-
1
-
-
36749100015
-
Genome-wide analyses of human perisylvian cerebral cortical patterning
-
Abrahams B.S., Tentler D., Perederiy J.V., Oldham M.C., Coppola G., Geschwind D.H. Genome-wide analyses of human perisylvian cerebral cortical patterning. Proceedings of the National Academy of Sciences of the United States of America 2007, 104(45):17849-17854.
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.45
, 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
-
2
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
Alarcon M., Abrahams B.S., Stone J.L., Duvall J.A., Perederiy J.V., Bomar J.M., et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. American Journal of Human Genetics 2008, 82(1):150-159.
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.1
, pp. 150-159
-
-
Alarcon, M.1
Abrahams, B.S.2
Stone, J.L.3
Duvall, J.A.4
Perederiy, J.V.5
Bomar, J.M.6
-
3
-
-
0036138102
-
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
-
Alarcon M., Cantor R.M., Liu J., Gilliam T.C., Geschwind D.H. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. American Journal of Human Genetics 2002, 70(1):60-71.
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.1
, pp. 60-71
-
-
Alarcon, M.1
Cantor, R.M.2
Liu, J.3
Gilliam, T.C.4
Geschwind, D.H.5
-
4
-
-
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., Love D.R. Amino-terminal microdeletion within the CNTNAP2 gene associated with variable expressivity of speech delay. Case Reports in Genetics 2012, 2012:172408.
-
(2012)
Case Reports in Genetics
, vol.2012
, pp. 172408
-
-
Al-Murrani, A.1
Ashton, F.2
Aftimos, S.3
George, A.M.4
Love, D.R.5
-
5
-
-
84868121906
-
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
-
Anderson G.R., Galfin T., Xu W., Aoto J., Malenka R.C., Sudhof T.C. Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development. Proceedings of the National Academy of Sciences of the United States of America 2012, 109(44):18120-18125.
-
(2012)
Proceedings of the National Academy of Sciences of the United States of America
, vol.109
, Issue.44
, pp. 18120-18125
-
-
Anderson, G.R.1
Galfin, T.2
Xu, W.3
Aoto, J.4
Malenka, R.C.5
Sudhof, T.C.6
-
6
-
-
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., Teslovich T.M., West K., Ikeda M., et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics 2008, 82(1):160-164.
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.1
, pp. 160-164
-
-
Arking, D.E.1
Cutler, D.J.2
Brune, C.W.3
Teslovich, T.M.4
West, K.5
Ikeda, M.6
-
7
-
-
84871877593
-
Mouse vocal communication system: Are ultrasounds learned or innate?
-
Arriaga G., Jarvis E.D. Mouse vocal communication system: Are ultrasounds learned or innate?. Brain and Language 2013, 124(1):96-116.
-
(2013)
Brain and Language
, vol.124
, Issue.1
, pp. 96-116
-
-
Arriaga, G.1
Jarvis, E.D.2
-
8
-
-
84867340347
-
Of mice, birds, and men: The mouse ultrasonic song system has some features similar to humans and song-learning birds
-
Arriaga G., Zhou E.P., Jarvis E.D. Of mice, birds, and men: The mouse ultrasonic song system has some features similar to humans and song-learning birds. PLoS One 2012, 7(10):e46610.
-
(2012)
PLoS One
, vol.7
, Issue.10
-
-
Arriaga, G.1
Zhou, E.P.2
Jarvis, E.D.3
-
9
-
-
84867581362
-
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
-
Bacon C., Rappold G.A. The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders. Human Genetics 2012, 131(11):1687-1698.
-
(2012)
Human Genetics
, vol.131
, Issue.11
, pp. 1687-1698
-
-
Bacon, C.1
Rappold, G.A.2
-
10
-
-
38749099110
-
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
-
Bakkaloglu B., O'Roak B.J., Louvi A., Gupta A.R., Abelson J.F., Morgan T.M., et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. American Journal of Human Genetics 2008, 82(1):165-173.
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.1
, pp. 165-173
-
-
Bakkaloglu, B.1
O'Roak, B.J.2
Louvi, A.3
Gupta, A.R.4
Abelson, J.F.5
Morgan, T.M.6
-
11
-
-
78650886933
-
A big-world network in ASD: Dynamical connectivity analysis reflects a deficit in long-range connections and an excess of short-range connections
-
Barttfeld P., Wicker B., Cukier S., Navarta S., Lew S., Sigman M. A big-world network in ASD: Dynamical connectivity analysis reflects a deficit in long-range connections and an excess of short-range connections. Neuropsychologia 2011, 49(2):254-263.
-
(2011)
Neuropsychologia
, vol.49
, Issue.2
, pp. 254-263
-
-
Barttfeld, P.1
Wicker, B.2
Cukier, S.3
Navarta, S.4
Lew, S.5
Sigman, M.6
-
12
-
-
58149178561
-
AutDB: A gene reference resource for autism research
-
Database issue
-
Basu S.N., Kollu R., Banerjee-Basu S. AutDB: A gene reference resource for autism research. Nucleic Acids Research 2009, 37(Database issue):D832-D836.
-
(2009)
Nucleic Acids Research
, vol.37
-
-
Basu, S.N.1
Kollu, R.2
Banerjee-Basu, S.3
-
13
-
-
0038638149
-
Cortical area and species differences in dendritic spine morphology
-
Benavides-Piccione R., Ballesteros-Yanez I., DeFelipe J., Yuste R. Cortical area and species differences in dendritic spine morphology. Journal of Neurocytology 2002, 31(3-5):337-346.
-
(2002)
Journal of Neurocytology
, vol.31
, Issue.3-5
, pp. 337-346
-
-
Benavides-Piccione, R.1
Ballesteros-Yanez, I.2
DeFelipe, J.3
Yuste, R.4
-
14
-
-
84864335157
-
Autism genetics: Searching for specificity and convergence
-
Berg J.M., Geschwind D.H. Autism genetics: Searching for specificity and convergence. Genome Biology 2012, 13(7):247.
-
(2012)
Genome Biology
, vol.13
, Issue.7
, pp. 247
-
-
Berg, J.M.1
Geschwind, D.H.2
-
15
-
-
77952827032
-
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
-
Berkel S., Marshall C.R., Weiss B., Howe J., Roeth R., Moog U., et al. Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nature Genetics 2010, 42(6):489-491.
-
(2010)
Nature Genetics
, vol.42
, Issue.6
, pp. 489-491
-
-
Berkel, S.1
Marshall, C.R.2
Weiss, B.3
Howe, J.4
Roeth, R.5
Moog, U.6
-
16
-
-
84888407891
-
ASD-relevant animal models of the Foxp family of transcription factors
-
Bowers J.M., Konopka G. ASD-relevant animal models of the Foxp family of transcription factors. Autism Open Access 2012, S1(10). 10.4172/2165-7890.S1-010.
-
(2012)
Autism Open Access
, Issue.10 SUPPL. 1
-
-
Bowers, J.M.1
Konopka, G.2
-
17
-
-
84872299260
-
The role of the FOXP family of transcription factors in ASD
-
Bowers J.M., Konopka G. The role of the FOXP family of transcription factors in ASD. Disease Markers 2012, 33(5):251-260.
-
(2012)
Disease Markers
, vol.33
, Issue.5
, pp. 251-260
-
-
Bowers, J.M.1
Konopka, G.2
-
18
-
-
84874199672
-
Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval
-
Bowers J.M., Perez-Pouchoulen M., Edwards N.S., McCarthy M.M. Foxp2 mediates sex differences in ultrasonic vocalization by rat pups and directs order of maternal retrieval. Journal of Neuroscience 2013, 33(8):3276-3283.
-
(2013)
Journal of Neuroscience
, vol.33
, Issue.8
, pp. 3276-3283
-
-
Bowers, J.M.1
Perez-Pouchoulen, M.2
Edwards, N.S.3
McCarthy, M.M.4
-
19
-
-
67349154764
-
Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder
-
Campbell D.B., Li C., Sutcliffe J.S., Persico A.M., Levitt P. Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder. Autism Research 2008, 1(3):159-168.
-
(2008)
Autism Research
, vol.1
, Issue.3
, pp. 159-168
-
-
Campbell, D.B.1
Li, C.2
Sutcliffe, J.S.3
Persico, A.M.4
Levitt, P.5
-
20
-
-
77949812715
-
Aberrant expression of the neuronal transcription factor FOXP2 in neoplastic plasma cells
-
Campbell A.J., Lyne L., Brown P.J., Launchbury R.J., Bignone P., Chi J., et al. Aberrant expression of the neuronal transcription factor FOXP2 in neoplastic plasma cells. British Journal of Haematology 2010, 149(2):221-230.
-
(2010)
British Journal of Haematology
, vol.149
, Issue.2
, pp. 221-230
-
-
Campbell, A.J.1
Lyne, L.2
Brown, P.J.3
Launchbury, R.J.4
Bignone, P.5
Chi, J.6
-
21
-
-
77958510976
-
Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency
-
Carr C.W., Moreno-De-Luca D., Parker C., Zimmerman H.H., Ledbetter N., Martin C.L., et al. Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency. European Journal of Human Genetics 2010, 18(11):1216-1220.
-
(2010)
European Journal of Human Genetics
, vol.18
, Issue.11
, pp. 1216-1220
-
-
Carr, C.W.1
Moreno-De-Luca, D.2
Parker, C.3
Zimmerman, H.H.4
Ledbetter, N.5
Martin, C.L.6
-
22
-
-
84860879137
-
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
-
Casey J.P., Magalhaes T., Conroy J.M., Regan R., Shah N., Anney R., et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics 2012, 131(4):565-579.
-
(2012)
Human Genetics
, vol.131
, Issue.4
, pp. 565-579
-
-
Casey, J.P.1
Magalhaes, T.2
Conroy, J.M.3
Regan, R.4
Shah, N.5
Anney, R.6
-
23
-
-
79960466733
-
Association study of the CNS patterning genes and autism in Han Chinese in Taiwan
-
Chien Y.L., Wu Y.Y., Chiu Y.N., Liu S.K., Tsai W.C., Lin P.I., et al. Association study of the CNS patterning genes and autism in Han Chinese in Taiwan. Progress in Neuro-Psychopharmacology and Biological Psychiatry 2011, 35(6):1512-1517.
-
(2011)
Progress in Neuro-Psychopharmacology and Biological Psychiatry
, vol.35
, Issue.6
, pp. 1512-1517
-
-
Chien, Y.L.1
Wu, Y.Y.2
Chiu, Y.N.3
Liu, S.K.4
Tsai, W.C.5
Lin, P.I.6
-
24
-
-
84873729095
-
Multiplex genome engineering using CRISPR/Cas systems
-
Cong L., Ran F.A., Cox D., Lin S., Barretto R., Habib N., et al. Multiplex genome engineering using CRISPR/Cas systems. Science 2013, 339(6121):819-823.
-
(2013)
Science
, vol.339
, Issue.6121
, pp. 819-823
-
-
Cong, L.1
Ran, F.A.2
Cox, D.3
Lin, S.4
Barretto, R.5
Habib, N.6
-
25
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
Cook E.H., Scherer S.W. Copy-number variations associated with neuropsychiatric conditions. Nature 2008, 455(7215):919-923.
-
(2008)
Nature
, vol.455
, Issue.7215
, pp. 919-923
-
-
Cook, E.H.1
Scherer, S.W.2
-
26
-
-
50249084956
-
Genomic imprinting in the development and evolution of psychotic spectrum conditions
-
Crespi B. Genomic imprinting in the development and evolution of psychotic spectrum conditions. Biological Reviews of the Cambridge Philosophical Society 2008, 83(4):441-493.
-
(2008)
Biological Reviews of the Cambridge Philosophical Society
, vol.83
, Issue.4
, pp. 441-493
-
-
Crespi, B.1
-
27
-
-
45449089030
-
Psychosis and autism as diametrical disorders of the social brain
-
discussion 261-320
-
Crespi B., Badcock C. Psychosis and autism as diametrical disorders of the social brain. Behavioral and Brain Sciences 2008, 31(3):241-261. discussion 261-320.
-
(2008)
Behavioral and Brain Sciences
, vol.31
, Issue.3
, pp. 241-261
-
-
Crespi, B.1
Badcock, C.2
-
29
-
-
85027946970
-
Thalamic mechanisms in language: A reconsideration based on recent findings and concepts
-
Crosson B. Thalamic mechanisms in language: A reconsideration based on recent findings and concepts. Brain and Language 2013, 126(1):73-88.
-
(2013)
Brain and Language
, vol.126
, Issue.1
, pp. 73-88
-
-
Crosson, B.1
-
30
-
-
0031578929
-
Is schizophrenia the price that Homo sapiens pays for language?
-
Crow T.J. Is schizophrenia the price that Homo sapiens pays for language?. Schizophrenia Research 1997, 28(2-3):127-141.
-
(1997)
Schizophrenia Research
, vol.28
, Issue.2-3
, pp. 127-141
-
-
Crow, T.J.1
-
31
-
-
47749149893
-
Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1
-
Dasen J.S., De Camilli A., Wang B., Tucker P.W., Jessell T.M. Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1. Cell 2008, 134(2):304-316.
-
(2008)
Cell
, vol.134
, Issue.2
, pp. 304-316
-
-
Dasen, J.S.1
De Camilli, A.2
Wang, B.3
Tucker, P.W.4
Jessell, T.M.5
-
32
-
-
79954947943
-
Aberrant striatal functional connectivity in children with autism
-
Di Martino A., Kelly C., Grzadzinski R., Zuo X.N., Mennes M., Mairena M.A., et al. Aberrant striatal functional connectivity in children with autism. Biological Psychiatry 2011, 69(9):847-856.
-
(2011)
Biological Psychiatry
, vol.69
, Issue.9
, pp. 847-856
-
-
Di Martino, A.1
Kelly, C.2
Grzadzinski, R.3
Zuo, X.N.4
Mennes, M.5
Mairena, M.A.6
-
34
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
Dunham I., Kundaje A., Aldred S.F., Collins P.J., Davis C.A., Doyle F., et al. An integrated encyclopedia of DNA elements in the human genome. Nature 2012, 489(7414):57-74.
-
(2012)
Nature
, vol.489
, Issue.7414
, pp. 57-74
-
-
Dunham, I.1
Kundaje, A.2
Aldred, S.F.3
Collins, P.J.4
Davis, C.A.5
Doyle, F.6
-
35
-
-
79951568560
-
The autism risk genes MET and PLAUR differentially impact cortical development
-
Eagleson K.L., Campbell D.B., Thompson B.L., Bergman M.Y., Levitt P. The autism risk genes MET and PLAUR differentially impact cortical development. Autism Research 2011, 4(1):68-83.
-
(2011)
Autism Research
, vol.4
, Issue.1
, pp. 68-83
-
-
Eagleson, K.L.1
Campbell, D.B.2
Thompson, B.L.3
Bergman, M.Y.4
Levitt, P.5
-
36
-
-
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. Behavior Genetics 2005, 35(1):19-29.
-
(2005)
Behavior Genetics
, vol.35
, Issue.1
, pp. 19-29
-
-
Ehret, G.1
-
38
-
-
65849256049
-
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
-
Enard W., Gehre S., Hammerschmidt K., Holter S.M., Blass T., Somel M., et al. A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell 2009, 137(5):961-971.
-
(2009)
Cell
, vol.137
, Issue.5
, pp. 961-971
-
-
Enard, W.1
Gehre, S.2
Hammerschmidt, K.3
Holter, S.M.4
Blass, T.5
Somel, M.6
-
39
-
-
0037158715
-
Molecular evolution of FOXP2, a gene involved in speech and language
-
Enard W., Przeworski M., Fisher S.E., Lai C.S., Wiebe V., Kitano T., et al. Molecular evolution of FOXP2, a gene involved in speech and language. Nature 2002, 418(6900):869-872.
-
(2002)
Nature
, vol.418
, Issue.6900
, pp. 869-872
-
-
Enard, W.1
Przeworski, M.2
Fisher, S.E.3
Lai, C.S.4
Wiebe, V.5
Kitano, T.6
-
40
-
-
77449127289
-
Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development
-
Feng X., Ippolito G.C., Tian L., Wiehagen K., Oh S., Sambandam A., et al. Foxp1 is an essential transcriptional regulator for the generation of quiescent naive T cells during thymocyte development. Blood 2010, 115(3):510-518.
-
(2010)
Blood
, vol.115
, Issue.3
, pp. 510-518
-
-
Feng, X.1
Ippolito, G.C.2
Tian, L.3
Wiehagen, K.4
Oh, S.5
Sambandam, A.6
-
41
-
-
0037467540
-
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain
-
Ferland R.J., Cherry T.J., Preware P.O., Morrisey E.E., Walsh C.A. Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. Journal of Comparative Neurology 2003, 460(2):266-279.
-
(2003)
Journal of Comparative Neurology
, vol.460
, Issue.2
, pp. 266-279
-
-
Ferland, R.J.1
Cherry, T.J.2
Preware, P.O.3
Morrisey, E.E.4
Walsh, C.A.5
-
42
-
-
33751113031
-
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
-
Feuk L., Kalervo A., Lipsanen-Nyman M., Skaug J., Nakabayashi K., Finucane B., et al. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. American Journal of Human Genetics 2006, 79(5):965-972.
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.5
, pp. 965-972
-
-
Feuk, L.1
Kalervo, A.2
Lipsanen-Nyman, M.3
Skaug, J.4
Nakabayashi, K.5
Finucane, B.6
-
43
-
-
84876754538
-
Broca's area and its striatal and thalamic connections: A diffusion-MRI tractography study
-
Ford A.A., Triplett W., Sudhyadhom A., Gullett J., McGregor K., Fitzgerald D.B., et al. Broca's area and its striatal and thalamic connections: A diffusion-MRI tractography study. Frontiers in Neuroanatomy 2013, 7:8.
-
(2013)
Frontiers in Neuroanatomy
, vol.7
, pp. 8
-
-
Ford, A.A.1
Triplett, W.2
Sudhyadhom, A.3
Gullett, J.4
McGregor, K.5
Fitzgerald, D.B.6
-
44
-
-
34547653713
-
Generation of mice with a conditional Foxp2 null allele
-
French C.A., Groszer M., Preece C., Coupe A.M., Rajewsky K., Fisher S.E. Generation of mice with a conditional Foxp2 null allele. Genesis 2007, 45(7):440-446.
-
(2007)
Genesis
, vol.45
, Issue.7
, pp. 440-446
-
-
French, C.A.1
Groszer, M.2
Preece, C.3
Coupe, A.M.4
Rajewsky, K.5
Fisher, S.E.6
-
45
-
-
84879264708
-
ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering
-
Gaj T., Gersbach C.A., Barbas C.F. ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering. Trends in Biotechnology 2013, 31(7):397-405.
-
(2013)
Trends in Biotechnology
, vol.31
, Issue.7
, pp. 397-405
-
-
Gaj, T.1
Gersbach, C.A.2
Barbas, C.F.3
-
46
-
-
77952992862
-
The structure of innate vocalizations in Foxp2-deficient mouse pups
-
Gaub S., Groszer M., Fisher S.E., Ehret G. The structure of innate vocalizations in Foxp2-deficient mouse pups. Genes, Brain and Behavior 2010, 9(4):390-401.
-
(2010)
Genes, Brain and Behavior
, vol.9
, Issue.4
, pp. 390-401
-
-
Gaub, S.1
Groszer, M.2
Fisher, S.E.3
Ehret, G.4
-
47
-
-
0037487188
-
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder
-
Gauthier J., Joober R., Mottron L., Laurent S., Fuchs M., De Kimpe V., et al. Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. American Journal of Medical Genetics Part A 2003, 118A(2):172-175.
-
(2003)
American Journal of Medical Genetics Part A
, vol.118 A
, Issue.2
, pp. 172-175
-
-
Gauthier, J.1
Joober, R.2
Mottron, L.3
Laurent, S.4
Fuchs, M.5
De Kimpe, V.6
-
48
-
-
67749106611
-
Knockout rats via embryo microinjection of zinc-finger nucleases
-
Geurts A.M., Cost G.J., Freyvert Y., Zeitler B., Miller J.C., Choi V.M., et al. Knockout rats via embryo microinjection of zinc-finger nucleases. Science 2009, 325(5939):433.
-
(2009)
Science
, vol.325
, Issue.5939
, pp. 433
-
-
Geurts, A.M.1
Cost, G.J.2
Freyvert, Y.3
Zeitler, B.4
Miller, J.C.5
Choi, V.M.6
-
49
-
-
84882282383
-
Evidence for a dysregulated immune system in the etiology of psychiatric disorders
-
Gibney S.M., Drexhage H.A. Evidence for a dysregulated immune system in the etiology of psychiatric disorders. Journal of NeuroImmune Pharmacology 2013, 8(4):900-920.
-
(2013)
Journal of NeuroImmune Pharmacology
, vol.8
, Issue.4
, pp. 900-920
-
-
Gibney, S.M.1
Drexhage, H.A.2
-
50
-
-
77957118061
-
The ESSENCE in child psychiatry: Early symptomatic syndromes eliciting neurodevelopmental clinical examinations
-
Gillberg C. The ESSENCE in child psychiatry: Early symptomatic syndromes eliciting neurodevelopmental clinical examinations. Research in Developmental Disabilities 2010, 31(6):1543-1551.
-
(2010)
Research in Developmental Disabilities
, vol.31
, Issue.6
, pp. 1543-1551
-
-
Gillberg, C.1
-
51
-
-
11144357511
-
Association between the FOXP2 gene and autistic disorder in Chinese population
-
Gong X., Jia M., Ruan Y., Shuang M., Liu J., Wu S., et al. Association between the FOXP2 gene and autistic disorder in Chinese population. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2004, 127B(1):113-116.
-
(2004)
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
, vol.127 B
, Issue.1
, pp. 113-116
-
-
Gong, X.1
Jia, M.2
Ruan, Y.3
Shuang, M.4
Liu, J.5
Wu, S.6
-
52
-
-
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(12):e321.
-
(2007)
PLoS Biology
, vol.5
, Issue.12
-
-
Haesler, S.1
Rochefort, C.2
Georgi, B.3
Licznerski, P.4
Osten, P.5
Scharff, C.6
-
53
-
-
0031667247
-
Genetic and developmental influences on infant mouse ultrasonic calling. II. Developmental patterns in the calls of mice 2-12 days of age
-
Hahn M.E., Karkowski L., Weinreb L., Henry A., Schanz N., Hahn E.M. Genetic and developmental influences on infant mouse ultrasonic calling. II. Developmental patterns in the calls of mice 2-12 days of age. Behavior Genetics 1998, 28(4):315-325.
-
(1998)
Behavior Genetics
, vol.28
, Issue.4
, pp. 315-325
-
-
Hahn, M.E.1
Karkowski, L.2
Weinreb, L.3
Henry, A.4
Schanz, N.5
Hahn, E.M.6
-
54
-
-
13644256065
-
A review of the methods of studies on infant ultrasound production and maternal retrieval in small rodents
-
Hahn M.E., Lavooy M.J. A review of the methods of studies on infant ultrasound production and maternal retrieval in small rodents. Behavior Genetics 2005, 35(1):31-52.
-
(2005)
Behavior Genetics
, vol.35
, Issue.1
, pp. 31-52
-
-
Hahn, M.E.1
Lavooy, M.J.2
-
55
-
-
78249268820
-
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
-
Hamdan F.F., Daoud H., Rochefort D., Piton A., Gauthier J., Langlois M., et al. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. American Journal of Human Genetics 2010, 87(5):671-678.
-
(2010)
American Journal of Human Genetics
, vol.87
, Issue.5
, pp. 671-678
-
-
Hamdan, F.F.1
Daoud, H.2
Rochefort, D.3
Piton, A.4
Gauthier, J.5
Langlois, M.6
-
56
-
-
70349284541
-
Female mice respond to male ultrasonic 'songs' with approach behaviour
-
Hammerschmidt K., Radyushkin K., Ehrenreich H., Fischer J. Female mice respond to male ultrasonic 'songs' with approach behaviour. Biology Letters 2009, 5(5):589-592.
-
(2009)
Biology Letters
, vol.5
, Issue.5
, pp. 589-592
-
-
Hammerschmidt, K.1
Radyushkin, K.2
Ehrenreich, H.3
Fischer, J.4
-
57
-
-
0037159541
-
The faculty of language: What is it, who has it, and how did it evolve?
-
Hauser M.D., Chomsky N., Fitch W.T. The faculty of language: What is it, who has it, and how did it evolve?. Science 2002, 298(5598):1569-1579.
-
(2002)
Science
, vol.298
, Issue.5598
, pp. 1569-1579
-
-
Hauser, M.D.1
Chomsky, N.2
Fitch, W.T.3
-
58
-
-
84866518216
-
An anatomically comprehensive atlas of the adult human brain transcriptome
-
Hawrylycz M.J., Lein E.S., Guillozet-Bongaarts A.L., Shen E.H., Ng L., Miller J.A., et al. An anatomically comprehensive atlas of the adult human brain transcriptome. Nature 2012, 489(7416):391-399.
-
(2012)
Nature
, vol.489
, Issue.7416
, pp. 391-399
-
-
Hawrylycz, M.J.1
Lein, E.S.2
Guillozet-Bongaarts, A.L.3
Shen, E.H.4
Ng, L.5
Miller, J.A.6
-
59
-
-
84863052622
-
Molecular microcircuitry underlies functional specification in a Basal Ganglia circuit dedicated to vocal learning
-
Hilliard A.T., Miller J.E., Fraley E.R., Horvath S., White S.A. Molecular microcircuitry underlies functional specification in a Basal Ganglia circuit dedicated to vocal learning. Neuron 2012, 73(3):537-552.
-
(2012)
Neuron
, vol.73
, Issue.3
, pp. 537-552
-
-
Hilliard, A.T.1
Miller, J.E.2
Fraley, E.R.3
Horvath, S.4
White, S.A.5
-
60
-
-
29144444606
-
Ultrasonic songs of male mice
-
Holy T.E., Guo Z. Ultrasonic songs of male mice. PLoS Biology 2005, 3(12):e386.
-
(2005)
PLoS Biology
, vol.3
, Issue.12
-
-
Holy, T.E.1
Guo, Z.2
-
61
-
-
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., Moog U., Lorenz-Depiereux B., Eck S., et al. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human Mutation 2010, 31(11):E1851-E1860.
-
(2010)
Human Mutation
, vol.31
, Issue.11
-
-
Horn, D.1
Kapeller, J.2
Rivera-Brugues, N.3
Moog, U.4
Lorenz-Depiereux, B.5
Eck, S.6
-
62
-
-
33746150775
-
Foxp1 is an essential transcriptional regulator of B cell development
-
Hu H., Wang B., Borde M., Nardone J., Maika S., Allred L., et al. Foxp1 is an essential transcriptional regulator of B cell development. Nature Immunology 2006, 7(8):819-826.
-
(2006)
Nature Immunology
, vol.7
, Issue.8
, pp. 819-826
-
-
Hu, H.1
Wang, B.2
Borde, M.3
Nardone, J.4
Maika, S.5
Allred, L.6
-
63
-
-
79953647406
-
Beyond knockout rats: New insights into finer genome manipulation in rats
-
Huang G., Tong C., Kumbhani D.S., Ashton C., Yan H., Ying Q.L. Beyond knockout rats: New insights into finer genome manipulation in rats. Cell Cycle 2011, 10(7):1059-1066.
-
(2011)
Cell Cycle
, vol.10
, Issue.7
, pp. 1059-1066
-
-
Huang, G.1
Tong, C.2
Kumbhani, D.S.3
Ashton, C.4
Yan, H.5
Ying, Q.L.6
-
64
-
-
62149099978
-
Gene associated with seizures, autism, and hepatomegaly in an Amish girl
-
Jackman C., Horn N.D., Molleston J.P., Sokol D.K. Gene associated with seizures, autism, and hepatomegaly in an Amish girl. Pediatric Neurology 2009, 40(4):310-313.
-
(2009)
Pediatric Neurology
, vol.40
, Issue.4
, pp. 310-313
-
-
Jackman, C.1
Horn, N.D.2
Molleston, J.P.3
Sokol, D.K.4
-
65
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Jamain S., Quach H., Betancur C., Rastam M., Colineaux C., Gillberg I.C., et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nature Genetics 2003, 34(1):27-29.
-
(2003)
Nature Genetics
, vol.34
, Issue.1
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Rastam, M.4
Colineaux, C.5
Gillberg, I.C.6
-
66
-
-
40349096250
-
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
-
Jamain S., Radyushkin K., Hammerschmidt K., Granon S., Boretius S., Varoqueaux F., et al. Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism. Proceedings of the National Academy of Sciences of the United States of America 2008, 105(5):1710-1715.
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.5
, pp. 1710-1715
-
-
Jamain, S.1
Radyushkin, K.2
Hammerschmidt, K.3
Granon, S.4
Boretius, S.5
Varoqueaux, F.6
-
67
-
-
0020008093
-
The thalamus and aphasia, including transcortical aphasia: A review
-
Jonas S. The thalamus and aphasia, including transcortical aphasia: A review. Journal of Communication Disorders 1982, 15(1):31-41.
-
(1982)
Journal of Communication Disorders
, vol.15
, Issue.1
, pp. 31-41
-
-
Jonas, S.1
-
68
-
-
62349125448
-
Broca's area: Nomenclature, anatomy, typology and asymmetry
-
Keller S.S., Crow T., Foundas A., Amunts K., Roberts N. Broca's area: Nomenclature, anatomy, typology and asymmetry. Brain and Language 2009, 109(1):29-48.
-
(2009)
Brain and Language
, vol.109
, Issue.1
, pp. 29-48
-
-
Keller, S.S.1
Crow, T.2
Foundas, A.3
Amunts, K.4
Roberts, N.5
-
69
-
-
79952315874
-
Is schizophrenia on the autism spectrum?
-
King B.H., Lord C. Is schizophrenia on the autism spectrum?. Brain Research 2011, 1380:34-41.
-
(2011)
Brain Research
, vol.1380
, pp. 34-41
-
-
King, B.H.1
Lord, C.2
-
70
-
-
70449653431
-
Human-specific transcriptional regulation of CNS development genes by FOXP2
-
Konopka G., Bomar J.M., Winden K., Coppola G., Jonsson Z.O., Gao F., et al. Human-specific transcriptional regulation of CNS development genes by FOXP2. Nature 2009, 462(7270):213-217.
-
(2009)
Nature
, vol.462
, Issue.7270
, pp. 213-217
-
-
Konopka, G.1
Bomar, J.M.2
Winden, K.3
Coppola, G.4
Jonsson, Z.O.5
Gao, F.6
-
71
-
-
84865374280
-
Human-specific transcriptional networks in the brain
-
Konopka G., Friedrich T., Davis-Turak J., Winden K., Oldham M.C., Gao F., et al. Human-specific transcriptional networks in the brain. Neuron 2012, 75(4):601-617.
-
(2012)
Neuron
, vol.75
, Issue.4
, pp. 601-617
-
-
Konopka, G.1
Friedrich, T.2
Davis-Turak, J.3
Winden, K.4
Oldham, M.C.5
Gao, F.6
-
72
-
-
84856218706
-
Modeling the functional genomics of autism using human neurons
-
Konopka G., Wexler E., Rosen E., Mukamel Z., Osborn G.E., Chen L., et al. Modeling the functional genomics of autism using human neurons. Molecular Psychiatry 2012, 17(2):202-214.
-
(2012)
Molecular Psychiatry
, vol.17
, Issue.2
, pp. 202-214
-
-
Konopka, G.1
Wexler, E.2
Rosen, E.3
Mukamel, Z.4
Osborn, G.E.5
Chen, L.6
-
73
-
-
84868125261
-
CNTNAP2 and language processing in healthy individuals as measured with ERPs
-
Kos M., van den Brink D., Snijders T.M., Rijpkema M., Franke B., Fernandez G., et al. CNTNAP2 and language processing in healthy individuals as measured with ERPs. PLoS One 2012, 7(10):e46995.
-
(2012)
PLoS One
, vol.7
, Issue.10
-
-
Kos, M.1
van den Brink, D.2
Snijders, T.M.3
Rijpkema, M.4
Franke, B.5
Fernandez, G.6
-
74
-
-
67649406057
-
Non-motor basal ganglia functions: A review and proposal for a model of sensory predictability in auditory language perception
-
Kotz S.A., Schwartze M., Schmidt-Kassow M. Non-motor basal ganglia functions: A review and proposal for a model of sensory predictability in auditory language perception. Cortex 2009, 45(8):982-990.
-
(2009)
Cortex
, vol.45
, Issue.8
, pp. 982-990
-
-
Kotz, S.A.1
Schwartze, M.2
Schmidt-Kassow, M.3
-
75
-
-
0035807360
-
A forkhead-domain gene is mutated in a severe speech and language disorder
-
Lai C.S., Fisher S.E., Hurst J.A., Vargha-Khadem F., Monaco A.P. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001, 413(6855):519-523.
-
(2001)
Nature
, vol.413
, Issue.6855
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
76
-
-
60549111634
-
WGCNA: An R package for weighted correlation network analysis
-
Langfelder P., Horvath S. WGCNA: An R package for weighted correlation network analysis. BMC Bioinformatics 2008, 9:559.
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 559
-
-
Langfelder, P.1
Horvath, S.2
-
77
-
-
57149124362
-
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders
-
Laroche F., Ramoz N., Leroy S., Fortin C., Rousselot-Paillet B., Philippe A., et al. Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders. Psychiatric Genetics 2008, 18(6):295-301.
-
(2008)
Psychiatric Genetics
, vol.18
, Issue.6
, pp. 295-301
-
-
Laroche, F.1
Ramoz, N.2
Leroy, S.3
Fortin, C.4
Rousselot-Paillet, B.5
Philippe, A.6
-
78
-
-
80053617549
-
Autism: A "critical period" disorder?
-
LeBlanc J.J., Fagiolini M. Autism: A "critical period" disorder?. Neural Plasticity 2011, 2011:921680.
-
(2011)
Neural Plasticity
, vol.2011
, pp. 921680
-
-
LeBlanc, J.J.1
Fagiolini, M.2
-
79
-
-
62349138572
-
Language pathway abnormalities in schizophrenia: A review of fMRI and other imaging studies
-
Li X., Branch C.A., DeLisi L.E. Language pathway abnormalities in schizophrenia: A review of fMRI and other imaging studies. Current Opinion in Psychiatry 2009, 22(2):131-139.
-
(2009)
Current Opinion in Psychiatry
, vol.22
, Issue.2
, pp. 131-139
-
-
Li, X.1
Branch, C.A.2
DeLisi, L.E.3
-
80
-
-
77953808897
-
Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
-
Li X., Hu Z., He Y., Xiong Z., Long Z., Peng Y., et al. Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population. Psychiatric Genetics 2010, 20(3):113-117.
-
(2010)
Psychiatric Genetics
, vol.20
, Issue.3
, pp. 113-117
-
-
Li, X.1
Hu, Z.2
He, Y.3
Xiong, Z.4
Long, Z.5
Peng, Y.6
-
81
-
-
79960034141
-
Modularly assembled designer TAL effector nucleases for targeted gene knockout and gene replacement in eukaryotes
-
Li T., Huang S., Zhao X., Wright D.A., Carpenter S., Spalding M.H., et al. Modularly assembled designer TAL effector nucleases for targeted gene knockout and gene replacement in eukaryotes. Nucleic Acids Research 2011, 39(14):6315-6325.
-
(2011)
Nucleic Acids Research
, vol.39
, Issue.14
, pp. 6315-6325
-
-
Li, T.1
Huang, S.2
Zhao, X.3
Wright, D.A.4
Carpenter, S.5
Spalding, M.H.6
-
82
-
-
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 E.E. 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(2):809-822.
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.2
, pp. 809-822
-
-
Li, S.1
Weidenfeld, J.2
Morrisey, E.E.3
-
83
-
-
14644415479
-
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
-
Li H., Yamagata T., Mori M., Momoi M.Y. Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients. Brain Dev 2005, 27(3):207-210.
-
(2005)
Brain Dev
, vol.27
, Issue.3
, pp. 207-210
-
-
Li, H.1
Yamagata, T.2
Mori, M.3
Momoi, M.Y.4
-
84
-
-
0039482686
-
On the nature and evolution of the neural bases of human language
-
Lieberman P. On the nature and evolution of the neural bases of human language. The American Journal of Physical Anthropology 2002, 35(Suppl.):36-62.
-
(2002)
The American Journal of Physical Anthropology
, vol.35
, Issue.SUPPL.
, pp. 36-62
-
-
Lieberman, P.1
-
85
-
-
84860503081
-
The WNT2 gene polymorphism associated with speech delay inherent to autism
-
Lin P.I., Chien Y.L., Wu Y.Y., Chen C.H., Gau S.S., Huang Y.S., et al. The WNT2 gene polymorphism associated with speech delay inherent to autism. Research in Developmental Disabilities 2012, 33(5):1533-1540.
-
(2012)
Research in Developmental Disabilities
, vol.33
, Issue.5
, pp. 1533-1540
-
-
Lin, P.I.1
Chien, Y.L.2
Wu, Y.Y.3
Chen, C.H.4
Gau, S.S.5
Huang, Y.S.6
-
86
-
-
84878675954
-
Stepwise acquisition of vocal combinatorial capacity in songbirds and human infants
-
Lipkind D., Marcus G.F., Bemis D.K., Sasahara K., Jacoby N., Takahasi M., et al. Stepwise acquisition of vocal combinatorial capacity in songbirds and human infants. Nature 2013, 498(7452):104-108.
-
(2013)
Nature
, vol.498
, Issue.7452
, pp. 104-108
-
-
Lipkind, D.1
Marcus, G.F.2
Bemis, D.K.3
Sasahara, K.4
Jacoby, N.5
Takahasi, M.6
-
87
-
-
84859541449
-
Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques
-
Liu X., Somel M., Tang L., Yan Z., Jiang X., Guo S., et al. Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques. Genome Research 2012, 22(4):611-622.
-
(2012)
Genome Research
, vol.22
, Issue.4
, pp. 611-622
-
-
Liu, X.1
Somel, M.2
Tang, L.3
Yan, Z.4
Jiang, X.5
Guo, S.6
-
88
-
-
84873734105
-
RNA-guided human genome engineering via Cas9
-
Mali P., Yang L., Esvelt K.M., Aach J., Guell M., DiCarlo J.E., et al. RNA-guided human genome engineering via Cas9. Science 2013, 339(6121):823-826.
-
(2013)
Science
, vol.339
, Issue.6121
, pp. 823-826
-
-
Mali, P.1
Yang, L.2
Esvelt, K.M.3
Aach, J.4
Guell, M.5
DiCarlo, J.E.6
-
89
-
-
84875614116
-
A recent evolutionary change affects a regulatory element in the human FOXP2 gene
-
Maricic T., Gunther V., Georgiev O., Gehre S., Curlin M., Schreiweis C., et al. A recent evolutionary change affects a regulatory element in the human FOXP2 gene. Molecular Biology and Evolution 2013, 30(4):844-852.
-
(2013)
Molecular Biology and Evolution
, vol.30
, Issue.4
, pp. 844-852
-
-
Maricic, T.1
Gunther, V.2
Georgiev, O.3
Gehre, S.4
Curlin, M.5
Schreiweis, C.6
-
90
-
-
33847242598
-
Foxp3 occupancy and regulation of key target genes during T-cell stimulation
-
Marson A., Kretschmer K., Frampton G.M., Jacobsen E.S., Polansky J.K., MacIsaac K.D., et al. Foxp3 occupancy and regulation of key target genes during T-cell stimulation. Nature 2007, 445(7130):931-935.
-
(2007)
Nature
, vol.445
, Issue.7130
, pp. 931-935
-
-
Marson, A.1
Kretschmer, K.2
Frampton, G.M.3
Jacobsen, E.S.4
Polansky, J.K.5
MacIsaac, K.D.6
-
91
-
-
23044492611
-
No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population
-
Marui T., Koishi S., Funatogawa I., Yamamoto K., Matsumoto H., Hashimoto O., et al. No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population. Neuroscience Research 2005, 53(1):91-94.
-
(2005)
Neuroscience Research
, vol.53
, Issue.1
, pp. 91-94
-
-
Marui, T.1
Koishi, S.2
Funatogawa, I.3
Yamamoto, K.4
Matsumoto, H.5
Hashimoto, O.6
-
92
-
-
77956628767
-
Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
-
Mefford H.C., Muhle H., Ostertag P., von Spiczak S., Buysse K., Baker C., et al. Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genetics 2010, 6(5):e1000962.
-
(2010)
PLoS Genetics
, vol.6
, Issue.5
-
-
Mefford, H.C.1
Muhle, H.2
Ostertag, P.3
von Spiczak, S.4
Buysse, K.5
Baker, C.6
-
93
-
-
84865837474
-
Immune system gene dysregulation in autism and schizophrenia
-
Michel M., Schmidt M.J., Mirnics K. Immune system gene dysregulation in autism and schizophrenia. Developmental Neurobiology 2012, 72(10):1277-1287.
-
(2012)
Developmental Neurobiology
, vol.72
, Issue.10
, pp. 1277-1287
-
-
Michel, M.1
Schmidt, M.J.2
Mirnics, K.3
-
94
-
-
33847682924
-
Targeted gene addition into a specified location in the human genome using designed zinc finger nucleases
-
Moehle E.A., Rock J.M., Lee Y.L., Jouvenot Y., DeKelver R.C., Gregory P.D., et al. Targeted gene addition into a specified location in the human genome using designed zinc finger nucleases. Proceedings of the National Academy of Sciences of the United States of America 2007, 104(9):3055-3060.
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.9
, pp. 3055-3060
-
-
Moehle, E.A.1
Rock, J.M.2
Lee, Y.L.3
Jouvenot, Y.4
DeKelver, R.C.5
Gregory, P.D.6
-
95
-
-
34547131606
-
Ultrasonic vocalizations emitted during dyadic interactions in female mice: A possible index of sociability?
-
Moles A., Costantini F., Garbugino L., Zanettini C., D'Amato F.R. Ultrasonic vocalizations emitted during dyadic interactions in female mice: A possible index of sociability?. Behavioural Brain Research 2007, 182(2):223-230.
-
(2007)
Behavioural Brain Research
, vol.182
, Issue.2
, pp. 223-230
-
-
Moles, A.1
Costantini, F.2
Garbugino, L.3
Zanettini, C.4
D'Amato, F.R.5
-
96
-
-
67349087393
-
Abnormalities of intrinsic functional connectivity in autism spectrum disorders
-
Monk C.S., Peltier S.J., Wiggins J.L., Weng S.J., Carrasco M., Risi S., et al. Abnormalities of intrinsic functional connectivity in autism spectrum disorders. NeuroImage 2009, 47(2):764-772.
-
(2009)
NeuroImage
, vol.47
, Issue.2
, pp. 764-772
-
-
Monk, C.S.1
Peltier, S.J.2
Wiggins, J.L.3
Weng, S.J.4
Carrasco, M.5
Risi, S.6
-
97
-
-
84864500142
-
Human-like brain hemispheric dominance in birdsong learning
-
Moorman S., Gobes S.M., Kuijpers M., Kerkhofs A., Zandbergen M.A., Bolhuis J.J. Human-like brain hemispheric dominance in birdsong learning. Proceedings of the National Academy of Sciences of the United States of America 2012, 109(31):12782-12787.
-
(2012)
Proceedings of the National Academy of Sciences of the United States of America
, vol.109
, Issue.31
, pp. 12782-12787
-
-
Moorman, S.1
Gobes, S.M.2
Kuijpers, M.3
Kerkhofs, A.4
Zandbergen, M.A.5
Bolhuis, J.J.6
-
98
-
-
0020572334
-
Language complexity and age of onset of schizophrenia
-
Morice R.D., Igram J.C. Language complexity and age of onset of schizophrenia. Psychiatry Research 1983, 9(3):233-242.
-
(1983)
Psychiatry Research
, vol.9
, Issue.3
, pp. 233-242
-
-
Morice, R.D.1
Igram, J.C.2
-
99
-
-
80051569371
-
Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk
-
Mukamel Z., Konopka G., Wexler E., Osborn G.E., Dong H., Bergman M.Y., et al. Regulation of MET by FOXP2, genes implicated in higher cognitive dysfunction and autism risk. Journal of Neuroscience 2011, 31(32):11437-11442.
-
(2011)
Journal of Neuroscience
, vol.31
, Issue.32
, pp. 11437-11442
-
-
Mukamel, Z.1
Konopka, G.2
Wexler, E.3
Osborn, G.E.4
Dong, H.5
Bergman, M.Y.6
-
100
-
-
84878829307
-
Impaired thalamocortical connectivity in autism spectrum disorder: A study of functional and anatomical connectivity
-
Nair A., Treiber J.M., Shukla D.K., Shih P., Muller R.A. Impaired thalamocortical connectivity in autism spectrum disorder: A study of functional and anatomical connectivity. Brain 2013, 136(Pt 6):1942-1955.
-
(2013)
Brain
, vol.136
, Issue.PART 6
, pp. 1942-1955
-
-
Nair, A.1
Treiber, J.M.2
Shukla, D.K.3
Shih, P.4
Muller, R.A.5
-
101
-
-
84880213877
-
Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets
-
Nelson C.S., Fuller C.K., Fordyce P.M., Greninger A.L., Li H., Derisi J.L. Microfluidic affinity and ChIP-seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets. Nucleic Acids Research 2013, 41(12):5991-6004.
-
(2013)
Nucleic Acids Research
, vol.41
, Issue.12
, pp. 5991-6004
-
-
Nelson, C.S.1
Fuller, C.K.2
Fordyce, P.M.3
Greninger, A.L.4
Li, H.5
Derisi, J.L.6
-
102
-
-
18344368187
-
FOXP2 is not a major susceptibility gene for autism or specific language impairment
-
Newbury D.F., Bonora E., Lamb J.A., Fisher S.E., Lai C.S., Baird G., et al. FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics 2002, 70(5):1318-1327.
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.5
, pp. 1318-1327
-
-
Newbury, D.F.1
Bonora, E.2
Lamb, J.A.3
Fisher, S.E.4
Lai, C.S.5
Baird, G.6
-
103
-
-
0025943787
-
Cortical organization of language
-
Ojemann G.A. Cortical organization of language. Journal of Neuroscience 1991, 11(8):2281-2287.
-
(1991)
Journal of Neuroscience
, vol.11
, Issue.8
, pp. 2281-2287
-
-
Ojemann, G.A.1
-
104
-
-
79957589237
-
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
-
O'Roak B.J., Deriziotis P., Lee C., Vives L., Schwartz J.J., Girirajan S., et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature Genetics 2011, 43(6):585-589.
-
(2011)
Nature Genetics
, vol.43
, Issue.6
, pp. 585-589
-
-
O'Roak, B.J.1
Deriziotis, P.2
Lee, C.3
Vives, L.4
Schwartz, J.J.5
Girirajan, S.6
-
105
-
-
84871448593
-
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders
-
O'Roak B.J., Vives L., Fu W., Egertson J.D., Stanaway I.B., Phelps I.G., et al. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science 2012, 338(6114):1619-1622.
-
(2012)
Science
, vol.338
, Issue.6114
, pp. 1619-1622
-
-
O'Roak, B.J.1
Vives, L.2
Fu, W.3
Egertson, J.D.4
Stanaway, I.B.5
Phelps, I.G.6
-
106
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
O'Roak B.J., Vives L., Girirajan S., Karakoc E., Krumm N., Coe B.P., et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012, 485(7397):246-250.
-
(2012)
Nature
, vol.485
, Issue.7397
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
Coe, B.P.6
-
107
-
-
77952158569
-
Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds
-
Panaitof S.C., Abrahams B.S., Dong H., Geschwind D.H., White S.A. Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds. Journal of Comparative Neurology 2010, 518(11):1995-2018.
-
(2010)
Journal of Comparative Neurology
, vol.518
, Issue.11
, pp. 1995-2018
-
-
Panaitof, S.C.1
Abrahams, B.S.2
Dong, H.3
Geschwind, D.H.4
White, S.A.5
-
108
-
-
67349164801
-
A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
-
Pariani M.J., Spencer A., Graham J.M., Rimoin D.L. 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(2-3):123-127.
-
(2009)
European Journal of Medical Genetics
, vol.52
, Issue.2-3
, pp. 123-127
-
-
Pariani, M.J.1
Spencer, A.2
Graham, J.M.3
Rimoin, D.L.4
-
109
-
-
80053540965
-
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
-
Penagarikano O., Abrahams B.S., Herman E.I., Winden K.D., Gdalyahu A., Dong H., et al. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell 2011, 147(1):235-246.
-
(2011)
Cell
, vol.147
, Issue.1
, pp. 235-246
-
-
Penagarikano, O.1
Abrahams, B.S.2
Herman, E.I.3
Winden, K.D.4
Gdalyahu, A.5
Dong, H.6
-
110
-
-
43749107081
-
Darwin's mistake: Explaining the discontinuity between human and nonhuman minds
-
discussion 130-178
-
Penn D.C., Holyoak K.J., Povinelli D.J. Darwin's mistake: Explaining the discontinuity between human and nonhuman minds. Behavioral and Brain Sciences 2008, 31(2):109-130. discussion 130-178.
-
(2008)
Behavioral and Brain Sciences
, vol.31
, Issue.2
, pp. 109-130
-
-
Penn, D.C.1
Holyoak, K.J.2
Povinelli, D.J.3
-
111
-
-
84879956588
-
Developmental vulnerability of synapses and circuits associated with neuropsychiatric disorders
-
Penzes P., Buonanno A., Passafaro M., Sala C., Sweet R.A. Developmental vulnerability of synapses and circuits associated with neuropsychiatric disorders. Journal of Neurochemistry 2013, 126(2):165-182.
-
(2013)
Journal of Neurochemistry
, vol.126
, Issue.2
, pp. 165-182
-
-
Penzes, P.1
Buonanno, A.2
Passafaro, M.3
Sala, C.4
Sweet, R.A.5
-
112
-
-
84869219473
-
Birds, primates, and spoken language origins: Behavioral phenotypes and neurobiological substrates
-
Petkov C.I., Jarvis E.D. Birds, primates, and spoken language origins: Behavioral phenotypes and neurobiological substrates. Frontiers in Evolutionary Neuroscience 2012, 4:12.
-
(2012)
Frontiers in Evolutionary Neuroscience
, vol.4
, pp. 12
-
-
Petkov, C.I.1
Jarvis, E.D.2
-
113
-
-
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(2):201-236.
-
(2005)
Cognition
, vol.95
, Issue.2
, pp. 201-236
-
-
Pinker, S.1
Jackendoff, R.2
-
114
-
-
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., 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(4):1037-1047.
-
(1999)
Neuron
, vol.24
, Issue.4
, pp. 1037-1047
-
-
Poliak, S.1
Gollan, L.2
Martinez, R.3
Custer, A.4
Einheber, S.5
Salzer, J.L.6
-
115
-
-
0141433266
-
Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1
-
Poliak S., Salomon D., Elhanany H., Sabanay H., Kiernan B., Pevny L., et al. Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1. Journal of Cell Biology 2003, 162(6):1149-1160.
-
(2003)
Journal of Cell Biology
, vol.162
, Issue.6
, pp. 1149-1160
-
-
Poliak, S.1
Salomon, D.2
Elhanany, H.3
Sabanay, H.4
Kiernan, B.5
Pevny, L.6
-
116
-
-
0020511314
-
Female behavior is affected by male ultrasonic vocalizations in house mice
-
Pomerantz S.M., Nunez A.A., Bean N.J. Female behavior is affected by male ultrasonic vocalizations in house mice. Physiology and Behavior 1983, 31(1):91-96.
-
(1983)
Physiology and Behavior
, vol.31
, Issue.1
, pp. 91-96
-
-
Pomerantz, S.M.1
Nunez, A.A.2
Bean, N.J.3
-
117
-
-
76549104658
-
Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder
-
Poot M., Beyer V., Schwaab I., Damatova N., Van't Slot R., Prothero J., et al. Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics 2010, 11(1):81-89.
-
(2010)
Neurogenetics
, vol.11
, Issue.1
, pp. 81-89
-
-
Poot, M.1
Beyer, V.2
Schwaab, I.3
Damatova, N.4
Van't Slot, R.5
Prothero, J.6
-
119
-
-
18444385647
-
The neurodevelopmental model of schizophrenia: Update 2005
-
Rapoport J.L., Addington A.M., Frangou S., Psych M.R. The neurodevelopmental model of schizophrenia: Update 2005. Molecular Psychiatry 2005, 10(5):434-449.
-
(2005)
Molecular Psychiatry
, vol.10
, Issue.5
, pp. 434-449
-
-
Rapoport, J.L.1
Addington, A.M.2
Frangou, S.3
Psych, M.R.4
-
120
-
-
33646691531
-
Autism and ultraconserved non-coding sequence on chromosome 7q
-
Richler E., Reichert J.G., Buxbaum J.D., McInnes L.A. Autism and ultraconserved non-coding sequence on chromosome 7q. Psychiatric Genetics 2006, 16(1):19-23.
-
(2006)
Psychiatric Genetics
, vol.16
, Issue.1
, pp. 19-23
-
-
Richler, E.1
Reichert, J.G.2
Buxbaum, J.D.3
McInnes, L.A.4
-
121
-
-
84876819814
-
Is autism a disease of the cerebellum? An integration of clinical and pre-clinical research
-
Rogers T.D., McKimm E., Dickson P.E., Goldowitz D., Blaha C.D., Mittleman G. Is autism a disease of the cerebellum? An integration of clinical and pre-clinical research. Frontiers in Systems Neuroscience 2013, 7:15.
-
(2013)
Frontiers in Systems Neuroscience
, vol.7
, pp. 15
-
-
Rogers, T.D.1
McKimm, E.2
Dickson, P.E.3
Goldowitz, D.4
Blaha, C.D.5
Mittleman, G.6
-
122
-
-
78649477258
-
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
-
Roll P., Vernes S.C., Bruneau N., Cillario J., Ponsole-Lenfant M., Massacrier A., et al. Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Human Molecular Genetics 2010, 19(24):4848-4860.
-
(2010)
Human Molecular Genetics
, vol.19
, Issue.24
, pp. 4848-4860
-
-
Roll, P.1
Vernes, S.C.2
Bruneau, N.3
Cillario, J.4
Ponsole-Lenfant, M.5
Massacrier, A.6
-
123
-
-
47749129203
-
Coordinated actions of the forkhead protein Foxp1 and Hox proteins in the columnar organization of spinal motor neurons
-
Rousso D.L., Gaber Z.B., Wellik D., Morrisey E.E., Novitch B.G. Coordinated actions of the forkhead protein Foxp1 and Hox proteins in the columnar organization of spinal motor neurons. Neuron 2008, 59(2):226-240.
-
(2008)
Neuron
, vol.59
, Issue.2
, pp. 226-240
-
-
Rousso, D.L.1
Gaber, Z.B.2
Wellik, D.3
Morrisey, E.E.4
Novitch, B.G.5
-
124
-
-
79958204980
-
Protein interactome reveals converging molecular pathways among autism disorders
-
Sakai Y., Shaw C.A., Dawson B.C., Dugas D.V., Al-Mohtaseb Z., Hill D.E., et al. Protein interactome reveals converging molecular pathways among autism disorders. Science Translational Medicine 2011, 3(86):86ra49.
-
(2011)
Science Translational Medicine
, vol.3
, Issue.86
-
-
Sakai, Y.1
Shaw, C.A.2
Dawson, B.C.3
Dugas, D.V.4
Al-Mohtaseb, Z.5
Hill, D.E.6
-
125
-
-
11844254379
-
FOXP2 polymorphisms in patients with schizophrenia
-
Sanjuan J., Tolosa A., Gonzalez J.C., Aguilar E.J., Molto M.D., Najera C., et al. FOXP2 polymorphisms in patients with schizophrenia. Schizophrenia Research 2005, 73(2-3):253-256.
-
(2005)
Schizophrenia Research
, vol.73
, Issue.2-3
, pp. 253-256
-
-
Sanjuan, J.1
Tolosa, A.2
Gonzalez, J.C.3
Aguilar, E.J.4
Molto, M.D.5
Najera, C.6
-
126
-
-
33749253516
-
Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations
-
Sanjuan J., Tolosa A., Gonzalez J.C., Aguilar E.J., Perez-Tur J., Najera C., et al. Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. Psychiatric Genetics 2006, 16(2):67-72.
-
(2006)
Psychiatric Genetics
, vol.16
, Issue.2
, pp. 67-72
-
-
Sanjuan, J.1
Tolosa, A.2
Gonzalez, J.C.3
Aguilar, E.J.4
Perez-Tur, J.5
Najera, C.6
-
127
-
-
84862274500
-
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2
-
Schmeisser M.J., Ey E., Wegener S., Bockmann J., Stempel A.V., Kuebler A., et al. Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2. Nature 2012, 486(7402):256-260.
-
(2012)
Nature
, vol.486
, Issue.7402
, pp. 256-260
-
-
Schmeisser, M.J.1
Ey, E.2
Wegener, S.3
Bockmann, J.4
Stempel, A.V.5
Kuebler, A.6
-
128
-
-
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., Sonnenblick L.I., Rudie J.D., Ghahremani D., et al. Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Science Translational Medicine 2010, 2(56):56ra80.
-
(2010)
Science Translational Medicine
, vol.2
, Issue.56
-
-
Scott-Van Zeeland, A.A.1
Abrahams, B.S.2
Alvarez-Retuerto, A.I.3
Sonnenblick, L.I.4
Rudie, J.D.5
Ghahremani, D.6
-
129
-
-
84875478700
-
Corticostriatal connectivity and its role in disease
-
Shepherd G.M. Corticostriatal connectivity and its role in disease. Nature Reviews Neuroscience 2013, 14(4):278-291.
-
(2013)
Nature Reviews Neuroscience
, vol.14
, Issue.4
, pp. 278-291
-
-
Shepherd, G.M.1
-
130
-
-
84877631590
-
Altered modular organization of structural cortical networks in children with autism
-
Shi F., Wang L., Peng Z., Wee C.Y., Shen D. Altered modular organization of structural cortical networks in children with autism. PLoS One 2013, 8(5):e63131.
-
(2013)
PLoS One
, vol.8
, Issue.5
-
-
Shi, F.1
Wang, L.2
Peng, Z.3
Wee, C.Y.4
Shen, D.5
-
131
-
-
22144496080
-
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
-
Shu W., Cho J.Y., Jiang Y., Zhang M., Weisz D., Elder G.A., et al. Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. Proceedings of the National Academy of Sciences of the United States of America 2005, 102(27):9643-9648.
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.27
, pp. 9643-9648
-
-
Shu, W.1
Cho, J.Y.2
Jiang, Y.3
Zhang, M.4
Weisz, D.5
Elder, G.A.6
-
132
-
-
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 M.M., Morrisey E.E. Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors. Journal of Biological Chemistry 2001, 276(29):27488-27497.
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.29
, pp. 27488-27497
-
-
Shu, W.1
Yang, H.2
Zhang, L.3
Lu, M.M.4
Morrisey, E.E.5
-
133
-
-
36749050396
-
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain
-
Spiteri E., Konopka G., Coppola G., Bomar J., Oldham M., Ou J., et al. Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. American Journal of Human Genetics 2007, 81(6):1144-1157.
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.6
, pp. 1144-1157
-
-
Spiteri, E.1
Konopka, G.2
Coppola, G.3
Bomar, J.4
Oldham, M.5
Ou, J.6
-
134
-
-
77955357758
-
Wernicke's area homologue in chimpanzees (Pan troglodytes) and its relation to the appearance of modern human language
-
Spocter M.A., Hopkins W.D., Garrison A.R., Bauernfeind A.L., Stimpson C.D., Hof P.R., et al. Wernicke's area homologue in chimpanzees (Pan troglodytes) and its relation to the appearance of modern human language. Proceedings of the Biological Sciences 2010, 277(1691):2165-2174.
-
(2010)
Proceedings of the Biological Sciences
, vol.277
, Issue.1691
, pp. 2165-2174
-
-
Spocter, M.A.1
Hopkins, W.D.2
Garrison, A.R.3
Bauernfeind, A.L.4
Stimpson, C.D.5
Hof, P.R.6
-
135
-
-
82255192290
-
The conundrums of understanding genetic risks for autism spectrum disorders
-
State M.W., Levitt P. The conundrums of understanding genetic risks for autism spectrum disorders. Nature Neuroscience 2011, 14(12):1499-1506.
-
(2011)
Nature Neuroscience
, vol.14
, Issue.12
, pp. 1499-1506
-
-
State, M.W.1
Levitt, P.2
-
136
-
-
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., et al. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. The New England Journal of Medicine 2006, 354(13):1370-1377.
-
(2006)
The New England Journal of Medicine
, vol.354
, Issue.13
, 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
-
137
-
-
80053610180
-
Autism spectrum disorders and schizophrenia: Meta-analysis of the neural correlates of social cognition
-
Sugranyes G., Kyriakopoulos M., Corrigall R., Taylor E., Frangou S. Autism spectrum disorders and schizophrenia: Meta-analysis of the neural correlates of social cognition. PLoS One 2011, 6(10):e25322.
-
(2011)
PLoS One
, vol.6
, Issue.10
-
-
Sugranyes, G.1
Kyriakopoulos, M.2
Corrigall, R.3
Taylor, E.4
Frangou, S.5
-
138
-
-
80155148101
-
Patterns of spinal sensory-motor connectivity prescribed by a dorsoventral positional template
-
Surmeli G., Akay T., Ippolito G.C., Tucker P.W., Jessell T.M. Patterns of spinal sensory-motor connectivity prescribed by a dorsoventral positional template. Cell 2011, 147(3):653-665.
-
(2011)
Cell
, vol.147
, Issue.3
, pp. 653-665
-
-
Surmeli, G.1
Akay, T.2
Ippolito, G.C.3
Tucker, P.W.4
Jessell, T.M.5
-
139
-
-
0038054082
-
Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum
-
Takahashi K., Liu F.C., Hirokawa K., Takahashi H. Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum. Journal of Neuroscience Research 2003, 73(1):61-72.
-
(2003)
Journal of Neuroscience Research
, vol.73
, Issue.1
, pp. 61-72
-
-
Takahashi, K.1
Liu, F.C.2
Hirokawa, K.3
Takahashi, H.4
-
140
-
-
57049112633
-
Expression of Foxp4 in the developing and adult rat forebrain
-
Takahashi K., Liu F.C., Hirokawa K., Takahashi H. Expression of Foxp4 in the developing and adult rat forebrain. Journal of Neuroscience Research 2008, 86(14):3106-3116.
-
(2008)
Journal of Neuroscience Research
, vol.86
, Issue.14
, pp. 3106-3116
-
-
Takahashi, K.1
Liu, F.C.2
Hirokawa, K.3
Takahashi, H.4
-
141
-
-
46949099804
-
Expression of FOXP2 in the developing monkey forebrain: Comparison with the expression of the genes FOXP1, PBX3, and MEIS2
-
Takahashi K., Liu F.C., Oishi T., Mori T., Higo N., Hayashi M., et al. Expression of FOXP2 in the developing monkey forebrain: Comparison with the expression of the genes FOXP1, PBX3, and MEIS2. Journal of Comparative Neurology 2008, 509(2):180-189.
-
(2008)
Journal of Comparative Neurology
, vol.509
, Issue.2
, pp. 180-189
-
-
Takahashi, K.1
Liu, F.C.2
Oishi, T.3
Mori, T.4
Higo, N.5
Hayashi, M.6
-
142
-
-
84864012904
-
Forkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: Implications for transcriptional dysregulation in Huntington disease
-
Tang B., Becanovic K., Desplats P.A., Spencer B., Hill A.M., Connolly C., et al. Forkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: Implications for transcriptional dysregulation in Huntington disease. Human Molecular Genetics 2012, 21(14):3097-3111.
-
(2012)
Human Molecular Genetics
, vol.21
, Issue.14
, pp. 3097-3111
-
-
Tang, B.1
Becanovic, K.2
Desplats, P.A.3
Spencer, B.4
Hill, A.M.5
Connolly, C.6
-
143
-
-
1842610982
-
Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction
-
Teramitsu I., Kudo L.C., London S.E., Geschwind D.H., White S.A. Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. Journal of Neuroscience 2004, 24(13):3152-3163.
-
(2004)
Journal of Neuroscience
, vol.24
, Issue.13
, pp. 3152-3163
-
-
Teramitsu, I.1
Kudo, L.C.2
London, S.E.3
Geschwind, D.H.4
White, S.A.5
-
144
-
-
77954803062
-
FOXP2 gene and language impairment in schizophrenia: Association and epigenetic studies
-
Tolosa A., Sanjuan J., Dagnall A.M., Molto M.D., Herrero N., de Frutos R. FOXP2 gene and language impairment in schizophrenia: Association and epigenetic studies. BMC Medical Genetics 2010, 11:114.
-
(2010)
BMC Medical Genetics
, vol.11
, pp. 114
-
-
Tolosa, A.1
Sanjuan, J.2
Dagnall, A.M.3
Molto, M.D.4
Herrero, N.5
de Frutos, R.6
-
145
-
-
84874946486
-
Analysis of two language-related genes in autism: A case-control association study of FOXP2 and CNTNAP2
-
Toma C., Hervas A., Torrico B., Balmana N., Salgado M., Maristany M., et al. Analysis of two language-related genes in autism: A case-control association study of FOXP2 and CNTNAP2. Psychiatric Genetics 2013, 23(2):82-85.
-
(2013)
Psychiatric Genetics
, vol.23
, Issue.2
, pp. 82-85
-
-
Toma, C.1
Hervas, A.2
Torrico, B.3
Balmana, N.4
Salgado, M.5
Maristany, M.6
-
146
-
-
84871770267
-
FoxP2 regulates neurogenesis during embryonic cortical development
-
Tsui D., Vessey J.P., Tomita H., Kaplan D.R., Miller F.D. FoxP2 regulates neurogenesis during embryonic cortical development. Journal of Neuroscience 2013, 33(1):244-258.
-
(2013)
Journal of Neuroscience
, vol.33
, Issue.1
, pp. 244-258
-
-
Tsui, D.1
Vessey, J.P.2
Tomita, H.3
Kaplan, D.R.4
Miller, F.D.5
-
147
-
-
68949180394
-
Schizophrenia
-
van Os J., Kapur S. Schizophrenia. Lancet 2009, 374(9690):635-645.
-
(2009)
Lancet
, vol.374
, Issue.9690
, pp. 635-645
-
-
van Os, J.1
Kapur, S.2
-
148
-
-
13244292715
-
FOXP2 and the neuroanatomy of speech and language
-
Vargha-Khadem F., Gadian D.G., Copp A., Mishkin M. FOXP2 and the neuroanatomy of speech and language. Nature Reviews Neuroscience 2005, 6(2):131-138.
-
(2005)
Nature Reviews Neuroscience
, vol.6
, Issue.2
, pp. 131-138
-
-
Vargha-Khadem, F.1
Gadian, D.G.2
Copp, A.3
Mishkin, M.4
-
149
-
-
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. Proceedings of the National Academy of Sciences of the United States of America 1995, 92(3):930-933.
-
(1995)
Proceedings of the National Academy of Sciences of the United States of America
, vol.92
, Issue.3
, pp. 930-933
-
-
Vargha-Khadem, F.1
Watkins, K.2
Alcock, K.3
Fletcher, P.4
Passingham, R.5
-
150
-
-
57149090343
-
A functional genetic link between distinct developmental language disorders
-
Vernes S.C., Newbury D.F., Abrahams B.S., Winchester L., Nicod J., Groszer M., et al. A functional genetic link between distinct developmental language disorders. The New England Journal of Medicine 2008, 359(22):2337-2345.
-
(2008)
The New England Journal of Medicine
, vol.359
, Issue.22
, pp. 2337-2345
-
-
Vernes, S.C.1
Newbury, D.F.2
Abrahams, B.S.3
Winchester, L.4
Nicod, J.5
Groszer, M.6
-
151
-
-
79960955811
-
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
-
Vernes S.C., Oliver P.L., Spiteri E., Lockstone H.E., Puliyadi R., Taylor J.M., et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genetics 2011, 7(7):e1002145.
-
(2011)
PLoS Genetics
, vol.7
, Issue.7
-
-
Vernes, S.C.1
Oliver, P.L.2
Spiteri, E.3
Lockstone, H.E.4
Puliyadi, R.5
Taylor, J.M.6
-
152
-
-
36749013035
-
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
-
Vernes S.C., Spiteri E., Nicod J., Groszer M., Taylor J.M., Davies K.E., et al. High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. American Journal of Human Genetics 2007, 81(6):1232-1250.
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.6
, pp. 1232-1250
-
-
Vernes, S.C.1
Spiteri, E.2
Nicod, J.3
Groszer, M.4
Taylor, J.M.5
Davies, K.E.6
-
153
-
-
16244408961
-
Reduced functional connectivity between V1 and inferior frontal cortex associated with visuomotor performance in autism
-
Villalobos M.E., Mizuno A., Dahl B.C., Kemmotsu N., Muller R.A. Reduced functional connectivity between V1 and inferior frontal cortex associated with visuomotor performance in autism. NeuroImage 2005, 25(3):916-925.
-
(2005)
NeuroImage
, vol.25
, Issue.3
, pp. 916-925
-
-
Villalobos, M.E.1
Mizuno, A.2
Dahl, B.C.3
Kemmotsu, N.4
Muller, R.A.5
-
154
-
-
79959262465
-
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
-
Voineagu I., Wang X., Johnston P., Lowe J.K., Tian Y., Horvath S., et al. Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature 2011, 474(7351):380-384.
-
(2011)
Nature
, vol.474
, Issue.7351
, pp. 380-384
-
-
Voineagu, I.1
Wang, X.2
Johnston, P.3
Lowe, J.K.4
Tian, Y.5
Horvath, S.6
-
155
-
-
84863507705
-
The DISC1 promoter: Characterization and regulation by FOXP2
-
Walker R.M., Hill A.E., Newman A.C., Hamilton G., Torrance H.S., Anderson S.M., et al. The DISC1 promoter: Characterization and regulation by FOXP2. Human Molecular Genetics 2012, 21(13):2862-2872.
-
(2012)
Human Molecular Genetics
, vol.21
, Issue.13
, pp. 2862-2872
-
-
Walker, R.M.1
Hill, A.E.2
Newman, A.C.3
Hamilton, G.4
Torrance, H.S.5
Anderson, S.M.6
-
156
-
-
77957916569
-
Allelic diversity in human developmental neurogenetics: Insights into biology and disease
-
Walsh C.A., Engle E.C. Allelic diversity in human developmental neurogenetics: Insights into biology and disease. Neuron 2010, 68(2):245-253.
-
(2010)
Neuron
, vol.68
, Issue.2
, pp. 245-253
-
-
Walsh, C.A.1
Engle, E.C.2
-
157
-
-
84877907898
-
Decoding human gene expression signatures in the brain
-
Wang G.Z., Konopka G. Decoding human gene expression signatures in the brain. Transcription 2013, 4(3):102-108.
-
(2013)
Transcription
, vol.4
, Issue.3
, pp. 102-108
-
-
Wang, G.Z.1
Konopka, G.2
-
158
-
-
6944232153
-
Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation
-
Wang B., Weidenfeld J., Lu M.M., Maika S., Kuziel W.A., Morrisey E.E., et al. Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation. Development 2004, 131(18):4477-4487.
-
(2004)
Development
, vol.131
, Issue.18
, pp. 4477-4487
-
-
Wang, B.1
Weidenfeld, J.2
Lu, M.M.3
Maika, S.4
Kuziel, W.A.5
Morrisey, E.E.6
-
159
-
-
0037043075
-
Evaluation of FOXP2 as an autism susceptibility gene
-
Wassink T.H., Piven J., Vieland V.J., Pietila J., Goedken R.J., Folstein S.E., et al. Evaluation of FOXP2 as an autism susceptibility gene. American Journal of Medical Genetics 2002, 114(5):566-569.
-
(2002)
American Journal of Medical Genetics
, vol.114
, Issue.5
, pp. 566-569
-
-
Wassink, T.H.1
Piven, J.2
Vieland, V.J.3
Pietila, J.4
Goedken, R.J.5
Folstein, S.E.6
-
160
-
-
0036190947
-
Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia
-
Watkins K.E., Dronkers N.F., Vargha-Khadem F. Behavioural analysis of an inherited speech and language disorder: Comparison with acquired aphasia. Brain 2002, 125(Pt. 3):452-464.
-
(2002)
Brain
, vol.125
, Issue.PART. 3
, pp. 452-464
-
-
Watkins, K.E.1
Dronkers, N.F.2
Vargha-Khadem, F.3
-
161
-
-
30344478870
-
A global map of p53 transcription-factor binding sites in the human genome
-
Wei C.L., Wu Q., Vega V.B., Chiu K.P., Ng P., Zhang T., et al. A global map of p53 transcription-factor binding sites in the human genome. Cell 2006, 124(1):207-219.
-
(2006)
Cell
, vol.124
, Issue.1
, pp. 207-219
-
-
Wei, C.L.1
Wu, Q.2
Vega, V.B.3
Chiu, K.P.4
Ng, P.5
Zhang, T.6
-
163
-
-
84862224852
-
AutismKB: An evidence-based knowledgebase of autism genetics
-
Database issue
-
Xu L.M., Li J.R., Huang Y., Zhao M., Tang X., Wei L. AutismKB: An evidence-based knowledgebase of autism genetics. Nucleic Acids Research 2011, 40(Database issue):D1016-D1022.
-
(2011)
Nucleic Acids Research
, vol.40
-
-
Xu, L.M.1
Li, J.R.2
Huang, Y.3
Zhao, M.4
Tang, X.5
Wei, L.6
-
164
-
-
80052563319
-
Neocortical excitation/inhibition balance in information processing and social dysfunction
-
Yizhar O., Fenno L.E., Prigge M., Schneider F., Davidson T.J., O'Shea D.J., et al. Neocortical excitation/inhibition balance in information processing and social dysfunction. Nature 2011, 477(7363):171-178.
-
(2011)
Nature
, vol.477
, Issue.7363
, pp. 171-178
-
-
Yizhar, O.1
Fenno, L.E.2
Prigge, M.3
Schneider, F.4
Davidson, T.J.5
O'Shea, D.J.6
-
166
-
-
0036959262
-
Accelerated protein evolution and origins of human-specific features: Foxp2 as an example
-
Zhang J., Webb D.M., Podlaha O. Accelerated protein evolution and origins of human-specific features: Foxp2 as an example. Genetics 2002, 162(4):1825-1835.
-
(2002)
Genetics
, vol.162
, Issue.4
, pp. 1825-1835
-
-
Zhang, J.1
Webb, D.M.2
Podlaha, O.3
-
167
-
-
72149095158
-
CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila
-
Zweier C., de Jong E.K., Zweier M., Orrico A., Ousager L.B., Collins A.L., et al. CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila. American Journal of Human Genetics 2009, 85(5):655-666.
-
(2009)
American Journal of Human Genetics
, vol.85
, Issue.5
, pp. 655-666
-
-
Zweier, C.1
de Jong, E.K.2
Zweier, M.3
Orrico, A.4
Ousager, L.B.5
Collins, A.L.6
|