-
1
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
Abrahams B. S., and, Geschwind D. H., (2008) Advances in autism genetics: on the threshold of a new neurobiology. Nat. Rev. Genet. 9, 341-355.
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
2
-
-
0036336931
-
Mice that lack astrotactin have slowed neuronal migration
-
Adams N. C., Tomoda T., Cooper M., Dietz G., and, Hatten M. E., (2002) Mice that lack astrotactin have slowed neuronal migration. Development 129, 965-972.
-
(2002)
Development
, vol.129
, pp. 965-972
-
-
Adams, N.C.1
Tomoda, T.2
Cooper, M.3
Dietz, G.4
Hatten, M.E.5
-
3
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
Alarcon M., Abrahams B. S., Stone J. L., et al,. (2008) Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am. J. Hum. Genet. 82, 150-159.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 150-159
-
-
Alarcon, M.1
Abrahams, B.S.2
Stone, J.L.3
-
4
-
-
77952888049
-
Neurons derive from the more apical daughter in asymmetric divisions in the zebrafish neural tube
-
Alexandre P., Reugels A. M., Barker D., Blanc E., and, Clarke J. D., (2010) Neurons derive from the more apical daughter in asymmetric divisions in the zebrafish neural tube. Nat. Neurosci. 13, 673-679.
-
(2010)
Nat. Neurosci.
, vol.13
, pp. 673-679
-
-
Alexandre, P.1
Reugels, A.M.2
Barker, D.3
Blanc, E.4
Clarke, J.D.5
-
5
-
-
79955824315
-
Human mutations in NDE1 cause extreme microcephaly with lissencephaly
-
Alkuraya F. S., Cai X., Emery C., et al,. (2011) Human mutations in NDE1 cause extreme microcephaly with lissencephaly. Am. J. Hum. Genet. 88, 538-547.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 538-547
-
-
Alkuraya, F.S.1
Cai, X.2
Emery, C.3
-
6
-
-
80052510244
-
Cytoplasmic dynein
-
Allan V. J., (2011) Cytoplasmic dynein. Biochem. Soc. Trans. 39, 1169-1178.
-
(2011)
Biochem. Soc. Trans.
, vol.39
, pp. 1169-1178
-
-
Allan, V.J.1
-
7
-
-
84877809255
-
Amino-terminal microdeletion within the CNTNAP2 gene associated with variable expressivity of speech delay
-
Al-Murrani A., Ashton F., Aftimos S., George A. M., and, Love D. R., (2012) Amino-terminal microdeletion within the CNTNAP2 gene associated with variable expressivity of speech delay. Case Rep. Genet. 2012, 172408.
-
(2012)
Case Rep. Genet.
, vol.2012
, pp. 172408
-
-
Al-Murrani, A.1
Ashton, F.2
Aftimos, S.3
George, A.M.4
Love, D.R.5
-
8
-
-
84896319374
-
De novo single exon deletion of AUTS2 in a patient with speech and language disorder: A review of disrupted AUTS2 and further evidence for its role in neurodevelopmental disorders
-
Amarillo I. E., Li W. L., Li X., Vilain E., and, Kantarci S., (2014) De novo single exon deletion of AUTS2 in a patient with speech and language disorder: a review of disrupted AUTS2 and further evidence for its role in neurodevelopmental disorders. Am. J. Med. Genet. A 164A, 958-965.
-
(2014)
Am. J. Med. Genet. A
, vol.164 A
, pp. 958-965
-
-
Amarillo, I.E.1
Li, W.L.2
Li, X.3
Vilain, E.4
Kantarci, S.5
-
9
-
-
0030698872
-
Interneuron migration from basal forebrain to neocortex: Dependence on Dlx genes
-
Anderson S. A., Eisenstat D. D., Shi L., and, Rubenstein J. L., (1997) Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science 278, 474-476.
-
(1997)
Science
, vol.278
, pp. 474-476
-
-
Anderson, S.A.1
Eisenstat, D.D.2
Shi, L.3
Rubenstein, J.L.4
-
10
-
-
0032826751
-
Differential origins of neocortical projection and local circuit neurons: Role of Dlx genes in neocortical interneuronogenesis
-
Anderson S., Mione M., Yun K., and, Rubenstein J. L., (1999) Differential origins of neocortical projection and local circuit neurons: role of Dlx genes in neocortical interneuronogenesis. Cereb. Cortex 9, 646-654.
-
(1999)
Cereb. Cortex
, vol.9
, pp. 646-654
-
-
Anderson, S.1
Mione, M.2
Yun, K.3
Rubenstein, J.L.4
-
11
-
-
0035123289
-
Distinct cortical migrations from the medial and lateral ganglionic eminences
-
(Cambridge, England).
-
Anderson S. A., Marin O., Horn C., Jennings K., and, Rubenstein J. L., (2001) Distinct cortical migrations from the medial and lateral ganglionic eminences. Development (Cambridge, England), 128, 353-363.
-
(2001)
Development
, vol.128
, pp. 353-363
-
-
Anderson, S.A.1
Marin, O.2
Horn, C.3
Jennings, K.4
Rubenstein, J.L.5
-
12
-
-
0344334400
-
Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse
-
Angevine J. B., and, Sidman R. L., (1961) Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse. Nature 192, 766-768.
-
(1961)
Nature
, vol.192
, pp. 766-768
-
-
Angevine, J.B.1
Sidman, R.L.2
-
13
-
-
84867829870
-
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
-
Anney R., Klei L., Pinto D., et al,. (2012) Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum. Mol. Genet. 21, 4781-4792.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 4781-4792
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
-
14
-
-
1842527386
-
Radial glia serve as neuronal progenitors in all regions of the central nervous system
-
Anthony T. E., Klein C., Fishell G., and, Heintz N., (2004) Radial glia serve as neuronal progenitors in all regions of the central nervous system. Neuron 41, 881-890.
-
(2004)
Neuron
, vol.41
, pp. 881-890
-
-
Anthony, T.E.1
Klein, C.2
Fishell, G.3
Heintz, N.4
-
15
-
-
38749096303
-
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
-
Arking D. E., Cutler D. J., Brune C. W., et al,. (2008) A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am. J. Hum. Genet. 82, 160-164.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 160-164
-
-
Arking, D.E.1
Cutler, D.J.2
Brune, C.W.3
-
16
-
-
84911387083
-
The clinical significance of small copy number variants in neurodevelopmental disorders
-
Asadollahi R., Oneda B., Joset P., et al,. (2014) The clinical significance of small copy number variants in neurodevelopmental disorders. J. Med. Genet. 51, 677-688.
-
(2014)
J. Med. Genet.
, vol.51
, pp. 677-688
-
-
Asadollahi, R.1
Oneda, B.2
Joset, P.3
-
17
-
-
0003472502
-
-
Association American Psychiatric, American Psychiatric Publishing, USA.
-
Association American Psychiatric, (2013) Diagnostic and Statistical Manual of Mental Disorders (DSM-5), pp. 1-999. American Psychiatric Publishing, USA.
-
(2013)
Diagnostic and Statistical Manual of Mental Disorders (DSM-5)
, pp. 1-999
-
-
-
18
-
-
77957956298
-
Abnormal cell patterning at the cortical gray-white matter boundary in autism spectrum disorders
-
Avino T. A., and, Hutsler J. J., (2010) Abnormal cell patterning at the cortical gray-white matter boundary in autism spectrum disorders. Brain Res. 1360, 138-146.
-
(2010)
Brain Res.
, vol.1360
, pp. 138-146
-
-
Avino, T.A.1
Hutsler, J.J.2
-
19
-
-
33846040831
-
Trekking across the brain: The journey of neuronal migration
-
Ayala R., Shu T., and, Tsai L. H., (2007) Trekking across the brain: the journey of neuronal migration. Cell 128, 29-43.
-
(2007)
Cell
, vol.128
, pp. 29-43
-
-
Ayala, R.1
Shu, T.2
Tsai, L.H.3
-
20
-
-
0031897162
-
A clinicopathological study of autism
-
Bailey A., Luthert P., Dean A., Harding B., Janota I., Montgomery M., Rutter M., and, Lantos P., (1998) A clinicopathological study of autism. Brain 121 (Pt 5), 889-905.
-
(1998)
Brain
, vol.121
, pp. 889-905
-
-
Bailey, A.1
Luthert, P.2
Dean, A.3
Harding, B.4
Janota, I.5
Montgomery, M.6
Rutter, M.7
Lantos, P.8
-
21
-
-
79955789917
-
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis
-
Bakircioglu M., Carvalho O. P., Khurshid M., et al,. (2011) The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis. Am. J. Hum. Genet. 88, 523-535.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 523-535
-
-
Bakircioglu, M.1
Carvalho, O.P.2
Khurshid, M.3
-
22
-
-
38749099110
-
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
-
Bakkaloglu B., O'Roak B. J., Louvi A., et al,. (2008) Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am. J. Hum. Genet. 82, 165-173.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 165-173
-
-
Bakkaloglu, B.1
O'Roak, B.J.2
Louvi, A.3
-
23
-
-
84867229875
-
Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism
-
Baudouin S. J., Gaudias J., Gerharz S., et al,. (2012) Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism. Science 338, 128-132.
-
(2012)
Science
, vol.338
, pp. 128-132
-
-
Baudouin, S.J.1
Gaudias, J.2
Gerharz, S.3
-
24
-
-
53949085577
-
Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development
-
Bayatti N., Sarma S., Shaw C., Eyre J. A., Vouyiouklis D. A., Lindsay S., and, Clowry G. J., (2008) Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development. Eur. J. Neuorsci. 28, 1449-1456.
-
(2008)
Eur. J. Neuorsci.
, vol.28
, pp. 1449-1456
-
-
Bayatti, N.1
Sarma, S.2
Shaw, C.3
Eyre, J.A.4
Vouyiouklis, D.A.5
Lindsay, S.6
Clowry, G.J.7
-
25
-
-
34249680737
-
Autism- highly heritable but not inherited
-
Beaudet A. L., (2007) Autism- highly heritable but not inherited. Nat. Med. 13, 534-536.
-
(2007)
Nat. Med.
, vol.13
, pp. 534-536
-
-
Beaudet, A.L.1
-
26
-
-
77955642202
-
Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex
-
Bedogni F., Hodge R. D., Elsen G. E., Nelson B. R., Daza R. A., Beyer R. P., Bammler T. K., Rubenstein J. L., and, Hevner R. F., (2010a) Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex. Proc. Natl Acad. Sci. USA 107, 13129-13134.
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 13129-13134
-
-
Bedogni, F.1
Hodge, R.D.2
Elsen, G.E.3
Nelson, B.R.4
Daza, R.A.5
Beyer, R.P.6
Bammler, T.K.7
Rubenstein, J.L.8
Hevner, R.F.9
-
27
-
-
73749086083
-
Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology
-
Bedogni F., Hodge R. D., Nelson B. R., Frederick E. A., Shiba N., Daza R. A., and, Hevner R. F., (2010b) Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology. Gene Expr. Patterns 10, 9-15.
-
(2010)
Gene Expr. Patterns
, vol.10
, pp. 9-15
-
-
Bedogni, F.1
Hodge, R.D.2
Nelson, B.R.3
Frederick, E.A.4
Shiba, N.5
Daza, R.A.6
Hevner, R.F.7
-
28
-
-
80052233376
-
Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression
-
Ben-David E., Granot-Hershkovitz E., Monderer-Rothkoff G., Lerer E., Levi S., Yaari M., Ebstein R. P., Yirmiya N., and, Shifman S., (2011) Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression. Hum. Mol. Genet. 20, 3632-3641.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 3632-3641
-
-
Ben-David, E.1
Granot-Hershkovitz, E.2
Monderer-Rothkoff, G.3
Lerer, E.4
Levi, S.5
Yaari, M.6
Ebstein, R.P.7
Yirmiya, N.8
Shifman, S.9
-
29
-
-
84855413477
-
Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology
-
Berkel S., Tang W., Trevino M., et al,. (2012) Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology. Hum. Mol. Genet. 21, 344-357.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 344-357
-
-
Berkel, S.1
Tang, W.2
Trevino, M.3
-
30
-
-
84873732078
-
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
-
Beunders G., Voorhoeve E., Golzio C., et al,. (2013) Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. Am. J. Hum. Genet. 92, 210-220.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 210-220
-
-
Beunders, G.1
Voorhoeve, E.2
Golzio, C.3
-
31
-
-
84929263387
-
Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome
-
Beunders G., de Munnik S. A., Van der Aa N., et al,. (2015) Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome. Eur. J. Hum. Genet. 23, 803-807.
-
(2015)
Eur. J. Hum. Genet.
, vol.23
, pp. 803-807
-
-
Beunders, G.1
De Munnik, S.A.2
Van Der Aa, N.3
-
32
-
-
59149099919
-
Increased LIS1 expression affects human and mouse brain development
-
Bi W., Sapir T., Shchelochkov O. A., et al,. (2009) Increased LIS1 expression affects human and mouse brain development. Nat. Genet. 41, 168-177.
-
(2009)
Nat. Genet.
, vol.41
, pp. 168-177
-
-
Bi, W.1
Sapir, T.2
Shchelochkov, O.A.3
-
33
-
-
80755168331
-
Genetic and epigenetic networks in intellectual disabilities
-
van Bokhoven H., (2011) Genetic and epigenetic networks in intellectual disabilities. Annu. Rev. Genet. 45, 81-104.
-
(2011)
Annu. Rev. Genet.
, vol.45
, pp. 81-104
-
-
Van Bokhoven, H.1
-
34
-
-
10744220777
-
Analysis of reelin as a candidate gene for autism
-
Bonora E., Beyer K. S., Lamb J. A., et al,. (2003) Analysis of reelin as a candidate gene for autism. Mol. Psychiatry 8, 885-892.
-
(2003)
Mol. Psychiatry
, vol.8
, pp. 885-892
-
-
Bonora, E.1
Beyer, K.S.2
Lamb, J.A.3
-
35
-
-
56349168458
-
DISC1, PDE4B, and NDE1 at the centrosome and synapse
-
Bradshaw N. J., Ogawa F., Antolin-Fontes B., Chubb J. E., Carlyle B. C., Christie S., Claessens A., Porteous D. J., and, Millar J. K., (2008) DISC1, PDE4B, and NDE1 at the centrosome and synapse. Biochem. Biophys. Res. Commun. 377, 1091-1096.
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.377
, pp. 1091-1096
-
-
Bradshaw, N.J.1
Ogawa, F.2
Antolin-Fontes, B.3
Chubb, J.E.4
Carlyle, B.C.5
Christie, S.6
Claessens, A.7
Porteous, D.J.8
Millar, J.K.9
-
36
-
-
80055075492
-
Clonal production and organization of inhibitory interneurons in the neocortex
-
Brown K. N., Chen S., Han Z., et al,. (2011) Clonal production and organization of inhibitory interneurons in the neocortex. Science 334, 480-486.
-
(2011)
Science
, vol.334
, pp. 480-486
-
-
Brown, K.N.1
Chen, S.2
Han, Z.3
-
37
-
-
48249116693
-
Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: Evidence of epistasis and competitive binding
-
Burdick K. E., Kamiya A., Hodgkinson C. A., et al,. (2008) Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding. Hum. Mol. Genet. 17, 2462-2473.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2462-2473
-
-
Burdick, K.E.1
Kamiya, A.2
Hodgkinson, C.A.3
-
38
-
-
84875511495
-
A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14
-
Burrage L. C., Eble T. N., Hixson P. M., Roney E. K., Cheung S. W., and, Franco L. M., (2013) A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14. Am. J. Med. Genet. A 161A, 841-844.
-
(2013)
Am. J. Med. Genet. A
, vol.161 A
, pp. 841-844
-
-
Burrage, L.C.1
Eble, T.N.2
Hixson, P.M.3
Roney, E.K.4
Cheung, S.W.5
Franco, L.M.6
-
39
-
-
84920911050
-
Whole exome sequencing in females with autism implicates novel and candidate genes
-
Butler M. G., Rafi S. K., Hossain W., Stephan D. A., and, Manzardo A. M., (2015) Whole exome sequencing in females with autism implicates novel and candidate genes. Int. J. Mol. Sci. 16, 1312-1335.
-
(2015)
Int. J. Mol. Sci.
, vol.16
, pp. 1312-1335
-
-
Butler, M.G.1
Rafi, S.K.2
Hossain, W.3
Stephan, D.A.4
Manzardo, A.M.5
-
40
-
-
33748741962
-
Reduced minicolumns in the frontal cortex of patients with autism
-
Buxhoeveden D. P., Semendeferi K., Buckwalter J., Schenker N., Switzer R., and, Courchesne E., (2006) Reduced minicolumns in the frontal cortex of patients with autism. Neuropathol. Appl. Neurobiol. 32, 483-491.
-
(2006)
Neuropathol. Appl. Neurobiol.
, vol.32
, pp. 483-491
-
-
Buxhoeveden, D.P.1
Semendeferi, K.2
Buckwalter, J.3
Schenker, N.4
Switzer, R.5
Courchesne, E.6
-
41
-
-
14344276586
-
Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization
-
Cahana A., Escamez T., Nowakowski R. S., et al,. (2001) Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization. Proc. Natl Acad. Sci. USA 98, 6429-6434.
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 6429-6434
-
-
Cahana, A.1
Escamez, T.2
Nowakowski, R.S.3
-
42
-
-
0036568734
-
Radial glia: Multi-purpose cells for vertebrate brain development
-
Campbell K., and, Gotz M., (2002) Radial glia: multi-purpose cells for vertebrate brain development. Trends Neurosci. 25, 235-238.
-
(2002)
Trends Neurosci.
, vol.25
, pp. 235-238
-
-
Campbell, K.1
Gotz, M.2
-
43
-
-
0029787920
-
Dynamics of cell migration from the lateral ganglionic eminence in the rat
-
de Carlos J. A., Lopez-Mascaraque L., and, Valverde F., (1996) Dynamics of cell migration from the lateral ganglionic eminence in the rat. J. Neurosci. 16, 6146-6156.
-
(1996)
J. Neurosci.
, vol.16
, pp. 6146-6156
-
-
De Carlos, J.A.1
Lopez-Mascaraque, L.2
Valverde, F.3
-
44
-
-
84901068440
-
Autism as a sequence: From heterochronic germinal cell divisions to abnormalities of cell migration and cortical dysplasias
-
Casanova M. F., (2014) Autism as a sequence: from heterochronic germinal cell divisions to abnormalities of cell migration and cortical dysplasias. Med. Hypotheses 83, 32-38.
-
(2014)
Med. Hypotheses
, vol.83
, pp. 32-38
-
-
Casanova, M.F.1
-
45
-
-
84923477745
-
The Neuropathology of Autism
-
in (Casanova M. F. and El-Baz A. S. and Suri J. S. eds), Springer New York, USA.
-
Casanova M., and, Pickett J., (2013) The Neuropathology of Autism, in Imaging the Brain in Autism (, Casanova M. F., and, El-Baz A. S., and, Suri J. S., eds), pp. 27-43. Springer New York, USA.
-
(2013)
Imaging the Brain in Autism
, pp. 27-43
-
-
Casanova, M.1
Pickett, J.2
-
46
-
-
0037065826
-
Minicolumnar pathology in autism
-
Casanova M. F., Buxhoeveden D. P., Switala A. E., and, Roy E., (2002) Minicolumnar pathology in autism. Neurology 58, 428-432.
-
(2002)
Neurology
, vol.58
, pp. 428-432
-
-
Casanova, M.F.1
Buxhoeveden, D.P.2
Switala, A.E.3
Roy, E.4
-
47
-
-
0020326426
-
3H] thymidine autoradiography
-
3H] thymidine autoradiography. Brain Res. 4, 293-302.
-
(1982)
Brain Res.
, vol.4
, pp. 293-302
-
-
Caviness, V.S.1
-
48
-
-
84880996033
-
Genetic analysis of AUTS2 as a susceptibility gene of heroin dependence
-
Chen Y. H., Liao D. L., Lai C. H., and, Chen C. H., (2013) Genetic analysis of AUTS2 as a susceptibility gene of heroin dependence. Drug Alcohol Depend. 128, 238-242.
-
(2013)
Drug Alcohol Depend.
, vol.128
, pp. 238-242
-
-
Chen, Y.H.1
Liao, D.L.2
Lai, C.H.3
Chen, C.H.4
-
49
-
-
84921917284
-
The emerging picture of autism spectrum disorder: Genetics and pathology
-
Chen J. A., Penagarikano O., Belgard T. G., Swarup V., and, Geschwind D. H., (2015) The emerging picture of autism spectrum disorder: genetics and pathology. Annu. Rev. Pathol. 10, 111-144.
-
(2015)
Annu. Rev. Pathol.
, vol.10
, pp. 111-144
-
-
Chen, J.A.1
Penagarikano, O.2
Belgard, T.G.3
Swarup, V.4
Geschwind, D.H.5
-
50
-
-
84880251662
-
An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk
-
Cheng Y., Quinn J. F., and, Weiss L. A., (2013) An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk. Hum. Mol. Genet. 22, 2960-2972.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 2960-2972
-
-
Cheng, Y.1
Quinn, J.F.2
Weiss, L.A.3
-
51
-
-
84874251894
-
Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene
-
Chojnicka I., Gajos K., Strawa K., et al,. (2013) Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene. PLoS ONE 8, e57199.
-
(2013)
PLoS ONE
, vol.8
, pp. e57199
-
-
Chojnicka, I.1
Gajos, K.2
Strawa, K.3
-
52
-
-
84940436447
-
T-Brain-1 - A Potential Master Regulator in Autism Spectrum Disorders
-
Chuang H. C., Huang T. N., and, Hsueh Y. P., (2015) T-Brain-1-A Potential Master Regulator in Autism Spectrum Disorders. Autism research: official journal of the International Society for Autism Research 4, 412-426.
-
(2015)
Autism Research: Official Journal of the International Society for Autism Research
, vol.4
, pp. 412-426
-
-
Chuang, H.C.1
Huang, T.N.2
Hsueh, Y.P.3
-
53
-
-
77952914565
-
P62/SQSTM1 and ALFY interact to facilitate the formation of p62 bodies/ALIS and their degradation by autophagy
-
Clausen T. H., Lamark T., Isakson P., et al,. (2010) p62/SQSTM1 and ALFY interact to facilitate the formation of p62 bodies/ALIS and their degradation by autophagy. Autophagy 6, 330-344.
-
(2010)
Autophagy
, vol.6
, pp. 330-344
-
-
Clausen, T.H.1
Lamark, T.2
Isakson, P.3
-
54
-
-
84869038551
-
Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses
-
Clement J. P., Aceti M., Creson T. K., et al,. (2012) Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses. Cell 151, 709-723.
-
(2012)
Cell
, vol.151
, pp. 709-723
-
-
Clement, J.P.1
Aceti, M.2
Creson, T.K.3
-
55
-
-
84879152374
-
SYNGAP1 links the maturation rate of excitatory synapses to the duration of critical-period synaptic plasticity
-
Clement J. P., Ozkan E. D., Aceti M., Miller C. A., and, Rumbaugh G., (2013) SYNGAP1 links the maturation rate of excitatory synapses to the duration of critical-period synaptic plasticity. J. Neurosci. 33, 10447-10452.
-
(2013)
J. Neurosci.
, vol.33
, pp. 10447-10452
-
-
Clement, J.P.1
Ozkan, E.D.2
Aceti, M.3
Miller, C.A.4
Rumbaugh, G.5
-
56
-
-
23044437148
-
Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy
-
Cobos I., Calcagnotto M. E., Vilaythong A. J., Thwin M. T., Noebels J. L., Baraban S. C., and, Rubenstein J. L., (2005) Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy. Nat. Neurosci. 8, 1059-1068.
-
(2005)
Nat. Neurosci.
, vol.8
, pp. 1059-1068
-
-
Cobos, I.1
Calcagnotto, M.E.2
Vilaythong, A.J.3
Thwin, M.T.4
Noebels, J.L.5
Baraban, S.C.6
Rubenstein, J.L.7
-
57
-
-
54849441959
-
Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons
-
Colasante G., Collombat P., Raimondi V., et al,. (2008) Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons. J. Neurosci. 28, 10674-10686.
-
(2008)
J. Neurosci.
, vol.28
, pp. 10674-10686
-
-
Colasante, G.1
Collombat, P.2
Raimondi, V.3
-
58
-
-
2442713977
-
The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing
-
Comoletti D., De Jaco A., Jennings L. L., Flynn R. E., Gaietta G., Tsigelny I., Ellisman M. H., and, Taylor P., (2004) The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing. J. Neurosci. 24, 4889-4893.
-
(2004)
J. Neurosci.
, vol.24
, pp. 4889-4893
-
-
Comoletti, D.1
De Jaco, A.2
Jennings, L.L.3
Flynn, R.E.4
Gaietta, G.5
Tsigelny, I.6
Ellisman, M.H.7
Taylor, P.8
-
59
-
-
84888232303
-
Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning
-
Condro M. C., and, White S. A., (2014) Distribution of language-related Cntnap2 protein in neural circuits critical for vocal learning. J. Comp. Neurol. 522, 169-185.
-
(2014)
J. Comp. Neurol.
, vol.522
, pp. 169-185
-
-
Condro, M.C.1
White, S.A.2
-
60
-
-
84890929160
-
Genetic risk factors in two Utah pedigrees at high risk for suicide
-
Coon H., Darlington T., Pimentel R., et al,. (2013) Genetic risk factors in two Utah pedigrees at high risk for suicide. Transl. Psychiat. 3, e325.
-
(2013)
Transl. Psychiat.
, vol.3
, pp. e325
-
-
Coon, H.1
Darlington, T.2
Pimentel, R.3
-
61
-
-
0036235403
-
LIS1, CLIP-170's key to the dynein/dynactin pathway
-
Coquelle F. M., Caspi M., Cordelieres F. P., et al,. (2002) LIS1, CLIP-170's key to the dynein/dynactin pathway. Mol. Cell. Biol. 22, 3089-3102.
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 3089-3102
-
-
Coquelle, F.M.1
Caspi, M.2
Cordelieres, F.P.3
-
62
-
-
84883465830
-
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
-
Cross-Disorder Group of the Psychiatric Genomics Consortium
-
Cross-Disorder Group of the Psychiatric Genomics Consortium, Lee S. H., Ripke S., et al,. (2013) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat. Genet. 45, 984-994.
-
(2013)
Nat. Genet.
, vol.45
, pp. 984-994
-
-
Lee, S.H.1
Ripke, S.2
-
63
-
-
84914149532
-
The evidence for the contribution of the autism susceptibility candidate 2 (AUTS2) gene in heroin dependence susceptibility
-
Dang W., Zhang Q., Zhu Y. S., and, Lu X. Y., (2014) The evidence for the contribution of the autism susceptibility candidate 2 (AUTS2) gene in heroin dependence susceptibility. J. Mol. Neurosci. 54, 811-819.
-
(2014)
J. Mol. Neurosci.
, vol.54
, pp. 811-819
-
-
Dang, W.1
Zhang, Q.2
Zhu, Y.S.3
Lu, X.Y.4
-
64
-
-
0028940096
-
A protein related to extracellular matrix proteins deleted in the mouse mutant reeler
-
D'Arcangelo G., Miao G. G., Chen S. C., Soares H. D., Morgan J. I., and, Curran T., (1995) A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374, 719-723.
-
(1995)
Nature
, vol.374
, pp. 719-723
-
-
D'Arcangelo, G.1
Miao, G.G.2
Chen, S.C.3
Soares, H.D.4
Morgan, J.I.5
Curran, T.6
-
65
-
-
84912144889
-
Synaptic, transcriptional and chromatin genes disrupted in autism
-
De Rubeis S., He X., Goldberg A. P., et al,. (2014) Synaptic, transcriptional and chromatin genes disrupted in autism. Nature 515, 209-215.
-
(2014)
Nature
, vol.515
, pp. 209-215
-
-
De Rubeis, S.1
He, X.2
Goldberg, A.P.3
-
66
-
-
0035203309
-
The adhesion molecule TAG-1 mediates the migration of cortical interneurons from the ganglionic eminence along the corticofugal fiber system
-
Denaxa M., Chan C.-H., Schachner M., Parnavelas J. G., and, Karagogeos D., (2001) The adhesion molecule TAG-1 mediates the migration of cortical interneurons from the ganglionic eminence along the corticofugal fiber system. Development 128, 4635-4644.
-
(2001)
Development
, vol.128
, pp. 4635-4644
-
-
Denaxa, M.1
Chan, C.-H.2
Schachner, M.3
Parnavelas, J.G.4
Karagogeos, D.5
-
67
-
-
84923327027
-
De novo TBR1 mutations in sporadic autism disrupt protein functions
-
Deriziotis P., O'Roak B. J., Graham S. A., et al,. (2014) De novo TBR1 mutations in sporadic autism disrupt protein functions. Nat. Commun. 5, 4954.
-
(2014)
Nat. Commun.
, vol.5
, pp. 4954
-
-
Deriziotis, P.1
O'Roak, B.J.2
Graham, S.A.3
-
68
-
-
33745964945
-
The developmental neurobiology of autism spectrum disorder
-
DiCicco-Bloom E., (2006) The developmental neurobiology of autism spectrum disorder. J. Neurosci. 26, 6897-6906.
-
(2006)
J. Neurosci.
, vol.26
, pp. 6897-6906
-
-
DiCicco-Bloom, E.1
-
69
-
-
0035102502
-
Tbr1 conducts the orchestration of early cortical development
-
Dwyer N. D., and, O'Leary D. D., (2001) Tbr1 conducts the orchestration of early cortical development. Neuron 29, 309-311.
-
(2001)
Neuron
, vol.29
, pp. 309-311
-
-
Dwyer, N.D.1
O'Leary, D.D.2
-
71
-
-
0023949611
-
Astrotactin: A novel neuronal cell surface antigen that mediates neuron-astroglial interactions in cerebellar microcultures
-
Edmondson J. C., Liem R. K., Kuster J. E., and, Hatten M. E., (1988) Astrotactin: a novel neuronal cell surface antigen that mediates neuron-astroglial interactions in cerebellar microcultures. J. Cell Biol. 106, 505-517.
-
(1988)
J. Cell Biol.
, vol.106
, pp. 505-517
-
-
Edmondson, J.C.1
Liem, R.K.2
Kuster, J.E.3
Hatten, M.E.4
-
72
-
-
0031835025
-
A screen for dynein synthetic lethals in Aspergillus nidulans identifies spindle assembly checkpoint genes and other genes involved in mitosis
-
Efimov V. P., and, Morris N. R., (1998) A screen for dynein synthetic lethals in Aspergillus nidulans identifies spindle assembly checkpoint genes and other genes involved in mitosis. Genetics 149, 101-116.
-
(1998)
Genetics
, vol.149
, pp. 101-116
-
-
Efimov, V.P.1
Morris, N.R.2
-
73
-
-
0034618076
-
The LIS1-related NUDF protein of Aspergillus nidulans interacts with the coiled-coil domain of the NUDE/RO11 protein
-
Efimov V. P., and, Morris N. R., (2000) The LIS1-related NUDF protein of Aspergillus nidulans interacts with the coiled-coil domain of the NUDE/RO11 protein. J. Cell Biol. 150, 681-688.
-
(2000)
J. Cell Biol.
, vol.150
, pp. 681-688
-
-
Efimov, V.P.1
Morris, N.R.2
-
74
-
-
33745381601
-
CLIP-170 Homologue and NUDE Play Overlapping Roles in NUDF Localization in Aspergillus nidulans
-
Efimov V. P., Zhang J., and, Xiang X., (2006) CLIP-170 Homologue and NUDE Play Overlapping Roles in NUDF Localization in Aspergillus nidulans. Mol. Biol. Cell 17, 2021-2034.
-
(2006)
Mol. Biol. Cell
, vol.17
, pp. 2021-2034
-
-
Efimov, V.P.1
Zhang, J.2
Xiang, X.3
-
75
-
-
84900490782
-
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families
-
Egger G., Roetzer K. M., Noor A., et al,. (2014) Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families. Neurogenetics 15, 117-127.
-
(2014)
Neurogenetics
, vol.15
, pp. 117-127
-
-
Egger, G.1
Roetzer, K.M.2
Noor, A.3
-
76
-
-
77952887857
-
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
-
Elia J., Gai X., Xie H. M., et al,. (2010) Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol. Psychiatry 15, 637-646.
-
(2010)
Mol. Psychiatry
, vol.15
, pp. 637-646
-
-
Elia, J.1
Gai, X.2
Xie, H.M.3
-
77
-
-
12144266963
-
Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex
-
Englund C., Fink A., Lau C., Pham D., Daza R. A., Bulfone A., Kowalczyk T., and, Hevner R. F., (2005) Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex. J. Neurosci. 25, 247-251.
-
(2005)
J. Neurosci.
, vol.25
, pp. 247-251
-
-
Englund, C.1
Fink, A.2
Lau, C.3
Pham, D.4
Daza, R.A.5
Bulfone, A.6
Kowalczyk, T.7
Hevner, R.F.8
-
78
-
-
65749318026
-
Two new mutants, 'trembler' and 'reeler', with neurological actions in the house mouse (Mus Musculus L.)
-
Falconer D. S., (1951) Two new mutants, 'trembler' and 'reeler', with neurological actions in the house mouse (Mus Musculus L.). J. Genet. 50, 192-201.
-
(1951)
J. Genet.
, vol.50
, pp. 192-201
-
-
Falconer, D.S.1
-
79
-
-
16844370707
-
Reelin signaling is impaired in autism
-
Fatemi S. H., Snow A. V., Stary J. M., Araghi-Niknam M., Reutiman T. J., Lee S., Brooks A. I., and, Pearce D. A., (2005) Reelin signaling is impaired in autism. Biol. Psychiatry 57, 777-787.
-
(2005)
Biol. Psychiatry
, vol.57
, pp. 777-787
-
-
Fatemi, S.H.1
Snow, A.V.2
Stary, J.M.3
Araghi-Niknam, M.4
Reutiman, T.J.5
Lee, S.6
Brooks, A.I.7
Pearce, D.A.8
-
80
-
-
5144222593
-
Mitotic spindle regulation by Nde1 controls cerebral cortical size
-
Feng Y., and, Walsh C. A., (2004) Mitotic spindle regulation by Nde1 controls cerebral cortical size. Neuron 44, 279-293.
-
(2004)
Neuron
, vol.44
, pp. 279-293
-
-
Feng, Y.1
Walsh, C.A.2
-
81
-
-
0034517593
-
LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome
-
Feng Y., Olson E. C., Stukenberg P. T., Flanagan L. A., Kirschner M. W., and, Walsh C. A., (2000) LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome. Neuron 28, 665-679.
-
(2000)
Neuron
, vol.28
, pp. 665-679
-
-
Feng, Y.1
Olson, E.C.2
Stukenberg, P.T.3
Flanagan, L.A.4
Kirschner, M.W.5
Walsh, C.A.6
-
82
-
-
79952067750
-
Cortical progenitor expansion, self-renewal and neurogenesis-A polarized perspective
-
Fietz S. A., and, Huttner W. B., (2011) Cortical progenitor expansion, self-renewal and neurogenesis-a polarized perspective. Curr. Opin. Neurobiol. 21, 23-35.
-
(2011)
Curr. Opin. Neurobiol.
, vol.21
, pp. 23-35
-
-
Fietz, S.A.1
Huttner, W.B.2
-
83
-
-
77952867780
-
OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling
-
Fietz S. A., Kelava I., Vogt J., et al,. (2010) OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling. Nat. Neurosci. 13, 690-699.
-
(2010)
Nat. Neurosci.
, vol.13
, pp. 690-699
-
-
Fietz, S.A.1
Kelava, I.2
Vogt, J.3
-
84
-
-
77950903972
-
The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy
-
Filimonenko M., Isakson P., Finley K. D., et al,. (2010) The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy. Mol. Cell 38, 265-279.
-
(2010)
Mol. Cell
, vol.38
, pp. 265-279
-
-
Filimonenko, M.1
Isakson, P.2
Finley, K.D.3
-
85
-
-
77957927440
-
The Simons Simplex Collection: A resource for identification of autism genetic risk factors
-
Fischbach G. D., and, Lord C., (2010) The Simons Simplex Collection: a resource for identification of autism genetic risk factors. Neuron 68, 192-195.
-
(2010)
Neuron
, vol.68
, pp. 192-195
-
-
Fischbach, G.D.1
Lord, C.2
-
86
-
-
53049092469
-
Making bigger brains-The evolution of neural-progenitor-cell division
-
Fish J. L., Dehay C., Kennedy H., and, Huttner W. B., (2008) Making bigger brains-the evolution of neural-progenitor-cell division. J. Cell Sci. 121, 2783-2793.
-
(2008)
J. Cell Sci.
, vol.121
, pp. 2783-2793
-
-
Fish, J.L.1
Dehay, C.2
Kennedy, H.3
Huttner, W.B.4
-
87
-
-
0025990092
-
Astrotactin provides a receptor system for CNS neuronal migration
-
Fishell G., and, Hatten M. E., (1991) Astrotactin provides a receptor system for CNS neuronal migration. Development 113, 755-765.
-
(1991)
Development
, vol.113
, pp. 755-765
-
-
Fishell, G.1
Hatten, M.E.2
-
88
-
-
84875216807
-
The involvement of Reelin in neurodevelopmental disorders
-
Folsom T. D., and, Fatemi S. H., (2012) The involvement of Reelin in neurodevelopmental disorders. Neuropharmacology 68, 122-135.
-
(2012)
Neuropharmacology
, vol.68
, pp. 122-135
-
-
Folsom, T.D.1
Fatemi, S.H.2
-
89
-
-
84893919352
-
De novo mutations in schizophrenia implicate synaptic networks
-
Fromer M., Pocklington A. J., Kavanagh D. H., et al,. (2014) De novo mutations in schizophrenia implicate synaptic networks. Nature 506, 179-184.
-
(2014)
Nature
, vol.506
, pp. 179-184
-
-
Fromer, M.1
Pocklington, A.J.2
Kavanagh, D.H.3
-
90
-
-
56049110230
-
Identification of Arx transcriptional targets in the developing basal forebrain
-
Fulp C. T., Cho G., Marsh E. D., Nasrallah I. M., Labosky P. A., and, Golden J. A., (2008) Identification of Arx transcriptional targets in the developing basal forebrain. Hum. Mol. Genet. 17, 3740-3760.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3740-3760
-
-
Fulp, C.T.1
Cho, G.2
Marsh, E.D.3
Nasrallah, I.M.4
Labosky, P.A.5
Golden, J.A.6
-
91
-
-
84859009895
-
Rare structural variation of synapse and neurotransmission genes in autism
-
Gai X., Xie H. M., Perin J. C., et al,. (2012) Rare structural variation of synapse and neurotransmission genes in autism. Mol. Psychiatry 17, 402-411.
-
(2012)
Mol. Psychiatry
, vol.17
, pp. 402-411
-
-
Gai, X.1
Xie, H.M.2
Perin, J.C.3
-
92
-
-
32544445546
-
Molecular and morphological heterogeneity of neural precursors in the mouse neocortical proliferative zones
-
Gal J. S., Morozov Y. M., Ayoub A. E., Chatterjee M., Rakic P., and, Haydar T. F., (2006) Molecular and morphological heterogeneity of neural precursors in the mouse neocortical proliferative zones. J. Neurosci. 26, 1045-1056.
-
(2006)
J. Neurosci.
, vol.26
, pp. 1045-1056
-
-
Gal, J.S.1
Morozov, Y.M.2
Ayoub, A.E.3
Chatterjee, M.4
Rakic, P.5
Haydar, T.F.6
-
93
-
-
0037336882
-
Multiple dose-dependent effects of Lis1 on cerebral cortical development
-
Gambello M. J., Darling D. L., Yingling J., Tanaka T., Gleeson J. G., and, Wynshaw-Boris A., (2003) Multiple dose-dependent effects of Lis1 on cerebral cortical development. J. Neurosci. 23, 1719-1729.
-
(2003)
J. Neurosci.
, vol.23
, pp. 1719-1729
-
-
Gambello, M.J.1
Darling, D.L.2
Yingling, J.3
Tanaka, T.4
Gleeson, J.G.5
Wynshaw-Boris, A.6
-
94
-
-
84922217833
-
An AUTS2-Polycomb complex activates gene expression in the CNS
-
Gao Z., Lee P., Stafford J. M., von Schimmelmann M., Schaefer A., and, Reinberg D., (2014) An AUTS2-Polycomb complex activates gene expression in the CNS. Nature 516, 349-354.
-
(2014)
Nature
, vol.516
, pp. 349-354
-
-
Gao, Z.1
Lee, P.2
Stafford, J.M.3
Von Schimmelmann, M.4
Schaefer, A.5
Reinberg, D.6
-
95
-
-
77953748360
-
Generation of interneuron diversity in the mouse cerebral cortex
-
Epub 2010 Jun 2137.
-
Gelman D. M., and, Marin O., (2010) Generation of interneuron diversity in the mouse cerebral cortex. Eur. J. Neurosci. 31, 2136-2141. Epub 2010 Jun 2137.
-
(2010)
Eur. J. Neurosci.
, vol.31
, pp. 2136-2141
-
-
Gelman, D.M.1
Marin, O.2
-
96
-
-
67651177570
-
The embryonic preoptic area is a novel source of cortical GABAergic interneurons
-
Gelman D. M., Martini F. J., Nobrega-Pereira S., Pierani A., Kessaris N., and, Marin O., (2009) The embryonic preoptic area is a novel source of cortical GABAergic interneurons. J. Neurosci. 29, 9380-9389.
-
(2009)
J. Neurosci.
, vol.29
, pp. 9380-9389
-
-
Gelman, D.M.1
Martini, F.J.2
Nobrega-Pereira, S.3
Pierani, A.4
Kessaris, N.5
Marin, O.6
-
97
-
-
54549086639
-
Autism: Many genes, common pathways?
-
Geschwind D. H., (2008) Autism: many genes, common pathways? Cell 135, 391-395.
-
(2008)
Cell
, vol.135
, pp. 391-395
-
-
Geschwind, D.H.1
-
98
-
-
34248326896
-
Distinct cis-regulatory elements from the Dlx1/Dlx2 locus mark different progenitor cell populations in the ganglionic eminences and different subtypes of adult cortical interneurons
-
Ghanem N., Yu M., Long J., Hatch G., Rubenstein J. L., and, Ekker M., (2007) Distinct cis-regulatory elements from the Dlx1/Dlx2 locus mark different progenitor cell populations in the ganglionic eminences and different subtypes of adult cortical interneurons. J. Neurosci. 27, 5012-5022.
-
(2007)
J. Neurosci.
, vol.27
, pp. 5012-5022
-
-
Ghanem, N.1
Yu, M.2
Long, J.3
Hatch, G.4
Rubenstein, J.L.5
Ekker, M.6
-
99
-
-
79958035893
-
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
-
Gilman S. R., Iossifov I., Levy D., Ronemus M., Wigler M., and, Vitkup D., (2011) Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron 70, 898-907.
-
(2011)
Neuron
, vol.70
, pp. 898-907
-
-
Gilman, S.R.1
Iossifov, I.2
Levy, D.3
Ronemus, M.4
Wigler, M.5
Vitkup, D.6
-
100
-
-
84873731200
-
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder
-
Girirajan S., Dennis M. Y., Baker C., et al,. (2013) Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder. Am. J. Hum. Genet. 92, 221-237.
-
(2013)
Am. J. Hum. Genet.
, vol.92
, pp. 221-237
-
-
Girirajan, S.1
Dennis, M.Y.2
Baker, C.3
-
101
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner J. T., Wang K., Cai G., et al,. (2009) Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 459, 569-573.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
-
102
-
-
0021709654
-
Architectonic and hodological organization of the cerebellum in reeler mutant mice
-
Goffinet A. M., So K. F., Yamamoto M., Edwards M., and, Caviness V. S. J., (1984) Architectonic and hodological organization of the cerebellum in reeler mutant mice. Brain Res. 318, 263-276.
-
(1984)
Brain Res.
, vol.318
, pp. 263-276
-
-
Goffinet, A.M.1
So, K.F.2
Yamamoto, M.3
Edwards, M.4
Caviness, V.S.J.5
-
103
-
-
24344510750
-
The cell biology of neurogenesis
-
Gotz M., and, Huttner W. B., (2005) The cell biology of neurogenesis. Nat. Rev. 6, 777-788.
-
(2005)
Nat. Rev.
, vol.6
, pp. 777-788
-
-
Gotz, M.1
Huttner, W.B.2
-
104
-
-
84863434758
-
Synaptopathies: Diseases of the synaptome
-
Grant S. G., (2012) Synaptopathies: diseases of the synaptome. Curr. Opin. Neurobiol. 22, 522-529.
-
(2012)
Curr. Opin. Neurobiol.
, vol.22
, pp. 522-529
-
-
Grant, S.G.1
-
105
-
-
84865017141
-
Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly
-
Guven A., Gunduz A., Bozoglu T. M., Yalcinkaya C., and, Tolun A., (2012) Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly. Neurogenetics 13, 189-194.
-
(2012)
Neurogenetics
, vol.13
, pp. 189-194
-
-
Guven, A.1
Gunduz, A.2
Bozoglu, T.M.3
Yalcinkaya, C.4
Tolun, A.5
-
106
-
-
33847266846
-
Reversal of neurological defects in a mouse model of Rett syndrome
-
Guy J., Gan J., Selfridge J., Cobb S., and, Bird A., (2007) Reversal of neurological defects in a mouse model of Rett syndrome. Science 315, 1143-1147.
-
(2007)
Science
, vol.315
, pp. 1143-1147
-
-
Guy, J.1
Gan, J.2
Selfridge, J.3
Cobb, S.4
Bird, A.5
-
107
-
-
27844568628
-
Analysis of four DLX homeobox genes in autistic probands
-
Hamilton S. P., Woo J. M., Carlson E. J., Ghanem N., Ekker M., and, Rubenstein J. L., (2005) Analysis of four DLX homeobox genes in autistic probands. BMC Genet. 6, 52.
-
(2005)
BMC Genet.
, vol.6
, pp. 52
-
-
Hamilton, S.P.1
Woo, J.M.2
Carlson, E.J.3
Ghanem, N.4
Ekker, M.5
Rubenstein, J.L.6
-
108
-
-
67650924855
-
Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept
-
Hamshere M. L., Green E. K., Jones I. R., et al,. (2009) Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. Br. J. Psychiatry 195, 23-29.
-
(2009)
Br. J. Psychiatry
, vol.195
, pp. 23-29
-
-
Hamshere, M.L.1
Green, E.K.2
Jones, I.R.3
-
109
-
-
79952592649
-
TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract
-
Han W., Kwan K. Y., Shim S., Lam M. M., Shin Y., Xu X., Zhu Y., Li M., and, Sestan N., (2011) TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract. Proc. Natl Acad. Sci. USA 108, 3041-3046.
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 3041-3046
-
-
Han, W.1
Kwan, K.Y.2
Shim, S.3
Lam, M.M.4
Shin, Y.5
Xu, X.6
Zhu, Y.7
Li, M.8
Sestan, N.9
-
110
-
-
0032965534
-
Central nervous system neuronal migration
-
Hatten M. E., (1999) Central nervous system neuronal migration. Annu. Rev. Neurosci. 22, 511-539.
-
(1999)
Annu. Rev. Neurosci.
, vol.22
, pp. 511-539
-
-
Hatten, M.E.1
-
111
-
-
0037031651
-
New directions in neuronal migration
-
Hatten M. E., (2002) New directions in neuronal migration. Science 297, 1660-1663.
-
(2002)
Science
, vol.297
, pp. 1660-1663
-
-
Hatten, M.E.1
-
112
-
-
1542297728
-
Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: A major site of neurogenesis
-
Haubensak W., Attardo A., Denk W., and, Huttner W. B., (2004) Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis. Proc. Natl Acad. Sci. USA 101, 3196-3201.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 3196-3201
-
-
Haubensak, W.1
Attardo, A.2
Denk, W.3
Huttner, W.B.4
-
113
-
-
52249097215
-
Lis1 and Ndel1 influence the timing of nuclear envelope breakdown in neural stem cells
-
Hebbar S., Mesngon M. T., Guillotte A. M., Desai B., Ayala R., and, Smith D. S., (2008) Lis1 and Ndel1 influence the timing of nuclear envelope breakdown in neural stem cells. J. Cell Biol. 182, 1063-1071.
-
(2008)
J. Cell Biol.
, vol.182
, pp. 1063-1071
-
-
Hebbar, S.1
Mesngon, M.T.2
Guillotte, A.M.3
Desai, B.4
Ayala, R.5
Smith, D.S.6
-
114
-
-
77952096810
-
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes
-
Heinzen E. L., Radtke R. A., Urban T. J., et al,. (2010) Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. Am. J. Hum. Genet. 86, 707-718.
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 707-718
-
-
Heinzen, E.L.1
Radtke, R.A.2
Urban, T.J.3
-
115
-
-
29844439285
-
From radial glia to pyramidal-projection neuron: Transcription factor cascades in cerebral cortex development
-
Hevner R. F., (2006) From radial glia to pyramidal-projection neuron: transcription factor cascades in cerebral cortex development. Mol. Neurobiol. 33, 33-50.
-
(2006)
Mol. Neurobiol.
, vol.33
, pp. 33-50
-
-
Hevner, R.F.1
-
116
-
-
17744398634
-
Tbr1 regulates differentiation of the preplate and layer 6
-
Hevner R. F., Shi L., Justice N., et al,. (2001) Tbr1 regulates differentiation of the preplate and layer 6. Neuron 29, 353-366.
-
(2001)
Neuron
, vol.29
, pp. 353-366
-
-
Hevner, R.F.1
Shi, L.2
Justice, N.3
-
117
-
-
0037140799
-
Cortical and thalamic axon pathfinding defects in Tbr1, Gbx2, and Pax6 mutant mice: Evidence that cortical and thalamic axons interact and guide each other
-
Hevner R. F., Miyashita-Lin E., and, Rubenstein J. L., (2002) Cortical and thalamic axon pathfinding defects in Tbr1, Gbx2, and Pax6 mutant mice: evidence that cortical and thalamic axons interact and guide each other. J. Comp. Neurol. 447, 8-17.
-
(2002)
J. Comp. Neurol.
, vol.447
, pp. 8-17
-
-
Hevner, R.F.1
Miyashita-Lin, E.2
Rubenstein, J.L.3
-
118
-
-
78449291189
-
Genetic mosaic dissection of Lis1 and Ndel1 in neuronal migration
-
Hippenmeyer S., Youn Y. H., Moon H. M., Miyamichi K., Zong H., Wynshaw-Boris A., and, Luo L., (2010) Genetic mosaic dissection of Lis1 and Ndel1 in neuronal migration. Neuron 68, 695-709.
-
(2010)
Neuron
, vol.68
, pp. 695-709
-
-
Hippenmeyer, S.1
Youn, Y.H.2
Moon, H.M.3
Miyamichi, K.4
Zong, H.5
Wynshaw-Boris, A.6
Luo, L.7
-
119
-
-
0029072876
-
The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons
-
Hirotsune S., Takahara T., Sasaki N., et al,. (1995) The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons. Nat. Genet. 10, 77-84.
-
(1995)
Nat. Genet.
, vol.10
, pp. 77-84
-
-
Hirotsune, S.1
Takahara, T.2
Sasaki, N.3
-
120
-
-
0031848149
-
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
-
Hirotsune S., Fleck M. W., Gambello M. J., Bix G. J., Chen A., Clark G. D., Ledbetter D. H., McBain C. J., and, Wynshaw-Boris A., (1998) Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat. Genet. 19, 333-339.
-
(1998)
Nat. Genet.
, vol.19
, pp. 333-339
-
-
Hirotsune, S.1
Fleck, M.W.2
Gambello, M.J.3
Bix, G.J.4
Chen, A.5
Clark, G.D.6
Ledbetter, D.H.7
McBain, C.J.8
Wynshaw-Boris, A.9
-
121
-
-
0342906570
-
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
-
Hong S. E., Shugart Y. Y., Huang D. T., Shahwan S. A., Grant P. E., Hourihane J. O., Martin N. D., and, Walsh C. A., (2000) Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat. Genet. 26, 93-96.
-
(2000)
Nat. Genet.
, vol.26
, pp. 93-96
-
-
Hong, S.E.1
Shugart, Y.Y.2
Huang, D.T.3
Shahwan, S.A.4
Grant, P.E.5
Hourihane, J.O.6
Martin, N.D.7
Walsh, C.A.8
-
122
-
-
84919875159
-
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis
-
Hori K., Nagai T., Shan W., et al,. (2014) Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis. Cell Rep. 9, 2166-2179.
-
(2014)
Cell Rep.
, vol.9
, pp. 2166-2179
-
-
Hori, K.1
Nagai, T.2
Shan, W.3
-
123
-
-
84902096048
-
Development and applications of CRISPR-Cas9 for genome engineering
-
Hsu P. D., Lander E. S., and, Zhang F., (2014) Development and applications of CRISPR-Cas9 for genome engineering. Cell 157, 1262-1278.
-
(2014)
Cell
, vol.157
, pp. 1262-1278
-
-
Hsu, P.D.1
Lander, E.S.2
Zhang, F.3
-
124
-
-
77955301410
-
A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism
-
Huang X. L., Zou Y. S., Maher T. A., Newton S., and, Milunsky J. M., (2010) A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism. Am. J. Med. Genet. A 152A, 2112-2114.
-
(2010)
Am. J. Med. Genet. A
, vol.152 A
, pp. 2112-2114
-
-
Huang, X.L.1
Zou, Y.S.2
Maher, T.A.3
Newton, S.4
Milunsky, J.M.5
-
125
-
-
84893751460
-
Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality
-
Huang T. N., Chuang H. C., Chou W. H., Chen C. Y., Wang H. F., Chou S. J., and, Hsueh Y. P., (2014) Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality. Nat. Neurosci. 17, 240-247.
-
(2014)
Nat. Neurosci.
, vol.17
, pp. 240-247
-
-
Huang, T.N.1
Chuang, H.C.2
Chou, W.H.3
Chen, C.Y.4
Wang, H.F.5
Chou, S.J.6
Hsueh, Y.P.7
-
126
-
-
33846604118
-
Histological and magnetic resonance imaging assessment of cortical layering and thickness in autism spectrum disorders
-
Hutsler J. J., Love T., and, Zhang H., (2007) Histological and magnetic resonance imaging assessment of cortical layering and thickness in autism spectrum disorders. Biol. Psychiatry 61, 449-457.
-
(2007)
Biol. Psychiatry
, vol.61
, pp. 449-457
-
-
Hutsler, J.J.1
Love, T.2
Zhang, H.3
-
127
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
International Molecular Genetic Study of Autism Consortium.
-
International Molecular Genetic Study of Autism Consortium (2001) A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am. J. Hum. Genet. 69, 570-581.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 570-581
-
-
-
128
-
-
84860297457
-
De novo gene disruptions in children on the autistic spectrum
-
Iossifov I., Ronemus M., Levy D., et al,. (2012) De novo gene disruptions in children on the autistic spectrum. Neuron 74, 285-299.
-
(2012)
Neuron
, vol.74
, pp. 285-299
-
-
Iossifov, I.1
Ronemus, M.2
Levy, D.3
-
129
-
-
84912101541
-
The contribution of de novo coding mutations to autism spectrum disorder
-
Iossifov I., O'Roak B. J., Sanders S. J., et al,. (2014) The contribution of de novo coding mutations to autism spectrum disorder. Nature 515, 216-221.
-
(2014)
Nature
, vol.515
, pp. 216-221
-
-
Iossifov, I.1
O'Roak, B.J.2
Sanders, S.J.3
-
130
-
-
62149099978
-
Gene associated with seizures, autism, and hepatomegaly in an Amish girl
-
Jackman C., Horn N. D., Molleston J. P., and, Sokol D. K., (2009) Gene associated with seizures, autism, and hepatomegaly in an Amish girl. Pediatr. Neurol. 40, 310-313.
-
(2009)
Pediatr. Neurol.
, vol.40
, pp. 310-313
-
-
Jackman, C.1
Horn, N.D.2
Molleston, J.P.3
Sokol, D.K.4
-
131
-
-
33751257500
-
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
-
Jacquemont M. L., Sanlaville D., Redon R., et al,. (2006) Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. J. Med. Genet. 43, 843-849.
-
(2006)
J. Med. Genet.
, vol.43
, pp. 843-849
-
-
Jacquemont, M.L.1
Sanlaville, D.2
Redon, R.3
-
132
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Jamain S., Quach H., Betancur C., et al,. (2003) Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat. Genet. 34, 27-29.
-
(2003)
Nat. Genet.
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
-
133
-
-
84893844183
-
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
-
Jeste S. S., and, Geschwind D. H., (2014) Disentangling the heterogeneity of autism spectrum disorder through genetic findings. Nat. Rev. Neurol. 10, 74-81.
-
(2014)
Nat. Rev. Neurol.
, vol.10
, pp. 74-81
-
-
Jeste, S.S.1
Geschwind, D.H.2
-
134
-
-
0036534772
-
Tangential migration in neocortical development
-
Jimenez D., Lopez-Mascaraque L. M., Valverde F., and, De Carlos J. A., (2002) Tangential migration in neocortical development. Dev. Biol. 244, 155-169.
-
(2002)
Dev. Biol.
, vol.244
, pp. 155-169
-
-
Jimenez, D.1
Lopez-Mascaraque, L.M.2
Valverde, F.3
De Carlos, J.A.4
-
135
-
-
84878231980
-
De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review
-
Jolley A., Corbett M., McGregor L., Waters W., Brown S., Nicholl J., and, Yu S., (2013) De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: a case report and literature review. Am. J. Med. Genet. A 161A, 1508-1512.
-
(2013)
Am. J. Med. Genet. A
, vol.161 A
, pp. 1508-1512
-
-
Jolley, A.1
Corbett, M.2
McGregor, L.3
Waters, W.4
Brown, S.5
Nicholl, J.6
Yu, S.7
-
136
-
-
0025997752
-
Complex segregation analysis of autism
-
Jorde L. B., Hasstedt S. J., Ritvo E. R., et al,. (1991) Complex segregation analysis of autism. Am. J. Hum. Genet. 49, 932-938.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 932-938
-
-
Jorde, L.B.1
Hasstedt, S.J.2
Ritvo, E.R.3
-
137
-
-
34147145963
-
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation
-
Kalscheuer V. M., FitzPatrick D., Tommerup N., et al,. (2007) Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation. Hum. Genet. 121, 501-509.
-
(2007)
Hum. Genet.
, vol.121
, pp. 501-509
-
-
Kalscheuer, V.M.1
FitzPatrick, D.2
Tommerup, N.3
-
138
-
-
84884907240
-
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks
-
Kapoor M., Wang J. C., Wetherill L., et al,. (2013) A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. Hum. Genet. 132, 1141-1151.
-
(2013)
Hum. Genet.
, vol.132
, pp. 1141-1151
-
-
Kapoor, M.1
Wang, J.C.2
Wetherill, L.3
-
139
-
-
70450228589
-
Regulators of the cytoplasmic dynein motor
-
Kardon J. R., and, Vale R. D., (2009) Regulators of the cytoplasmic dynein motor. Nat. Rev. 10, 854-865.
-
(2009)
Nat. Rev.
, vol.10
, pp. 854-865
-
-
Kardon, J.R.1
Vale, R.D.2
-
140
-
-
84898486639
-
Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD
-
Kim D.-S., Ross P. J., Zaslavsky K., and, Ellis J., (2014) Optimizing neuronal differentiation from induced pluripotent stem cells to model ASD. Front. Cell Neurosci. 8, 109. doi: 10.3389/fncel.2014.00109.
-
(2014)
Front. Cell Neurosci
, vol.8
, pp. 109
-
-
Kim, D.-S.1
Ross, P.J.2
Zaslavsky, K.3
Ellis, J.4
-
141
-
-
0034637504
-
Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE
-
Kitagawa M., Umezu M., Aoki J., Koizumi H., Arai H., and, Inoue K., (2000) Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE. FEBS Lett. 479, 57-62.
-
(2000)
FEBS Lett.
, vol.479
, pp. 57-62
-
-
Kitagawa, M.1
Umezu, M.2
Aoki, J.3
Koizumi, H.4
Arai, H.5
Inoue, K.6
-
142
-
-
70350517377
-
Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007
-
Kogan M. D., Blumberg S. J., Schieve L. A., et al,. (2009) Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007. Pediatrics 124, 1395-1403.
-
(2009)
Pediatrics
, vol.124
, pp. 1395-1403
-
-
Kogan, M.D.1
Blumberg, S.J.2
Schieve, L.A.3
-
143
-
-
28344455348
-
A unique subpopulation of Tbr1-expressing deep layer neurons in the developing cerebral cortex
-
Kolk S. M., Whitman M. C., Yun M. E., Shete P., and, Donoghue M. J., (2005) A unique subpopulation of Tbr1-expressing deep layer neurons in the developing cerebral cortex. Mol. Cell Neurosci. 30, 538-551.
-
(2005)
Mol. Cell Neurosci.
, vol.30
, pp. 538-551
-
-
Kolk, S.M.1
Whitman, M.C.2
Yun, M.E.3
Shete, P.4
Donoghue, M.J.5
-
144
-
-
37749022460
-
Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis
-
Konno D., Shioi G., Shitamukai A., Mori A., Kiyonari H., Miyata T., and, Matsuzaki F., (2008) Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis. Nat. Cell Biol. 10, 93-101.
-
(2008)
Nat. Cell Biol.
, vol.10
, pp. 93-101
-
-
Konno, D.1
Shioi, G.2
Shitamukai, A.3
Mori, A.4
Kiyonari, H.5
Miyata, T.6
Matsuzaki, F.7
-
145
-
-
3042541528
-
Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells
-
Kosodo Y., Roper K., Haubensak W., Marzesco A. M., Corbeil D., and, Huttner W. B., (2004) Asymmetric distribution of the apical plasma membrane during neurogenic divisions of mammalian neuroepithelial cells. EMBO J. 23, 2314-2324.
-
(2004)
EMBO J.
, vol.23
, pp. 2314-2324
-
-
Kosodo, Y.1
Roper, K.2
Haubensak, W.3
Marzesco, A.M.4
Corbeil, D.5
Huttner, W.B.6
-
146
-
-
74249088463
-
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
-
de Kovel C. G., Trucks H., Helbig I., et al,. (2010) Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies. Brain 133, 23-32.
-
(2010)
Brain
, vol.133
, pp. 23-32
-
-
De Kovel, C.G.1
Trucks, H.2
Helbig, I.3
-
147
-
-
3042638932
-
Patterns of neuronal migration in the embryonic cortex
-
Kriegstein A. R., and, Noctor S. C., (2004) Patterns of neuronal migration in the embryonic cortex. Trends Neurosci. 27, 392-399.
-
(2004)
Trends Neurosci.
, vol.27
, pp. 392-399
-
-
Kriegstein, A.R.1
Noctor, S.C.2
-
148
-
-
77954517607
-
Genome variation and complexity in the autism spectrum
-
van de Lagemaat L. N., and, Grant S. G. N., (2010) Genome variation and complexity in the autism spectrum. Neuron 67, 8-10.
-
(2010)
Neuron
, vol.67
, pp. 8-10
-
-
Van De Lagemaat, L.N.1
Grant, S.G.N.2
-
149
-
-
73849148044
-
Functional interplay between LIS1, NDE1 and NDEL1 in dynein-dependent organelle positioning
-
Lam C., Vergnolle M. A., Thorpe L., Woodman P. G., and, Allan V. J., (2010) Functional interplay between LIS1, NDE1 and NDEL1 in dynein-dependent organelle positioning. J. Cell Sci. 123, 202-212.
-
(2010)
J. Cell Sci.
, vol.123
, pp. 202-212
-
-
Lam, C.1
Vergnolle, M.A.2
Thorpe, L.3
Woodman, P.G.4
Allan, V.J.5
-
151
-
-
84884414984
-
Cerebral organoids model human brain development and microcephaly
-
Lancaster M. A., Renner M., Martin C.-A., et al,. (2013) Cerebral organoids model human brain development and microcephaly. Nature 501, 373-379.
-
(2013)
Nature
, vol.501
, pp. 373-379
-
-
Lancaster, M.A.1
Renner, M.2
Martin, C.-A.3
-
152
-
-
84877834489
-
Spatially dependent dynamic MAPK modulation by the nde1-lis1-brap complex patterns Mammalian CNS
-
Lanctot A. A., Peng C. Y., Pawlisz A. S., Joksimovic M., and, Feng Y., (2013) Spatially dependent dynamic MAPK modulation by the nde1-lis1-brap complex patterns Mammalian CNS. Dev. Cell 25, 241-255.
-
(2013)
Dev. Cell
, vol.25
, pp. 241-255
-
-
Lanctot, A.A.1
Peng, C.Y.2
Pawlisz, A.S.3
Joksimovic, M.4
Feng, Y.5
-
153
-
-
0033568857
-
The medial ganglionic eminence gives rise to a population of early neurons in the developing cerebral cortex
-
Lavdas A. A., Grigoriou M., Pachnis V., and, Parnavelas J. G., (1999) The medial ganglionic eminence gives rise to a population of early neurons in the developing cerebral cortex. J. Neurosci. 19, 7881-7888.
-
(1999)
J. Neurosci.
, vol.19
, pp. 7881-7888
-
-
Lavdas, A.A.1
Grigoriou, M.2
Pachnis, V.3
Parnavelas, J.G.4
-
154
-
-
80054031512
-
Neurogenesis at the brain-cerebrospinal fluid interface
-
Lehtinen M. K., and, Walsh C. A., (2011) Neurogenesis at the brain-cerebrospinal fluid interface. Annu. Rev. Cell Dev. Biol. 27, 653-679.
-
(2011)
Annu. Rev. Cell Dev. Biol.
, vol.27
, pp. 653-679
-
-
Lehtinen, M.K.1
Walsh, C.A.2
-
155
-
-
55349128167
-
Molecular genetics of adult ADHD: Converging evidence from genome-wide association and extended pedigree linkage studies
-
Lesch K. P., Timmesfeld N., Renner T. J., et al,. (2008) Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. J. Neural. Transm. 115, 1573-1585.
-
(2008)
J. Neural. Transm.
, vol.115
, pp. 1573-1585
-
-
Lesch, K.P.1
Timmesfeld, N.2
Renner, T.J.3
-
156
-
-
0037030677
-
Origin of GABAergic neurons in the human neocortex
-
Letinic K., Zoncu R., and, Rakic P., (2002) Origin of GABAergic neurons in the human neocortex. Nature 417, 645-649.
-
(2002)
Nature
, vol.417
, pp. 645-649
-
-
Letinic, K.1
Zoncu, R.2
Rakic, P.3
-
157
-
-
79958032110
-
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
-
Levy D., Ronemus M., Yamrom B., et al,. (2011) Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron 70, 886-897.
-
(2011)
Neuron
, vol.70
, pp. 886-897
-
-
Levy, D.1
Ronemus, M.2
Yamrom, B.3
-
158
-
-
84898772564
-
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
-
Lionel A. C., Tammimies K., Vaags A. K., et al,. (2014) Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Hum. Mol. Genet. 23, 2752-2768.
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 2752-2768
-
-
Lionel, A.C.1
Tammimies, K.2
Vaags, A.K.3
-
159
-
-
58349091226
-
The DLX1and DLX2 genes and susceptibility to autism spectrum disorders
-
Liu X., Novosedlik N., Wang A., Hudson M. L., Cohen I. L., Chudley A. E., Forster-Gibson C. J., Lewis S. M., and, Holden J. J., (2009) The DLX1and DLX2 genes and susceptibility to autism spectrum disorders. Eur. J. Hum. Genet. 17, 228-235.
-
(2009)
Eur. J. Hum. Genet.
, vol.17
, pp. 228-235
-
-
Liu, X.1
Novosedlik, N.2
Wang, A.3
Hudson, M.L.4
Cohen, I.L.5
Chudley, A.E.6
Forster-Gibson, C.J.7
Lewis, S.M.8
Holden, J.J.9
-
160
-
-
84929943707
-
De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review
-
Liu Y., Zhao D., Dong R., Yang X., Zhang Y., Tammimies K., Uddin M., Scherer S. W., and, Gai Z., (2015) De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review. Am. J. Med. Genet. A 167, 1381-1385.
-
(2015)
Am. J. Med. Genet. A
, vol.167
, pp. 1381-1385
-
-
Liu, Y.1
Zhao, D.2
Dong, R.3
Yang, X.4
Zhang, Y.5
Tammimies, K.6
Uddin, M.7
Scherer, S.W.8
Gai, Z.9
-
161
-
-
84859133061
-
Disrupted-in-schizophrenia (DISC1) functions presynaptically at glutamatergic synapses
-
Maher B. J., and, LoTurco J. J., (2012) Disrupted-in-schizophrenia (DISC1) functions presynaptically at glutamatergic synapses. PLoS ONE 7, e34053.
-
(2012)
PLoS ONE
, vol.7
, pp. e34053
-
-
Maher, B.J.1
LoTurco, J.J.2
-
162
-
-
0034518641
-
Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage
-
Malatesta P., Hartfuss E., and, Gotz M., (2000) Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage. Development 127, 5253-5263.
-
(2000)
Development
, vol.127
, pp. 5253-5263
-
-
Malatesta, P.1
Hartfuss, E.2
Gotz, M.3
-
163
-
-
0037421992
-
Neuronal or glial progeny: Regional differences in radial glia fate
-
Malatesta P., Hack M. A., Hartfuss E., Kettenmann H., Klinkert W., Kirchhoff F., and, Gotz M., (2003) Neuronal or glial progeny: regional differences in radial glia fate. Neuron 37, 751-764.
-
(2003)
Neuron
, vol.37
, pp. 751-764
-
-
Malatesta, P.1
Hack, M.A.2
Hartfuss, E.3
Kettenmann, H.4
Klinkert, W.5
Kirchhoff, F.6
Gotz, M.7
-
164
-
-
58149343267
-
Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder
-
Manent J.-B., Wang Y., Chang Y., Paramasivam M., and, LoTurco J. J., (2009) Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder. Nat. Med. 15, 84-90.
-
(2009)
Nat. Med.
, vol.15
, pp. 84-90
-
-
Manent, J.-B.1
Wang, Y.2
Chang, Y.3
Paramasivam, M.4
LoTurco, J.J.5
-
165
-
-
0035511906
-
A long, remarkable journey: Tangential migration in the telencephalon
-
Marin O., and, Rubenstein J. L., (2001) A long, remarkable journey: tangential migration in the telencephalon. Nat. Rev. Neurosci. 2, 780-790.
-
(2001)
Nat. Rev. Neurosci.
, vol.2
, pp. 780-790
-
-
Marin, O.1
Rubenstein, J.L.2
-
167
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall C. R., Noor A., Vincent J. B., et al,. (2008) Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 82, 477-488.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
-
168
-
-
84878733905
-
Cellular and molecular basis of cerebellar development
-
Martinez S., Andreu A., Mecklenburg N., and, Echevarria D., (2013) Cellular and molecular basis of cerebellar development. Front. Neuroanat. 7, 18.
-
(2013)
Front. Neuroanat.
, vol.7
, pp. 18
-
-
Martinez, S.1
Andreu, A.2
Mecklenburg, N.3
Echevarria, D.4
-
169
-
-
84901246368
-
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
-
McCarthy S. E., Gillis J., Kramer M., et al,. (2014) De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability. Mol. Psychiatry 19, 652-658.
-
(2014)
Mol. Psychiatry
, vol.19
, pp. 652-658
-
-
McCarthy, S.E.1
Gillis, J.2
Kramer, M.3
-
170
-
-
0026011638
-
The generation of neuronal diversity in the central nervous system
-
McConnell S. K., (1991) The generation of neuronal diversity in the central nervous system. Annu. Rev. Neurosci. 14, 269-300.
-
(1991)
Annu. Rev. Neurosci.
, vol.14
, pp. 269-300
-
-
McConnell, S.K.1
-
171
-
-
78651498771
-
Tbr1 and Fezf2 regulate alternate corticofugal neuronal identities during neocortical development
-
McKenna W. L., Betancourt J., Larkin K. A., Abrams B., Guo C., Rubenstein J. L., and, Chen B., (2011) Tbr1 and Fezf2 regulate alternate corticofugal neuronal identities during neocortical development. J. Neurosci. 31, 549-564.
-
(2011)
J. Neurosci.
, vol.31
, pp. 549-564
-
-
McKenna, W.L.1
Betancourt, J.2
Larkin, K.A.3
Abrams, B.4
Guo, C.5
Rubenstein, J.L.6
Chen, B.7
-
172
-
-
77951701022
-
LIS1 and NudE induce a persistent dynein force-producing state
-
McKenney R. J., Vershinin M., Kunwar A., Vallee R. B., and, Gross S. P., (2010) LIS1 and NudE induce a persistent dynein force-producing state. Cell 141, 304-314.
-
(2010)
Cell
, vol.141
, pp. 304-314
-
-
McKenney, R.J.1
Vershinin, M.2
Kunwar, A.3
Vallee, R.B.4
Gross, S.P.5
-
173
-
-
77956628767
-
Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
-
Mefford H. C., Muhle H., Ostertag P., et al,. (2010) Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet. 6, e1000962.
-
(2010)
PLoS Genet.
, vol.6
, pp. e1000962
-
-
Mefford, H.C.1
Muhle, H.2
Ostertag, P.3
-
174
-
-
78650882587
-
The T-box brain 1 (Tbr1) transcription factor inhibits astrocyte formation in the olfactory bulb and regulates neural stem cell fate
-
Mendez-Gomez H. R., Vergano-Vera E., Abad J. L., Bulfone A., Moratalla R., de Pablo F., and, Vicario-Abejon C., (2011) The T-box brain 1 (Tbr1) transcription factor inhibits astrocyte formation in the olfactory bulb and regulates neural stem cell fate. Mol. Cell Neurosci. 46, 108-121.
-
(2011)
Mol. Cell Neurosci.
, vol.46
, pp. 108-121
-
-
Mendez-Gomez, H.R.1
Vergano-Vera, E.2
Abad, J.L.3
Bulfone, A.4
Moratalla, R.5
De Pablo, F.6
Vicario-Abejon, C.7
-
175
-
-
84871595000
-
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation
-
Michaelson J. J., Shi Y., Gujral M., et al,. (2012) Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. Cell 151, 1431-1442.
-
(2012)
Cell
, vol.151
, pp. 1431-1442
-
-
Michaelson, J.J.1
Shi, Y.2
Gujral, M.3
-
176
-
-
79955030459
-
Autism spectrum disorders-A genetics review
-
Miles J. H., (2011) Autism spectrum disorders-a genetics review. Genet. Med. 13, 278-294.
-
(2011)
Genet. Med.
, vol.13
, pp. 278-294
-
-
Miles, J.H.1
-
177
-
-
0035855758
-
Asymmetric inheritance of radial glial fibers by cortical neurons
-
Miyata T., Kawaguchi A., Okano H., and, Ogawa M., (2001) Asymmetric inheritance of radial glial fibers by cortical neurons. Neuron 31, 727-741.
-
(2001)
Neuron
, vol.31
, pp. 727-741
-
-
Miyata, T.1
Kawaguchi, A.2
Okano, H.3
Ogawa, M.4
-
178
-
-
4043142765
-
Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells
-
Miyata T., Kawaguchi A., Saito K., Kawano M., Muto T., and, Ogawa M., (2004) Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells. Development 131, 3133-3145.
-
(2004)
Development
, vol.131
, pp. 3133-3145
-
-
Miyata, T.1
Kawaguchi, A.2
Saito, K.3
Kawano, M.4
Muto, T.5
Ogawa, M.6
-
179
-
-
76149146046
-
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons
-
Miyoshi G., Hjerling-Leffler J., Karayannis T., Sousa V. H., Butt S. J. B., Battiste J., Johnson J. E., Machold R. P., and, Fishell G., (2010) Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. J. Neurosci. 30, 1582-1594.
-
(2010)
J. Neurosci.
, vol.30
, pp. 1582-1594
-
-
Miyoshi, G.1
Hjerling-Leffler, J.2
Karayannis, T.3
Sousa, V.H.4
Butt, S.J.B.5
Battiste, J.6
Johnson, J.E.7
MacHold, R.P.8
Fishell, G.9
-
180
-
-
0142123055
-
Subpallial origin of a population of projecting pioneer neurons during corticogenesis
-
Morante-Oria J., Carleton A., Ortino B., Kremer E. J., Fairén A., and, Lledo P.-M., (2003) Subpallial origin of a population of projecting pioneer neurons during corticogenesis. Proc. Natl Acad. Sci. 100, 12468-12473.
-
(2003)
Proc. Natl Acad. Sci.
, vol.100
, pp. 12468-12473
-
-
Morante-Oria, J.1
Carleton, A.2
Ortino, B.3
Kremer, E.J.4
Fairén, A.5
Lledo, P.-M.6
-
181
-
-
29144469234
-
The novel roles of glial cells revisited: The contribution of radial glia and astrocytes to neurogenesis
-
Mori T., Buffo A., and, Gotz M., (2005) The novel roles of glial cells revisited: the contribution of radial glia and astrocytes to neurogenesis. Curr. Top. Dev. Biol. 69, 67-99.
-
(2005)
Curr. Top. Dev. Biol.
, vol.69
, pp. 67-99
-
-
Mori, T.1
Buffo, A.2
Gotz, M.3
-
182
-
-
84879883914
-
Recent developments in the genetics of autism spectrum disorders
-
Murdoch J. D., and, State M. W., (2013) Recent developments in the genetics of autism spectrum disorders. Curr. Opin. Genet. Dev. 23, 310-315.
-
(2013)
Curr. Opin. Genet. Dev.
, vol.23
, pp. 310-315
-
-
Murdoch, J.D.1
State, M.W.2
-
183
-
-
0036594138
-
Modes of neuronal migration in the developing cerebral cortex
-
Nadarajah B., and, Parnavelas J. G., (2002) Modes of neuronal migration in the developing cerebral cortex. Nat. Rev. Neurosci. 3, 423-432.
-
(2002)
Nat. Rev. Neurosci.
, vol.3
, pp. 423-432
-
-
Nadarajah, B.1
Parnavelas, J.G.2
-
184
-
-
79951810239
-
Phenotypic manifestations of copy number variation in chromosome 16p13.11
-
Nagamani S. C., Erez A., Bader P., et al,. (2011) Phenotypic manifestations of copy number variation in chromosome 16p13.11. Eur. J. Hum. Genet. 19, 280-286.
-
(2011)
Eur. J. Hum. Genet.
, vol.19
, pp. 280-286
-
-
Nagamani, S.C.1
Erez, A.2
Bader, P.3
-
185
-
-
84874113937
-
Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders
-
Nagamani S. C., Erez A., Ben-Zeev B., et al,. (2013) Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders. Eur. J. Hum. Genet. 21, 343-346.
-
(2013)
Eur. J. Hum. Genet.
, vol.21
, pp. 343-346
-
-
Nagamani, S.C.1
Erez, A.2
Ben-Zeev, B.3
-
186
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
Neale B. M., Kou Y., Liu L., et al,. (2012) Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 485, 242-245.
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
-
187
-
-
0036898691
-
The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations
-
Nery S., Fishell G., and, Corbin J. G., (2002) The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations. Nat. Neurosci. 5, 1279-1287.
-
(2002)
Nat. Neurosci.
, vol.5
, pp. 1279-1287
-
-
Nery, S.1
Fishell, G.2
Corbin, J.G.3
-
188
-
-
0034520636
-
NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein
-
Niethammer M., Smith D. S., Ayala R., Peng J., Ko J., Lee M. S., Morabito M., and, Tsai L. H., (2000) NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein. Neuron 28, 697-711.
-
(2000)
Neuron
, vol.28
, pp. 697-711
-
-
Niethammer, M.1
Smith, D.S.2
Ayala, R.3
Peng, J.4
Ko, J.5
Lee, M.S.6
Morabito, M.7
Tsai, L.H.8
-
189
-
-
0035825670
-
Neurons derived from radial glial cells establish radial units in neocortex
-
Noctor S. C., Flint A. C., Weissman T. A., Dammerman R. S., and, Kriegstein A. R., (2001) Neurons derived from radial glial cells establish radial units in neocortex. Nature 409, 714-720.
-
(2001)
Nature
, vol.409
, pp. 714-720
-
-
Noctor, S.C.1
Flint, A.C.2
Weissman, T.A.3
Dammerman, R.S.4
Kriegstein, A.R.5
-
190
-
-
1642458489
-
Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases
-
Noctor S. C., Martinez-Cerdeno V., Ivic L., and, Kriegstein A. R., (2004) Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases. Nat. Neurosci. 7, 136-144.
-
(2004)
Nat. Neurosci.
, vol.7
, pp. 136-144
-
-
Noctor, S.C.1
Martinez-Cerdeno, V.2
Ivic, L.3
Kriegstein, A.R.4
-
191
-
-
42149188826
-
Distinct behaviors of neural stem and progenitor cells underlie cortical neurogenesis
-
Noctor S. C., Martinez-Cerdeno V., and, Kriegstein A. R., (2008) Distinct behaviors of neural stem and progenitor cells underlie cortical neurogenesis. J. Comp. Neurol. 508, 28-44.
-
(2008)
J. Comp. Neurol.
, vol.508
, pp. 28-44
-
-
Noctor, S.C.1
Martinez-Cerdeno, V.2
Kriegstein, A.R.3
-
192
-
-
84884416967
-
The role of AUTS2 in neurodevelopment and human evolution
-
Oksenberg N., and, Ahituv N., (2013) The role of AUTS2 in neurodevelopment and human evolution. Trends Genet. 29, 600-608.
-
(2013)
Trends Genet.
, vol.29
, pp. 600-608
-
-
Oksenberg, N.1
Ahituv, N.2
-
193
-
-
84873506311
-
Function and regulation of AUTS2, a gene implicated in autism and human evolution
-
Oksenberg N., Stevison L., Wall J. D., and, Ahituv N., (2013) Function and regulation of AUTS2, a gene implicated in autism and human evolution. PLoS Genet. 9, e1003221.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003221
-
-
Oksenberg, N.1
Stevison, L.2
Wall, J.D.3
Ahituv, N.4
-
194
-
-
84871448593
-
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders
-
O'Roak B. J., Vives L., Fu W., et al,. (2012a) Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science 338, 1619-1622.
-
(2012)
Science
, vol.338
, pp. 1619-1622
-
-
O'Roak, B.J.1
Vives, L.2
Fu, W.3
-
195
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
O'Roak B. J., Vives L., Girirajan S., et al,. (2012b) Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 485, 246-250.
-
(2012)
Nature
, vol.485
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
-
196
-
-
84943528737
-
Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology
-
Orosco L. A., Ross A. P., Cates S. L., et al,. (2014) Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology. Nat. Commun. 5, 4692.
-
(2014)
Nat. Commun.
, vol.5
, pp. 4692
-
-
Orosco, L.A.1
Ross, A.P.2
Cates, S.L.3
-
197
-
-
84879464555
-
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption
-
Paciorkowski A. R., Keppler-Noreuil K., Robinson L., et al,. (2013) Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption. Am. J. Med. Genet. A 161, 1523-1530.
-
(2013)
Am. J. Med. Genet. A
, vol.161
, pp. 1523-1530
-
-
Paciorkowski, A.R.1
Keppler-Noreuil, K.2
Robinson, L.3
-
198
-
-
84856250437
-
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies
-
Pagnamenta A. T., Lise S., Harrison V., et al,. (2012) Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies. J. Hum. Genet. 57, 70-72.
-
(2012)
J. Hum. Genet.
, vol.57
, pp. 70-72
-
-
Pagnamenta, A.T.1
Lise, S.2
Harrison, V.3
-
199
-
-
84894235667
-
TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion
-
Palumbo O., Fichera M., Palumbo P., Rizzo R., Mazzolla E., Cocuzza D. M., Carella M., and, Mattina T., (2014) TBR1 is the candidate gene for intellectual disability in patients with a 2q24.2 interstitial deletion. Am. J. Med. Genet. A 164A, 828-833.
-
(2014)
Am. J. Med. Genet. A
, vol.164 A
, pp. 828-833
-
-
Palumbo, O.1
Fichera, M.2
Palumbo, P.3
Rizzo, R.4
Mazzolla, E.5
Cocuzza, D.M.6
Carella, M.7
Mattina, T.8
-
200
-
-
80055055519
-
Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes
-
Pawlisz A. S., and, Feng Y., (2011) Three-dimensional regulation of radial glial functions by Lis1-Nde1 and dystrophin glycoprotein complexes. PLoS Biol. 9, e1001172.
-
(2011)
PLoS Biol.
, vol.9
, pp. e1001172
-
-
Pawlisz, A.S.1
Feng, Y.2
-
201
-
-
48249085262
-
Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and lamination
-
Pawlisz A. S., Mutch C., Wynshaw-Boris A., Chenn A., Walsh C. A., and, Feng Y., (2008) Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and lamination. Hum. Mol. Genet. 17, 2441-2455.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2441-2455
-
-
Pawlisz, A.S.1
Mutch, C.2
Wynshaw-Boris, A.3
Chenn, A.4
Walsh, C.A.5
Feng, Y.6
-
202
-
-
80053540965
-
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
-
Penagarikano O., Abrahams B. S., Herman E. I., et al,. (2011) Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell 147, 235-246.
-
(2011)
Cell
, vol.147
, pp. 235-246
-
-
Penagarikano, O.1
Abrahams, B.S.2
Herman, E.I.3
-
203
-
-
17744393442
-
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
-
Persico A. M., D'Agruma L., Maiorano N., et al,. (2001) Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder. Mol. Psychiatry 6, 150-159.
-
(2001)
Mol. Psychiatry
, vol.6
, pp. 150-159
-
-
Persico, A.M.1
D'Agruma, L.2
Maiorano, N.3
-
204
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
Pinto D., Pagnamenta A. T., Klei L., et al,. (2010) Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466, 368-372.
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
-
205
-
-
0033396331
-
Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels
-
Poliak S., Gollan L., Martinez R., Custer A., Einheber S., Salzer J. L., Trimmer J. S., Shrager P., and, Peles E., (1999) Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels. Neuron 24, 1037-1047.
-
(1999)
Neuron
, vol.24
, pp. 1037-1047
-
-
Poliak, S.1
Gollan, L.2
Martinez, R.3
Custer, A.4
Einheber, S.5
Salzer, J.L.6
Trimmer, J.S.7
Shrager, P.8
Peles, E.9
-
206
-
-
0141433266
-
Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1
-
Poliak S., Salomon D., Elhanany H., et al,. (2003) Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. J. Cell Biol. 162, 1149-1160.
-
(2003)
J. Cell Biol.
, vol.162
, pp. 1149-1160
-
-
Poliak, S.1
Salomon, D.2
Elhanany, H.3
-
207
-
-
0036337484
-
Control of cortical interneuron migration by neurotrophins and PI3-kinase signaling
-
(Cambridge, England).
-
Polleux F., Whitford K. L., Dijkhuizen P. A., Vitalis T., and, Ghosh A., (2002) Control of cortical interneuron migration by neurotrophins and PI3-kinase signaling. Development (Cambridge, England), 129, 3147-3160.
-
(2002)
Development
, vol.129
, pp. 3147-3160
-
-
Polleux, F.1
Whitford, K.L.2
Dijkhuizen, P.A.3
Vitalis, T.4
Ghosh, A.5
-
208
-
-
77649134493
-
Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction
-
Pramparo T., Youn Y. H., Yingling J., Hirotsune S., and, Wynshaw-Boris A., (2010) Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction. J. Neurosci. 30, 3002-3012.
-
(2010)
J. Neurosci.
, vol.30
, pp. 3002-3012
-
-
Pramparo, T.1
Youn, Y.H.2
Yingling, J.3
Hirotsune, S.4
Wynshaw-Boris, A.5
-
209
-
-
79953735108
-
Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects
-
Pramparo T., Libiger O., Jain S., Li H., Youn Y. H., Hirotsune S., Schork N. J., and, Wynshaw-Boris A., (2011) Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects. PLoS Genet. 7, e1001331.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1001331
-
-
Pramparo, T.1
Libiger, O.2
Jain, S.3
Li, H.4
Youn, Y.H.5
Hirotsune, S.6
Schork, N.J.7
Wynshaw-Boris, A.8
-
210
-
-
0015340401
-
Mode of cell migration to the superficial layers of fetal monkey neocortex
-
Rakic P., (1972) Mode of cell migration to the superficial layers of fetal monkey neocortex. J. Comp. Neurol. 145, 61-84.
-
(1972)
J. Comp. Neurol.
, vol.145
, pp. 61-84
-
-
Rakic, P.1
-
211
-
-
79960804293
-
16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders
-
Ramalingam A., Zhou X. G., Fiedler S. D., Brawner S. J., Joyce J. M., Liu H. Y., and, Yu S., (2011) 16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders. J. Hum. Genet. 56, 541-544.
-
(2011)
J. Hum. Genet.
, vol.56
, pp. 541-544
-
-
Ramalingam, A.1
Zhou, X.G.2
Fiedler, S.D.3
Brawner, S.J.4
Joyce, J.M.5
Liu, H.Y.6
Yu, S.7
-
212
-
-
0034517634
-
LIS1. Let's interact sometimes. (part 1)
-
Reiner O., (2000) LIS1. let's interact sometimes. (part 1). Neuron 28, 633-636.
-
(2000)
Neuron
, vol.28
, pp. 633-636
-
-
Reiner, O.1
-
213
-
-
84885587729
-
LIS1 and DCX: Implications for brain development and human disease in relation to microtubules
-
Reiner O., (2013) LIS1 and DCX: implications for brain development and human disease in relation to microtubules. Scientifica 2013, 393975.
-
(2013)
Scientifica
, vol.2013
, pp. 393975
-
-
Reiner, O.1
-
214
-
-
84892965281
-
Nucleokinesis
-
in, 1, (Rubinstein J. R. and Marin O. eds), Elsevier Limited, Oxford, UK.
-
Reiner O., and, Gerlitz G., (2013) Nucleokinesis, in Developmental Neuroscience: A Comprehensive Reference, Vol. 1, (, Rubinstein J. R., and, Marin O., eds), pp. 1-15. Elsevier Limited, Oxford, UK.
-
(2013)
Developmental Neuroscience: A Comprehensive Reference
, pp. 1-15
-
-
Reiner, O.1
Gerlitz, G.2
-
215
-
-
84887410391
-
LIS1 functions in normal development and disease
-
Reiner O., and, Sapir T., (2013) LIS1 functions in normal development and disease. Curr. Opin. Neurobiol. 23, 951-956.
-
(2013)
Curr. Opin. Neurobiol.
, vol.23
, pp. 951-956
-
-
Reiner, O.1
Sapir, T.2
-
216
-
-
0027176708
-
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats
-
Reiner O., Carrozzo R., Shen Y., Wehnert M., Faustinella F., Dobyns W. B., Caskey C. T., and, Ledbetter D. H., (1993) Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature 364, 717-721.
-
(1993)
Nature
, vol.364
, pp. 717-721
-
-
Reiner, O.1
Carrozzo, R.2
Shen, Y.3
Wehnert, M.4
Faustinella, F.5
Dobyns, W.B.6
Caskey, C.T.7
Ledbetter, D.H.8
-
217
-
-
33645470190
-
Asymmetric localization of Numb:EGFP in dividing neuroepithelial cells during neurulation in Danio rerio
-
Reugels A. M., Boggetti B., Scheer N., and, Campos-Ortega J. A., (2006) Asymmetric localization of Numb:EGFP in dividing neuroepithelial cells during neurulation in Danio rerio. Dev. Dyn. 235, 934-948.
-
(2006)
Dev. Dyn.
, vol.235
, pp. 934-948
-
-
Reugels, A.M.1
Boggetti, B.2
Scheer, N.3
Campos-Ortega, J.A.4
-
218
-
-
84892799819
-
The role of de novo mutations in the genetics of autism spectrum disorders
-
Ronemus M., Iossifov I., Levy D., and, Wigler M., (2014) The role of de novo mutations in the genetics of autism spectrum disorders. Nat. Rev. Genet. 15, 133-141.
-
(2014)
Nat. Rev. Genet.
, vol.15
, pp. 133-141
-
-
Ronemus, M.1
Iossifov, I.2
Levy, D.3
Wigler, M.4
-
219
-
-
0345734339
-
Behavioral phenotype of the reeler mutant mouse: Effects of RELN gene dosage and social isolation
-
Salinger W. L., Ladrow P., and, Wheeler C., (2003) Behavioral phenotype of the reeler mutant mouse: effects of RELN gene dosage and social isolation. Behav. Neurosci. 117, 1257-1275.
-
(2003)
Behav. Neurosci.
, vol.117
, pp. 1257-1275
-
-
Salinger, W.L.1
Ladrow, P.2
Wheeler, C.3
-
220
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
Sanders S. J., Ercan-Sencicek A. G., Hus V., et al,. (2011) Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 70, 863-885.
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
Ercan-Sencicek, A.G.2
Hus, V.3
-
221
-
-
84860780495
-
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
-
Sanders S. J., Murtha M. T., Gupta A. R., et al,. (2012) De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature 485, 237-241.
-
(2012)
Nature
, vol.485
, pp. 237-241
-
-
Sanders, S.J.1
Murtha, M.T.2
Gupta, A.R.3
-
222
-
-
0034520597
-
A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system
-
Sasaki S., Shionoya A., Ishida M., Gambello M. J., Yingling J., Wynshaw-Boris A., and, Hirotsune S., (2000) A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system. Neuron 28, 681-696.
-
(2000)
Neuron
, vol.28
, pp. 681-696
-
-
Sasaki, S.1
Shionoya, A.2
Ishida, M.3
Gambello, M.J.4
Yingling, J.5
Wynshaw-Boris, A.6
Hirotsune, S.7
-
223
-
-
79958071067
-
Solving the autism puzzle a few pieces at a time
-
Schaaf C. P., and, Zoghbi H. Y., (2011) Solving the autism puzzle a few pieces at a time. Neuron 70, 806-808.
-
(2011)
Neuron
, vol.70
, pp. 806-808
-
-
Schaaf, C.P.1
Zoghbi, H.Y.2
-
224
-
-
79955569025
-
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
-
Schumann G., Coin L. J., Lourdusamy A., et al,. (2011) Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proc. Natl Acad. Sci. USA 108, 7119-7124.
-
(2011)
Proc. Natl Acad. Sci. USA
, vol.108
, pp. 7119-7124
-
-
Schumann, G.1
Coin, L.J.2
Lourdusamy, A.3
-
225
-
-
78149301263
-
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
-
Scott-Van Zeeland A. A., Abrahams B. S., Alvarez-Retuerto A. I., et al,. (2010) Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Sci. Transl. Med. 2, 56ra80.
-
(2010)
Sci. Transl. Med.
, vol.2
, pp. 56ra80
-
-
Scott-Van Zeeland, A.A.1
Abrahams, B.S.2
Alvarez-Retuerto, A.I.3
-
226
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J., Lakshmi B., Malhotra D., et al,. (2007) Strong association of de novo copy number mutations with autism. Science 316, 445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
-
227
-
-
84912535199
-
How does Reelin control neuronal migration and layer formation in the developing mammalian neocortex?
-
Sekine K., Kubo K., and, Nakajima K., (2014) How does Reelin control neuronal migration and layer formation in the developing mammalian neocortex? Neurosci. Res. 86, 50-58.
-
(2014)
Neurosci. Res.
, vol.86
, pp. 50-58
-
-
Sekine, K.1
Kubo, K.2
Nakajima, K.3
-
228
-
-
0030948938
-
Concurrent cellular output from two proliferative populations in the early embryonic mouse corpus striatum
-
Sheth A. N., and, Bhide P. G., (1997) Concurrent cellular output from two proliferative populations in the early embryonic mouse corpus striatum. J. Comp. Neurol. 383, 220-230.
-
(1997)
J. Comp. Neurol.
, vol.383
, pp. 220-230
-
-
Sheth, A.N.1
Bhide, P.G.2
-
229
-
-
84860244323
-
Control of asymmetric cell division of mammalian neural progenitors
-
Shitamukai A., and, Matsuzaki F., (2012) Control of asymmetric cell division of mammalian neural progenitors. Dev. Growth Differ. 54, 277-286.
-
(2012)
Dev. Growth Differ.
, vol.54
, pp. 277-286
-
-
Shitamukai, A.1
Matsuzaki, F.2
-
230
-
-
79952381377
-
Oblique radial glial divisions in the developing mouse neocortex induce self-renewing progenitors outside the germinal zone that resemble primate outer subventricular zone progenitors
-
Shitamukai A., Konno D., and, Matsuzaki F., (2011) Oblique radial glial divisions in the developing mouse neocortex induce self-renewing progenitors outside the germinal zone that resemble primate outer subventricular zone progenitors. J. Neurosci. 31, 3683-3695.
-
(2011)
J. Neurosci.
, vol.31
, pp. 3683-3695
-
-
Shitamukai, A.1
Konno, D.2
Matsuzaki, F.3
-
231
-
-
75649100553
-
Ndel1 palmitoylation: A new mean to regulate cytoplasmic dynein activity
-
Shmueli A., Segal M., Sapir T., et al,. (2010) Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activity. EMBO J. 29, 107-119.
-
(2010)
EMBO J.
, vol.29
, pp. 107-119
-
-
Shmueli, A.1
Segal, M.2
Sapir, T.3
-
232
-
-
5144228139
-
Ndel1 operates in a common pathway with LIS1 and cytoplasmic dynein to regulate cortical neuronal positioning
-
Shu T., Ayala R., Nguyen M. D., Xie Z., Gleeson J. G., and, Tsai L. H., (2004) Ndel1 operates in a common pathway with LIS1 and cytoplasmic dynein to regulate cortical neuronal positioning. Neuron 44, 263-277.
-
(2004)
Neuron
, vol.44
, pp. 263-277
-
-
Shu, T.1
Ayala, R.2
Nguyen, M.D.3
Xie, Z.4
Gleeson, J.G.5
Tsai, L.H.6
-
233
-
-
77951667779
-
The exon junction complex component Magoh controls brain size by regulating neural stem cell division
-
Silver D. L., Watkins-Chow D. E., Schreck K. C., et al,. (2010) The exon junction complex component Magoh controls brain size by regulating neural stem cell division. Nat. Neurosci. 13, 551-558.
-
(2010)
Nat. Neurosci.
, vol.13
, pp. 551-558
-
-
Silver, D.L.1
Watkins-Chow, D.E.2
Schreck, K.C.3
-
234
-
-
4944247868
-
Alfy, a novel FYVE-domain-containing protein associated with protein granules and autophagic membranes
-
Simonsen A., Birkeland H. C., Gillooly D. J., Mizushima N., Kuma A., Yoshimori T., Slagsvold T., Brech A., and, Stenmark H., (2004) Alfy, a novel FYVE-domain-containing protein associated with protein granules and autophagic membranes. J. Cell Sci. 117, 4239-4251.
-
(2004)
J. Cell Sci.
, vol.117
, pp. 4239-4251
-
-
Simonsen, A.1
Birkeland, H.C.2
Gillooly, D.J.3
Mizushima, N.4
Kuma, A.5
Yoshimori, T.6
Slagsvold, T.7
Brech, A.8
Stenmark, H.9
-
235
-
-
0015746089
-
Proliferative characteristics of the ependymal layer during the early development of the mouse neocortex: A pilot study based on recording the number, location and plane of cleavage of mitotic figures
-
Smart I. H., (1973) Proliferative characteristics of the ependymal layer during the early development of the mouse neocortex: a pilot study based on recording the number, location and plane of cleavage of mitotic figures. J. Anat. 116, 67-91.
-
(1973)
J. Anat.
, vol.116
, pp. 67-91
-
-
Smart, I.H.1
-
236
-
-
0036133288
-
Unique morphological features of the proliferative zones and postmitotic compartments of the neural epithelium giving rise to striate and extrastriate cortex in the monkey
-
Smart I. H., Dehay C., Giroud P., Berland M., and, 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.
-
(2002)
Cereb. Cortex
, vol.12
, pp. 37-53
-
-
Smart, I.H.1
Dehay, C.2
Giroud, P.3
Berland, M.4
Kennedy, H.5
-
237
-
-
84869213888
-
Synapse dysfunction in autism: A molecular medicine approach to drug discovery in neurodevelopmental disorders
-
Spooren W., Lindemann L., Ghosh A., and, Santarelli L., (2012) Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disorders. Trends Pharmacol. Sci. 33, 669-684.
-
(2012)
Trends Pharmacol. Sci.
, vol.33
, pp. 669-684
-
-
Spooren, W.1
Lindemann, L.2
Ghosh, A.3
Santarelli, L.4
-
238
-
-
84869852219
-
A network of genetic repression and derepression specifies projection fates in the developing neocortex
-
Srinivasan K., Leone D. P., Bateson R. K., Dobreva G., Kohwi Y., Kohwi-Shigematsu T., Grosschedl R., and, McConnell S. K., (2012) A network of genetic repression and derepression specifies projection fates in the developing neocortex. Proc. Natl Acad. Sci. USA 109, 19071-19078.
-
(2012)
Proc. Natl Acad. Sci. USA
, vol.109
, pp. 19071-19078
-
-
Srinivasan, K.1
Leone, D.P.2
Bateson, R.K.3
Dobreva, G.4
Kohwi, Y.5
Kohwi-Shigematsu, T.6
Grosschedl, R.7
McConnell, S.K.8
-
239
-
-
77952642527
-
Heterogeneity in ventricular zone neural precursors contributes to neuronal fate diversity in the postnatal neocortex
-
Stancik E. K., Navarro-Quiroga I., Sellke R., and, Haydar T. F., (2010) Heterogeneity in ventricular zone neural precursors contributes to neuronal fate diversity in the postnatal neocortex. J. Neurosci. 30, 7028-7036.
-
(2010)
J. Neurosci.
, vol.30
, pp. 7028-7036
-
-
Stancik, E.K.1
Navarro-Quiroga, I.2
Sellke, R.3
Haydar, T.F.4
-
240
-
-
77949831756
-
Structural variation in the human genome and its role in disease
-
Stankiewicz P., and, Lupski J. R., (2010) Structural variation in the human genome and its role in disease. Annu. Rev. Med. 61, 437-455.
-
(2010)
Annu. Rev. Med.
, vol.61
, pp. 437-455
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
241
-
-
34547958546
-
NudE and NudEL are required for mitotic progression and are involved in dynein recruitment to kinetochores
-
Stehman S. A., Chen Y., McKenney R. J., and, Vallee R. B., (2007) NudE and NudEL are required for mitotic progression and are involved in dynein recruitment to kinetochores. J. Cell Biol. 178, 583-594.
-
(2007)
J. Cell Biol.
, vol.178
, pp. 583-594
-
-
Stehman, S.A.1
Chen, Y.2
McKenney, R.J.3
Vallee, R.B.4
-
242
-
-
79954605497
-
A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits
-
Stein M. B., Yang B. Z., Chavira D. A., Hitchcock C. A., Sung S. C., Shipon-Blum E., and, Gelernter J., (2011) A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits. Biol. Psychiatry 69, 825-831.
-
(2011)
Biol. Psychiatry
, vol.69
, pp. 825-831
-
-
Stein, M.B.1
Yang, B.Z.2
Chavira, D.A.3
Hitchcock, C.A.4
Sung, S.C.5
Shipon-Blum, E.6
Gelernter, J.7
-
243
-
-
84896829795
-
A genotype-first approach to defining the subtypes of a complex disease
-
Stessman H. A., Bernier R., and, Eichler E. E., (2014) A genotype-first approach to defining the subtypes of a complex disease. Cell 156, 872-877.
-
(2014)
Cell
, vol.156
, pp. 872-877
-
-
Stessman, H.A.1
Bernier, R.2
Eichler, E.E.3
-
244
-
-
0025224928
-
Antibodies that recognize astrotactin block granule neuron binding to astroglia
-
Stitt T. N., and, Hatten M. E., (1990) Antibodies that recognize astrotactin block granule neuron binding to astroglia. Neuron 5, 639-649.
-
(1990)
Neuron
, vol.5
, pp. 639-649
-
-
Stitt, T.N.1
Hatten, M.E.2
-
245
-
-
84896918827
-
Patches of disorganization in the neocortex of children with autism
-
Stoner R., Chow M. L., Boyle M. P., et al,. (2014) Patches of disorganization in the neocortex of children with autism. N. Engl. J. Med. 370, 1209-1219.
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 1209-1219
-
-
Stoner, R.1
Chow, M.L.2
Boyle, M.P.3
-
246
-
-
33645415686
-
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2
-
Strauss K. A., Puffenberger E. G., Huentelman M. J., Gottlieb S., Dobrin S. E., Parod J. M., Stephan D. A., and, Morton D. H., (2006) Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. N. Engl. J. Med. 354, 1370-1377.
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 1370-1377
-
-
Strauss, K.A.1
Puffenberger, E.G.2
Huentelman, M.J.3
Gottlieb, S.4
Dobrin, S.E.5
Parod, J.M.6
Stephan, D.A.7
Morton, D.H.8
-
247
-
-
0036020705
-
Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX
-
Stromme P., Mangelsdorf M. E., Scheffer I. E., and, Gecz J., (2002) Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX. Brain Dev. 24, 266-268.
-
(2002)
Brain Dev.
, vol.24
, pp. 266-268
-
-
Stromme, P.1
Mangelsdorf, M.E.2
Scheffer, I.E.3
Gecz, J.4
-
248
-
-
0036993811
-
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins
-
Sultana R., Yu C. E., Yu J., et al,. (2002) Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics 80, 129-134.
-
(2002)
Genomics
, vol.80
, pp. 129-134
-
-
Sultana, R.1
Yu, C.E.2
Yu, J.3
-
249
-
-
84856281267
-
Cytoarchitecture of mouse and human subventricular zone in developing cerebral neocortex
-
Tabata H., Yoshinaga S., and, Nakajima K., (2012) Cytoarchitecture of mouse and human subventricular zone in developing cerebral neocortex. Exp. Brain Res. 216, 161-168.
-
(2012)
Exp. Brain Res.
, vol.216
, pp. 161-168
-
-
Tabata, H.1
Yoshinaga, S.2
Nakajima, K.3
-
250
-
-
4644245980
-
Compromised generation of GABAergic interneurons in the brains of Vax1-/- mice
-
Epub 2004 Jul 4227.
-
Taglialatela P., Soria J. M., Caironi V., Moiana A., and, Bertuzzi S., (2004) Compromised generation of GABAergic interneurons in the brains of Vax1-/- mice. Development 131, 4239-4249. Epub 2004 Jul 4227.
-
(2004)
Development
, vol.131
, pp. 4239-4249
-
-
Taglialatela, P.1
Soria, J.M.2
Caironi, V.3
Moiana, A.4
Bertuzzi, S.5
-
251
-
-
0029052830
-
Early ontogeny of the secondary proliferative population of the embryonic murine cerebral wall
-
Takahashi T., Nowakowski R. S., and, Caviness V. S. Jr, (1995) Early ontogeny of the secondary proliferative population of the embryonic murine cerebral wall. J. Neurosci. 15, 6058-6068.
-
(1995)
J. Neurosci.
, vol.15
, pp. 6058-6068
-
-
Takahashi, T.1
Nowakowski, R.S.2
Caviness, V.S.3
-
252
-
-
36248966518
-
Induction of pluripotent stem cells from adult human fibroblasts by defined factors
-
Takahashi K., Tanabe K., Ohnuki M., Narita M., Ichisaka T., Tomoda K., and, Yamanaka S., (2007) Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell, 131, 861-872.
-
(2007)
Cell
, vol.131
, pp. 861-872
-
-
Takahashi, K.1
Tanabe, K.2
Ohnuki, M.3
Narita, M.4
Ichisaka, T.5
Tomoda, K.6
Yamanaka, S.7
-
253
-
-
84860347597
-
Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries
-
Talkowski M. E., Rosenfeld J. A., Blumenthal I., et al,. (2012) Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell 149, 525-537.
-
(2012)
Cell
, vol.149
, pp. 525-537
-
-
Talkowski, M.E.1
Rosenfeld, J.A.2
Blumenthal, I.3
-
254
-
-
84886297061
-
Neocortical neurogenesis and neuronal migration
-
Tan X., and, Shi S.-H., (2012) Neocortical neurogenesis and neuronal migration. Wiley Interdiscip. Rev. Dev. Biol. 2, 443-459.
-
(2012)
Wiley Interdiscip. Rev. Dev. Biol.
, vol.2
, pp. 443-459
-
-
Tan, X.1
Shi, S.-H.2
-
255
-
-
0032142774
-
Separate progenitors for radial and tangential cell dispersion during development of the cerebral neocortex
-
Tan S. S., Kalloniatis M., Sturm K., Tam P. P., Reese B. E., and, Faulkner-Jones B., (1998) Separate progenitors for radial and tangential cell dispersion during development of the cerebral neocortex. Neuron 21, 295-304.
-
(1998)
Neuron
, vol.21
, pp. 295-304
-
-
Tan, S.S.1
Kalloniatis, M.2
Sturm, K.3
Tam, P.P.4
Reese, B.E.5
Faulkner-Jones, B.6
-
256
-
-
80053128156
-
A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex
-
Taniguchi H., He M., Wu P., et al,. (2011) A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex. Neuron 71, 995-1013.
-
(2011)
Neuron
, vol.71
, pp. 995-1013
-
-
Taniguchi, H.1
He, M.2
Wu, P.3
-
257
-
-
84871921706
-
The spatial and temporal origin of chandelier cells in mouse neocortex
-
Taniguchi H., Lu J., and, Huang Z. J., (2013) The spatial and temporal origin of chandelier cells in mouse neocortex. Science 339, 70-74.
-
(2013)
Science
, vol.339
, pp. 70-74
-
-
Taniguchi, H.1
Lu, J.2
Huang, Z.J.3
-
258
-
-
84874946486
-
Analysis of two language-related genes in autism: A case-control association study of FOXP2 and CNTNAP2
-
Toma C., Hervas A., Torrico B., et al,. (2013) Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2. Psychiatr. Genet. 23, 82-85.
-
(2013)
Psychiatr. Genet.
, vol.23
, pp. 82-85
-
-
Toma, C.1
Hervas, A.2
Torrico, B.3
-
259
-
-
77955093058
-
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
-
Toro R., Konyukh M., Delorme R., et al,. (2010) Key role for gene dosage and synaptic homeostasis in autism spectrum disorders. Trends Genet. 26, 363-372.
-
(2010)
Trends Genet.
, vol.26
, pp. 363-372
-
-
Toro, R.1
Konyukh, M.2
Delorme, R.3
-
260
-
-
84866536266
-
Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions
-
Traylor R. N., Dobyns W. B., Rosenfeld J. A., et al,. (2012) Investigation of TBR1 Hemizygosity: four Individuals with 2q24 Microdeletions. Mol. Syndromol. 3, 102-112.
-
(2012)
Mol. Syndromol.
, vol.3
, pp. 102-112
-
-
Traylor, R.N.1
Dobyns, W.B.2
Rosenfeld, J.A.3
-
261
-
-
84876337451
-
Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders
-
Tropeano M., Ahn J. W., Dobson R. J., et al,. (2013) Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders. PLoS ONE 8, e61365.
-
(2013)
PLoS ONE
, vol.8
, pp. e61365
-
-
Tropeano, M.1
Ahn, J.W.2
Dobson, R.J.3
-
262
-
-
18144364317
-
Nucleokinesis in neuronal migration
-
Tsai L. H., and, Gleeson J. G., (2005) Nucleokinesis in neuronal migration. Neuron 46, 383-388.
-
(2005)
Neuron
, vol.46
, pp. 383-388
-
-
Tsai, L.H.1
Gleeson, J.G.2
-
263
-
-
24944431844
-
LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages
-
Tsai J. W., Chen Y., Kriegstein A. R., and, Vallee R. B., (2005) LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages. J. Cell Biol. 170, 935-945.
-
(2005)
J. Cell Biol.
, vol.170
, pp. 935-945
-
-
Tsai, J.W.1
Chen, Y.2
Kriegstein, A.R.3
Vallee, R.B.4
-
264
-
-
34547533825
-
Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue
-
Tsai J. W., Bremner K. H., and, Vallee R. B., (2007) Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue. Nat. Neurosci. 10, 970-979.
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 970-979
-
-
Tsai, J.W.1
Bremner, K.H.2
Vallee, R.B.3
-
265
-
-
0036837658
-
Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation
-
Turner G., Partington M., Kerr B., Mangelsdorf M., and, Gecz J., (2002) Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation. Am. J. Med. Genet. 112, 405-411.
-
(2002)
Am. J. Med. Genet.
, vol.112
, pp. 405-411
-
-
Turner, G.1
Partington, M.2
Kerr, B.3
Mangelsdorf, M.4
Gecz, J.5
-
266
-
-
84926357413
-
Loss of delta-catenin function in severe autism
-
Turner T. N., Sharma K., Oh E. C., et al,. (2015) Loss of delta-catenin function in severe autism. Nature 520, 51-56.
-
(2015)
Nature
, vol.520
, pp. 51-56
-
-
Turner, T.N.1
Sharma, K.2
Oh, E.C.3
-
267
-
-
34447278070
-
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
-
Ullmann R., Turner G., Kirchhoff M., et al,. (2007) Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Hum. Mutat. 28, 674-682.
-
(2007)
Hum. Mutat.
, vol.28
, pp. 674-682
-
-
Ullmann, R.1
Turner, G.2
Kirchhoff, M.3
-
268
-
-
84906934598
-
Neuropathology of the anterior midcingulate cortex in young children with autism
-
Uppal N., Wicinski B., Buxbaum J. D., Heinsen H., Schmitz C., and, Hof P. R., (2014) Neuropathology of the anterior midcingulate cortex in young children with autism. J. Neuropathol. Exp. Neurol. 73, 891-902.
-
(2014)
J. Neuropathol. Exp. Neurol.
, vol.73
, pp. 891-902
-
-
Uppal, N.1
Wicinski, B.2
Buxbaum, J.D.3
Heinsen, H.4
Schmitz, C.5
Hof, P.R.6
-
269
-
-
77049125263
-
Neuronal migration mechanisms in development and disease
-
Valiente M., and, Marin O., (2010) Neuronal migration mechanisms in development and disease. Curr. Opin. Neurobiol. 20, 68-78.
-
(2010)
Curr. Opin. Neurobiol.
, vol.20
, pp. 68-78
-
-
Valiente, M.1
Marin, O.2
-
270
-
-
84857717466
-
Multiple modes of cytoplasmic dynein regulation
-
Vallee R. B., McKenney R. J., and, Ori-McKenney K. M., (2012) Multiple modes of cytoplasmic dynein regulation. Nat. Cell Biol. 14, 224-230.
-
(2012)
Nat. Cell Biol.
, vol.14
, pp. 224-230
-
-
Vallee, R.B.1
McKenney, R.J.2
Ori-McKenney, K.M.3
-
271
-
-
34250833558
-
Cenp-F links kinetochores to Ndel1/Nde1/Lis1/dynein microtubule motor complexes
-
Vergnolle M. A., and, Taylor S. S., (2007) Cenp-F links kinetochores to Ndel1/Nde1/Lis1/dynein microtubule motor complexes. Curr. Biol. 17, 1173-1179.
-
(2007)
Curr. Biol.
, vol.17
, pp. 1173-1179
-
-
Vergnolle, M.A.1
Taylor, S.S.2
-
272
-
-
57149090343
-
A functional genetic link between distinct developmental language disorders
-
Vernes S. C., Newbury D. F., Abrahams B. S., et al,. (2008) A functional genetic link between distinct developmental language disorders. N. Engl. J. Med. 359, 2337-2345.
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 2337-2345
-
-
Vernes, S.C.1
Newbury, D.F.2
Abrahams, B.S.3
-
273
-
-
32844460507
-
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
-
Vorstman J. A., Staal W. G., van Daalen E., van Engeland H., Hochstenbach P. F., and, Franke L., (2006) Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol. Psychiatry 11, 18-28.
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 18-28
-
-
Vorstman, J.A.1
Staal, W.G.2
Van Daalen, E.3
Van Engeland, H.4
Hochstenbach, P.F.5
Franke, L.6
-
274
-
-
34447559959
-
Transitin, a nestin-like intermediate filament protein, mediates cortical localization and the lateral transport of Numb in mitotic avian neuroepithelial cells
-
Wakamatsu Y., Nakamura N., Lee J. A., Cole G. J., and, Osumi N., (2007) Transitin, a nestin-like intermediate filament protein, mediates cortical localization and the lateral transport of Numb in mitotic avian neuroepithelial cells. Development 134, 2425-2433.
-
(2007)
Development
, vol.134
, pp. 2425-2433
-
-
Wakamatsu, Y.1
Nakamura, N.2
Lee, J.A.3
Cole, G.J.4
Osumi, N.5
-
275
-
-
54949129840
-
Autism and Brain Development
-
Walsh C. A., Morrow E. M., and, Rubenstein J. L. R., (2008) Autism and Brain Development. Cell 135, 396-400.
-
(2008)
Cell
, vol.135
, pp. 396-400
-
-
Walsh, C.A.1
Morrow, E.M.2
Rubenstein, J.L.R.3
-
276
-
-
79955455586
-
A new subtype of progenitor cell in the mouse embryonic neocortex
-
Wang X., Tsai J.-W., LaMonica B., and, Kriegstein A. R., (2011) A new subtype of progenitor cell in the mouse embryonic neocortex. Nat. Neurosci. 14, 555-561.
-
(2011)
Nat. Neurosci.
, vol.14
, pp. 555-561
-
-
Wang, X.1
Tsai, J.-W.2
LaMonica, B.3
Kriegstein, A.R.4
-
277
-
-
84928663819
-
Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer's disease
-
Wang K.-S., Tonarelli S., Luo X., et al,. (2014a) Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer's disease. J. Neural. Transm. 122, 701-708.
-
(2014)
J. Neural. Transm.
, vol.122
, pp. 701-708
-
-
Wang, K.-S.1
Tonarelli, S.2
Luo, X.3
-
278
-
-
84893510629
-
Reelin gene variants and risk of autism spectrum disorders: An integrated meta-analysis
-
Wang Z., Hong Y., Zou L., et al,. (2014b) Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis. Am. J. Med. Genet. B Neuropsychiatr. Genet. 165B, 192-200.
-
(2014)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.165 B
, pp. 192-200
-
-
Wang, Z.1
Hong, Y.2
Zou, L.3
-
279
-
-
0032826750
-
Coexistence of widespread clones and large radial clones in early embryonic ferret cortex
-
Ware M. L., Tavazoie S. F., Reid C. B., and, Walsh C. A., (1999) Coexistence of widespread clones and large radial clones in early embryonic ferret cortex. Cereb. Cortex 9, 636-645.
-
(1999)
Cereb. Cortex
, vol.9
, pp. 636-645
-
-
Ware, M.L.1
Tavazoie, S.F.2
Reid, C.B.3
Walsh, C.A.4
-
280
-
-
77953028667
-
The neuropathology of autism: Defects of neurogenesis and neuronal migration, and dysplastic changes
-
Wegiel J., Kuchna I., Nowicki K., et al,. (2010) The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes. Acta Neuropathol. 119, 755-770.
-
(2010)
Acta Neuropathol.
, vol.119
, pp. 755-770
-
-
Wegiel, J.1
Kuchna, I.2
Nowicki, K.3
-
281
-
-
80054847541
-
Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals. American journal of medical genetics
-
Whalley H. C., O'Connell G., Sussmann J. E., et al,. (2011) Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals. American journal of medical genetics. Am. J. Med. Genet. B Neuropsychiatr. Genet. 156B, 941-948.
-
(2011)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.156 B
, pp. 941-948
-
-
Whalley, H.C.1
O'Connell, G.2
Sussmann, J.E.3
-
282
-
-
0034773221
-
In utero fate mapping reveals distinct migratory pathways and fates of neurons born in the mammalian basal forebrain
-
(Cambridge, England).
-
Wichterle H., Turnbull D. H., Nery S., Fishell G., and, Alvarez-Buylla A., (2001) In utero fate mapping reveals distinct migratory pathways and fates of neurons born in the mammalian basal forebrain. Development (Cambridge, England), 128, 3759-3771.
-
(2001)
Development
, vol.128
, pp. 3759-3771
-
-
Wichterle, H.1
Turnbull, D.H.2
Nery, S.3
Fishell, G.4
Alvarez-Buylla, A.5
-
283
-
-
78049303903
-
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: A genome-wide analysis
-
Williams N. M., Zaharieva I., Martin A., et al,. (2010) Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet 376, 1401-1408.
-
(2010)
Lancet
, vol.376
, pp. 1401-1408
-
-
Williams, N.M.1
Zaharieva, I.2
Martin, A.3
-
284
-
-
84889583293
-
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
-
Willsey A. J., Sanders S. J., Li M., et al,. (2013) Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell 155, 997-1007.
-
(2013)
Cell
, vol.155
, pp. 997-1007
-
-
Willsey, A.J.1
Sanders, S.J.2
Li, M.3
-
285
-
-
77954138932
-
Astn2, A Novel Member of the Astrotactin Gene Family, Regulates the Trafficking of ASTN1 during Glial-Guided Neuronal Migration
-
Wilson P. M., Fryer R. H., Fang Y., and, Hatten M. E., (2010) Astn2, A Novel Member of the Astrotactin Gene Family, Regulates the Trafficking of ASTN1 during Glial-Guided Neuronal Migration. J. Neurosci. 30, 8529-8540.
-
(2010)
J. Neurosci.
, vol.30
, pp. 8529-8540
-
-
Wilson, P.M.1
Fryer, R.H.2
Fang, Y.3
Hatten, M.E.4
-
286
-
-
18844362115
-
Cortical interneurons and their origins
-
Wonders C., and, Anderson S. A., (2005) Cortical interneurons and their origins. Neuroscientist 11, 199-205.
-
(2005)
Neuroscientist
, vol.11
, pp. 199-205
-
-
Wonders, C.1
Anderson, S.A.2
-
287
-
-
33747614577
-
The origin and specification of cortical interneurons
-
Wonders C. P., and, Anderson S. A., (2006) The origin and specification of cortical interneurons. Nat. Rev. Neurosci. 7, 687-696.
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 687-696
-
-
Wonders, C.P.1
Anderson, S.A.2
-
288
-
-
1642313606
-
Origins of cortical interneuron subtypes
-
Xu Q., Cobos I., De La Cruz E., Rubenstein J. L., and, Anderson S. A., (2004) Origins of cortical interneuron subtypes. J. Neurosci. 24, 2612-2622.
-
(2004)
J. Neurosci.
, vol.24
, pp. 2612-2622
-
-
Xu, Q.1
Cobos, I.2
De La Cruz, E.3
Rubenstein, J.L.4
Anderson, S.A.5
-
289
-
-
0037315489
-
Human Nudel and NudE as regulators of cytoplasmic dynein in poleward protein transport along the mitotic spindle
-
Yan X., Li F., Liang Y., Shen Y., Zhao X., Huang Q., and, Zhu X., (2003) Human Nudel and NudE as regulators of cytoplasmic dynein in poleward protein transport along the mitotic spindle. Mol. Cell. Biol. 23, 1239-1250.
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 1239-1250
-
-
Yan, X.1
Li, F.2
Liang, Y.3
Shen, Y.4
Zhao, X.5
Huang, Q.6
Zhu, X.7
-
290
-
-
38849091345
-
Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division
-
Yingling J., Youn Y. H., Darling D., Toyo-Oka K., Pramparo T., Hirotsune S., and, Wynshaw-Boris A., (2008) Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division. Cell 132, 474-486.
-
(2008)
Cell
, vol.132
, pp. 474-486
-
-
Yingling, J.1
Youn, Y.H.2
Darling, D.3
Toyo-Oka, K.4
Pramparo, T.5
Hirotsune, S.6
Wynshaw-Boris, A.7
-
291
-
-
80052563319
-
Neocortical excitation/inhibition balance in information processing and social dysfunction
-
Yizhar O., Fenno L. E., Prigge M., et al,. (2011) Neocortical excitation/inhibition balance in information processing and social dysfunction. Nature 477, 171-178.
-
(2011)
Nature
, vol.477
, pp. 171-178
-
-
Yizhar, O.1
Fenno, L.E.2
Prigge, M.3
-
292
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan A. L., Alarcon M., Cheng R., et al,. (2003) A genomewide screen of 345 families for autism-susceptibility loci. Am. J. Hum. Genet. 73, 886-897.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
-
293
-
-
71849090031
-
Distinct dose-dependent cortical neuronal migration and neurite extension defects in Lis1 and Ndel1 mutant mice
-
Youn Y. H., Pramparo T., Hirotsune S., and, Wynshaw-Boris A., (2009) Distinct dose-dependent cortical neuronal migration and neurite extension defects in Lis1 and Ndel1 mutant mice. J. Neurosci. 29, 15520-15530.
-
(2009)
J. Neurosci.
, vol.29
, pp. 15520-15530
-
-
Youn, Y.H.1
Pramparo, T.2
Hirotsune, S.3
Wynshaw-Boris, A.4
-
294
-
-
23444447456
-
The caudal migratory stream: A novel migratory stream of interneurons derived from the caudal ganglionic eminence in the developing mouse forebrain
-
Yozu M., Tabata H., and, Nakajima K., (2005) The caudal migratory stream: a novel migratory stream of interneurons derived from the caudal ganglionic eminence in the developing mouse forebrain. J. Neurosci. 25, 7268-7277.
-
(2005)
J. Neurosci.
, vol.25
, pp. 7268-7277
-
-
Yozu, M.1
Tabata, H.2
Nakajima, K.3
-
295
-
-
24344486768
-
Contributions of cortical subventricular zone to the development of the human cerebral cortex
-
Zecevic N., Chen Y., and, Filipovic R., (2005) Contributions of cortical subventricular zone to the development of the human cerebral cortex. J. Comp. Neurol. 491, 109-122.
-
(2005)
J. Comp. Neurol.
, vol.491
, pp. 109-122
-
-
Zecevic, N.1
Chen, Y.2
Filipovic, R.3
-
296
-
-
0036428852
-
Reelin gene alleles and susceptibility to autism spectrum disorders
-
Zhang H., Liu X., Zhang C., Mundo E., Macciardi F., Grayson D. R., Guidotti A. R., and, Holden J. J., (2002) Reelin gene alleles and susceptibility to autism spectrum disorders. Mol. Psychiatry 7, 1012-1017.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 1012-1017
-
-
Zhang, H.1
Liu, X.2
Zhang, C.3
Mundo, E.4
MacCiardi, F.5
Grayson, D.R.6
Guidotti, A.R.7
Holden, J.J.8
-
297
-
-
84919871854
-
Association study identifying a new susceptibility gene (AUTS2) for schizophrenia
-
Zhang B., Xu Y. H., Wei S. G., Zhang H. B., Fu D. K., Feng Z. F., Guan F. L., Zhu Y. S., and, Li S. B., (2014) Association study identifying a new susceptibility gene (AUTS2) for schizophrenia. Int. J. Mol. Sci. 15, 19406-19416.
-
(2014)
Int. J. Mol. Sci.
, vol.15
, pp. 19406-19416
-
-
Zhang, B.1
Xu, Y.H.2
Wei, S.G.3
Zhang, H.B.4
Fu, D.K.5
Feng, Z.F.6
Guan, F.L.7
Zhu, Y.S.8
Li, S.B.9
-
298
-
-
34547886497
-
A unified genetic theory for sporadic and inherited autism
-
Zhao X., Leotta A., Kustanovich V., et al,. (2007) A unified genetic theory for sporadic and inherited autism. Proc. Natl Acad. Sci. USA 104, 12831-12836.
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 12831-12836
-
-
Zhao, X.1
Leotta, A.2
Kustanovich, V.3
-
299
-
-
0029947209
-
CNS gene encoding astrotactin, which supports neuronal migration along glial fibers
-
Zheng C., Heintz N., and, Hatten M. E., (1996) CNS gene encoding astrotactin, which supports neuronal migration along glial fibers. Science 272, 417-419.
-
(1996)
Science
, vol.272
, pp. 417-419
-
-
Zheng, C.1
Heintz, N.2
Hatten, M.E.3
-
300
-
-
84862659562
-
Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities
-
Zoghbi H. Y., and, Bear M. F., (2012) Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities. Cold Spring Harb. Perspect. Biol. 4, a009886.
-
(2012)
Cold Spring Harb. Perspect. Biol.
, vol.4
, pp. a009886
-
-
Zoghbi, H.Y.1
Bear, M.F.2
|