-
2
-
-
33745818375
-
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The Special Needs and Autism Project (SNAP
-
Baird G, Simonoff E, Pickles A, et al. Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP). Lancet. 2006; 368: 210-215.
-
(2006)
Lancet
, vol.368
, pp. 210-215
-
-
Baird, G.1
Simonoff, E.2
Pickles, A.3
-
3
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Szatmari P, Paterson AD, Zwaigenbaum L, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature genetics. 2007; 39: 319-328.
-
(2007)
Nature Genetics
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
-
5
-
-
31144444162
-
Epidemiology of autistic disorder and other pervasive developmental disorders
-
Fombonne E. Epidemiology of autistic disorder and other pervasive developmental disorders. The Journal of clinical psychiatry. 2005; 66(Suppl 10): 3-8.
-
(2005)
The Journal of Clinical Psychiatry
, vol.66
, Issue.SUPPL. 10
, pp. 3-8
-
-
Fombonne, E.1
-
7
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I, et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychological medicine. 1995; 25: 63-77.
-
(1995)
Psychological Medicine
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
-
8
-
-
79955494719
-
A systematic review of early intensive intervention for autism spectrum disorders
-
Warren Z, McPheeters ML, Sathe N, Foss-Feig JH, Glasser A, Veenstra-Vanderweele J. A systematic review of early intensive intervention for autism spectrum disorders. Pediatrics. 2011; 127: e1303-1311.
-
(2011)
Pediatrics
, vol.127
-
-
Warren, Z.1
McPheeters, M.L.2
Sathe, N.3
Foss-Feig, J.H.4
Glasser, A.5
Veenstra-Vanderweele, J.6
-
9
-
-
42349095075
-
Advances in autism genetics: On the threshold of a new neurobiology
-
Abrahams BS, Geschwind DH. Advances in autism genetics: on the threshold of a new neurobiology. Nat Rev Genet. 2008; 9: 341-355.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
10
-
-
67651010456
-
Genetic advances in autism: Heterogeneity and convergence on shared pathways
-
Bill BR, Geschwind DH. Genetic advances in autism: Heterogeneity and convergence on shared pathways. Curr Opin Genet Dev. 2009; 19: 271-278.
-
(2009)
Curr Opin Genet Dev
, vol.19
, pp. 271-278
-
-
Bill, B.R.1
Geschwind, D.H.2
-
11
-
-
35348822496
-
Human and animal cognition: Continuity and discontinuity
-
Premack D. Human and animal cognition: continuity and discontinuity. Proc Natl Acad Sci USA. 2007; 104: 13861-13867.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 13861-13867
-
-
Premack, D.1
-
12
-
-
43749107081
-
Darwin's mistake: Explaining the discontinuity between human and nonhuman minds
-
discussion 130-178
-
Penn DC, Holyoak KJ, Povinelli DJ. Darwin's mistake: explaining the discontinuity between human and nonhuman minds. Behav Brain Sci. 2008; 31: 109-130; discussion 130-178.
-
(2008)
Behav Brain Sci
, vol.31
, pp. 109-130
-
-
Penn, D.C.1
Holyoak, K.J.2
Povinelli, D.J.3
-
13
-
-
13444311847
-
The faculty of language: What's special about it?
-
Pinker S, Jackendoff R. The faculty of language: What's special about it? Cognition. 2005; 95: 201-236.
-
(2005)
Cognition
, vol.95
, pp. 201-236
-
-
Pinker, S.1
Jackendoff, R.2
-
14
-
-
0037159541
-
The faculty of language: What is it, who has it, and how did it evolve?
-
Hauser MD, Chomsky N, FitchWT. The faculty of language: what is it, who has it, and how did it evolve? Science. 2002; 298: 1569-1579.
-
(2002)
Science
, vol.298
, pp. 1569-1579
-
-
Hauser, M.D.1
Chomsky, N.2
Fitch, W.T.3
-
15
-
-
0031455924
-
Prevalence of specific language impairment in kindergarten children
-
Tomblin JB, Records NL, Buckwalter P, Zhang X, Smith E, O'Brien M. Prevalence of specific language impairment in kindergarten children. J Speech Lang Hear Res. 1997; 40: 1245-1260.
-
(1997)
J Speech Lang Hear Res
, vol.40
, pp. 1245-1260
-
-
Tomblin, J.B.1
Records, N.L.2
Buckwalter, P.3
Zhang, X.4
Smith, E.5
O'Brien, M.6
-
16
-
-
0035991532
-
The role of genes in the etiology of specific language impairment
-
Bishop DV. The role of genes in the etiology of specific language impairment. J Commun Disord. 2002; 35: 311-328.
-
(2002)
J Commun Disord
, vol.35
, pp. 311-328
-
-
Bishop, D.V.1
-
17
-
-
33751298803
-
What Causes Specific Language Impairment in Children?
-
Bishop DV. What Causes Specific Language Impairment in Children? Current directions in psychological science. 2006; 15: 217-221.
-
(2006)
Current Directions in Psychological Science
, vol.15
, pp. 217-221
-
-
Bishop, D.V.1
-
19
-
-
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, et al. Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels. Neuron. 1999; 24: 1037-1047.
-
(1999)
Neuron
, vol.24
, pp. 1037-1047
-
-
Poliak, S.1
Gollan, L.2
Martinez, R.3
-
20
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
Alarcon M, Abrahams BS, Stone JL, et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet. 2008; 82: 150-159.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 150-159
-
-
Alarcon, M.1
Abrahams, B.S.2
Stone, J.L.3
-
21
-
-
38749096303
-
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
-
Arking DE, Cutler DJ, Brune CW, et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet. 2008; 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
-
22
-
-
38749099110
-
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autismspectrum disorders
-
Bakkaloglu B, O'Roak BJ, Louvi A, et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autismspectrum disorders. AmJHum Genet. 2008; 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
-
-
76549104658
-
Disruption of CNTNAP2 and additional structural genome changes in a boywith speech delay and autism spectrum disorder
-
Poot M, Beyer V, Schwaab I, et al. Disruption of CNTNAP2 and additional structural genome changes in a boywith speech delay and autism spectrum disorder. Neurogenetics. 2010; 11: 81-89.
-
(2010)
Neurogenetics
, vol.11
, pp. 81-89
-
-
Poot, M.1
Beyer, V.2
Schwaab, I.3
-
24
-
-
77953808897
-
Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
-
Li X, Hu Z, He Y, et al. Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population. Psychiatr Genet. 2010; 20: 113-117.
-
(2010)
Psychiatr Genet
, vol.20
, pp. 113-117
-
-
Li, X.1
Hu, Z.2
He, Y.3
-
25
-
-
36749100015
-
Genome-wide analyses of human perisylvian cerebral cortical patterning
-
Abrahams BS, Tentler D, Perederiy JV, Oldham MC, Coppola G, Geschwind DH. Genome-wide analyses of human perisylvian cerebral cortical patterning. Proc Natl Acad Sci USA. 2007; 104: 17849-17854.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 17849-17854
-
-
Abrahams, B.S.1
Tentler, D.2
Perederiy, J.V.3
Oldham, M.C.4
Coppola, G.5
Geschwind, D.H.6
-
26
-
-
80053540965
-
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
-
Penagarikano O, Abrahams BS, Herman EI, et al. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell. 2011; 147: 235-246.
-
(2011)
Cell
, vol.147
, pp. 235-246
-
-
Penagarikano, O.1
Abrahams, B.S.2
Herman, E.I.3
-
28
-
-
0028870054
-
Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
-
Vargha-Khadem F, Watkins K, Alcock K, Fletcher P, Passingham R. Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proc Natl Acad Sci USA. 1995; 92: 930-933.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 930-933
-
-
Vargha-Khadem, F.1
Watkins, K.2
Alcock, K.3
Fletcher, P.4
Passingham, R.5
-
29
-
-
0036190947
-
Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia
-
Watkins KE, Dronkers NF, Vargha-Khadem F. Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. Brain. 2002; 125: 452-464.
-
(2002)
Brain
, vol.125
, pp. 452-464
-
-
Watkins, K.E.1
Dronkers, N.F.2
Vargha-Khadem, F.3
-
30
-
-
0033865944
-
The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
-
Lai CS, Fisher SE, Hurst JA, et al. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. Am J Hum Genet. 2000; 67: 357-368.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 357-368
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
-
31
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F,Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001; 413: 519-523.
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem Fmonaco, A.P.4
-
32
-
-
0347986673
-
Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions
-
Li S, Weidenfeld J, Morrisey EE. Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions. Molecular and cellular biology. 2004; 24: 809-822.
-
(2004)
Molecular and Cellular Biology
, vol.24
, pp. 809-822
-
-
Li, S.1
Weidenfeld, J.2
Morrisey, E.E.3
-
33
-
-
33749867547
-
Functional genetic analysis of mutations implicated in a human speech and language disorder
-
Vernes SC, Nicod J, Elahi FM, et al. Functional genetic analysis of mutations implicated in a human speech and language disorder. Hum Mol Genet. 2006; 15: 3154-3167.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3154-3167
-
-
Vernes, S.C.1
Nicod, J.2
Elahi, F.M.3
-
34
-
-
84857853508
-
Foxp2mutations impair auditorymotor association learning
-
Kurt S, Fisher SE, Ehret G. Foxp2mutations impair auditorymotor association learning. PloS one. 2012; 7: e33130.
-
(2012)
PloS One
, vol.7
-
-
Kurt, S.1
Fisher, S.E.2
Ehret, G.3
-
35
-
-
33751113031
-
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
-
Feuk L, Kalervo A, Lipsanen-Nyman M, et al. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet. 2006; 79: 965-972.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 965-972
-
-
Feuk, L.1
Kalervo, A.2
Lipsanen-Nyman, M.3
-
36
-
-
34147120769
-
Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review
-
Lennon PA, CooperML, Peiffer DA, et al. Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. Am J Med Genet A. 2007; 143A: 791-798.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 791-798
-
-
Lennon, P.A.1
Cooper, M.L.2
Peiffer, D.A.3
-
37
-
-
21044445447
-
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
-
MacDermot KD, Bonora E, Sykes N, et al. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet. 2005; 76: 1074-1080.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1074-1080
-
-
MacDermot, K.D.1
Bonora, E.2
Sykes, N.3
-
38
-
-
33749869970
-
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2
-
Shriberg LD, Ballard KJ, Tomblin JB, Duffy JR, Odell KH, Williams CA. Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2. J Speech Lang Hear Res. 2006; 49: 500-525.
-
(2006)
J Speech Lang Hear Res
, vol.49
, pp. 500-525
-
-
Shriberg, L.D.1
Ballard, K.J.2
Tomblin, J.B.3
Duffy, J.R.4
Odell, K.H.5
Williams, C.A.6
-
39
-
-
33644860165
-
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2
-
Zeesman S, Nowaczyk MJ, Teshima I, et al. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am JMed Genet A. 2006; 140: 509-514.
-
(2006)
Am JMed Genet A
, vol.140
, pp. 509-514
-
-
Zeesman, S.1
Nowaczyk, M.J.2
Teshima, I.3
-
41
-
-
0035920153
-
Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors
-
Shu W, Yang H, Zhang L, Lu MM, Morrisey EE. Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors. J Biol Chem. 2001; 276: 27488-27497.
-
(2001)
J Biol Chem
, vol.276
, pp. 27488-27497
-
-
Shu, W.1
Yang, H.2
Zhang, L.3
Lu, M.M.4
Morrisey, E.E.5
-
42
-
-
1842610982
-
Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction
-
Teramitsu I, Kudo LC, London SE, Geschwind DH, White SA. Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. The Journal of neuroscience: The official journal of the Society for Neuroscience. 2004; 24: 3152-3163.
-
(2004)
The Journal of Neuroscience: The Official Journal of the Society for Neuroscience
, vol.24
, pp. 3152-3163
-
-
Teramitsu, I.1
Kudo, L.C.2
London, S.E.3
Geschwind, D.H.4
White, S.A.5
-
44
-
-
0037467540
-
Preware PO,Morrisey EE,Walsh CA. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
Ferland RJ, Cherry TJ, Preware PO,Morrisey EE,Walsh CA. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. The Journal of comparative neurology. 2003; 460: 266-279.
-
(2003)
The Journal of Comparative Neurology
, vol.460
, pp. 266-279
-
-
Ferland, R.J.1
Cherry, T.J.2
-
45
-
-
0142153166
-
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
-
Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ. FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain. 2003; 126: 2455-2462.
-
(2003)
Brain
, vol.126
, pp. 2455-2462
-
-
Lai, C.S.1
Gerrelli, D.2
Monaco, A.P.3
Fisher, S.E.4
Copp, A.J.5
-
46
-
-
80054993342
-
Spatio-temporal transcriptome of the human brain
-
Kang HJ, Kawasawa YI, Cheng F, et al. Spatio-temporal transcriptome of the human brain. Nature. 2011; 478: 483-489.
-
(2011)
Nature
, vol.478
, pp. 483-489
-
-
Kang, H.J.1
Kawasawa, Y.I.2
Cheng, F.3
-
47
-
-
0037487188
-
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder
-
Gauthier J, Joober R,Mottron L, et al. Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. Am J Med Genet A. 2003; 118A: 172-175.
-
(2003)
Am J Med Genet A
, vol.118 A
, pp. 172-175
-
-
Gauthier, J.1
Joober Rmottron, L.2
-
48
-
-
18344368187
-
FOXP2 is not a major susceptibility gene for autism or specific language impairment
-
Newbury DF, Bonora E, Lamb JA, et al. FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet. 2002; 70: 1318-1327.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1318-1327
-
-
Newbury, D.F.1
Bonora, E.2
Lamb, J.A.3
-
49
-
-
0037043075
-
Evaluation of FOXP2 as an autism susceptibility gene
-
Wassink TH, Piven J, Vieland VJ, et al. Evaluation of FOXP2 as an autism susceptibility gene. Am JMed Genet. 2002; 114: 566-569.
-
(2002)
Am JMed Genet
, vol.114
, pp. 566-569
-
-
Wassink, T.H.1
Piven, J.2
Vieland, V.J.3
-
50
-
-
38849126088
-
Recurrent 16p11.2 microdeletions in autism
-
KumarRA, KaraMohamed S, Sudi J, et al. Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008; 17: 628-638.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 628-638
-
-
Kumar, R.A.1
Kara Mohamed, S.2
Sudi, J.3
-
51
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall CR, Noor A, Vincent JB, et al. Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet. 2008; 82: 477-488.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
-
52
-
-
39049163023
-
Association between microdeletion and microduplication at 16p11.2 and autism
-
Weiss LA, Shen Y, Korn JM, et al. Association between microdeletion and microduplication at 16p11.2 and autism. N Engl J Med. 2008; 358: 667-675.
-
(2008)
N Engl J Med
, vol.358
, pp. 667-675
-
-
Weiss, L.A.1
Shen, Y.2
Korn, J.M.3
-
53
-
-
65449184161
-
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1
-
Ma D, Salyakina D, Jaworski JM, et al. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Ann Hum Genet. 2009; 73: 263-273.
-
(2009)
Ann Hum Genet
, vol.73
, pp. 263-273
-
-
Ma, D.1
Salyakina, D.2
Jaworski, J.M.3
-
54
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
Wang K, Zhang H, Ma D, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 2009; 459: 528-533.
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
-
55
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
Anney R, Klei L, Pinto D, et al. A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet. 2010.
-
(2010)
Hum Mol Genet
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
-
56
-
-
77950899212
-
Connecting genes to brain in the autism spectrum disorders
-
Abrahams BS, Geschwind DH. Connecting genes to brain in the autism spectrum disorders. Arch Neurol. 2010; 67: 395-399.
-
(2010)
Arch Neurol
, vol.67
, pp. 395-399
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
57
-
-
11144357511
-
Association between the FOXP2 gene and autistic disorder in Chinese population
-
Gong X, JiaM,RuanY, et al. Association between the FOXP2 gene and autistic disorder in Chinese population. Am J Med Genet B Neuropsychiatr Genet. 2004; 127B: 113-116.
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.127 B
, pp. 113-116
-
-
Gong, X.1
Jia, M.2
Ruan, Y.3
-
58
-
-
57149124362
-
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders
-
Laroche F,Ramoz N, Leroy S, et al. Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders. Psychiatr Genet. 2008; 18: 295-301.
-
(2008)
Psychiatr Genet
, vol.18
, pp. 295-301
-
-
Laroche, F.1
Ramoz, N.2
Leroy, S.3
-
59
-
-
14644415479
-
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
-
Li H,Yamagata T, Mori M,MomoiMY. Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients. Brain Dev. 2005; 27: 207-210.
-
(2005)
Brain Dev
, vol.27
, pp. 207-210
-
-
Li, H.1
Yamagata, T.2
Mori, M.3
Momoi, M.Y.4
-
60
-
-
23044492611
-
No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population
-
Marui T, Koishi S, Funatogawa I, et al. No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population. Neurosci Res. 2005; 53: 91-94.
-
(2005)
Neurosci Res
, vol.53
, pp. 91-94
-
-
Marui, T.1
Koishi, S.2
Funatogawa, I.3
-
62
-
-
0036705625
-
FOXP2: Novel exons, splice variants, and CAG repeat length stability
-
Bruce HA, Margolis RL. FOXP2: novel exons, splice variants, and CAG repeat length stability. Human genetics. 2002; 111: 136-144.
-
(2002)
Human Genetics
, vol.111
, pp. 136-144
-
-
Bruce, H.A.1
Margolis, R.L.2
-
64
-
-
70449653431
-
Human-specific transcriptional regulation of CNS development genes by FOXP2
-
Konopka G, Bomar JM, Winden K, et al. Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature. 2009; 462: 213-217.
-
(2009)
Nature
, vol.462
, pp. 213-217
-
-
Konopka, G.1
Bomar, J.M.2
Winden, K.3
-
66
-
-
67349154764
-
Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder
-
Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P. Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder. Autism Res. 2008; 1: 159-168.
-
(2008)
Autism Res
, vol.1
, pp. 159-168
-
-
Campbell, D.B.1
Li, C.2
Sutcliffe, J.S.3
Persico, A.M.4
Levitt, P.5
-
68
-
-
70349323427
-
Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder
-
Jackson PB, Boccuto L, Skinner C, et al. Further evidence that the rs1858830 C variant in the promoter region of the MET gene is associated with autistic disorder. Autism Res. 2009; 2: 232-236.
-
(2009)
Autism Res
, vol.2
, pp. 232-236
-
-
Jackson, P.B.1
Boccuto, L.2
Skinner, C.3
-
69
-
-
33750962208
-
A genetic variant that disrupts MET transcription is associated with autism
-
Campbell DB, Sutcliffe JS, Ebert PJ, et al. A genetic variant that disrupts MET transcription is associated with autism. Proc Natl Acad Sci USA. 2006; 103: 16834-16839.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 16834-16839
-
-
Campbell, D.B.1
Sutcliffe, J.S.2
Ebert, P.J.3
-
70
-
-
34948876359
-
Disruption of cerebral cortex MET signaling in autism spectrum disorder
-
Campbell DB, D'Oronzio R, Garbett K, et al. Disruption of cerebral cortex MET signaling in autism spectrum disorder. Ann Neurol. 2007; 62: 243-250.
-
(2007)
Ann Neurol
, vol.62
, pp. 243-250
-
-
Campbell, D.B.1
D'Oronzio, R.2
Garbett, K.3
-
71
-
-
64549151568
-
Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain
-
Judson MC, Bergman MY, Campbell DB, Eagleson KL, Levitt P. Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain. J Comp Neurol. 2009; 513: 511-531.
-
(2009)
J Comp Neurol
, vol.513
, pp. 511-531
-
-
Judson, M.C.1
Bergman, M.Y.2
Campbell, D.B.3
Eagleson, K.L.4
Levitt, P.5
-
72
-
-
33845566076
-
Loss of embryonic MET signaling alters profiles of hippocampal interneurons
-
Martins GJ, Plachez C, Powell EM. Loss of embryonic MET signaling alters profiles of hippocampal interneurons. Dev Neurosci. 2007; 29: 143-158.
-
(2007)
Dev Neurosci
, vol.29
, pp. 143-158
-
-
Martins, G.J.1
Plachez, C.2
Powell, E.M.3
-
73
-
-
0037198923
-
Localization and functional role of hepatocyte growth factor (HGF) and its receptor c-met in the rat developing cerebral cortex
-
Sun W, Funakoshi H, Nakamura T. Localization and functional role of hepatocyte growth factor (HGF) and its receptor c-met in the rat developing cerebral cortex. Brain Res Mol Brain Res. 2002; 103: 36-48.
-
(2002)
Brain Res Mol Brain Res
, vol.103
, pp. 36-48
-
-
Sun, W.1
Funakoshi, H.2
Nakamura, T.3
-
74
-
-
34147096333
-
Hepatocyte growth factor (HGF) promotes oligodendrocyte progenitor cell proliferation and inhibits its differentiation during postnatal development in the rat
-
Ohya W, Funakoshi H, Kurosawa T, Nakamura T. Hepatocyte growth factor (HGF) promotes oligodendrocyte progenitor cell proliferation and inhibits its differentiation during postnatal development in the rat. Brain Res. 2007; 1147: 51-65.
-
(2007)
Brain Res
, vol.1147
, pp. 51-65
-
-
Ohya, W.1
Funakoshi, H.2
Kurosawa, T.3
Nakamura, T.4
-
75
-
-
0036955831
-
Foxp4: A novel member of the Foxp subfamily of winged-helix genes co-expressed with Foxp1 and Foxp2 in pulmonary and gut tissues
-
Lu MM, Li S, Yang H, Morrisey EE. Foxp4: a novel member of the Foxp subfamily of winged-helix genes co-expressed with Foxp1 and Foxp2 in pulmonary and gut tissues. Gene Expr Patterns. 2002; 2: 223-228.
-
(2002)
Gene Expr Patterns
, vol.2
, pp. 223-228
-
-
Lu, M.M.1
Li, S.2
Yang, H.3
Morrisey, E.E.4
-
77
-
-
46949099804
-
Expression of FOXP2 in the developing monkey forebrain: Comparison with the expression of the genes FOXP1, PBX3, and MEIS2
-
Takahashi K, Liu FC, Oishi T, et al. Expression of FOXP2 in the developing monkey forebrain: comparison with the expression of the genes FOXP1, PBX3, and MEIS2. The Journal of Comparative Neurology. 2008; 509: 180-189.
-
(2008)
The Journal of Comparative Neurology
, vol.509
, pp. 180-189
-
-
Takahashi, K.1
Liu, F.C.2
Oishi, T.3
-
79
-
-
78650736911
-
Foxp4 is essential in maintenance of Purkinje cell dendritic arborization in the mouse cerebellum
-
TamWY, Leung CK, Tong KK,Kwan KM. Foxp4 is essential in maintenance of Purkinje cell dendritic arborization in the mouse cerebellum. Neuroscience. 2011; 172: 562-571.
-
(2011)
Neuroscience
, vol.172
, pp. 562-571
-
-
Tam, W.Y.1
Leung, C.K.2
Tong, K.K.3
Kwan, K.M.4
-
80
-
-
33750608171
-
Cerebellar 'transcriptome' reveals cell-type and stage-specific expression during postnatal development and tumorigenesis
-
Schuller U, Kho AT, Zhao Q, Ma Q, Rowitch DH. Cerebellar 'transcriptome' reveals cell-type and stage-specific expression during postnatal development and tumorigenesis. Molecular and cellular neurosciences. 2006; 33: 247-259.
-
(2006)
Molecular and Cellular Neurosciences
, vol.33
, pp. 247-259
-
-
Schuller, U.1
Kho, A.T.2
Zhao, Q.3
Ma, Q.4
Rowitch, D.H.5
-
81
-
-
78249268820
-
De novo mutations in FOXP1 in cases with intellectual disability autism and language impairment
-
Hamdan FF, Daoud H, Rochefort D, et al. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. American journal of human genetics. 2010; 87: 671-678.
-
(2010)
American Journal of Human Genetics
, vol.87
, pp. 671-678
-
-
Hamdan, F.F.1
Daoud, H.2
Rochefort, D.3
-
82
-
-
67349164801
-
A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
-
ParianiMJ, Spencer A, Graham JM, Jr., Rimoin DL.A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis. European journal of medical genetics. 2009; 52: 123-127.
-
(2009)
European Journal of Medical Genetics
, vol.52
, pp. 123-127
-
-
Pariani, M.J.1
Spencer, A.2
Graham Jr., J.M.3
Rimoin, D.L.4
-
83
-
-
77957896206
-
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
-
Horn D, Kapeller J, Rivera-Brugues N, et al. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human mutation. 2010; 31: E1851-1860.
-
(2010)
Human Mutation
, vol.31
-
-
Horn, D.1
Kapeller, J.2
Rivera-Brugues, N.3
-
84
-
-
79957589237
-
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
-
O'Roak BJ, Deriziotis P, Lee C, et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature genetics. 2011; 43: 585-589.
-
(2011)
Nature Genetics
, vol.43
, pp. 585-589
-
-
O'Roak, B.J.1
Deriziotis, P.2
Lee, C.3
-
85
-
-
84859430008
-
Animal Models of Autism: An Epigenetic and Environmental Viewpoint
-
Iwata K, Matsuzaki H, Takei N, Manabe T, Mori N. Animal Models of Autism: An Epigenetic and Environmental Viewpoint. Journal of Central Nervous System Disease. 2010; 2: 37.
-
(2010)
Journal of Central Nervous System Disease
, vol.2
, pp. 37
-
-
Iwata, K.1
Matsuzaki, H.2
Takei, N.3
Manabe, T.4
Mori, N.5
-
87
-
-
0034758125
-
Accelerated nervous system development contributes to behavioral efficiency in the laboratory mouse: A behavioral review and theoretical proposal
-
Whishaw IQ, Metz GA, Kolb B, Pellis SM. Accelerated nervous system development contributes to behavioral efficiency in the laboratory mouse: a behavioral review and theoretical proposal. Developmental psychobiology. 2001; 39: 151-170.
-
(2001)
Developmental Psychobiology
, vol.39
, pp. 151-170
-
-
Whishaw, I.Q.1
Metz, G.A.2
Kolb, B.3
Pellis, S.M.4
-
88
-
-
34548348780
-
The mouse ascending: Perspectives for human-diseasemodels
-
Rosenthal N, Brown S. The mouse ascending: Perspectives for human-diseasemodels. Nature cell biology. 2007; 9: 993-999.
-
(2007)
Nature Cell Biology
, vol.9
, pp. 993-999
-
-
Rosenthal, N.1
Brown, S.2
-
89
-
-
70349840881
-
Animal models of autism spectrum disorders: Information for neurotoxicologists
-
Halladay AK, Amaral D, Aschner M, et al. Animal models of autism spectrum disorders: information for neurotoxicologists. Neurotoxicology. 2009; 30: 811-821.
-
(2009)
Neurotoxicology
, vol.30
, pp. 811-821
-
-
Halladay, A.K.1
Amaral, D.2
Aschner, M.3
-
91
-
-
32444451616
-
Mousemodels of autism spectrum disorders: The challenge for behavioral genetics
-
Moy SS, Nadler JJ, Magnuson TR, Crawley JN.Mousemodels of autism spectrum disorders: The challenge for behavioral genetics. American journal of medical genetics Part C, Seminars in medical genetics. 2006; 142C: 40-51.
-
(2006)
American Journal of Medical Genetics Part C, Seminars in Medical Genetics
, vol.142 C
, pp. 40-51
-
-
Moy, S.S.1
Nadler, J.J.2
Magnuson, T.R.3
Crawley, J.N.4
-
92
-
-
40349093351
-
Autism-like behavioral phenotypes in BTBR T+tf/J mice
-
McFarlane HG, Kusek GK, Yang M, Phoenix JL, Bolivar VJ, Crawley JN. Autism-like behavioral phenotypes in BTBR T+tf/J mice. Genes, brain, and behavior. 2008; 7: 152-163.
-
(2008)
Genes, Brain, and Behavior
, vol.7
, pp. 152-163
-
-
McFarlane, H.G.1
Kusek, G.K.2
Yang, M.3
Phoenix, J.L.4
Bolivar, V.J.5
Crawley, J.N.6
-
93
-
-
84863052622
-
Molecular microcircuitry underlies functional specification in a basal ganglia circuit dedicated to vocal learning
-
Hilliard AT, Miller JE, Fraley ER, Horvath S, White SA. Molecular microcircuitry underlies functional specification in a basal ganglia circuit dedicated to vocal learning. Neuron. 2012; 73: 537-552.
-
(2012)
Neuron
, vol.73
, pp. 537-552
-
-
Hilliard, A.T.1
Miller, J.E.2
Fraley, E.R.3
Horvath, S.4
White, S.A.5
-
94
-
-
0035829366
-
Ultrasonic vocalisation emitted by infant rodents: A tool for assessment of neurobehavioural development
-
Branchi I, SantucciD,Alleva E.Ultrasonic vocalisation emitted by infant rodents: A tool for assessment of neurobehavioural development. Behav Brain Res. 2001; 125: 49-56.
-
(2001)
Behav Brain Res
, vol.125
, pp. 49-56
-
-
Branchi, I.1
Santucci, D.2
Alleva, E.3
-
95
-
-
13644263307
-
Infant rodent ultrasounds-a gate to the understanding of sound communication
-
Ehret G. Infant rodent ultrasounds-a gate to the understanding of sound communication. Behav Genet. 2005; 35: 19-29.
-
(2005)
Behav Genet
, vol.35
, pp. 19-29
-
-
Ehret, G.1
-
96
-
-
0032892152
-
Sonographic structure of isolation-induced ultrasonic calls of rat pups
-
Brudzynski SM, Kehoe P, Callahan M. Sonographic structure of isolation-induced ultrasonic calls of rat pups. Developmental psychobiology. 1999; 34: 195-204.
-
(1999)
Developmental Psychobiology
, vol.34
, pp. 195-204
-
-
Brudzynski, S.M.1
Kehoe, P.2
Callahan, M.3
-
97
-
-
42949179575
-
Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells
-
Fujita E, Tanabe Y, Shiota A, et al. Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells. Proc Natl Acad Sci USA. 2008; 105: 3117-3122.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 3117-3122
-
-
Fujita, E.1
Tanabe, Y.2
Shiota, A.3
-
98
-
-
40149112272
-
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
-
Groszer M, Keays DA, Deacon RM, et al. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol. 2008; 18: 354-362.
-
(2008)
Curr Biol
, vol.18
, pp. 354-362
-
-
Groszer, M.1
Keays, D.A.2
Deacon, R.M.3
-
99
-
-
77952992862
-
The structure of innate vocalizations in Foxp2-deficient mouse pups
-
Gaub S, Groszer M, Fisher SE, Ehret G. The structure of innate vocalizations in Foxp2-deficient mouse pups. Genes Brain Behav. 2010; 9: 390-401.
-
(2010)
Genes Brain Behav
, vol.9
, pp. 390-401
-
-
Gaub, S.1
Groszer, M.2
Fisher, S.E.3
Ehret, G.4
-
102
-
-
0036638050
-
The effects of cold, rotation, and genotype on the production of ultrasonic calls in infant mice
-
Hahn ME, Schanz N. The effects of cold, rotation, and genotype on the production of ultrasonic calls in infant mice. Behavior genetics. 2002; 32: 267-273.
-
(2002)
Behavior Genetics
, vol.32
, pp. 267-273
-
-
Hahn, M.E.1
Schanz, N.2
-
103
-
-
79960807951
-
A role for strain differences in waveforms of ultrasonic vocalizations during malefemale interaction
-
Sugimoto H, Okabe S, Kato M, et al. A role for strain differences in waveforms of ultrasonic vocalizations during malefemale interaction. PloS one. 2011; 6: e22093.
-
(2011)
PloS One
, vol.6
-
-
Sugimoto, H.1
Okabe, S.2
Kato, M.3
-
104
-
-
79952388376
-
Cross fostering experiments suggest that mice songs are innate
-
Kikusui T, Nakanishi K, Nakagawa R, Nagasawa M, Mogi K, Okanoya K. Cross fostering experiments suggest that mice songs are innate. PloS one. 2011; 6: e17721.
-
(2011)
PloS One
, vol.6
-
-
Kikusui, T.1
Nakanishi, K.2
Nakagawa, R.3
Nagasawa, M.4
Mogi, K.5
Okanoya, K.6
-
105
-
-
79960955811
-
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
-
Vernes SC, Oliver PL, Spiteri E, et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS genetics. 2011; 7: e1002145.
-
(2011)
PLoS Genetics
, vol.7
-
-
Vernes, S.C.1
Oliver, P.L.2
Spiteri, E.3
-
106
-
-
65849256049
-
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
-
Enard W, Gehre S, Hammerschmidt K, et al. A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell. 2009; 137: 961-971.
-
(2009)
Cell
, vol.137
, pp. 961-971
-
-
Enard, W.1
Gehre, S.2
Hammerschmidt, K.3
-
107
-
-
1842454166
-
FoxP2 expression in avian vocal learners and non-learners
-
Haesler S, Wada K, Nshdejan A, et al. FoxP2 expression in avian vocal learners and non-learners. J Neurosci. 2004; 24: 3164-3175.
-
(2004)
J Neurosci
, vol.24
, pp. 3164-3175
-
-
Haesler, S.1
Wada, K.2
Nshdejan, A.3
-
108
-
-
33746083657
-
FoxP2 regulation during undirected singing in adult songbirds
-
Teramitsu I, White SA. FoxP2 regulation during undirected singing in adult songbirds. J Neurosci. 2006; 26: 7390-7394.
-
(2006)
J Neurosci
, vol.26
, pp. 7390-7394
-
-
Teramitsu, I.1
White, S.A.2
-
109
-
-
57349177015
-
Birdsong decreases protein levels of FoxP2, a molecule required for human speech
-
Miller JE, Spiteri E, Condro MC, Dosumu-Johnson RT, Geschwind DH,White SA. Birdsong decreases protein levels of FoxP2, a molecule required for human speech. J Neurophysiol. 2008; 100: 2015-2025.
-
(2008)
J Neurophysiol
, vol.100
, pp. 2015-2025
-
-
Miller, J.E.1
Spiteri, E.2
Condro, M.C.3
Dosumu-Johnson, R.T.4
Geschwind Dhwhite, S.A.5
-
110
-
-
38549176222
-
Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X
-
Haesler S, Rochefort C, Georgi B, Licznerski P, Osten P, Scharff C. Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X. PLoS biology. 2007; 5: e321.
-
(2007)
PLoS Biology
, vol.5
-
-
Haesler, S.1
Rochefort, C.2
Georgi, B.3
Licznerski, P.4
Osten, P.5
Scharff, C.6
-
111
-
-
77958498211
-
Knockdown of FoxP2 alters spine density in Area X of the zebra finch
-
Schulz SB, Haesler S, Scharff C, Rochefort C. Knockdown of FoxP2 alters spine density in Area X of the zebra finch. Genes, brain, and behavior. 2010; 9: 732-740.
-
(2010)
Genes, Brain, and Behavior
, vol.9
, pp. 732-740
-
-
Schulz, S.B.1
Haesler, S.2
Scharff, C.3
Rochefort, C.4
-
112
-
-
80155148101
-
Patterns of spinal sensory-motor connectivity prescribed by a dorsoventral positional template
-
Surmeli G, Akay T, Ippolito GC, Tucker PW, Jessell TM. Patterns of spinal sensory-motor connectivity prescribed by a dorsoventral positional template. Cell. 2011; 147: 653-665.
-
(2011)
Cell
, vol.147
, pp. 653-665
-
-
Surmeli, G.1
Akay, T.2
Ippolito, G.C.3
Tucker, P.W.4
Jessell, T.M.5
|