lavenex P (2007) The dentate gyrus: functional neuroanatomical organization. Prog Brain Res 163:3–22
Amaral DG, Schumann CM, Nordahl CW (2008) Neuroanatomy of autism. Trends Neurosci 31:137–145
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23:185–188
Amir RE, Van den Veyver IB, Schultz R, Malicki DM, Tran CQ, Dahle EJ et al (2000) Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Ann Neurol 47:670–679
Amunts K, Schleicher A, Bürgel U, Mohlberg H, Uylings HBM, Zilles K (1999) Broca’s Region revisited: cytoarchitecture and intersubject variability. J Comp Neurol 412:319–341
Anderson SA, Mione M, Yun K, Rubinstein JLR (1999) Differential origins of neocortical projection and local circuit neurons: Role of Dlx genes in neocortical interneuronogenesis. Cereb Cortex 9:646–654
Anderson SA, Marín O, Horn C, Jennings K, Rubinstein JLR (2001) Distinct cortical migrations from the medial and lateral ganglionic eminences. Development 128:353–363
Andres C (2002) Molecular genetics and animal models in autistic disorder. Brain Res Bull 57:109–119
Andrews W, Liapi A, Plachez C, Camurri L, Zhang J, Mori S et al (2006) Robo1 regulates the development of major axontracts and interneuron migration in the forebrain. Development 133:2243–2252
Ang ES Jr, Haydar TF, Gluncic V, Rakic P (2003) Four-dimensional migratory coordinates of GABAergic interneurons in the developing mouse cortex. J Neurosci 23:5805–5815
Angevine JB Jr (1965) Time of neuron origin in the hippocampal region. Exp Neurol 2(Suppl):1–70
Angevine JB Jr, Sidman RL (1961) Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse. Nature 192:766–768
Ariani F, Hayek G, Rondinella D, Artuso R, Mencarelli MA, Spanhol-Rosseto A (2008) FOXG1 is responsible for the congenital variant of Rett syndrome. Am J Hum Genet 83:89–93
Armand J (1982) The origin, course and termination of corticospinal fibers in various mammals. Prog Brain Res 57:329–360
Armstrong DD (1992) The neuropathology of the Rett syndrome. Brain Dev 14(Suppl):S89–S98
Armstrong DD (2001) Rett syndrome neuropathology review 2000. Brain Dev 23(Suppl 1):S72–S76
Armstrong DD, Dunn JK, Antalffy B, Trivedi R (1995a) Selective dendritic alterations in the cortex of Rett syndrome. J Neuropathol Exp Neurol 54:195–201
Armstrong E, Schleicher A, Omran H, Curtis M, Zilles K (1995b) The ontogeny of human gyrification. Cereb Cortex 1:56–63
Armstrong DD, Dunn JK, Schultz RJ, Herbert DA, Glaze DG, Motil KJ (1999) Organ growth in Rett syndrome: a postmortem examination analysis. Pediatr Neurol 20:125–129
Armstrong DD, Deguchi K, Antalffy B (2003) Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain. J Child Neurol 18:683–687
Arnold SE, Trojanowski JQ (1996a) Human fetal hippocampal development. I. Cytoarchitecture, myeloarchitecture, and neuronal morphologic features. J Comp Neurol 367:274–292
Arnold SE, Trojanowski JQ (1996b) Human fetal hippocampal development. II. The neuronal cytoskeleton. J Comp Neurol 367:293–30
Aronica E, Toering ST, Boer K, de Groot M, Troost D, Heimans JJ et al (2009) Expression patterns of synaptic vesicle protein 2A in focal cortical dysplasia and TSC-cortical tubers. Epilepsia 50:1409–1418
Aronica E, Becker AJ, Spreafico R (2012) Malformations of cortical development. Brain Pathol 22:380–401
Bagri A, Marín O, Plump AS, Mak Y, Pleasure SJ, Rubinstein JLR, Tessier-Lavigne M (2002) Slit proteins pevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain. Neuron 33:233–248
Bahi-Buisson N, Souville I, Fourniol FJ, Toussaint A, Moores CA, Houdusse A et al (2013) New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum. Brain 136:223–244
Bailey P, van Bonin G (1951) The isocortex of man. University of Illinois Press, Urbana, IL
Baker K, Northam GB, Chong WK, Banks T, Beales P, Baldeweg T (2010) Neocortical and hippocampal volume loss in a human ciliopathy: a quantitative MRI study in bardet-biedl syndrome. Am J Med Genet A 155:1–8
Bar I, Lambert de Rouvroit C, Royaux I, Kritzman DB, Dernoncourt C, Ruelle D et al (1995) A YAC contig containing the reeler locus with preliminary characterization of candidate gene fragments. Genomics 26:543–549
Bardoni B, Mandel J-L (2002) Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X-linked mental retardation genes. Curr Opin Genet Dev 12:284–293
Barkovich AJ (1990) Apparent atypical callosal dysgenesis: analysis of MR findings in six cases and their relationship to holoprosencephaly. AJNR Am J Neuroradiol 11:333–340
Barkovich AJ (1998) Neuroimaging manifestations and classification of congenital muscular dystrophies. AJNR Am J Neuroradiol 19:1389–1396
Barkovich AJ (2000) Pediatric neuroimaging, 3rd edn. Lippincott, Philadelphia, PA
Barkovich AJ (2003) Anomalies of the corpus callosum and cortical malformations. In: Barth PG (ed) Disorders of neuronal migration. Mac Keith, London, pp 83–103
Barkovich AJ (2010) Current concepts of polymicrogyria. Neuroradiology 52:479–487
Barkovich AJ, Kjos BO (1992a) Gray matter heterotopias: MR characteristics and correlation with developmental and neurologic manifestations. Radiology 182:493–499
Barkovich AJ, Kjos BO (1992b) Schizencephaly: correlation of clinical findings with MR characteristics. AJNR Am J Neuroradiol 13:85–94
Barkovich AJ, Kuzniecky RI (2000) Gray matter heterotopia. Neurology 55:1603–1608
Barkovich AJ, Koch TK, Carroll CL (1991) The spectrum of lissencephaly: report of ten cases analyzed by magnetic resonance imaging. Ann Neurol 30:139–146
Barkovich AJ, Gressens P, Evrard P (1992a) Formation, maturation, and disorders of brain neocortex. AJNR Am J Neuroradiol 13:423–446
Barkovich AJ, Lyon G, Evrard P (1992b) Formation, maturation, and disorders of white matter. AJNR Am J Neuroradiol 13:447–461
Barkovich AJ, Rowley H, Boller A (1995) Correlation of prenatal events with the development of polymicrogyria. AJNR Am J Neuroradiol 16:822–827
Barkovich AJ, Ferreiro DM, Barr RM, Gressens P, Dobyns WB, Truwit CL, Evrard P (1998) Microlissencephaly: a heterogeneous malformation of cortical development. Neuropediatrics 29:113–119
Barkovich AJ, Hevner R, Guerrini R (1999) Syndromes of bilateral symmetrical polymicrogyria. AJNR Am J Neuroradiol 20:1814–1821
Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB (2001) Classification system for malformations of cortical development. Update 2001. Neurology 57:2168–2178
Barkovich AJ, Guerrini R, Kuzniecky RI, Jackson GD, Dobyns WB (2012) A developmental and genetic classification for malformations of cortical development: update 2012. Brain 135:1348–1369
Barth PG (1987) Disorders of neuronal migration. Can J Neurol Sci 14:1–16
Battaglia G, Arcelli P, Granata T, Selvaggio M, Andermann F, Dubeau F et al (1996) Neuronal migration disorders and epilepsy: a morphological analysis of three surgically treated patients. Epilepsy Res 26:49–58
Bauman ML (1991) Microscopic neuroanatomic abnormalities in autism. Pediatrics 87:791–796
Bauman ML, Kemper TL (1985) Histoanatomic observations of the brain in early infantile autism. Neurology 35:866–874
Bauman ML, Kemper TL, Arin DM (1995) Pervasive neuroanatomic abnormalities of the brain in three cases of Rett’s syndrome. Neurology 45:1581–1586
Bauman ML, Filipek PA, Kemper TL (1997) Early infantile autism. Int Rev Neurobiol 41:367–386
Bayatti N, Moss JA, Sun L, Ambrose P, Ward JF, Lindsey S, Clowry GJ (2008) A molecular neuroanatomical study of the developing human neocortex from to 17 postconceptional weeks revealing the early differentiation of the subplate and subventricular zone. Cereb Cortex 18:1536–1548
Bayer SA (1980a) Development of the hippocampal region in the rat. I. Neurogenesis examined with 3H-thymidine autoradiography. J Comp Neurol 190:87–114
Bayer SA (1980b) Development of the hippocampal region in the rat. II. Morphogenesis during embryonic and early postnatal life. J Comp Neurol 190:115–134
Bayer SA, Altman J (1990) Development of layer I and subplate in the rat neocortex. Exp Neurol 107:48–62
Bayer SA, Altman J (1991) Neocortical development. Raven, New York
Belgard TG, Marques AC, Oliver PL, Abacu HO, Sirey TM, Hoerder-Suabedissen A et al (2011) A transcriptome atlas of mouse neocortical layers. Neuron 71:605–616
Belichenko PV, Oldfors A, Hagberg B, Dahlström A (1994) Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents. Neuroreport 5:1509–1513
Belichenko PV, Wright EE, Belichenko NP, Masliah E, Li HH, Mobley WC, Francke U (2009) Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks. J Comp Neurol 514:240–258
Bellugi U, Lichtenberger L, Mills D, Galaburda A, Korenberg JR (1999) Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome. Trends Neurosci 22:197–209
Beltrán-Valero de Bernabé D, Currier S, Steinbrecher A, Celli J, van Beusekom E, van der Zwaag B et al (2002) Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. Am J Hum Genet 71:1033–1043
Ben-Ari Y (2001) Developing networks play a similar melody. Trends Neurosci 24:353–360
Ben-Ari Y (2002) Excitatory actions of GABA during development: the nature of the nurture. Nat Rev Neurosci 3:728–739
Benavides-Piccione R, Ballesteros-Yáñez I, Martínez de Lagrán M, Elston G, Estivill X, Fillat C et al (2004) On dendrites in Down syndrome and DS murine models: a spiny way to learn. Prog Neurobiol 74:111–126
Benes FM, Berretta S (2001) GABAergic interneurons: implications for understanding schizophrenia and bipolar disorder. Neuropsychopharmacology 25:1–27
Benes FM, Taylor JB, Cunningham MC (2000) Convergence and plasticity of monoaminergic systems in the medial prefrontal cortex during the postnatal period: implications for the development of psychopathology. Cereb Cortex 10:1014–1027
Berger B, Alvarez C (1996) Neurochemical development of the hippocampal region in the fetal rhesus monkey. III. Calbindin D28k, calretinin and parvalbumin with special mention of Cajal-Retzius cells and the retrosplenial cortex. J Comp Neurol 366:674–699
Berger B, Alvarez C, Goldman-Rakic P (1993) Ibid. Early appearance of peptides, calcium-binding proteins, DARPP-32, and the monoamine innervation in the entorhinal cortex during the first half of gestation (E47 to E90). Hippocampus 3:279–305
Bernard A, Lubbers LS, Taris KQ, Luo R, Podtelezhnikov AA, Finney EM et al (2012) Transcriptional architecture of the primate neocortex. Neuron 73:1083–1099
Berry M, Rogers AW (1965) The migration of neuroblasts in the developing cerebral cortex. J Anat (Lond) 99:691–709
Billette de Villemeur T, Chiron C, Robain O (1992) Unlayered polymicrogyria and agenesis of the corpus callosum: a relevant association? Acta Neuropathol (Berl) 83:265–270
Blaschke AJ, Staley K, Chun J (1996) Widespread programmed cell death in proliferative and postmitotic regions of the fetal cerebral cortex. Development 122:1165–1174
Blaschke AJ, Weiner JA, Chun J (1998) Programmed cell death is a universal feature of embryonic and postnatal neuroproliferative regions throughout the central nervous system. J Comp Neurol 396:39–50
Blümcke I, Spreafico R (2011) An international consensus classification for focal cortical dysplasias. Lancet Neurol 10:26–27
Blümcke I, Zuschratter W, Schewe J-C, Suter B, Lie AA, Riederer BM et al (1999) Cellular pathology of hilar neurons in Ammon’s horn sclerosis. J Comp Neurol 414:437–453
Blümcke I, Thom M, Wiestler OD (2002) Ammon’s Horn sclerosis: a maldevelopmental disorder associated with temporal lobe epilepsy. Brain Pathol 12:199–211
Blümcke I, Vinters HV, Armstrong D, Aronica E, Thom M, Spreafico R (2009) Malformations of cortical development and epilepsies: neuropathological findings with emphasis on focal cortical dysplasia. Epileptic Disord 11:181–193
Blümcke I, Pieper T, Pauli E, Hildebrandt M, Kudernatsch M, Winkler P et al (2010) A distinct variant of focal cortical dysplasia type I characterized by magnetic resonance imaging and neuropathological examination in children with severe epilepsies. Epileptic Disord 12:172–180
Blümcke I, Thom M, Aronica E, Armstrong DD, Vinters HV, Palmini A et al (2011) The clinicopathologic spectrum of cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia 52:158–174
Bodensteiner JB, Schaefer GB, Craft JM (1998) Cavum septum pellucidi and cavum Vergae in normal and developmentally delayed populations. J Child Neurol 13:120–121
Boer K, Troost D, Spliet WG, Redeker S, Crino PB, Aronica E (2007) A neuropathological study of two autopsy cases of syndromic hemimegalencephaly. Neuropathol Appl Neurobiol 33:455–470
Boer K, Troost D, Jansen F, Nellist M, van den Ouweland AM, Geurts JJ et al (2008) Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex. Neuropathology 28:577–590
Boer K, Crino PB, Gorter JA, Nellist M, Jansen FE, Spliet WG et al (2010) Gene expression analysis of tuberous sclerosis complex cortical tubers reveals increased expression of adhesion and inflammatory factors. Brain Pathol 20:704–719
Bogerts B, Meertz E, Schönfeld-Bausch R (1985) Basal ganglia and limbic system pathology in schizophrenia. A morphometric study of brain volume and shrinkage. Arch Gen Psychiatry 42:784–791
Bogerts B, Falkai P, Greve B, Schneider T, Pfeiffer U (1993) The neuropathology of schizophrenia: past and present. J Hirnforsch 34:193–205
Bourneville DM (1880) Contributions à l’étude de l’idiotie. III. Sclérose tubéreuse des circonvolutions cérébrales. Arch Int Neurol 1:81–91
Braak H (1976) A primitive gigantopyramidal field buried in the depth of the cingulate sulcus of the human brain. Brain Res 109:219–233
Braak H (1979) Pigment architecture of the human telencephalic cortex. V. Regio anterogenualis. Cell Tissue Res 204:441–451
Braak H (1980) Architectonics of the human telencephalic cortex. Springer, Berlin Heidelberg New York
Braak H, Braak E (1992) The human entorhinal cortex: normal morphology and lamina-specific pathology in various diseases. Neurosci Res 15:6–31
Braak H, Braak E, Yilmazer D, Bohl J (1996) Functional anatomy of human hippocampal formation and related structures. J Child Neurol 11:265–275
Brambati SM, Termine C, Ruffino M, Stella G, Fazio F, Cappa S, Perani D (2004) Regional reductions of gray matter volume in familial dyslexia. Neurology 63:742–745
Brambilla P, Hardan A, Ucelli di Nemi S, Perez J, Soares JC, Barale F (2003) Brain anatomy and development in autism: review of structural MRI studies. Brain Res Bull 61:557–569
Brauer J, Friederici AD (2007) Functional neural networks of semantic and syntactic processes in the developing brain. J Cogn Neurosci 19:1609–1623
Brauer J, Neumann J, Friederici AD (2008) Temporal dynamics of perisylvian activation during language processing in children and adults. Neuroimage 41:1484–1492
Brauer J, Anwander A, Friederici AD (2011) Neuroanatomical prerequisites for language functions in the maturing brain. Cereb Cortex 21:459–466
Brazel CY, Romanenko MJ, Rothstein RP, Levison SW (2003) Roles of the mammalian subventricular zone in brain development. Prog Neurobiol 69:49–69
Brinks H, Conrad S, Vogt J, Oldekamp J, Sierra A, Deitinghoff L et al (2004) The repulsive guidance molecule RGMa is involved in the formation of afferent connections in the dentate gyrus. J Neurosci 24:3862–3869
Broca P (1878) Anatomie comparée des circonvolutions cérébrales. Le grand lobe limbique et la scissure limbique dans la série des mammifères. Rev Antropol 1:385–498
Brodmann K (1909) Vergleichende Lokalisationslehre der Grosshirnrinde in ihren Prinzipien dargestellt auf Grund des Zellenbaues. Barth, Leipzig; English translation by LJ Garey (1999) Brodmann’s ‘Localisation in the Cerebral Cortex’. Imperial College Press, London
Brown WT (2002) The molecular biology of the fragile X mutation. In: Hagerman RJ, Hagerman PJ (eds) Fragile X syndrome: diagnosis, treatment and research, 3rd edn. Johns Hopkins University Press, Baltimore, MD, pp 110–135
Brun A (1965) The subpial granular layer of the foetal cerebral cortex in man. Its ontogeny and significance in congenital cortical malformations Acta Pathol Microbiol Scand 179(Suppl):1–98
Brunner HG, Nelen MR, Breakefield XO, Ropers H-H, van Oost BA (1993a) Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase a. Science 262:578–586
Brunner HG, Nelen MR, van Zandvoort P, Abeling NG, van Gennip AH, Wolters EC et al (1993b) X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism. Am J Hum Genet 52:1032–1039
Bruyn GW (1977) Agenesis septi pellucidi, cavum septi pellucidi, and cavum Vergae, and cavum veli interpositi. Handb Clin Neurol 30:299–336
Bürgel U, Amunts K, Hoemke L, Mohlberg H, Gilsbach JM, Zilles K (2006) White matter tracts of the human brain: three-dimensional mapping at microscopic resolution, topography and intersubject variability. Neuroimage 29:1092–1105
Bürgel U, Mädler B, Honey CR, Thron A, Gilsbach J, Coenen V (2009) Fiber tracking with distinct software tools results in a clear diversity in anatomical fiber tract portrayal. Cent Eur Neurosurg 70:27–35
Buxhoeveden DP, Casanova MF (2002) The minicolumn hypothesis in neuroscience. Brain 125:935–951
Bystron I, Rakic P, Molnár Z, Blakemore C (2006) The first neurons of the human cerebral cortex. Nat Neurosci 9:880–886
Bystron I, Blakemore C, Rakic P (2008) Development of the human cerebral cortex: Boulder Committee revisited. Nat Rev Neurosci 9:110–122
Cabrero-Socorro A, Hernandez-Acosta NC, Gonzalez-Gomez MG (2007) Comparative aspects of p73 and reelin expression in Cajal-Retzius cells and the cortical hem in lizard, mouse and human. Brain Res 1132:59–70
Cameron HE, McKay RDG (2001) Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus. J Comp Neurol 435:406–417
Cannon M, Jones PB, Murray RM (2002) Obstetric complications and schizophrenia: historical and meta-analytic review. Am J Psychiatry 159:1080–1092
Cao QL, Yan XX, Luo XG, Garey LJ (1996) Prenatal development of parvalbumin immunoreactivity in the human striate cortex. Cereb Cortex 6:620–630
Casanova MF (1997) Functional and anatomical aspects of prefrontal pathology and schizophrenia. Schizophr Bull 23:517–519
Casanova MF, Buxhoeveden DP, Switala AE, Roy EL (2002a) Minicolumnar pathology in autism. Neurology 58:428–432
Casanova MF, Buxhoeveden DP, Cohen M, Switala AE, Roy EL (2002b) Minicolumnar pathology in dyslexia. Ann Neurol 52:108–110
Casanova MF, van Kooten IAJ, Switala AE, van Engeland H, Heinsen H, Steinbusch HWM et al (2006) Minicolumnar abnormalities in autism. Acta Neuropathol (Berl) 112:287–303
Cases O, Seif I, Grimsby J, Gaspar P, Chen K, Pournin S et al (1995) Agressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA. Science 268:1763–1776
Caspi A, McClay J, Moffitt TE, Mill J, Martin J, Craig IW et al (2002) Role of genotype in the cycle of violence in maltreated children. Science 297:851–854
Catani M, Thiebaut de Schotten M (2008) A diffusion tensor tractography atlas for virtual in vivo dissections. Cortex 44:1105–1132
Catani M, Thiebaut de Schotten M (2012) Atlas of human brain connections. Oxford University Press, Oxford
Catani M, Jones DK, Ffytche DH (2005) Perisylvian language networks of the human brain. Ann Neurol 57:8–16
Caviness VS Jr (1973) Time of neuron origin in the hippocampus and dentate gyrus of normal and reeler mutant mice: an autoradiographic analysis. J Comp Neurol 151:113–120
Caviness VS Jr (1982) Neocortical histogenesis in normal and reeler mice: a developmental study based upon [3H]thymidine autoradiography. Dev Brain Res 4:293–302
Caviness VS Jr, Sidman RL (1973) Time of origin of corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis. J Comp Neurol 170:449–460
Caviness VS Jr, Takahashi T, Nowakowski RS (1995) Numbers, time and neocortical neurogenesis: a general developmental and evolutionary model. Trends Neurosci 18:379–393
Caviness VS Jr, Takahashi T, Nowakowski RS (2000) Neurogenesis and the early events of neocortical histogenesis. In: Goffinet AM, Rakic P (eds) Mouse brain development. Springer, Berlin Heidelberg New York, pp 107–143
Caviness VS Jr, Takahashi T, Nowakowski RS (2003) Morphogenesis of the human cerebral cortex. In: Barth PG (ed) Disorders of neuronal migration. Mac Keith, London, pp 1–23
Caviness VS Jr, Nowakowski RS, Bhide PG (2009) Neocortical neurogenesis: morphogenetic gradients and beyond. Trends Neurosci 32:443–450
Cecchi C, Boncinelli E (2000) Emx homeogenes and mouse brain development. Trends Neurosci 23:347–352
Chae T, Kwon YT, Bronson R, Dikkes P, Li E, Tsai L-H (1997) Mice lacking p35, a neuronal specific activator of cdk5, display cortical lamination defects, seizures and adult lethality. Neuron 18:29–42
Chahrour M, Zoghbi HY (2007) The story of Rett syndrome: from clinic to neurobiology. Neuron 8:422–437
Chan WY, Kostović I, Takashima S, Feldhaus C, Stoltenburg-Didinger G, Verney C et al (2002) Normal and abnormal development of the human cerebral cortex. Neuroembryology 1:78–90
Chang BS, Lowenstein DH (2003) Mechanisms of disease: epilepsy. N Engl J Med 349:1257–1266
Chang BS, Piao X, Giannini C, Cascino GD, Scheffer I, Wood CG et al (2004) Bilateral generalised polymicrogyria (BGP): a distinct syndrome of cortical malformation. Neurology 62:1722–1728
Chapleau CA, Calfa GD, Lane MC, Albertson AJ, Larimore JL, Kudo S et al (2009) Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations. Neurobiol Dis 35:219–233
Chédotal A, Del Rio JA, Ruiz M, He Z, Borrell V, de Castro F et al (1998) Semaphorins III and IV repel hippocampal axons via two distinct receptors. Development 125:4313–4323
Chelly J, Khelfaoui M, Francis F, Cheriff B, Bienvenu T (2006) Genetics and pathophysiology of mental retardation. Eur J Hum Genet 14:701–713
Chen H, Bagri A, Zupicich JA, Zou Y, Stoeckli E, Pleasure SJ et al (2000) Neuropilin-2 regulates the development of selective cranial and sensory nerves and hippocampal mossy fiber projections. Neuron 25:43–56
Chen H, Cheng Q, Lin Y, Meissner A, West AE, Griffith EC et al (2003) Depression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2. Science 302:885–889
Chenn A, McConnell SK (1995) Cleavage orientation and the asymmetric inheritance of Notch1 immunoreactivity in mammalian neurogenesis. Cell 82:631–641
Chenn A, Braisted JE, McConnell SK, O’Leary DDM (1997) Development of the cerebral cortex: mechanisms controlling cell fate, laminar and areal patterning, and axonal connectivity. In: Cowan WM, Jessell TM, Zipursky SL (eds) Molecular and cellular approach to neural development. Oxford University Press, New York, pp 440–473
Chi JG, Dooling EC, Gilles FH (1977) Gyral development of the human brain. Ann Neurol 1:86–93
Chiurazzi P, Oostra BA (2000) Genetics of mental retardation. Curr Opin Pediatr 12:529–535
Chiurazzi P, Schwartz CE, Gecz J, Neri G (2008) XLMR genes: update 2007. Eur J Hum Genet 16:422–434
Cho WH, Seidenwurm D, Barkovich AJ (1999) Adult-onset neurologic dysfunction associated with cortical malformations. AJNR Am J Neuroradiol 20:1037–1043
Cholfin JA, Rubinstein JLR (2008) Frontal cortex subdivision patterning is coordinately regulated by Fgf8, Fgf17, and Emx2. J Comp Neurol 509:144–155
Chow EWC, Zipursky RB, Mikulis DJ, Bassett AS (2002) Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biol Psychiatry 51:208–215
Clowry G, Molnár Z, Rakic P (2010) Renewed focus on the developing human neocortex. J Anat (Lond) 217:276–288
Colantuoni C, Lipska BK, Ye T, Hyde TM, Tao R, Leek JT et al (2011) Temporal dynamics and genetic control of transcription in the human prefrontal cortex. Nature 478:519–524
Comery TA, Harris JB, Willems PJ, Oostra BA, Irwin SA, Weiler IJ, Greenough WT (1997) Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits. Proc Natl Acad Sci U S A 94:5401–5404
Condé F, Lund JS, Lewis DA (1996) The hierarchical development of monkey visual cortical regions as revealed by the maturation of parvalbumin-immunoreactive neurons. Dev Brain Res 96:261–276
Conel JL (1939) The postnatal development of the human cerebral cortex. I. The cortex of the newborn. Harvard University Press, Cambridge
Conel JL (1941) The postnatal development of the human cerebral cortex, II. The cortex of the one-month infant. Harvard University Press, Cambridge
Conel JL (1947) The postnatal development of the human cerebral cortex. III. The cortex of the three-month infant. Harvard University Press, Cambridege
Conel JL (1951) The postnatal development of the human cerebral cortex. IV. The cortex of the six-month infant. Harvard University Press, Cambridge
Conel JL (1955) The postnatal development of the human cerebral cortex. V. The cortex of the fifteen-month infant. Harvard University Press, Cambridge
Conel JL (1959) The postnatal development of the human cerebral cortex. VI. The cortex of the twenty-four-month infant. Harvard University Press, Cambridge
Conel JL (1963) The postnatal development of the human cerebral cortex, VII. The cortex of the four-year child. Harvard University Press, Cambridge
Conel JL (1967) The postnatal development of the human cerebral cortex. VIII. The cortex of the six-year child. Harvard University Press, Cambridge
Connolly MB, Hendson G, Steinbok P (2006) Tuberous sclerosis complex: a review of the management of epilepsy with emphasis on surgical aspects. Childs Nerv Syst 22:896–908
Consortium ECTS (1993) Identification and characterization of the tuberous sclerosis gene on chromosome 16. Cell 75:1305–1315
Copp AJ, Harding BN (1999) Neuronal migration disorders in humans and in mouse models – an overview. Epilepsy Res 36:133–141
Costa E, Davis J, Pesold C, Tueting P, Guidotti A (2002) The heterozygote reeler mouse as a model for the development of a new generation of antipsychotics. Curr Opin Pharmacol 2:56–62
Counsell SJ, Dyet LE, Larkman DJ, Nunes RG, Boardman JP, Allsop JM et al (2007) Thalamo-cortical connectivity in children born preterm mapped using probabilistic magnetic resonance imaging. Neuroimage 34:896–904
Courchesne E (1997) Brainstem, cerebellum and limbic neuroanatomical abnormalities in autism. Curr Opin Neurobiol 7:269–278
Courchesne E, Pierce K (2005) Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection. Curr Opin Neurobiol 15:225–230
Courchesne E, Carper R, Akshoomoff N (2003) Evidence of brain overgrowth in the first year of life in autism. JAMA 290:337–344
Craig AD (2002) How do you feel? Interoception: the sense of the physiological condition of the body. Nat Rev Neurosci 3:665–666
Craig AD (2009) How do you feel – now? The anterior insula and human awareness. Nat Rev Neurosci 10:59–70
Crino PB, Henske EP (1999) New developments in the neurobiology of the tuberous sclerosis complex. Neurology 53:1384–1390
Crino PB, Duhaime A-C, Baltuch G, White R (2001) Differential expression of glutamate and GABA-A receptor subunit mRNA in cortical dysplasia. Neurology 56:906–913
Crino PB, Miyata H, Vinters HV (2002) Neurodevelopmental disorders as a cause of seizures: neuropathologic, genetic, and mechanistic considerations. Brain Pathol 12:212–233
Crino PB, Nathanson KL, Henske EP (2006) The tuberous sclerosis complex. N Engl J Med 355:1345–1356
Curatolo P, Verdecchia M, Bombardieri R (2002) Tuberous sclerosis complex: a review of neurological aspects. Eur J Paediatr Neurol 6:15–23
Cushion TD, Dobyns WB, Mullins JGL, Stoodley N, Chung S-K, Fry AE et al (2013) Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain 136:536–548
D’Agostino MD, Bernasconi A, Das S, Bastos A, Valerio RM, Palmini A et al (2002) Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females. Brain 125:2507–2522
D’Arcangelo G, Miao GG, Chen S-C, Soares HD, Morgan JI, Curran T (1995) A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374:719–723
D’Arcangelo G, Nakajima K, Miyata T, Ogawa M, Mikoshiba K, Curran T (1997) Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody. J Neurosci 17:23–31
Damasio AR, Maurer RG (1978) A neurological model for childhood autism. Arch Neurol 35:777–786
Danesin C, Houart C (2012) A Fox stops the Wnt: implications for forebrain development and diseases. Curr Opin Genet Dev 22:323–330
Darby JH (1976) Neuropathological aspects of psychosis in childhood. J Autism Childhood Schizophrenia 6:339–352
de Lacoste MC, Kirkpatrick JB, Ross ED (1985) Topography of the human corpus callosum. J Neuropathol Exp Neurol 44:578–591
de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T et al (2012) Diagnostic exome sequencing in persons with severe intellectual disability. N Engl J Med 367:1921–1929
deAzevedo LC, Hedin-Pereira C, Leht R (1997) Callosal neurons in the cingulate cortical plate and subplate of human fetuses. J Comp Neurol 386:60–70
Deb P, Sharma MC, Tripathi M, Sarat Chandra P, Gupta A, Sarkar C (2006) Expression of CD34 as a novel marker for glioneuronal lesions associated with chronic intractable epilepsy. Neuropathol Appl Neurobiol 32:461–468
DeFelipe J (2002) Cortical interneurons: from Cajal to 2001. Prog Brain Res 136:215–238
DeFelipe J, López-Cruz PL, Benavides-Piccione R, Bielar C, Larraňaga P et al (2013) New insights into the classification and nomenclature of cortical GABAergic interneurons. Nat Rev Neurosci 14:202–216
Deguchi K, Inoue K, Avila WE, Lopez-Terrada D, Antalffy BA, Quattrocchi CC et al (2003) Reelin and disabled-1 expression in developing and mature human cortical neurons. J Neuropathol Exp Neurol 62:676–684
Demb JB, Boynton GM, Heeger DJ (1998) Functional magnetic resonance imaging of early visual pathways in dyslexia. J Neurosci 18:6939–6951
Deng J, Elberger AJ (2001) The role of pioneer neurons in the development of mouse visual cortex and corpus callosum. Anat Embryol (Berl) 204:437–453
des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrié A et al (1998) A novel gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 92:51–61
Devisme L, Bouchet C, Gonzalès M, Alanio E, Bazin A, Bessières B et al (2012) Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies. Brain 135:469–482
Di Virgilio G, Clarke S (1997) Direct interhemispheric visual input to human speech areas. Hum Brain Mapp 5:347–354
Di Virgilio G, Clarke S, Pizzolatto G, Schaffner T (1999) Cortical regions contributing to the anterior commissure in man. Exp Brain Res 124:1–7
Dick AS, Tremblay P (2012) Beyond the arcuate fasciculus: consensus and controversy in the connectional anatomy of language. Brain 135:3529–3550
Dobyns WB, Truwit CL (1995) Lissencephaly and other malformations of cortical development: 1995 an update. Neuropediatrics 26:132–147
Dobyns WB, Stratton RF, Greenberg F (1984) Syndromes with lissencephaly. I. Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly. Am J Med Genet 18:509–526
Dobyns WB, Kirkpatrick JB, Hittner HM, Roberts RM, Kretzer FL (1985) Syndromes with lissencephaly. II. Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephaly. Am J Med Genet 22:157–195
Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A et al (1989) Diagnostic criteria for Walker-Warburg syndrome. Am J Med Genet 32:195–210
Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O et al (1996) X-linked malformations of neuronal migration. Neurology 47:331–339
Dobyns WB, Truwit CL, Ross ME, Matsumoto N, Pilz DT, Ledbetter DH et al (1999) Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly. Neurology 53:270–277
Donahoo A-LS, Richards LJ (2009) Understanding the mechanisms of callosal development through the use of transgenic mouse models. Semin Pediatr Neurol 16:217–242
Dooling EC, Chi JG, Gilles FH (1983) Telencephalic development: changing gyral patterns. In: Gilles FH, Leviton A, Dooling EC (eds) The developing human brain. Wright, Bristol, pp 94–104
Dover CJ, Le Couteur A (2007) How to diagnose autism. Arch Dis Child 92:540–545
DSM-IV (1994) Diagnostic and statistical manual of mental disorders, IV. American Psychiatric Association, Washington, DC
Dubeau F, Tampieri D, Lee N, Andermann E, Carpenter S, Leblanc R et al (1995) Periventricular and subcortical nodular heterotopia. A study of 33 patients. Brain 118:1273–1287
Dubois J, Benders M, Borradori-Tolsa C, Cachia A, Lazeyras F, Ha-Vinh Leuchter R et al (2008a) Primary cortical folding in the human newborn: an early marker of later functional development. Brain 131:2028–2041
Dubois J, Benders M, Cachia A, Lazeyras F, Ha-Vinh Leuchter R, Sizonenko SV et al (2008b) Mapping the early cortical folding process in the preterm newborn brain. Cereb Cortex 18:1444–1454
Dubois J, Benders M, Lazeyras F, Borradori-Tolsa C, Ha-Vinh Leuchter R, Mangin JF, Hüppi PS (2010) Structural asymmetries of perisylvian regions in the preterm newborn. Neuroimage 52:32–42
Duchowny M, Jayakar P, Levin B (2000) Aberrant neural circuits in malformations of cortical development and focal epilepsy. Neurology 55:423–428
Dudek FE, Sutula TP (2007) Epileptogenesis in the dentate gyrus: a critical perspective. Prog Brain Res 163:755–773
Duffau H (2008) The anatomo-functional connectivity of language revisited: New insights provided by electrostimulation and tractography. Neuropsychologia 46:927–934
Dum RP, Strick PL (1996) Spinal cord terminations of the medial motor areas in macaque monkeys. J Neurosci 15:6513–6525
Duvernoy HM (1992) Le cerveau humain. Surface, coupes sériée tridimensionelles et IRM. Springer, Paris
Duvernoy HM (1998) The human hippocampus. Functional anatomy, vascularization and serial sections with MRI, 2nd edn. Springer, Berlin Heidelberg New York
Ekşioğlu YZ, Scheffer IE, Cardenas P, Knoll J, DiMario F, Ramsby G et al (1996) Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical development. Neuron 16:77–87
Elliot Smith G (1897) The morphology of the indusium griseum and striae Lancisii. Anat Anz 13:23–27
Eriksson PS, Perfilieva E, Björk-Eriksson T, Alborn AM, Nordborg C, Peterson DA, Gage FH (1998) Neurogenesis in the adult human hippocampus. Nat Med 4:1313–1317
Eriksson SH, Thom M, Hefferman J, Lin WR, Harding BN, Squier MV, Sisodiya SM (2001) Persistent reelin-expressing Cajal-Retzius cells in polymicrogyria. Brain 124:1350–1361
Evrard P, Miladi N, Bonnier C, Gressens P (1992) Normal and abnormal development of the brain. In: Rapin I, Segalowitz SJ (eds) Child neuropsychology. Elsevier, Amsterdam, pp 11–44
Eyre JA, Miller S, Clowry GJ, Conway EA, Watts C (2000) Functionally corticospinal projections are established prenatally in the human foetus permitting involvement in the development of spinal motor centres. Brain 123:51–64
Falconer DS (1951) Two new mutants, “trembler” and “reeler”, with neurological actions in the house mouse (Mus musculus L). J Genet 50:192–201
Farah S, Sabry MA, Khuraibet A, Khaffagi S, Rudwan M, Hassan M et al (1997) Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome? Clin Genet 51:326–330
Fatemi SH (2002) The role of Reelin in the pathology of autism. Mol Psychiatry 7:919–920
Feess-Higgins A, Larroche J-C (1987) Le développement du cerveau foetal humain. Atlas anatomique, Masson, Paris
Ferland RJ, Batic LF, Neal J, Lian G, Bundock E, Lu J et al (2009) Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Hum Mol Genet 18:497–516
Ferreiro DM, Miller SP (2010) Imaging selective vulnerability in the developing nervous system. J Anat (Lond) 217:429–435
Fertuzinhos S, Krsnik Z, Kawasawa YI, Rašin M-R, Kwan KY, Chen J-G et al (2009) Selective depletion of molecularly defined cortical interneurons in human prosencephaly with severe striatal hypoplasia. Cereb Cortex 19:2196–2207
Fietz SA, Kelava I, Vogt J, Wilsch-Brauninger M, Nitsch R, Huttner WB (2010) OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling. Nat Neurosci 13:690–699
Filipovi B, Prostran M, Ilankovi N, Filipovi B (2004) Predictive potential of cavum septi pellucidi (CSP) in schizophrenics, alcoholics and persons with past head trauma. A postmortem study. Eur Arch Psychiatry Clin Neurosci 254:228–230
Fink GR, Frackowiak RSJ, Pietrzyk U, Passingham RF (1997) Multiple nonprimary motor areas in the human cortex. J Neurophysiol 77:2164–2174
Fishell G, Kriegstein AR (2003) Neuron from radial glia: the consequences of asymmetric inheritance. Curr Opin Neurobiol 13:34–41
Fisher SE, DeFries JC (2002) Developmental dyslexia: genetic dissection of a complex cognitive trait. Nat Rev Neurosci 3:767–780
Flores-Sarnat L (2002) Hemimegalencephaly: part 1. Genetic, clinical, and imaging aspects. J Child Neurol 17:373–384
Fox JW, Lamperti ED, Ekşioğlu YZ, Hong SE, Feng Y, Graham DA et al (1998) Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron 21:1315–1325
Franz DN, Bissler JJ, McCormack FX (2010) Tuberous sclerosis complex: Neurological, renal and pulmonary manifestations. Neuropediatrics 41:199–208
Frey S, Campbell JSW, Pike GB, Petrides M (2008) Dissociating the human language pathways with high angular resolution diffusion fiber tractography. J Neurosci 28:11435–11444
Friede RL (1989) Developmental neuropathology, 2nd edn. Springer, Berlin Heidelberg New York
Friederici AD (2009) Pathways to language: fiber tracts in the human brain. Trends Cogn Sci 13:175–181
Friederici AD (2012) The cortical language circuit: from auditory perception to sentence comprehension. Trends Cogn Sci 16:262–268
Friederici AD, Bahlmann J, Helm S, Schubotz RI, Anwander A (2006) The brain differentiates human and non-human grammars: functional localization and structural connectivity. Proc Natl Acad Sci U S A 103:2458–2463
Frotscher M (1997) Dual role of Cajal-Retzius cells and reelin in cortical development. Cell Tissue Res 290:315–322
Fukuyama Y, Osawa M, Suzuki H (1981) Congenital progressive muscular dystrophy of the Fukuyama type – clinical, genetic and pathological considerations. Brain Dev 3:1–29
Fukuzako H, Kodama S (1998) Cavum septum pellucidum in schizophrenia. Biol Psychiatry 43:466–469
Gadisseux J-F, Goffinet AM, Lyon G, Evrard P (1992) The human transient subpial granular layer: an optical, immunohistochemical, and ultrastructural analysis. J Comp Neurol 324:94–114
Galaburda AM (1999) Developmental dyslexia: a multilevel syndrome. Dyslexia 5:183–191
Galaburda AM, Kemper TL (1979) Cytoarchitectonic abnormalities in developmental dyslexia: a case study. Ann Neurol 6:94–100
Galaburda AM, Sherman GF, Rosen GD, Aboitiz F, Geschwind N (1985) Developmental dyslexia: four consecutive patients with cortical anomalies. Ann Neurol 18:222–233
Galaburda AM, Menard MT, Rosen GD (1994a) Evidence for aberrant auditory anatomy in developmental dyslexia. Proc Natl Acad Sci U S A 91:8010–8013
Galaburda AM, Wang PP, Bellugi U, Rossen M (1994b) Cytoarchitectonic anomalies in a genetically based disorder: Williams syndrome. Neuroreport 5:753–757
Galaburda AM, Schmitt JE, Atlas SW, Eliez S, Bellugi U (2001) Dorsal forebrain anomaly in Williams syndrome. Arch Neurol 58:1865–1869
Garel C (2004) MRI of the fetal brain. Normal development and cerebral pathologies. Springer, Berlin Heidelberg New York
Garey L (2010) When cortical development goes wrong: Schizophrenia as a neurodevelopmental disease of microcircuits. J Anat (Lond) 217:324–333
Geerdink N, Rotteveel JJ, Lammens M, Sistermans EA, Heikens GT, Gabreëls FJM et al (2002) MECP2 Mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings. Neuropediatrics 33:33–36
Geschwind DH, Levitt P (2007) Autism spectrum disorders: developmental disconnection syndromes. Curr Opin Neurobiol 17:103–111
Geyer S, Matelli M, Luppino G, Zilles K (2000) Functional neuroanatomy of the primate isocortical motor system. Anat Embryol (Berl) 202:443–474
Giedd JN, Blumenthal J, Jeffries NO, Castellanos FX, Liu H, Zijdenbos A et al (1999) Brain development during childhood and adolescence: a longitudinal MRI study. Nat Neurosci 2:861–863
Gilles FN, Nelson MD (2012) The developing human brain: growth and adversities. Mac Keith, London
Giraud A-L, Ramus F (2013) Neurogenetics and auditory processing in developmental dyslexia. Curr Opin Neurobiol 23:37–42
Glasser MF, Rilling JK (2008) DTI tractography of human brain’s language pathways. Cereb Cortex 18:2471–2482
Gleeson JG (2000) Classical lissencephaly and double cortex (subcortical band heterotopia): LIS1 and doublecortin. Curr Opin Neurol 13:121–125
Gleeson JG, Walsh CA (2000) Neuronal migration disorders: from genetic diseases to developmental mechanisms. Trends Neurosci 23:352–359
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic SF, Scheffer IE et al (1998) doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 92:63–72
Godfrey C, Clement E, Mein R, Brockington M, Smith J, Talim B et al (2007) Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. Brain 130:2725–2735
Godfrey C, Reghan Foley A, Clement A, Muntoni F (2011) Dystroglycanopathies: coming into focus. Curr Opin Genet Dev 21:278–285
Goffinet AM (1979) An early developmental defect in the cerebral cortex of the reeler mouse. Anat Embryol (Berl) 157:205–216
Goffinet AM (1984) Events governing organization of postmigratory neurons: studies on brain development in normal and reeler mice. Brain Res Rev 7:291–296
Goldberg EM, Coulter DA (2013) Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction. Nat Rev Neurosci 14:337–349
Goldowitz D, Cushing RC, Laywell E, D’Arcangelo G, Sheldon M, Sweet H et al (1997) Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin. J Neurosci 17:8767–8777
Gomez MR (1988) Tuberous sclerosis. Raven, New York
González JL, Russo CJ, Goldowitz D, Sweet HO, Davisson MT, Walsh CA (1997) Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype. J Neurosci 17:9204–9211
Gorman DG, Unützer J (1993) Brodmann’s “missing” numbers. Neurology 43:226–227
Götz M, Bolz J (1994) Differentiation of transmitter phenotypes in rat cerebral cortex. Eur J Neurosci 6:18–32
Gould E, Reeves AJ, Fallah M, Tanapat P, Gross CG, Fuchs E (1999) Hippocampal neurogenesis in adult Old World primates. Proc Natl Acad Sci U S A 96:5263–5267
Griffiths PD, Batty R, Reeves MJ, Connolly DJA (2009) Imaging the corpus callosum, septum pellucidum and fornix in children: normal anatomy and variations of normality. Neuroradiology 51:337–345
Groen WB, Zwiers MP, van der Gaag RJ, Buitelaar JK (2008) The phenotype and neural correlates of language in autism: an integrative review. Neurosci Biobehav Rev 32:1416–1425
Grove EA, Tole S (1999) Patterning events and specification signals in the developing hippocampus. Cereb Cortex 9:551–561
Grove EA, Tole S, Limon J, Yip L, Ragsdale CW (1998) The hem of the embryonic cerebral cortex is defined by the expression of multiple Wnt genes and is compromised in Gli3-deficient mice. Development 117:553–561
Guerrini R, Parrini E (2010) Neuronal migration disorders. Neurobiol Dis 38:154–166
Guerrini R, Dubeau F, Dulac O, Barkovich AJ, Kuzniecky R, Fett C et al (1997) Bilateral parasagittal parietooccipital polymicrogyria and epilepsy. Ann Neurol 41:65–73
Guerrini R, Barkovich AJ, Sztriha L, Dobyns WB (2000a) Bilateral frontal polymicrogyria: a newly recognized malformation syndrome. Neurology 54:909–913
Guerrini R, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K et al (2000b) Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment. Ann Neurol 48:39–48
Guerrini R, Sicca F, Parmeggiani L (2003) Epilepsy and malformations of the cerebral cortex. Epileptic Disord 9(Suppl 2):S9–S26
Guerrini R, Mei D, Sisodiya S, Sicca F, Harding B, Takahashi Y et al (2004) Germline and mosaic mutations of FLN1 in men with periventricular heterotopia. Neurology 63:51–56
Guerrini R, Dobyns WB, Barkovich AJ (2008) Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options. Trends Neurosci 31:154–162
Gutknecht L (2001) Full-genomic scans with autistic disorder: a review. Behav Genet 31:113–123
Gutmann DH, Zhang Y, Hasbani MJ, Goldberg MP, Plank TL, Henske EP (2000) Expression of the tuberous sclerosis complex gene products hamartin and tuberin in central nervous system tissues. Acta Neuropathol (Berl) 99:223–230
Habas PA, Scott JA, Roosta A, Rajagopalan V, Kim K, Rousseau F et al (2012) Early folding patterns and asymmetries of the normal human brain detected from in utero MRI. Cereb Cortex 22:13–25
Habib M (2000) The neurological basis of developmental dyslexia: an overview and working hypothesis. Brain 123:2373–2399
Hagberg B, Hagberg G (1997) Rett syndrome: epidemiology and geographical variability. Eur Child Adolesc Psychiatry 6:5–7
Hagberg B, Aicardi J, Dias K, Ramos O (1983) A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett’s syndrome: report of 35 cases. Ann Neurol 14:471–479
Hagerman RJ (2002) Physical and behavioral phenotype. In: Hagerman RJ, Hagerman PJ (eds) Fragile X syndrome: diagnosis, treatment and research, 3rd edn. Johns Hopkins University Press, Baltimore, MD
Hagerman RJ, Leehey M, Heinrichs W, Tassone F, Wilson R, Hills J et al (2001) Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 57:127–130
Hamel BCJ (1999) X-linked mental retardation – a clinical and molecular study. University of Nijmegen, Thesis
Hannan AJ, Servotte S, Katsnelson A, Sisodiya S, Blakemore C, Squier M, Molnár Z (1999) Characterization of nodular neuronal heterotopia in children. Brain 122:219–238
Hansen DV, Lui JH, Parker PR, Kriegstein AR (2010) Neurogenic radial glia in the outer subventricular zone of human neocortex. Nature 464:554–561
Harrison PJ, Law AJ (2006) Neuregulin 1 and schizophrenia: genetics, gene expression, and neurobiology. Biol Psychiatry 60:132–140
Hartmann D, De Strooper B, Saftig P (1999) Presenilin-1 deficiency leads to loss of Cajal-Retzius neurons and cortical dysplasia similar to human type 2 lissencephaly. Curr Biol 9:719–727
Hatanaka Y, Jones EG (1999) Novel genes expressed in the developing medial cortex. Cereb Cortex 9:577–585
Hawrylycz MJ, Lein ES, Guillozet-Bongaarts AL, Shen EH, Ng L, Miller JA et al (2012) An anatomical comprehensive atlas of the adult human brai transcriptome. Nature 489:391–399
Haydar TF, Kuan C-Y, Flavell RA, Rakic P (1999) The role of cell death in regulating the size and shape of the mammalian forebrain. Cereb Cortex 9:621–626
He S-Q, Dum RP, Strick PL (1993) Topographic organization of corticospinal projections from the frontal lobe: motor areas on the lateral surface of the hemisphere. J Neurosci 13:952–980
He S-Q, Dum RP, Strick PL (1995) Topographic organization of corticospinal projections from the frontal lobe: motor areas on the medial surface of the hemisphere. J Neurosci 14:3284–3306
Heimer L, Van Hoesen GW (2006) The limbic lobe and its output channels: implications for emotional functions and adaptive behaviour. Neurosci Biobehav Rev 30:126–147
Heimer L, de Olmos J, Alheid GF, Pearson J, Sakamoto N, Marksteiner J, Switzer RC (1999) The human basal forebrain, part 2. Handb Chem Neuroanat 15:57–226
Heimer L, Van Hoesen GW, Trimble M, Zahm DS (2008) Anatomy of neuropsychiatry. Elsevier, Amsterdam
Heimrich B, Vogt J, Simbürger E, Skutella T, Glumm R (2002) Axon guidance and the formation of specific connections in the hippocampus. Neuroembryology 1:154–160
Hengst M, Tücke J, Zerres M, Häusler M (2010) Megalencephaly, mega corpus callosum, and complete lack of motor development: delineation of a rare syndrome. Am J Med Genet A 152A:2360–2364
Hennou S, Khalilov I, Diabira D, Ben-Ari Y, Gozlan H (2002) Early sequential formation of functional GABAA and glutamatergic synapses in CA1 interneurons of the rat foetal hippocampus. Eur J Neurosci 16:197–208
Herbst DS, Miller JR (1980) Non-specific X-linked mental retardation. II. The frequency in British Columbia. Am J Med Genet 7:461–469
Hevner RF, Kinney HC (1996) Reciprocal entorhinal-hippocampal connections established by human fetal midgestation. J Comp Neurol 372:384–394
Hewitt W (1961) The development of the human internal capsule and lentiform nucleus. J Anat (Lond) 95:191–199
Hinton VJ, Brown WT, Wisniewski K, Rudelli RD (1991) Analysis of neocortex in three males with the fragile X syndrome. Am J Med Genet 41:289–294
Hirotsune S, Takahara T, Sasaki N, Hirose K, Yoshiki A, Ohashi T et al (1995) The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons. Nat Genet 10:77–83
His W (1904) Die Entwicklung des menschlichen Gehirns während der ersten Monate. Hirzel, Leipzig
Hochstetter F (1919) Beiträge zur Entwicklungsgeschichte des menschlichen Gehirns. I. Teil, Deuticke, Wien, Leipzig
Hofer S, Frahm J (2006) Topography of the human corpus callosum revisited – comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. Neuroimage 32:989–994
Homayouni R, Curran T (2000) Cortical development: Cdk5 gets into sticky situations. Curr Biol 10:331–334
Hong SE, Shugart YY, Huang DT, Al Shahwan S, Grant PE, Hourihane JO et al (2000) Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat Genet 26:93–96
Honig LS, Herrmann K, Shatz CJ (1996) Developmental changes revealed by immunohistochemical markers in human cerebral cortex. Cereb Cortex 6:794–806
Hori A (1996) Precocious cerebral development associated with agenesis of the corpus callosum in mid-fetal life: a transient syndrome? Acta Neuropathol (Berl) 91:120–125
Hori A (1997) Anatomical variants of brain structure: confused spatial relationship of the fornix to the corpus callosum and anterior commissure. Ann Anat 179:545–547
Hori A (1999) Morphology of brain malformations: beyond the classification, towards the integration. No Shinkei Geka (Neurol Surg) 27:969–985 (in Japanese)
Hori A, Stan AC (2004) Supracallosal longitudinal fiber bundle: heterotopic cingulum, dorsal fornix or Probst bundle? Neuropathology 24:56–59
Hori A, Friede RL, Fischer G (1983) Ventricular diverticles with localized dysgenesis of the temporal lobe in cloverleaf skull anomaly. Acta Neuropathol (Berl) 60:132–136
Hourihane JO, Bennett CP, Chaudhuri R, Robb SA, Martin ND (1993) A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema. Neuropediatrics 24:43–46
Houser CR (1990) Granule cell dispersion in the dentate gyrus of humans with temporal lobe epilepsy. Brain Res 535:195–204
Houser CR, Swartz BE, Walsh GO, Delgado-Escueta AV (1992) Granule cell disorganization in the dentate gyrus: possible alterations of neuronal migration in human temporal lobe epilepsy. Epilepsy Res Suppl 9:41–48
Howell BW, Hawkes R, Soriano P, Cooper JA (1997a) Neuronal position in the developing brain is regulated by mouse disabled-1. Nature 389:733–737
Howell BW, Herrick TM, Cooper JA (1997b) Reelin-induced tyrosine phosphorylation of disabled 1 during neuronal positioning. Genes Dev 13:643–648
Huang H, Zhang J, Wakana S, Zhang W, Ren T, Richards LJ et al (2006) White and grey matter development in human fetal, newborn and pediatric brains. Neuroimage 33:27–38
Huang H, Xue R, Zhang J, Ren T, Richards LJ, Yarowsky P et al (2009) Anatomical characterization of human fetal brain development with diffusion tensor magnetic resonance imaging. J Neurosci 29:4263–4273
Hubel DH, Wiesel TN (1962) Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex. J Physiol (Lond) 160:106–154
Hubel DH, Wiesel TN (1977) Functional architecture of macaque monkey visual cortex. Proc R Soc Lond B 198:1–59
Hubel DH, Wiesel TN, Stryker MP (1978) Anatomical demonstration of orientation columns in macaque monkey. J Comp Neurol 177:361–379
Humphrey T (1960) The development of the pyramidal tracts in human fetuses, correlated with cortical differentiation. In: Tower DB, Schadé JP (eds) Structure and function of the cerebral cortex. Elsevier, Amsterdam, pp 93–103
Humphrey T (1966a) The development of the human hippocampal formation correlated with some aspects of its phylogenetic history. In: Hassler R, Stephan H (eds) Evolution of the forebrain. Thieme, Stuttgart, pp 104–116
Humphrey T (1966b) Correlations between the development of the hippocampal formation and the differentiation of the olfactory bulbs. Alab J Med Sci 3:235–269
Humphreys P, Kaufmann WE, Galaburda AM (1990) Developmental dyslexia in women: neuropathological findings in three patients. Ann Neurol 28:727–738
Huttenlocher PR (1970) Dendritic development and mental defect. Neurology 20:381
Huttenlocher PR (1974) Dendritic development in neocortex of children with mental defect and infantile spasms. Neurology 24:203–210
Huttenlocher PR (1975) Synaptic and dendritic development and mental defect. In: Buchwald NA, Brazier MAB (eds) Brain mechanisms in mental retardation. Academic, New York, pp 123–140
Huttenlocher PR (1991) Dendritic and synaptic pathology in mental retrdation. Pediatr Neurol 7:79–85
Huttenlocher PR, Taravath S, Mojtahedi S (1994) Periventricular heterotopia and epilepsy. Neurology 44:51–55
Ikeda Y, Terashima T (1997) Corticospinal tract neurons are radially malpositioned in the sensory-motor cortex of the shaking rat Kawasaki. J Comp Neurol 383:370–380
Innocenti GM (1994) Some new trends in the study of the corpus callosum. Behav Brain Res 64:1–8
Inoue K, Lupski JR (2003) Genetics and genomics of behavioral and psychiatric disorders. Curr Opin Genet Dev 13:303–309
Insausti R, Amaral DG (2012) Hippocampal formation. In: Mai JK, Paxinos G (eds) The human nervous system. Elsevier, Amsterdam, pp 896–942
Insausti R, Amaral DG, Cowan WM (1987) The entorhinal cortex of the monkey: II. Cortical afferents. J Comp Neurol 264:356–395
Insausti R, Tuñón T, Sobreviela T, Insausti AM, Gonzalo LM (1995) The human entorhinal cortex: a cytoarchitectonic analysis. J Comp Neurol 355:171–198
Insausti R, Cebada-Sánchez S, Marcos P (2010) Postnatal development of the hippocampal formation. Adv Anat Embryol Cell Biol 206:1–89
Ip BK, Bayatti N, Howard NJ, Lindsay S, Clowry GJ (2011) The corticofugal neuron-associated genes ROBO1, SRGAP1, and CTIP2 exhibit an anterior to posterior gradient in early fetal human neocortex development. Cereb Cortex 21:1395–1407
Izzi L, Charron F (2011) Midline axon guidance and human genetic disorders. Clin Genet 80:226–234
Janssen A, Gressens P, Grabenbauer M, Baumgart E, Schad A, Vanhorebeek I et al (2003) Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues. J Neurosci 23:9732–9741
Jellinger K, Rett A (1976) Agyria-pachygyria (lissencephaly syndrome). Neuropediatrie 7:66–91
Jellinger K, Seitelberger F (1986) Neuropathology of Rett syndrome. Am J Med Genet Suppl 1(1986):259–288
Jeste SS (2011) The neurology of autism spectrum disorders. Curr Opin Neurol 24:132–139
Johnson MB, Kawasawa YI, Mason CE, Krsnik Z, Coppola G, Bogdanović D et al (2009) Functional and evolutionary insights onto human brain development through global transcriptome analysis. Neuron 62:494–509
Johnston MV, Mullaney B, Blue ME (2003) Neurobiology of Rett syndrome. J Child Neurol 18:688–692
Jonas R, Nguyen S, Hu B, Asarnow RF, LoPresti C, Curtiss S et al (2004) Cerebral hemispherectomy: hospital course, seizure, developmental, language, and motor outcomes. Neurology 62:1712–1721
Jones EG (2009) The origins of cortical interneurons: Mouse versus monkey and human cerebral cortex. Cereb Cortex 19:1953–1956
Judaš M, Radoš M, Jovanov-Milošević N et al (2005) Structural, immunohistochemical, and MR imaging properties of periventricular crossroads of growing cortical pathways in preterm infants. AJNR Am J Neuroradiol 26:2671–2684
Judaš M, Sedmak G, Pletikos M, Jovanov-Milošević N (2010) Populations of subplate and interstitial neurons in fetal and adult human telencephalon. J Anat (Lond) 217:381–399
Just MA, Cherkassy VL, Keller TA, Minshew NJ (2004) Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity. Brain 127:1811–1821
Kahle W (1969) Die Entwicklung der menschlichen Grosshirnhemisphäre. Schriftenr Neurol 1:1–116
Kaindl AM, Passemard M, Kumar P, Kraemer N, Issa L, Zwirner A et al (2009) Many roads lead to primary autosomal recessive microcephaly. Prog Neurobiol 90:363–383
Kakita A, Hayashi S, Moro F, Guerrini R, Ozawa T, Ono K et al (2002) Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex. Acta Neuropathol (Berl) 104:649–657
Kang HJ, Kawasawa YI, Cheng F, Zhu Y, Xu X, Li M et al (2011) Spatio-temporal transcriptome of the human brain. Nature 478:483–489
Kanner L (1943) Autistic disturbances of affective contact. Nervous Child 2:217–250
Kanold PO, Luhmann HJ (2010) The subplate and early cortical circuits. Annu Rev Neurosci 33:23–48
Kasprian G, Brugger PC, Schöpf V, Mitter C, Weber M, Hainfellner JA, Prayer D (2013) Assessing prenatal white matter connectivity in commissural agenesis. Brain 136:168–179
Kato M, Dobyns WB (2005) X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term ‘interneuronopathy’. J Child Neurol 20:392–397
Kaufmann WE, Galaburda AM (1989) Cerebrocortical microdysgenesis in neurologically normal subjects: a histopathological study. Neurology 39:238–244
Kaufmann WE, Moser HW (2000) Dendritic anomalies associated with mental retardation. Cereb Cortex 10:981–991
Keibel F, Mall FP (eds) (1911) Handbuch der Entwicklungsgeschichte des Menschen. Hirzel, Leipzig
Keibel F, Mall FP (eds) (1912) Manual of human embryology. Lippincott, Philadelphia, PA
Kemper TL, Bauman M (1998) Neuropathology of infantile autism. J Neuropathol Exp Neurol 57:645–652
Kempermann G, Jessberger S, Steiner B, Kronenberg G (2004) Milestones of neuronal development in the adult hippocampus. Trends Neurosci 27:447–452
Kerner B, Graham JM Jr, Golden JA, Pepkowitz SH, Dobyns WB (1999) Familial lissencephaly with cleft palate and severe cerebellar hypoplasia. Am J Med Genet 87:440–445
Khazipov R, Esclaper M, Caillard O, Bernard C, Khalilov I, Tyzio R et al (2001) Early development of neuronal activity in the primate hippocampus in utero. J Neurosci 21:9770–9781
Kilb W, Hartmann D, Saftig P, Luhmann HJ (2004) Altered morphological and electrophysiological properties of Cajal-Retzius cells in cerebral cortex of embryonic Presenilin-1 knockout mice. Eur J Neurosci 20:2749–2756
Kirkcaldie MTK (2012) Neocortex. In: Watson C, Paxinos G, Puelles L (eds) The mouse nervous system. Elsevier, Amsterdam, pp 52–111
Kleefstra T, Smidt M, Banning MJ, Oudakker AR, Van Esch H, de Brouwer AP et al (2005) Disruption of the gene euchromatin histone methyl transferase 1 (Eu-HMTase 1) is associated with the 9q34 subtelomeric deletion syndrome. J Med Genet 42:299–306
Kleefstra T, Brunner HG, Amiel J, Oudakker AR, Nillesen WM, Magee A et al (2006) Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome. Am J Hum Genet 79:370–377
Klingler J (1948) Die makroskopische Anatomie der Ammonsformation. Denkschriften der Schweizerischen Naturforschenden Gesellschaft, vol 78. Fretz, Zürich
Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondo-Iida E, Nomura Y et al (1998) An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 394:388–392
Koenderink MJT, Uylings HBM (1995) Postnatal maturation of layer V pyramidal neurons in the human prefrontal cortex. A quantitative Golgi analysis. Brain Res 678:233–243
Koenderink MJT, Uylings HBM, Mrzljak L (1994) Postnatal maturation of the layer III pyramidal neurons in the human prefrontal cortex: A quantitative Golgi analysis. Brain Res 653:173–182
Koester SE, O’Leary DDM (1994) Axons of early generating neurons in cingulate cortex pioneer the corpus callosum. J Neurosci 14:6608–6620
Kooy RF (2003) Of mice and the fragile X syndrome. Trends Genet 19:148–154
Kooy RF, Reyniers E, Verhoye M, Sijbers J, Bakker CE, Oostra BA et al (1999) Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging. Eur J Hum Genet 7:526–532
Kornack DR, Rakic P (1995) Radial and horizontal development of clonally related cells in the primate neocortex: relationship to distinct mitotic lineages. Neuron 15:311–321
Kostović I (1990a) Zentralnervensystem. In: Hinrichsen KV (ed) Humanembryologie. Lehrbuch und Atlas der vorgeburtlichen Entwicklung des Menschen. Springer, Berlin/Heidelberg/New York, pp 381–448
Kostović I (1990b) Structural and histochemical reorganization of the human prefrontal cortex during prenatal and postnatal life. Prog Brain Res 85:223–240
Kostović I, Goldman-Rakic PS (1983) Transient cholinesterase staining in the mediodorsal nucleus of the thalamus and its connectivity in the developing human and monkey brain. J Comp Neurol 219:431–447
Kostović I, Jovanov-Milošević N (2006) The development of cerebral connections during the first 20–45 weeks’ gestation. Semin Fetal Neonatal Med 11:415–422
Kostović I, Judaš M (2002) The role of the subplate zone in the structural plasticity of the developing human cerebral cortex. Neuroembryology 1:145–153
Kostović I, Judaš M (2007) Transient patterns of cortical lamination during prenatal life: Do they have implications in treatment? Neurosci Biobehav Rev 31:1157–1168
Kostović I, Judaš M (2010) The development of the subplate and thalamocortical connections in the human fetal brain. Acta Paediatr 99:1119–1127
Kostović I, Rakic P (1990) Developmental history of the transient subplate in the visual and somatosensory cortex of the macaque monkey and human brain. J Comp Neurol 297:441–470
Kostović I, Vasung L (2009) Insights from in vitro fetal magnetic resonance imaging of cerebral development. Semin Perinatol 33:220–233
Kostović I, Lukinovic N, Judaš M, Bogdanovich N, Mrzljak L, Zecevic N, Kubat M (1989) Structural basis of the developmental plasticity in the human cerebral cortex: the role of the transient subplate zone. Metab Brain Dis 4:17–23
Kotrla KJ, Sater AM, Weinberger DR (1997) Neuropathology, neurodevelopment and schizophrenia. In: Keshavan MS, Murray RM (eds) Neurodevelopment & adult psychopathology. Cambridge University Press, Cambridge, pp 187–198
Kriegstein AR, Alvarez-Buylla A (2009) The glial nature of embryonic and adult neural stem cells. Annu Rev Neurosci 32:149–184
Kriegstein AR, Noctor SC (2004) Patterns of neuronal migration in the embryonic cortex/Trends Neurosci 27:393–399
Krsek P, Pieper T, Karlmeier A, Hildebrandt M, Kolodziejczyk D, Winkler P et al (2009) Different presurgical characteristics and seizure outcomes in children with focal cortical dysplasia type I or II. Epilepsia 50:125–137
Kumar A, Juhasz C, Asano E, Sundaram SK, Makki MI, Chugani DC, Chugani HT (2009) Diffusion tensor imaging study of the cortical origin and course of the corticospinal tract in healthy children. AJNR Am J Neuroradiol 30:1963–1970
Kumar RA, Pilz DT, Babatz TD, Cushion TD, Harvey K, Topf M et al (2010) TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins. Hum Mol Genet 19:2817–2827
Kuypers HGJM (1981) Anatomy of the descending pathways. In: Brooks VB, Brookhart JM, Mountcastle VB (eds) Handbook of physiology – the nervous system, vol 2, Motor systems. American Physiological Society, Bethesda, MD, pp 597–666
Kuzniecky R, Andermann F, Guerrini R (1993) Congenital bilateral perisylvian syndrome: a study of 31 patients. The Congenital Bilateral Perisylvian Syndrome Multicenter Collaborative Study. Lancet 341:608–612
Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, Rasini MR et al (2012) Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex. Cell 149:899–911
Kwiatkowski DJ, Short MP (1994) Tuberous sclerosis. Arch Dermatol 130:348–354
Kwon YT, Tsai L-H (1998) A novel disruption of cortical development in p35-/- mice distinct from reeler. J Comp Neurol 395:510–522
Kwon JS, Shenton ME, Hirayasu Y, Salisbury DF, Fischer IA, Dickey CC et al (1998) MRI study of cavum septi pellicidi in schizophrenia, affective disorders, and schizotypal personality disorders. Am J Psychiatry 15:509–515
Kyin R, Hua Y, Baybis M, Scheithauer B, Kolson D, Uhlmann E et al (2001) Differential cellular expression of neurotrophins in cortical tubers of the tuberous sclerosis complex. Am J Pathol 159:1541–1554
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001) A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413:519–523
Lai G, Pantazatos SP, Schneider H, Hirsch J (2012) Neural systems for speech and song in autism. Brain 135:961–975
Lamantia AS, Rakic P (1990a) Axon overproduction and elimination in the corpus callosum of the developing rhesus monkey. J Neurosci 10:2165–2175
Lamantia AS, Rakic P (1990b) Cytological and quantitative characteristics of four cerebral commissures in the rhesus monkey. J Comp Neurol 291:520–537
Lambert de Rouvroit C, Goffinet AM (1998) The reeler mouse as a model of brain development. Adv Anat Embryol Cell Biol 150:1–108
Lammens M (2000) Neuronal migration disorders in man. Eur J Morphol 38:327–333
Lammens M, Hiel JAP, Gabreëls FJM, van Engelen BGM, van den Heuvel LPWJ, Weemaes CMR (2003) Nijmegen breakage syndrome: a neuropathological study. Neuropediatrics 34:189–193
LaMonica BE, Lui JH, Wang X, Kreigstein AR (2012) OSVZ progenitors in the human cortex: an updated perspective on neurodevelopmental disease. Curr Opin Neurobiol 22:747–753
Lamparello P, Baybis M, Pollard J, Hol EM, Eisenstat DD, Aronica E, Crino PB (2007) Developmental lineage of cell types in cortical dysplasia with balloon cells. Brain 130:2267–2276
Lavdas AA, Grigoriou M, Pachnis V, Parnavelas JG (1999) The medial ganglionic eminence gives rise to a population of early neurons in the developing cerebral cortex. J Neurosci 19:7881–7888
Lawes INC, Barrick TR, Murugam V, Spierings N, Evans DR, Song M, Clark CA (2008) Atlas-based segmentation of white matter tracts of the human brain using diffusion tensor tractography and comparison with classical dissection. Neuroimage 39:62–79
Laxova R, Ohara PT, Timothy JAD (1972) A further example of a lethal autosomal recessive condition in sibs. J Ment Defic Res 16:139–143
Lee KS, Schottler F, Collins JL, Lanzino G, Couture D, Rao A et al (1997) A genetic animal model of human neocortical heterotopia associated with seizures. J Neurosci 17:6236–6242
Lee KS, Collins JL, Anzivino MJ, Frankel EA, Schottler F (1998) Heterotopic neurogenesis in a rat with cortical heterotopia. J Neurosci 18:9365–9375
Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, Bernard A et al (2007) Genome-wide atlas of gene expression in the adult mouse brain. Nature 445:168–176
Lemire RJ, Loeser JJ, Leech RW, Alvord EC Jr (1975) Normal and abnormal development of the human nervous system. Harper & Row, Hagerstown
Lena G, van Calenberg F, Genitori L, Choux M (1995) Supratentorial interhemispheric cysts associated with callosal agenesis: surgical treatment and outcome in 16 children. Childs Nerv Syst 11:568–573
Lent R, Uziel D, Baudrimont M, Fallet C (2005) Cellular and molecular tunnels surrounding the forebrain commissures of human fetuses. J Comp Neurol 483:375–382
Letinić K, Zoncu R, Rakic P (2002) Origin of GABAergic neurons in the human neocortex. Nature 417:645–649
Leventer RJ, Dobyns WB (2003) Periventricular gray matter heterotopias: a heterogeneous group of malformations of cortical development. In: Barth PG (ed) Disorders of neuronal migration. Mac Keith, London, pp 72–82
Levine D, Barnes PD (1999) Cortical maturation in normal and abnormal fetuses as assessed with prenatal MR imaging. Radiology 210:751–758
Levitt P, Eagleson KL, Powell EM (2004) Regulation of neocortical interneuron development and the implications for neurodevelopmental disorders. Trends Neurosci 27:400–406
Lewis DA, Levitt P (2002) Schizophrenia as a disorder of neurodevelopment. Annu Rev Neurosci 25:409–432
Ligon KL, Echelard Y, Assimacopoulos S, Danielian PS, Kaing S, Grove EA et al (2003) Loss of Emx function leads to ectopic expression of Wnt1 in the developing telencephalon and cortical dysplasia. Development 130:2275–2287
Lim C, Blume HW, Madsen JR, Saper CB (1997a) Connections of the hippocampal formation in humans. I. The mossy fiber pathway. J Comp Neurol 385:325–351
Lim C, Mufson EJ, Kordower JW, Blume HW, Madsen JR, Saper CB (1997b) Connections of the hippocampal formation in humans. II. The endfolial fiber pathway. J Comp Neurol 385:352–371
Liu H, Abecasis GR, Heath SC, Knowles A, Demars S, Chen YJ et al (2002) Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci U S A 99:16859–16864
Livingstone MS, Rosen GD, Drislane FW, Galaburda AM (1991) Physiological and anatomical evidence for a magnocellular defect in developmental dyslexia. Proc Natl Acad Sci U S A 88:7943–7947
Loeser JD, Alvord EC Jr (1968) Agenesis of the corpus callosum. Brain 91:553–570
López-Bendito G, Molnár Z (2003) Thalamocortical development: how are we going to get there? Nat Rev Neurosci 4:276–289
López-Bendito G, Flames N, Ma L, Fouquet C, Di Meglio T, Chédotal A et al (2007) Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain. J Neurosci 27:3395–3407
Ludwig E, Klingler J (1956) Atlas cerebri humani. Karger, Basel
Lui JH, Hansen DV, Kriegstein AR (2011) Development and evolution of the human neocortex. Cell 146:18–36
Lund JS, Angelucci A, Bressloff PC (2003) Anatomical substrates for functional columns in macaque monkey primary visual cortex. Cereb Cortex 13:15–24
Luo R, Jeong S-J, Jin Z, Strokes N, Li S, Piao X (2011) G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination. Proc Natl Acad Sci U S A 108:12925–12930
Luskin MB, Pearlman AL, Sanes JR (1988) Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a recombinant retrovirus. Neuron 1:635–647
Mai JK, Berger K, Sofroniew MV (1993) Morphometric evaluation of neurophysin-immunoreactivity in the human brain: Pronounced inter-individual variability and evidence for altered staining patterns in schizophrenia. J Hirnforsch 34:133–154
Mallamaci A, Mercurio S, Muzio L, Cecchi C, Pardini CL, Gruss P, Boncinelli E (2000) The lack of Emx2 causes impairment of Reelin signaling and defects of neuronal migration in the developing cerebral cortex. J Neurosci 20:1109–1118
Manoranjan B, Provias JP (2010) Hemimegalencephaly: a fetal case with neuropathological confirmation and review of the literature. Acta Neuropathol (Berl) 120:117–130
Marcorelles P, Laquierrière A, Adde-Michel C, Marret S, Saugier-Veber P, Beldjord C, Friocourt G (2010) Evidence for tangential migration disturbances in human lissencephaly resulting from defects in LIS1, DCX and ARX genes. Acta Neuropathol (Berl) 120:503–515
Marcotte A, Aronica E, Baybis M, Crino PB (2012) Cytoarchitectural alterations are widespread in cerebral cortex in tuberous sclerosis complex. Acta Neuropathol (Berl) 123:685–693
Marín O (2012) Interneuron dysfunction in psychiatric disorders. Nat Rev Neurosci 13:107–120
Marín O, Rubinstein JLR (2001) A long, remarkable journey: tangential migration in the telencephalon. Nat Rev Neurosci 2:780–790
Marín O, Anderson SA, Rubinstein JLR (2000) Origin and molecular specification of striatal interneurons. J Neurosci 20:6063–6076
Marín O, Yaron A, Bagri A, Tessier-Lavigne M, Rubinstein JLR (2001) Sorting of striatal and cortical interneurons regulated by semaphorin-neuropilin interactions. Science 293:872–875
Marín-Padilla M (1971) Early prenatal ontogenesis of the cerebral cortex (neocortex) of the cat (Felis domestica): a Golgi study. I. The primordial neocortical organization. Z Anat Entw Gesch 134:117–145
Marín-Padilla M (1972) Structural abnormalities of the cerebral cortex in human chromosomal aberrations. A Golgi study. Brain Res 44:625–629
Marin-Padilla M (1976) Pyramidal cell abnormalities in the motor cortex of a child with Down’s syndrome. A Golgi study. J Comp Neurol 167:63–82
Marín-Padilla M (1978) The dual origin of the mammalian neocortex and evolution of the cortical plate. Anat Embryol 152:109–126
Marín-Padilla M (1990) Origin, formation, and prenatal maturation of the human cerebral cortex: an overview. J Craniofac Genet Dev Biol 10:137–146
Marín-Padilla M (1992) Ontogenesis of the pyramidal cell of the mammalian neocortex and developmental cytoarchitectonics: a unifying theory. J Comp Neurol 321:223–240
Marín-Padilla M (1996) Developmental neuropathology and impact of perinatal brain damage. I. Hemorrhagic lesions of neocortex. J Neuropathol Exp Neurol 55:758–773
Marín-Padilla M (1997) Developmental neuropathology and impact of perinatal brain damage. II. White matter lesions of neocortex. J Neuropathol Exp Neurol 56:219–235
Marín-Padilla M (1998) Cajal-Retzius cells and the development of the neocortex. Trends Neurosci 21:64–71
Marín-Padilla M (1999) Developmental neuropathology and impact of perinatal brain damage. III. Gray matter lesions of the neocortex. J Neuropathol Exp Neurol 58:407–429
Marshall CR, Noor A, Vincent JB, Lionel AC, Feuk L, Skaug J et al (2008) Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet 82:477–488
Matelli M, Luppino G, Geyer S, Zilles K (2004) Motor cortex. In: Paxinos G, Mai JK (eds) The human nervous system, 2nd edn. Elsevier, Amsterdam, pp 973–996
McConnell SK, Kaznowski CE (1991) Cell cycle dependence of laminar determination in developing cerebral cortex. Science 254:282–285
McConnell SK, Ghosh A, Shatz CJ (1989) Subplate neurons pioneer the first axon pathway from the cerebral cortex. Science 245:978–982
McConnell SK, Ghosh A, Shatz CJ (1994) Subplate pioneers and the formation of descending connections from cerebral cortex. J Neurosci 14:1892–1907
Meencke H-J (2000) Diagnosis of cortical and subcortical dysplasias in epilepsy. In: Schmidt D, Schachter SC (eds) Epilepsy – problemsolving in clinical practice. Dunitz, London, pp 95–109
Mesulam M-M (1985) Patterns in behavioral neuroanatomy: association areas, the limbic system, and hemispheric specialization. In: Mesulam M-M (ed) Principles of behavioral neurology. Davis, Philadelphia, PA, pp 1–70
Mesulam M-M (2000) Behavioral neuroanatomy: large-scale networks, association cortex, frontal syndromes, the limbic system, and hemispheric specializations. In: Mesulam M-M (ed) Principles of behavioral and cognitive neurology, 2nd edn. Oxford University Press, New York, pp 1–120
Mesulam M-M, Mufson EJ (1985) The insula of reil in man and monkey. Architectonics, connectivity and function. In: Peters A, Jones EG (eds) The cerebral cortex, vol 4. Plenum, New York, pp 179–226
Meyer G (2007) Genetic control of neuronal migrations in human cortical development. Adv Anat Embryol Cell Biol 189:1–114
Meyer G (2010) Building a human cortex: the evolutionary differentiation of Cajal-Retzius cells and the cortical hem. J Anat (Lond) 217:334–343
Meyer G, Goffinet AM (1998) Prenatal development of reelin-immunoreactive neurons in the human neocortex. J Comp Neurol 397:29–40
Meyer G, Gonzalez-Hernandez T (1993) Developmental changes in layer I of the human neocortex during prenatal life: a DiI-tracing and AChE and NADPH-d histochemical study. J Comp Neurol 338:317–336
Meyer G, Wahle P (1999) The paleocortical ventricle is the origin of reelin-expressing neurons in the marginal zone of the foetal human neocortex. Eur J Neurosci 11:3937–3944
Meyer G, Soria JM, Martínez-Galán JR, Martín-Clemente B, Fairén A (1998) Different origins and developmental histories of transient neurons in the marginal zone of the fetal and neonatal rat cortex. J Comp Neurol 397:493–518
Meyer G, Goffinet AM, Fairén A (1999) What is a Cajal-Retzius cell? A reassessment of a classical cell type based on recent observations in the developing neocortex. Cereb Cortex 9:765–775
Meyer G, Castro R, Soria JM, Fairén A (2000a) The subpial granular layer in the developing cerebral cortex of rodents. In: Goffinet AM, Rakic P (eds) Mouse brain development. Springer, Berlin/Heidelberg/New York, pp 277–291
Meyer G, Schaaps JP, Moreau L, Goffinet AM (2000b) Embryonic and early fetal development of the human neocortex. J Neurosci 20:1858–1868
Meyer G, Pérez-García CG, Abraham H, Coput D (2002) Expression of p73 and Reelin in the developing human cortex. J Neurosci 22:4973–4986
Meyer G, Lambert de Rouvroit C, Goffinet AM, Wahle P (2003) Disabled-1 mRNA and protein expression in developing human cortex. Eur J Neurosci 17:517–525
Meynert T (1872) Vom Gehirne der Säugethiere. In: Stricker’s Handbuch der Lehre von den Geweben des Menschen und der Thiere, Vol 2. Engelmann, Leipzig, pp 694–808 (English translation by Putnam JJ (1872) Stricker S (ed) Manual of histology, William Wood, New York, pp 650–766)
Miles JH (2011) Autism spectrum disorders – a genetics review. Genes Med 13:278–294
Miles JH, Takahashi TN, Bagby S, Schota PK, Vaslow DF, Wang CH et al (2005) Essential versus complex autism: definition of fundamental prognostic subtypes. Am J Hum Genet 135:171–180
Miller DT, Adams MP, Aradhya S, Biesecker LG, Brothman AR et al (2010) Consensus statement: chromosomal microarray is the first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 86:749–764
Mione MC, Cavanagh JFR, Harris B, Parnavelas JG (1997) Cell fate specification and symmetrical/asymmetrical divisions in the developing cerebral cortex. J Neurosci 17:2018–2029
Mirzaa GM, Conway RL, Gripp KW, Lorman-Sagic T, Siegel DH, de Vries LS et al (2012) Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis. Am J Med Genet A 158:269–291
Mirzaa GM, Rivière J-B, Dobyns WB (2013) Megalencephaly syndromes and activating mutations in the P13K-AKT pathway: MPPH and MCAP. Am J Med Genet C Semin Med Genet 163C:122–130
Mischel PS, Nguyen LP, Vinters HV (1995) Cerebral cortical dysplasias associated with pediatric epilepsy. Review of neuropathological features and proposal for a grading system. J Neuropathol Exp Neurol 54:137–153
Miyata T, Kawaguchi A, Okano H, Ogawa M (2001) Asymmetric inheritance of radial glial fibers by cortical neurons. Neuron 31:727–741
Miyata H, Chute DJ, Fink J, Villablanca P, Vinters HV (2004) Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia. Acta Neuropathol (Berl) 107:69–81
Mizuguchi M, Takahashi S, Ikeda K, Kato M, Hori A (2002) Loss of doublecortin in heterotopic gray matter of a fetus with subcortical laminar heterotopia. Neurology 59:143–144
Mochida GH (2009) Genetics and biology of microcephaly and lissencephaly. Semin Pediatr Neurol 16:120–126
Mochida GH, Walsh CA (2001) Molecular genetics of human microcephaly. Curr Opin Neurobiol 14:151–156
Molnár Z, Adams R, Goffinet AM, Blakemore C (1998) The role of the first postmitotic cortical cells in the development of thalamocortical innervation in the reeler mouse. J Neurosci 18:5746–5765
Molyneaux BJ, Arlotta P, Fame RM, MacDonald JL, MacQuarrie KL, Macklis JD (2009) Novel subtype-specific genes identify distinct populations of callosal projection neurons. J Neurosci 29:12343–12354
Moore CJ, Daly EM, Tassone F, Tysoe C, Schmitz N, Ng V et al (2004) The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy. Brain 127:2672–2681
Mori S, Wakana S, Nagae-Poetscher LM, van Zijl PC (2005) MRI atlas of human white matter. Elsevier, Amsterdam
Morris-Rosendahl DJ, Segel R, Born AP, Conrad C, Loeys B, Brooks SS et al (2008) New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish. Eur J Hum Genet 18:1100–1106
Mostofsky SH, Mazzocco MMM, Aakalu G, Warsofsky IS, Denckla MB, Reiss AL (1998) Decreased cerebellar posterior vermis size in fragile X syndrome. Correlation with neurocognitive performance. Neurology 50:121–130
Mountcastle VB (1957) Modality and topographic properties of single neurons of cat’s somatic sensory cortex. J Neurophysiol 20:408–434
Mountcastle VB (1997) The columnar organization of the neocortex. Brain 120:701–722
Mrzljak L, Uylings HBM, Kostović I, van Eden CG (1988) Prenatal development of neurons in the human prefrontal cortex. I. A qualitative Golgi study. J Comp Neurol 271:355–386
Mrzljak L, Uylings HBM, van Eden CG, Judaš M (1990) Neuronal development in human prefrontal cortex in prenatal and postnatal stages. Prog Brain Res 85:185–222
Muller RA (2007) The study of autism as a distributed disorder. Ment Retard Dev Disabil Res Rev 13:85–95
Nadarajah B, Brunstrom JE, Grutzendler J, Wong ROL, Pearlman AL (2001) Two modes of radial migration in early development of the cerebral cortex. Nat Neurosci 4:143–150
Nagano T, Morikubo S, Sato M (2004) Filamin A and FILIP (Filamin A-interacting protein) regulate cell polarity and motility in neocortical subventricular and intermediate zones during radial migration. J Neurosci 24:9648–9657
Naidu S (1997) Rett syndrome: a disorder affecting early brain growth. Ann Neurol 42:3–10
Naidu S, Bibat G, Kratz L, Kelley RI, Pevsner J, Hoffman E et al (2003) Clinical variability in Rett syndrome. J Child Neurol 18:662–668
Nance MA, Berry SA (1992) Cockayne syndrome: review of 140 cases. Am J Med Genet 42:68–84
Nathan PW, Smith MC, Deacon P (1990) The corticospinal tracts in man. Course and location of fibres at different segmental levels. Brain 113:303–324
Neu RL, Kajii T, Gardner LI, Nagyfy SF, King S (1971) A lethal syndrome of microcephaly with multiple congenital anomalies in three siblings. Pediatrics 47:610–612
Newton JM, Ward NS, Parker GJM, Deichmann R, Alexander DC, Friston KJ, Frackowiak RSJ (2006) Non-invasive mapping of corticofugal fibres from multiple motor areas – relevance to stroke recovery. Brain 129:1844–1858
Nguyen Ba-Charvet KT, Brose K, Marillat V, Kidd T, Goodman CS, Tessier-Lavigne M et al (1999) Slit2-mediated chemorepulsion and collapse of developing forebrain axons. Neuron 22:463–473
Nicolson RI, Fawcett AJ, Dean P (2001) A TINS debate – hindbrain versus the forebrain: a case for cerebellar deficit in developmental dyslexia. Trends Neurosci 24:508–516
Nieuwenhuys R (1994) The neocortex. An overview of its evolutionary development, structural organization and synaptology. Anat Embryol (Berl) 190:307–337
Nieuwenhuys R (1996) The greater limbic system, the emotional motor system and the brain. Prog Brain Res 107:551–580
Nieuwenhuys R (2013) The myeloarchitectonic studies on the human cerebral cortexof the Vogt-Vogt school, and their significance for the interpretation of functional neuroimaging data. Brain Struct Funct 218:303–352
Nieuwenhuys R, Voogd J, van Huijzen C (1988) The human central nervous system, 3rd edn. Springer, Berlin Heidelberg New York
Nikolic M, Dudek YT, Kwon YT, Ramos YFM, Tsai L-H (1996) The cdk5/p35 kinase is essential for neurite outgrowth during neuronal differentiation. Genes Dev 7:816–825
Nimchinski EA, Oberlander AM, Svoboda K (2001) Abnormal development of dendritic spines in FMR1 knock-out mice. J Neurosci 21:5139–5146
Noctor SC, Flint AC, Weissman TA, Dammerman RS, Kriegstein AR (2001) Neurons derived from radial glial cells establish radial units in neocortex. Nature 409:714–720
Noctor SC, Martínez-Cerdeňo V, Ivic L, Kriegstein AR (2004) Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases. Nat Neurosci 7:136–144
Noctor SC, Martínez-Cerdeňo V, Kriegstein AR (2007) Contribution of intermediate progenitor cells to cortical histogenesis. Arch Neurol 64:639–642
Noctor SC, Martínez-Cerdeňo V, Kriegstein AR (2008) Distinct behaviors of neural stem and progenitor cells underlie cortical neurogenesis. J Comp Neurol 508:28–44
Nopoulos PC, Giedd JN, Andreasen NC, Rapoport JL (1998) Frequency and severity of enlarged cavum septi pellucidi in childhood and schizophrenia. Am J Psychiatry 155:1074–1079
Norman MG, McGillivray BC, Kalousek DK, Hill A, Poskitt KJ (1995) Congenital malformations of the brain. Pathological, embryological, clinical, radiological and genetic aspects. Oxford University Press, New York
Nudo RJ, Masterton RB (1990) Descending pathways to the spinal cord. III. Sites of origin of the corticospinal tract. J Comp Neurol 296:559–583
O’Donnell WT, Warren ST (2002) A decade of molecular studies of fragile X syndrome. Annu Rev Neurosci 25:315–338
O’Leary DDM (1989) Do cortical areas emerge from a protocortex? Trends Neurosci 12:400–406
O’Leary DDM, Koester SE (1993) Development of projection neuron types, axon pathways, and patterned connections of the mammalian cortex. Neuron 10:991–1006
O’Leary DDM, Nakagawa Y (2002) Patterning centers, regulatory genes and extrinsic mechanisms controlling arealization of the neocortex. Curr Opin Neurobiol 12:14–25
O’Leary DDM, Sahara S (2008) Genetic regulation of arealization of the neocortex. Curr Opin Neurobiol 18:90–100
O’Rahilly R, Müller F (1999) The embryonic human brain. An atlas of developmental stages, 2nd edn. Wiley, New York
O’Rourke NA, Chenn A, McConnell SK (1997) Postmitotic neurons migrate tangentially in the cortical ventricular zone. Development 124:997–1005
Oba H, Barkovich AJ (1995) Holoprosencephaly: an analysis of callosal formation and its relation to development of the interhemispheric fissure. AJNR Am J Neuroradiol 16:453–456
Oeschger FM, Wang WZ, Lee S, García-Moreno F, Goffinet AM, Arbonés ML et al (2012) Gene expression analysis of the embryonic subplate. Cereb Cortex 22:1343–1359
Ogawa M, Miyata T, Nakajima K, Yagyu K, Seike M, Ikenaka K et al (1995) The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons. Neuron 14:899–912
Ohshima T, Ward JM, Huh CG, Longenecker G, Veeranna XX, Pant HC et al (1996) Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. Proc Natl Acad Sci U S A 93:11173–11178
Oishi K, Zilles K, Amunts K, Faria A, Jiang H, Li X et al (2008) Human brain white matter atlas: identification and assignment of common anatomical structures in superficial white matter. Neuroimage 43:447–457
Ono M, Kubik S, Abermathey CD (1990) Atlas of the cerebral sulci. Thieme, Stuttgart
Overy K, Molnar-Szakacs I (2009) Being together in time: musical experience and the mirror neuron system. Music Percept 26:489–504
Owens DF, Kriegstein AR (2002) Is there more to GABA than synaptic inhibition? Nat Rev Neurosci 3:715–727
Palmen SJMC, van Engeland H, Hof PR, Schmitz C (2004) Neuropathological findings in autism. Brain 127:2572–2583
Palmini A, Gambardella A, Andermann F, Dubeau F, da Costa JC, Olivier A et al (1995) Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results. Ann Neurol 37:476–487
Palmini A, Najm I, Avanzini G, Babb T, Guerrini R, Foldvary-Schaefer N et al (2004) Terminology and classification of the cortical dysplasias. Neurology 62:S2–S8
Pandya DN, Karol EA, Heilbronn D (1971) The topographical distribution of interhemispheric projections in the corpus callosum of the rhesus monkey. Brain Res 32:31–43
Parent JM (2007) Adult neurogenesis in the intact and epileptic dentate gyrus. Prog Brain Res 163:529–540
Parent JM, Lowenstein DH (1997) Mossy fiber reorganization in the epileptic hippocampus. Curr Opin Neurol 10:103–109
Parnavelas JG (2000) The origin and migration of cortical neurones: new vistas. Trends Neurosci 23:126–131
Parnavelas JG, Barfield JA, Franke E, Luskin MB (1991) Separate progenitor cells give rise to pyramidal and nonpyramidal neurons in the rat telencephalon. Cereb Cortex 1:463–468
Patel DR, Greydanus DE, Calles JL Jr, Pratt HD (2010) Developmental disabilities across the lifespan. Dis Mon 56:304–397
Paul LK, Brown WS, Adolphs R, Tyszka M, Richards LJ, Mukherjee P, Sgerr EH (2007) Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity. Nat Rev Neurosci 8:287–299
Pearlman AL, Faust PL, Hatten ME, Brunstrom JE (1998) New directions for neuronal migration. Curr Opin Neurobiol 8:45–54
Pena SDJ, Shokeir MHK (1974) Autosomal recessive cerebro-oculo-facio-skeletal (COFS) syndrome. Clin Genet 5:285–293
Penzes P, Cahill ME, Jones KA, Vanleeuwen JE, Woolfrey KM (2011) Dendritic spine pathology in neuropsychiatric disorders. Nat Neurosci 14:285–293
Perani D, Saccuman MC, Scifo P, Anwander A, Spada D, Baldoli C et al (2011) The neural language networks at birth. Proc Natl Acad Sci U S A 108:16056–16061
Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM et al (1998) LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet 13:2029–2037
Pilz D, Stoodley N, Golden JA (2002) Neuronal migration, cerebral cortical development, and cerebral cortical anomalies. J Neuropathol Exp Neurol 61:1–11
Pinard J-M, Feydy A, Carlier R, Perez N, Pierot L, Burnod Y (2000) Functional MRI in double cortex: functionality of heterotopia. Neurology 54:1531–1533
Pirozzi T, Tabolazzi E, Neri G (2011) The FRAXopathies: definition, overview and update. Am J Med Genet A 155:1803–1816
Poliakov GI (1949) Structural organisation of the human cerebral cortex during ontogenetic development. In: Sarkissov SA, Filimonoff IN, Preobraschenskaja SN (eds) Cytoarchitectonics of the cerebral cortex in man. Medgiz, Moscow, pp 33–92 (in Russian)
Poliakov GI (1959) Progressive neuron differentiation of the human cerebral cortex in ontogenesis. In: Sarkissov SA, Preobraschenskaja SN (eds) Development of the central nervous system. Medgiz, Moscow, pp 11–26 (in Russian)
Poliakov GI (1965) Development of the cerebral neocortex during the first half of intrauterine life. In: Sarkissov SA (ed) Development of the Child’s brain. Medicina, Leningrad, pp 22–52 (in Russian)
Porter R, Lemon R (1993) Corticospinal function and voluntary movements. Monographs of the physiological society, vol 45. Clarendon, Oxford
Porter BE, Brooks-Kayal A, Golden JA (2002) Disorders of cortical development and epilepsy. Arch Neurol 59:361–365
Poussaint TY, Fox JW, Dobyns WB, Radtke R, Scheffer IE, Berkovic SF et al (2000) Periventricular nodular heterotopia in a patiënt with filamin-1 gene mutation: neuroimaging findings. Pediatr Radiol 30:748–755
Povey S, Burley M, Attwood J, Benham F, Hunt D, Jeremiah SJ et al (1994) Two loci for tuberous sclerosis: one on 9q34 and one on 16p13. Ann Hum Genet 58:107–127
Powell EM, Campbell DB, Stanwood GD, Davis C, Noebels JL, Levitt P (2003) Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction. J Neurosci 23:622–631
Powers RE (1999) The neuropathology of schizophrenia. J Neuropathol Exp Neurol 58:679–690
Prayer D, Kasprian G, Krampl E, Ulm B, Witzani L, Prayer L, Brugger PC (2006) MRI of normal fetal brain development. Eur J Radiol 57:199–216
Price DJ, Thurlow L (1988) Cell lineage in the rat cerebral cortex: a study using retroviral-mediated gene transfer. Development 104:473–482
Price DJ, Willshaw DJ (2000) Mechanisms of cortical development. Monographs of the physiological society, vol 48. Oxford University Press, Oxford
Price DJ, Aslam S, Tasker L, Gillies K (1997) The fates of the earliest generated cells in the developing murine neocortex. J Comp Neurol 377:414–422
Probst M (1901) Ueber den Bau des vollständig balkenlosen Grosshirnes sowie über Mikrogyrie und Heterotopie der grauen Substanz. Arch Psychiatry 34:709–786
Pujol J (2006) Myelination of language-related networks at birth. Neurology 66:339–343
Purpura DP (1974) Dendritic spine ‘dysgenesis’ and mental retardation. Science 186:1126–1128
Purpura DP (1975a) Dendritic differentiation in human cerebral cortex: normal and aberrant developmental patterns. Adv Neurol 12:91–116
Purpura DP (1975b) Normal and aberrant neuronal development in the cerebral cortex of human fetus and young infant. In: Buchwald NA, Brazier MAB (eds) Brain mechanisms and mental retatdation. Academic, New York, pp 141–169
Rademacher J, Caviness VS Jr, Steinmetz H, Galaburda AM (1993) Topographical variation of the human primary cortices: Implications for neuroimaging, brain mapping, and neurobiology. Cereb Cortex 3:313–329
Rademacher J, Bürgel U, Geyer S, Schormann T, Schleicher A, Freund H-J, Zilles K (2001) Variability and asymmetry in the human precentral motor system. A cytoarchitectonic and myeloarchitectonic brain mapping study. Brain 124:2232–2258
Radoš M, Judaš M, Kostović I (2006) In vitro MRI of brain development. Eur J Radiol 57:187–198
Raedler E, Raedler A (1978) Autoradiographic study of early neurogenesis in rat neocortex. Anat Embryol (Berl) 154:267–284
Raedler TJ, Knable MB, Weinberger DR (1998) Schizophrenia as a developmental disorder of the cerebral cortex. Curr Opin Neurobiol 8:157–161
Ragsdale CW, Grove EA (2001) Patterning the mammalian cerebral cortex. Curr Opin Neurobiol 11:50–58
Rajarethinam R, Miedler J, De Quardo J, Smet CI, Brunberg J, Kirbat R, Tandon R (2001) Prevalence of cavum septum pellucidum in schizophrenics studied with MRI. Schizophr Res 48:201–205
Rakic P (1974) Neurons in rhesus monkey visual cortex: systemic relation between time of origin and eventual disposition. Science 183:425–427
Rakic P (1988) Specification of cerebral cortical areas. Science 241:170–176
Rakic P (1995) A small step for the cell, a giant leap for mankind: a hypothesis of neocortical expansion during evolution. Trends Neurosci 18:383–388
Rakic P (2009) Evolution of the neocortex: a perspective from developmental biology. Nat Rev Neurosci 10:724–735
Rakic P, Yakovlev PI (1968) Development of the corpus callosum and cavum septi in man. J Comp Neurol 132:45–72
Ramakers GJA (2002) Rho proteins, mental retardation and the cellular basis of cognition. Trends Neurosci 25:191–199
Ramón y Cajal S (1891) Sur la structure de l’écorce cérébrale de quelques mammifères. Cellule 7:123–176
Ramus F (2004) Neurobiology of dyslexia: a reinterpretation of the data. Trends Neurosci 27:720–726
Ramus F, Rosen S, Dakin SC, Day BL, Castelletto JM, White S, Frith U (2003) Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults. Brain 126:841–865
Ranke G (1910) Beiträge zur Kenntnis der normalen und pathologischen Hirnrindenbildung. Ziegl Beitr Path Anat 47:51–125
Ranson SW, Clark SL (1959) The anatomy of the nervous system. Its development and function. Saunders, Philadelphia
Rash BG, Richards LJ (2001) A role for cingulate pioneering axons in the development of the corpus callosum. J Comp Neurol 434:147–157
Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayer T et al (2012) Range of genetic mutations associated with severe non-syndromic spradic intellectual disability: an exome sequencing study. Lancet 380:1674–1682
Rauschecker AM, Deutsch GK, Ben-Shachar M, Schwartman A, Perry LM, Dougherty RF (2009) Reading impairment in a patient with missing arcuate fasciculus. Neuropsychologia 47:180–194
Raybaud CA (2010) The corpus callosum, the other great forebrain commissures, and the septum pellucidum: anatomy, development, and malformations. Neuroradiology 52:447–477
Raybaud CA, Girard N (1998) Étude anatomique par IRM des agénésies et dysplasies commissurales télencéphaliques. Neurochirurgie 44(Suppl 1):38–60
Raybaud CA, Girard N (1999) The developmental disorders of the commissural plate of the telencephalon: MR imaging study and morphologic classification. Nerv Syst Child 24:348–357
Raymond AA, Fish DR, Stevens JM, Sisodiya SM, Alsanjari N, Shorvon SD (1994) Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy. J Neurol Neurosurg Psychiatry 57:1195–1202
Reid CB, Liang I, Walsh C (1995) Systematic widespread clonal organization in cerebral cortex. Neuron 15:299–310
Reillo I, de Juan RC, Garcia-Cabezas MA, Borrell V (2011) A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex. Cereb Cortex 21:1674–1694
Reiss AL, Aylward E, Freund LS, Joshi PK, Bryan RN (1991a) Neuroanatomy of fragile X syndrome: the posterior fossa. Ann Neurol 29:26–32
Reiss AL, Freund L, Tseng JE, Joshi PK (1991b) Neuroanatomy in fragile X females: the posterior fossa. Am J Hum Genet 49:279–288
Reiss AL, Faruque F, Naidu S, Abrams M, Beaty T, Bryan RN, Moser H (1993) Neuroanatomy of Rett syndrome: a volumetric imaging study. Ann Neurol 34:227–234
Ren T, Anderson A, Shen WB, Huang H, Plachez C, Zhang J et al (2006) Imaging, anatomical, and molecular analysis of callosal formation in the developing fetal brain. Anat Rec 288:191–204
Rett A (1966) Über ein zerebral-atrophisches Syndrom bei Hyperammonemie. Wien Med Wochenschr 116:723–726
Retzius G (1893) Die Cajal’schen Zellen der Grosshirnrinde beim Menschen und bei Säugetieren. Biol Unter Neue Folge 5:1–8
Retzius G (1894) Weitere Beiträge zur Kenntnis der Cajal’schen Zellen der Grosshirnrinde des Menschen. Biol Unters Neue Folge 6:29–36
Reyniers E, Martin J-J, Cras P, Van Marck E, Handig I, Jorens HRJ et al (1999) Postmortem examination of two fragile X brothers with an FMR1 full mutation. Am J Med Genet 84:245–249
Rice DS, Curran T (2001) Role of the reelin signaling pathway in central nervous system development. Annu Rev Neurosci 24:1005–1039
Richter W (1980) Neurohistologische und morphometrische Untersuchungen der Ontogenese der Regio cingularis mesoneocorticalis der Ratte. J Hirnforsch 21:53–87
Rickmann M, Chronwall BM, Wolff JR (1977) On the development of non-pyramidal neurons and axons outside the cortical plate: the early marginal zone as a pallial anlage. Anat Embryol (Berl) 151:285–307
Rico B, Marín O (2011) Neuroregulin signaling, cortical circuitry development and schizophrenia. Curr Opin Genet Dev 21:262–270
Rilling JK, Glasser MF, Preuss TM, Ma X, Zhao T, Hu X, Behrens TEJ (2008) The evolution of the arcuate fasciculus revealed with comparative DTI. Nat Neurosci 11:426–428
Robain O, Gelot A (1996) Neuropathology of hemimegalencephaly. In: Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin BG, Pfanner P (eds) Dysplasia of cerebral cortex and epilepsy. Lippincott-Raven, Philadelphia, PA, pp 89–92
Robain O, Floquet J, Heldt N, Rozemberg F (1988) Hemimegalencephaly: a clinicopathological study of four cases. Neuropathol Appl Neurobiol 14:125–135
Roland PE, Zilles K (1996) Functions and structures of the motor cortices in humans. Curr Opin Neurobiol 6:773–781
Ropers H-H (2010) Genetics of early onset cognitive impairment. Annu Rev Genomics Hum Genet 11:161–187
Ropers H-H, Hamel B (2005) XLMR. Nat Rev Genet 6:46–58
Ropers H-H, Hoeltzenbein M, Kalscheuer V, Yntema H, Hamel B, Fryns J-P et al (2003) Nonsyndromic X-linked mental retardation: where are the missing mutations? Trends Genet 19:316–320
Rose M (1927a) Der Allocortex bei Tier und Mensch. I Teil J Psychol Neurol (Lpz) 34:1–111
Rose M (1927b) Die sog. Riechrinde beim Menschen und beim Affen. II. Teil des “Allocortex bei Tier und Mensch”. J Psychol Neurol (Lpz) 34:261–401
Rose J (1938) Zur normalen und pathologischen Architektonik der Ammonsformation. J Psychol Neurol (Lpz) 49:137–192
Ross CA, Pearlson GD (1996) Schizophrenia, the heteromodal association neocortex and development: potential for a neurogenetic approach. Trends Neurosci 19:171–176
Ross ME, Walsh CA (2001) Human brain malformations and their lessons for neuronal migration. Annu Rev Neurosci 24:1041–1070
Ross ME, Swanson K, Dobyns WB (2001) Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformation. Neuropediatrics 32:256–263
Rubinstein JLR (2010) Three hypotheses for developmental defects that may underlie some forms of autism spectrum disorder. Curr Opin Neurol 23:118–123
Rubinstein JLR, Anderson S, Shi L, Miyashita-Lin E, Bulfone A, Hevner R (1999) Genetic control of cortical regionalization and connectivity. Cereb Cortex 9:524–532
Rudelli RD, Brown WT, Wisniewski K, Jenkins EC, Laure-Kamionowska M, Connell F, Wisniewski HM (1985) Adult fragile X syndrome. Clinico-neuropathologic findings. Acta Neuropathol (Berl) 67:289–295
Ruoss K, Lövblad K, Schroth G, Moessinger AC, Fusch C (2001) Brain development (sulci and gyri) as assessed by early postnatal MR imaging in preterm and term newborn infants. Neuropediatrics 32:69–74
Sahyoun CP, Belliveau JW, Soulieres I, Schwartz S, Mody M (2009) Neuroimaging of functional and structural networks underlying visuospatial vs. linguistic reasoning in high-functioning autism. Neuropsychologia 48:86–95
Saito Y, Kobayashi M, Itoh M, Saito K, Mizuguchi M, Sasaki H et al (2003) Aberrant neuronal migration in the brainstem of Fukuyama-type congenital muscular dystrophy. J Neuropathol Exp Neurol 62:497–508
Saitoh O, Karns CM, Courchesne E (2001) Development of the hippocampal formation from 2 to 42 years. MRI evidence of smaller area dentata in autism. Brain 124:1317–1324
Sanchez MP, Frassoni C, Alvarez-Bolado G, Spreafico R, Fairén A (1992) Distribution of calbindin and parvalbumin in the developing somatosensory cortex and its primordium in the rat: an immunocytochemical study. J Neurocytol 21:717–736
Sanes JR, Yamagata M (1999) Formation of lamina-specific synaptic connections. Curr Opin Neurobiol 9:79–97
Santavuori P, Somer H, Sainio K, Rapola J, Kruus S, Nikitin T et al (1989) Muscle-eye-brain disease (MEB). Brain Dev 11:147–153
Sarkissov SA, Filimonoff IN, Kononowa EP, Preobraschenskaja SN, Kukuew LA (1955) Atlas of the cytoarchitecture of the human cerebral cortex. Medgiz, Moscow
Sarwar M (1989) The septum pellucidum: normal and abnormal. Am J Neuroradiol 10:989–1005
Saur D, Kreher BW, Schnell S, Kümmerer D, Kellmeyer P, Vay M-S et al (2008) Ventral and dorsal pathways for language. Proc Natl Acad Sci U S A 105:18035–18040
Saur D, Schelter B, Schnell S, Kratochvil D, Kupper H, Kellmeyer P et al (2010) Combining functional and anatomical connectivity reveals brain networks for auditory language comprehension. Neuroimage 49:3187–3197
Schaefer GB, Bodensteiner JB, Thompson JN (1994) Subtle anomalies of the septum pellucidum and neurodevelopmental deficits. Dev Med Child Neurol 36:554–559
Schanen NC, Kurczynski TW, Brunelle D, Woodcock MM, Dure LS, Percy AK (1998) Neonatal encephalopathy in two boys in families with recurrent Rett syndrome. J Child Neurol 13:229–231
Schmahmann JD, Pandya DN (2006) Fiber pathways of the brain. Oxford University Press, New York
Schmahmann JD, Pandya DN (2008) Disconnection syndromes of basal ganglia, thalamus, and cerebrocerebellar systems. Corte 44:1037–1066
Schmitt JE, Eliez S, Bellugi U, Reiss AL (2001) Analysis of cerebral shape in Williams syndrome. Arch Neurol 58:283–287
Schottler F, Couture D, Rao A, Kahn H, Lee KS (1998) Subcortical connections of normotopic and heterotopic neurons in sensory and motor cortices of the tish mutant rat. J Comp Neurol 395:29–42
Schumann CM, Amaral DG (2006) Stereological analysis of amygdala neuron number in autism. J Neurosci 26:7674–7679
Scott BS, Becker LE, Petit TL (1983) Neurobiology of Down’s syndrome. Prog Neurobiol 21:199–237
Scott TF, Price TRP, George MS, Brillman J, Rothfus W (1993) Midline cerebral malformation and schizophrenia. J Neuropsychiatry Clin Neurosci 5:287–293
Serafini T, Colamarino SA, Leonardo ED, Wang H, Beddington R, Skarnes WC, Tessier-Levigne M (1996) Netrin-1 is required for commissural axon guidance in the developing vertebrate nervous system. Cell 87:1001–1014
Seress L (2007) Comparative anatomy of he hippocampal dentate gyrus in adult and developing rodents, non-human primates and humans. Prog Brain Res 163:23–41
Seress L, Ábrahám H, Tornóczky T, Kosztolányi G (2001) Cell formation in the human hippocampal formation from mid-gestation to the late postnatal period. Neuroscience 105:831–843
Sessa A, Mao CA, Hadjantonakis AK, Klein WH, Broccoli V (2008) Tbr2 directs conversion of radial glia into basal precursors and guides neuronal amplification by indirect neurogenesis in the developing neocortex. Neuron 60:56–69
Shahbazian MD, Zoghbi HY (2002) Rett syndrome and MeCP2: Linking epigenetics and neuronal function. Am J Hum Genet 71:1259–1272
Shaw CM, Alvord EC Jr (1969) Cava septi pellucidi et Vergae: their normal and pathological states. Brain 92:213–224
Sheldon M, Rice DS, D’Arcangelo G, Yoneshima H, Nakajima K, Mikoshiba K et al (1997) Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice. Nature 389:730–733
Shepherd GMG, Katz DM (2011) Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met. Curr Opin Neurobiol 21:827–833
Shepherd MM, Özarslan E, Yachnis AT, King MA, Blackband SJ (2007) Diffusion tensor microscopy indicates the cytoarchitectural basis for diffusion anisotropy in the human hippocampus. AJNR Am J Neuroradiol 28:958–964
Shinozaki K, Miyagi T, Yoshida M, Miyata T, Ogawa M, Aizawa S, Suda Y (2002) Absence of Cajal-Retzius cells and subplate neurons associated with defects of tangential cell migration from ganglionic eminence in Emx1/2 double nutant cerebral cortex. Development 129:3479–3492
Short MP, Richardson EP, Haines J, Kwiatkowski DJ (1995) Clinical, neuropathological, and genetic aspects of the tuberous sclerosis complex. Brain Pathol 5:173–179
Shu T, Richards LJ (2001) Cortical axon guidance by the glial wedge during the development of the corpus callosum. J Neurosci 21:2749–2758
Shu T, Li Y, Keller A, Richards LJ (2003a) The glial sling is a migratory population of developing neurons. Development 130:2929–2937
Shu T, Butz KG, Pachez C, Gronostajski RM, Richards LJ (2003b) Abnormal development of forebrain midline glia and commissural projections in Nfia knock-out mice. J Neurosci 23:203–212
Shu T, Sundaresan V, McCarthy MM, Richards LJ (2003c) Slit2 guides both precrossing and postcrossing axons at the midline in vivo. J Neurosci 23:8176–8184
Sidman RL, Rakic P (1982) Development of the human central nervous system. In: Haymaker W, Adams RD (eds) Histology and histopathology of the nervous system. Thomas, Springfield, IL, pp 3–145
Silver J (1993) Glia-neuron interactions at the midline of the developing mammalian brain and spinal cord. Perspect Dev Neurobiol 1:227–236
Silver J, Lorenz S, Wahlsten D, Coughlin J (1982) Axonal guidance during development of the great commissures: descriptive and experimental studies, in vivo, on the role of preformed glial pathways. J Comp Neurol 210:10–29
Sisodiya SM (2000) Surgery for malformations of cortical development causing epilepsy. Brain 123:1075–1091
Sisodiya SM, Fauser S, Cross JH, Thom M (2009) Focal cortical dysplasia type II: biological features and clinical perspectives. Lancet Neurol 8:830–843
Skutella I, Nitsch R (2001) New molecules for hippocampal development. Trends Neurosci 24:107–113
Smart IHM, McSherry GM (1982) Growth patterns in the lateral wall of the mouse telencephalon. II. Histological changes during and subsequent to the period of isocortical neuron production. J Anat (Lond) 134:415–442
Smart IHM, Dehay C, Giroud P, Berland M, Kennedy H (2002) Unique morphological features of the proliferative zones and postmitotic compartments of the neural epithelium giving rise to striate and extrastriate cortex in the monkey. Cereb Cortex 12:37–53
Smith KM, Ohkuba Y, Maragnoli ME, Rasin MR, Schwartz ML, Sestan N, Vaccarino FM (2006) Midline radial glial translocation and corpus callosum formation require FGF signaling. Nat Neurosci 9:787–797
Solodkin A, Van Hoesen GW (1996) Entorhinal cortex modules of the human brain. J Comp Neurol 365:610–627
Sommer W (1880) Erkrankung des Ammonshorns als aetiologisches Moment der Epilepsie. Arch Psychiatry 10:631–675
Soriano E, Cobas A, Fairén A (1989) Neurogenesis of glutamic acid decarboxylase immunoreactive cells in the hippocampus of the mouse. I: regio superior and regio inferior. J Comp Neurol 281:586–602
Soriano E, Del Rio JA, Martinez A, Supèr H (1994) Organization of the embryonic and early postnatal murine hippocampus. I. Immunocytochemical characteristics of neuronal populations in the subplate and marginal zone. J Comp Neurol 340:1–25
Spreafico R, Blümcke I (2010) Focal cortical dysplasias: clinical implication of neuropathological classification systems. Acta Neuropathol (Berl) 120:359–367
Spreafico R, Frassoni C, Arcelli P, Selvaggio M, De Biasi S (1995) In situ labeling of apoptotic cell death in the cerebral cortex and thalamus of rats during development. J Comp Neurol 363:281–295
Spreafico R, Pasquier B, Minotti L, Garbelli R, Kahane P, Grand S et al (1998) Immunocytochemical investigation on dysplastic human tissue from epileptic patients. Epilepsy Res 32:34–48
Spreafico R, Arcelli P, Frassoni C, Canetti P, Giaccone G, Rizzuti T et al (1999) Development of layer I of the human cerebral cortex after midgestation: architectonic findings, immunocytochemical identification of neurons and glia, and in situ labeling of apoptotic cells. J Comp Neurol 410:126–142
Squier W, Jansen A (2010) Abnormal development of the human cerebral cortex. J Anat (Lond) 217:312–323
Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Ghosh S et al (2002) Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 71:877–892
Stein J, Walsh V (1997) To see but not to read; the magnocellular theory of dyslexia. Trends Neurosci 20:147–152
Stein E, Savashan NE, Ninnemann O, Nitsch R, Zhou R, Skutella T (1999) A role for the Eph ligand ephrin A3 in entorhino-hippocampal axon targeting. J Neurosci 19:8885–8893
Stephan H (1975) Allocortex. Handbuch der mikroskopischen Anatomie des Menschen, vol 4, Teil 9. Springer, Berlin Heidelberg New York
Steup A, Lohrum M, Hamsho N, Savashan NE, Ninnemann O, Nitsch R et al (2000) Semaphorin 3C and netrin-1 differentially affect axon growth in the hippocampal formation. Mol Cell Neurosci 15:141–155
Subramaniam B, Naidu S, Reiss AL (1997) Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa. Neurology 48:399–407
Supèr H, Soriano E (1994) The organization of the embryonic and early postnatal murine hippocampus. II. Development of entorhinal, commissural, and septal connections studied with the lipophilic tracer DiI. J Comp Neurol 344:101–120
Supèr H, Uylings HBM (2001) The early differentiation of the neocortex: a hypothesis on neocortical evolution. Cereb Cortex 11:1101–1109
Supèr H, Martínez A, Del Rio JA, Soriano E (1998a) Involvement of distinct pioneer neurons in the formation of layer-specific connections in the hippocampus. J Neurosci 18:4616–4626
Supèr H, Soriano E, Uylings HBM (1998b) The functions of the preplate in development and evolution of the neocortex and hippocampus. Brain Res Rev 27:40–64
Supprian T, Sian J, Heils A, Hoffmann E, Warmuth-Metz M, Solymosi L (1999) Isolated absence of the septum pellucidum. Neuroradiology 41:563–566
Suzuki WA, Amaral DG (2003) Where are the perirhinal and parahippocampal cortices? A historical overview of the nomenclature and boundaries applied to the primate medial temporal lobe. Neuroscience 120:893–906
Sweet HO, Bronson RT, Johnson KR, Cook SA, Davisson MT (1996) Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration. Mamm Genome 7:798–802
Takahashi T, Nowakowski RS, Caviness VS Jr (1995a) The cell cycle of the pseudostratified ventricular epithelium of the murine cerebral wall. J Neurosci 15:6046–6057
Takahashi T, Nowakowski RS, Caviness VS Jr (1995b) Early ontogeny of the secondary proliferative population of the embryonic murine cerebral wall. J Neurosci 15:6058–6068
Takahashi E, Folkerth RD, Galaburda AM, Grant PE (2012) Emerging cerebral connectivity in the human fetal brain: an MR tractography study. Cereb Cortex 22:455–464
Takiguchi-Hayashi K, Sekiguchi M, Ashigaki S, Takamatsu M, Hasegawa H, Suzuki-Migishima R et al (2004) Generation of reelin-positive marginal zone cells from the caudomedial wall of telencephalic vesicles. J Neurosci 24:2286–2295
Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A et al (2012) Sequencing chromosomal abnormalities reveals neurosevelopmental loci that confer across diagnostic boundaries. Cell 149:525–537
Talos DM, Kwiatkowski DJ, Cordero K, Black PM, Jensen FE (2008) Cell-specific alterations of glutamate receptor expression in tuberous sclerosis complex cortical tubers. Ann Neurol 63:454–465
Tan S-S, Kalloniatis M, Sturm K, Tam PPL, Reese BE, Faulkner-Jones B (1998) Separate progenitors for radial and tangential cell dispersion during development of the cerebral neocortex. Neuron 21:295–304
Tanaka D, Nakaya Y, Yanagawa Y, Obata K, Murakami F (2003) Multimodal tangential migration of neocortical GABAergic neurons independent of GPI-anchored proteins. Development 130:5803–5813
Tassi L, Garbelli R, Colombo N, Bramerio M, Lo Russo G, Deleo F et al (2010) Type I focal cortical dysplasia: surgical outcome is related to histopathology. Epileptic Disord 12:181–191
ten Donkelaar HJ (2000) Development and regenerative capacity of descending supraspinal pathways in tetrapods: a comparative approach. Adv Anat Embryol Cell Biol 154:1–145
ten Donkelaar HJ, Wesseling P, Semmekrot BA, Liem KD, Tuerlings J, Cruysberg JRM, de Wit PEJ (1999) Severe, non X-linked congenital microcephaly with absence of the pyramidal tracts in two saiblings. Acta Neuropathol (Berl) 98:203–211
ten Donkelaar HJ, Lammens M, Wesseling P, Hori A, Keyser A, Rotteveel J (2004) Development and malformations of the human pyramidal tract. J Neurol 251:1429–1442
ten Donkelaar HJ, Brabec J, Lammens M, Küsters B, Hashizume Y, Hori A (2011a) The limbic system. In: ten Donkelaar HJ (ed) Clinical neuroanatomy: brain circuitry and its disorders. Springer, Berlin Heidelberg New York, pp 633–710
ten Donkelaar HJ, van Domburg P, Eling P, Keyser A, Küsters B, Hori A (2011b) The cerebral cortex and complex cerebral functions. In: ten Donkelaar HJ (ed) Clinical neuroanatomy: brain circuitry and its disorders. Springer, Berlin Heidelberg New York, pp 711–809
Terashima T (1995) Anatomy, development and lesion-induced plasticity of rodent corticospinal tract. Neurosci Res 22:139–161
Thiebaut de Schotten M, Kinkingnéhun S, Delmaire C, Lehéricy S, Duffau H, Thivard L et al (2008) Visualization of disconnection syndromes in humans. Cortex 44:1097–1103
Thirumalai SS, Shubin RA, Robinson R (2002) Rapid eye movement sleep behavior disorder in children with autism. J Child Neurol 17:173–178
Thom M, Sisodiya SM, Harkness W, Scaravilli F (2001) Microdysgenesis in temporal lobe epilepsy. A quantitative and immunohistochemical study of white matter neurones. Brain 124:2299–2309
Thom M, Sisodiya SM, Beckett A, Martinian L, Lin W-R, Harkness W et al (2002) Cytoachitectural abnormalities in hippocampal sclerosis. J Neuropathol Exp Neurol 61:510–519
Thom M, Eriksson S, Martinian L, Caboclo LO, McEvoy AW, Duncan JS, Sisodiya SM (2009) Temporal lobe sclerosis associated with hippocampal sclerosis in temporal lobe epilepsy: neuropathological features. J Neuropathol Exp Neurol 68:928–938
Thom M, Blümcke I, Aronica E (2012) Long-term epilepsy-associated tumors. Brain Pathol 22:356–379
Thomaidou D, Mione MC, Cavanagh JFR, Parnavelas JG (1997) Apoptosis and its relation to the cell cycle in the developing cerebral cortex. J Neurosci 17:1075–1085
Thornton GK, Woods CG (2009) Primary microcephaly: do all roads lead to Rome? Trends Genet 25:501–510
Tinkle BT, Schorry EK, Franz DN, Crone KR, Saal HM (2005) Epidemiology of hemimegalencephaly: a case series and review. Am J Med Genet A 139A:204–211
Tissir F, Goffinet AM (2003) Reelin and brain development. Nat Rev Neurosci 4:496–505
Toda T, Kobayashi K, Takeda S, Sasaki J, Kurahashi H, Kano H et al (2003) Fukuyama-type congenital muscular dystrophy (FCMD) and α–dystroglycanopathy. Cong Anom 43:97–104
Tole S, Gutin G, Bhatnager L, Remedios R, Hebert JM (2006) Development of midline cell types and commissural axon tracts requires Fgfr1 in the cerebrum. Dev Biol 289:141–151
Tomaiuolo F, Di Paola M, Caravale B, Vicari S, Petrides M, Caltagirone C (2002) Morphology and morphometry of the corpus callosum in Williams syndrome: a T10weigted MRI study. Neuroreport 13:2281–2284
Toniolo D, D’Adamo P (2000) X-linked non-specific mental retardation. Curr Opin Genet Dev 10:280–285
Trommsdorff M, Gotthardt M, Hiesberger T, Sheldon J, Stockinger W, Nimpf J et al (1999) Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2. Cell 97:689–701
Tuchman R, Rapin I (2002) Epilepsy in autism. Lancet Neurol 1:352–358
Türe U, Yaşargil MG, Friedman AH, Al-Mefty O (2000) Fiber dissection technique: lateral aspects of the brain. Neuroimaging 47:417–427
Tyzio R, Represa A, Jorquera I, Ben-Ari Y, Hozlan H, Anikszteyn L (1999) The establishment of GABAergic and glutaminergic synapses on CA1 pyramidal neurons is sequential and correlates with the development of the apical dendrite. J Neurosci 19:10372–10382
Ulfig N, Chan WY (2002) Axonal patterns in the prosencephalon of the human developing brain. Neuroembryology 1:4–16
Ulfig N, Szabo A, Bohl J (2001) Effects of fetal hydrocephalus on the distribution patterns of calcium-binding proteins in the human occipital cortex. Pediatr Neurosurg 34:20–32
Utsunomiya H, Ogasawara T, Hayashi T, Hashimoto T, Okazaki M (1997) Dysgenesis of the corpus callosum and associated telencephalic anomalies: MRI. Neuroradiology 39:302–310
Uylings HBM (2001) The human cerebral cortex in development. In: Kalverboer AF, Gramsbergen A (eds) Handbook of brain and behaviour in human development. Kluwer, Dordrecht, pp 63–80
Uylings HBM, Delalle I, Petanjek Z, Koenderink MJT (2002) Structural and immunocytochemical differentiation of neurons in prenatal and postnatal human prefrontal cortex. Neuroembryology 1:176–186
Valiente M, Marín O (2010) Neuronal migration mechanisms in development and disease. Curr Opin Neurobiol 20:68–78
van Bokhoven H (2011) Genetic and epigenetic networks in intellectual disabilities. Annu Rev Genet 45:81–104
Van den Veyver IB, Zoghbi HY (2000) Methyl-CpG-binding protein 2 mutations in Rett syndrome. Curr Opin Genet Dev 10:275–279
van der Knaap MS, van Wezel-Meijler G, Barth PG, Barkhof F, Ader HJ, Valk J (1996) Normal gyration and sulcation in preterm and term neonates: appearances on MR images. Radiology 200:389–396
van der Knaap MS, Smit LME, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IFM (1997) MRI in classification of congenital muscular dystrophies with brain abnormalities. Ann Neurol 42:50–59
van Eden CG, Mrzljak L, Voorn P, Uylings HBM (1989) Prenatal development of GABAergic neurons in the neocortex of the rat. J Comp Neurol 289:213–227
van Karnebeek CDM, van Gelderen I, Nijhoff GJ, Abeling NG, Vreken P, Rederer EJ et al (2002) An aetiological study of 25 mentally retarded adults with autism. J Med Genet 39:205–214
Van Paesschen W, Révész T (1998) Hippocampal sclerosis. In: Scaravilli F (ed) Neuropathology of epilepsy. World Scientific, Singapore, pp 501–572
van Reeuwijk J, Janssen M, van den Elzen C, Beltrán-Valero de Bernabé D, Sabatelli P, Merlini L et al (2005) POMT2 mutations cause (alpha)-dystroglycan hypoglycosylation and Walker-Warburg syndrome. J Med Genet 42:907–912
van Reeuwijk J, Maugenre S, van den Elzen C, Verrips A, Bertini E, Muntoni F et al (2006) The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation. Hum Mutat 27:453–459
van Reeuwijk J, Grewal P, Salik M, Beltrán-Valero de Bernabé D, McLaughlan J, Michielse C et al (2007) Intragenic deletion in the LARGE gene cause Walker-Warburg syndrome. Hum Genet 121:685–690
van Reeuwijk J, Olderode-Berends MJW, van den Elzen C, Brouwer OF, Roscioli T, van Pampus MG et al (2010) A homozygous FKRP start codon mutation is associated with Walker-Warburg syndrome, the severe end of the clinical spectrum. Clin Genet 78:275–281
van Slegtenhorst M, de Hoogt R, Hermans C, Nellitt M, Janssen B, Verhoef S et al (1997) Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34. Science 277:805–808
Vandermosten M, Boets B, Poelmans H, Sunaert S, Wouters J, Ghesquière P (2012) A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing. Brain 135:935–948
Vasung L, Huang H, Jovanov-Milošević N, Pletikos M, Mori S, Kostović I (2010) Development of axonal pathways in the human fetal fronto-limbic brain: histochemical characterization and diffusion tensor imaging. J Anat (Lond) 217:400–417
Vasung L, Jovanov-Milošević N, Pletikos M, Mori S, Judaš M, Kostović I (2011) Prominent periventricular fiber system related to ganglionic eminence and striatum in the human fetal cerebrum. Brain Struct Funct 215:237–253
Verga A (1851) Sul ventriculo della volta e tre pilastri. Gazz Med Lombarda 2: Series 3, No 7 (quoted from Bruyn 1977)
Verhoeven JS, De Cock P, Lagae L, Sunaert S (2010) Neuroimaging of autism. Neuroradiology 52:3–14
Vissers LE, de Vries BB, Veltman JA (2010a) Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis. J Med Genet 47:289–297
Vissers LE, de Ligt J, Gilissen C, Janssen I, Steehouwer M, de Vries P et al (2010b) A de novo paradigm for mental retardation. Nat Genet 42:1109–1112
Voeller KKS (2004) Dyslexia. J Child Neurol 19:740–744
Vogt BA, Palomero-Gallagher N (2012) Cingulate cortex. In: Mai JK, Paxinos G (eds) The human nervous system, 3rd edn. Elsevier, Amsterdam, pp 943–987
Vogt C, Vogt O (1919) Allgemeinere Ergebnisse unserer Hirnforschung. J Psychol Neurol 25:279–461
Vogt BA, Nimchinsky EA, Vogt LJ, Hof PR (1995) Human cingulate cortex: surface features, flat maps, and cytoarchitecture. J Comp Neurol 359:490–506
von Economo C (1929) The cytoarchitectonics of the human cerebral cortex. Oxford University Press, London
von Economo C, Koskinas GN (1925) Die Cytoarchitektonik der Hirnrinde des erwachsenen Menschen. Springer, Berlin Heidelberg New York
Wahl M, Lauterbach-Soon B, Hattingen E, Jung P, Singer O, Volz S et al (2007) Human motor corpus callosum: topography, somatotopy and link between microstructure and function. J Neurosci 27:12132–12138
Wahl M, Strominger Z, Jeremy RJ, Barkovich AJ, Wakahiro M, Sherr EH, Mukherjee P (2009) Variability of homotypic and heterotopic callosal connectivity in partial agenesis of the corpus callosum: a 3 T diffusion tensor imaging and Q-ball tractography study. AJNR Am J Neuroradiol 30:282–289
Walker AE (1942) Lissencephaly. Arch Neurol Psychiatry 48:13–29
Walsh CA (1999) Genetic malformations of the human cerebral cortex. Neuron 23:19–29
Walsh CA, Cepko CL (1988) Clonally related cortical cells show several migration patterns. Science 241:1342–1345
Walsh CA, Cepko CL (1992) Widespread dispersion of neuronal clones across functional regions of the cerebral cortex. Science 255:434–440
Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM et al (2008) Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320:539–543
Wang WZ, Hoerder-Suabedissen A, Oeschger FM, Bayatti N, Ip BK, Lindsay S et al (2010) Subplate in the developing cortex of mouse and human. J Anat (Lond) 217:368–380
Wang X, Tsai JW, LaMonica B, Kriegstein AR (2011) A new subtype of progenitor cell in the mouse embryonic neocortex. Nat Neurosci 14:555–561
Ware ML, Fox JW, González JL, Davis NM, Lambert de Rouvroit C, Russo CJ et al (1997) Aberrant splicing of a mouse disabled homologue, mdab1, in the scrambler mouse. Neuron 19:239–249
Weinberger DR (1987) Implications of normal brain development for the pathogenesis of schizophrenia. Arch Gen Psychiatry 44:660–669
Weinberger DR, Egan MF, Bertolino A, Callicott JH, Mattay VS, Lipska BK et al (2001) Prefrontal neurons and the genetics of schizophrenia. Biol Psychiatry 50:825–844
Weiner HL, Carlson C, Ridgway EB, Zaroffi CM, Miles D, LaJoie J, Devinsky O (2006) Epilepsy surgery in young children with tuberous sclerosis: results of a novel approach. Pediatrics 117:1494–1502
White B, Hua Y, Scheithauer B, Lynch DR, Henske EP, Crino PB (2001) Selective alterations in glutamate and GABA receptor subunit mRNA expression in dysplastic neurons and giant cells in cortical tubers. Ann Neurol 49:6–78
Whitford KL, Dijkhuizen P, Polleux F, Ghosh A (2002) Molecular control of cortical dendrite development. Annu Rev Neurosci 25:127–149
WHO (1980) International classification of impairments. Disabilities and handicaps. World Health Organization, Genève
Willemsen MH, Rensen H, van Schrojenstein-Lantman de Valk H, Hamel BCJ, Kleefstra T (2012a) Adult phenotypes in Angelman- and Rett-like syndromes. Mol Syndromol 2(van Schrojenstein-Lantman de Valk H):217–234
Willemsen MH, Vissets LE, Willemsen MA, van Bon BW, Kroes T, de Ligt J et al (2012b) Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects. J Med Genet 49:179–183
Williams RS, Swisher CN, Jennings M, Ambler M, Caviness VS Jr (1984) Cerebro-ocular dysgenesis (Walker-Warburg syndrome): neuropathologic and etiologic analysis. Neurology 34:1531–1541
Winterer G, Weinberger DR (2004) Genes, dopamine and cortical signal-to-noise ratio in schizophrenia. Trends Neurosci 27:683–690
Wisniewski KE, Segan SM, Miezejeski CM, Sersen EA, Rudelli RD (1991) The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities. Am J Med Genet 38:476–480
Witelson SF (1989) Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain 112:799–835
Witter MP, Amaral DG (1991) Entorhinal cortex of the monkey: V. Projections to the dentate gyrus, hippocampus, and subicular complex. J Comp Neurol 307:437–459
Witter MP, Van Hoesen GW, Amaral DG (1989) Topographical organization of the entorhinal projection to the dentate gyrus of the monkey. J Neurosci 9:216–228
Woo TU, Whitehead RE, Melchitzky DS, Lewis DA (1998) A subclass of prefrontal gamma-aminobutyric acid axon terminals are selectively altered in schizophrenia. Proc Natl Acad Sci U S A 95:5341–5346
Xu X, Zecevic N (2011) Dorsal radial glial cells have the potential to generate cortical interneurons in human but not in mouse brain. J Neurosci 31:2413–2420
Xu Q, Cobos I, De La Cruz E, Rubinstein JL, Anderson SA (2004) Origins of cortical interneuron subtypes. J Neurosci 24:2612–2622
Yakovlev PI, Lecours A (1967) The myelogenetic cycles of regional maturation of the brain. In: Minkowski A (ed) Regional development of the brain in early life. Blackwell, Oxford, pp 3–70
Yamadori T (1965) Die Entwicklung der Thalamuskerne mit ihren ersten Fasersystemen bei menschlichen Embryonen. J Hirnforsch 7:393–413
Yamamoto T, Kato Y, Karita M, Takeiri H, Muramatsu F, Kobayashi M et al (2002) Fukutin expression in glial cells and neurons: Implication in the brain lesions of Fukuyama congenital muscular dystrophy. Acta Neuropathol (Berl) 104:217–224
Yamamoto T, Kato Y, Kawaguchi M, Shibata N, Kobayashi M (2004) Expression and localization of fukutin, POMGnT1, and POMT1 in the central nervous system: consideration for functions of fukutin. Med Electron Microsc 37:200–207
Ying Z, Babb TL, Comair YG, Bingaman W, Bushey M, Touhalisky K (1998) Induced expression of NMDAR2 proteins and differential expression of NMDAR1 splice variants in dysplastic neurons of human epileptic neocortex. J Neuropathol Exp Neurol 57:47–62
Ying Z, Gonzalez-Martinez J, Tilelli C, Bingaman W, Najim I (2005) Expression of neural stem cell surface marker CD133 in balloon cells of human focal cortical dysplasia. Epilepsia 46:1716–1723
Yoshida A, Kobayashi K, Manya H, Taniguchi K, Kano H, Mizuno M et al (2001) Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Dev Cell 1:717–724
Yu J, Baybis M, Lee A, McKhann S, Chugani D, Kupsky WJ et al (2005) Targeted gene expression analysis in hemimegalencephaly: activation of beta-catenin signaling. Brain Pathol 15:179–186
Yuste R, Bonhoeffer T (2004) Genesis of dendritic spines: insights from ultrastructural and imaging studies. Nat Rev Neurosci 5:24–34
Zaki PA, Quinn JC, Price DJ (2003) Mouse models of telencephalic development. Curr Opin Genet Dev 13:423–437
Zarei M, Johansen-Berg H, Smith S, Ciccarelli O, Thompson AJ, Matthews PM (2006) Functional anatomy of interhemispheric cortical connections in the human brain. J Anat (Lond) 209:311–320
Zecevic N, Milosevic A, Rakic S, Marín-Padilla M (1999) Early development and composition of the human primordial plexiform layer: an immunohistochemical study. J Comp Neurol 412:241–254
Zecevic N, Chen Y, Filipovic R (2005) Contributions of cortical ventricular zone to the development of the human cerebral cortex. J Comp Neurol 491:109–122
Zecevic N, Hu F, Jakovcevski I (2011) Interneurons in the developing human neocortex. Dev Neurobiol 71:18–33
Zeki S (1993) A vision of the brain. Blackwell, Oxford
Zilles K (2004) Architecture of the human cerebral cortex. In: Paxinos G, Mai JK (eds) The human nervous system, 2nd edn. Elsevier, Amsterdam, pp 997–1055
Zilles K, Amunts K (2009) Receptor mapping: architecture of the human cerebral cortex. Curr Opin Neurobiol 22:331–339
Zilles K, Amunts K (2012) Architecture of the cerebral cortex. In: Mai J, Paxinos G (eds) The human nervous system, 3rd edn. Elsevier, Amsterdam, pp 836–895
Zilles K, Palomero-Gallagher N, Schleicher A (2004) Transmitter receptors and functional anatomy of the cerebral cortex. J Anat (Lond) 205:417–432
Zilles K, Palomero-Gallagher N, Amunts K (2013) Developments of cortical folding during evolution and ontogeny. Trends Neurosci 36:275–284
Zuckerkandl E (1901) Zur Entwicklung des Balkens und des Gewölbes. Sitzber Akad Wissensch Wien, Math-Naturw Classe 110:233–307
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ten Donkelaar, H.J., Lammens, M., Aronica, E., van Bokhoven, H., Ulzen, K.Kv., Hori, A. (2014). Development and Developmental Disorders of the Cerebral Cortex. In: Clinical Neuroembryology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-54687-7_10
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