-
2
-
-
33846969944
-
-
ADDMNS, Autism and Developmental Disabilities Monitoring Network Surveillance Year 2002 Principal Investigators; Centers for Disease Control and Prevention (2007). Prevalence of autism spectrum disorders autism and developmental disabilities monitoring network, 14 sites, United States, 2002. MMWR Surveill Summ 56:12-28.
-
ADDMNS, Autism and Developmental Disabilities Monitoring Network Surveillance Year 2002 Principal Investigators; Centers for Disease Control and Prevention (2007). Prevalence of autism spectrum disorders autism and developmental disabilities monitoring network, 14 sites, United States, 2002. MMWR Surveill Summ 56:12-28.
-
-
-
-
3
-
-
3042775209
-
Autism as a disorder of neural information processing: Directions for research and targets for therapy
-
Belmonte MK, Cook EH Jr, Anderson GM, Rubenstein JL, Greenough WT, Beckel-Mitchener A, et al. (2004). Autism as a disorder of neural information processing: directions for research and targets for therapy. Mol Psychiatry 9:646-663.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 646-663
-
-
Belmonte, M.K.1
Cook Jr, E.H.2
Anderson, G.M.3
Rubenstein, J.L.4
Greenough, W.T.5
Beckel-Mitchener, A.6
-
4
-
-
27244454668
-
Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus
-
Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, et al. (2005). Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. Am J Hum Genet 77: 851-868.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 851-868
-
-
Benayed, R.1
Gharani, N.2
Rossman, I.3
Mancuso, V.4
Lazar, G.5
Kamdar, S.6
-
5
-
-
0034993195
-
Otx genes in the development and evolution of the vertebrate brain
-
Boyl PP, Signore M, Annino A, Barbera JP, Acampora D, Simeone A (2001). Otx genes in the development and evolution of the vertebrate brain. Int J Dev Neurosci 19:353-363.
-
(2001)
Int J Dev Neurosci
, vol.19
, pp. 353-363
-
-
Boyl, P.P.1
Signore, M.2
Annino, A.3
Barbera, J.P.4
Acampora, D.5
Simeone, A.6
-
6
-
-
0347418199
-
Alanine tracts: The expanding story of human illness and trinucleotide repeats
-
Brown LY, Brown SA (2004). Alanine tracts: the expanding story of human illness and trinucleotide repeats. Trends Genet 20:51-58.
-
(2004)
Trends Genet
, vol.20
, pp. 51-58
-
-
Brown, L.Y.1
Brown, S.A.2
-
7
-
-
0030065606
-
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
-
Brunelli S, Faiella A, Capra V, Nigro V, Simeone A, Cama A, et al. (1996). Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nat Genet 12:94-96.
-
(1996)
Nat Genet
, vol.12
, pp. 94-96
-
-
Brunelli, S.1
Faiella, A.2
Capra, V.3
Nigro, V.4
Simeone, A.5
Cama, A.6
-
8
-
-
34047249386
-
Mutation screening of the ARX gene in patients with autism
-
Chaste P, Nygren G, Anckarsater H, Rastam M, Coleman M, Leboyer M, et al. (2007). Mutation screening of the ARX gene in patients with autism. Am J Med Genet 144:228-230.
-
(2007)
Am J Med Genet
, vol.144
, pp. 228-230
-
-
Chaste, P.1
Nygren, G.2
Anckarsater, H.3
Rastam, M.4
Coleman, M.5
Leboyer, M.6
-
9
-
-
10744221938
-
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism
-
Conciatori M, Stodgell CJ, Hyman SL, O'Bara M, Militerni R, Bravaccio C, et al. (2004). Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism. Biol Psychiatry 55:413-419.
-
(2004)
Biol Psychiatry
, vol.55
, pp. 413-419
-
-
Conciatori, M.1
Stodgell, C.J.2
Hyman, S.L.3
O'Bara, M.4
Militerni, R.5
Bravaccio, C.6
-
10
-
-
0037044008
-
-
Devlin B, Bennett P, Cook EH Jr, Dawson G, Gonen D, Grigorenko EL, et al.; Collaborative Programs of Excellence in Autism (CPEA) Genetics Network (2002). No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network. Am J Med Genet 114:667-672.
-
Devlin B, Bennett P, Cook EH Jr, Dawson G, Gonen D, Grigorenko EL, et al.; Collaborative Programs of Excellence in Autism (CPEA) Genetics Network (2002). No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network. Am J Med Genet 114:667-672.
-
-
-
-
11
-
-
11144331051
-
Accelerated evolution of nervous system genes in the origin of Homo sapiens
-
Dorus S, Vallender EJ, Evans PD, Anderson JR, Gilbert SL, Mahowald M, et al. (2004). Accelerated evolution of nervous system genes in the origin of Homo sapiens. Cell 119:1027-1040.
-
(2004)
Cell
, vol.119
, pp. 1027-1040
-
-
Dorus, S.1
Vallender, E.J.2
Evans, P.D.3
Anderson, J.R.4
Gilbert, S.L.5
Mahowald, M.6
-
12
-
-
33845797961
-
The genetics of autistic disorders and its clinical relevance: A review of the literature
-
Freitag CM (2007). The genetics of autistic disorders and its clinical relevance: a review of the literature. Mol Psychiatry 12:2-22.
-
(2007)
Mol Psychiatry
, vol.12
, pp. 2-22
-
-
Freitag, C.M.1
-
13
-
-
0347993123
-
No association between allelic variants of HOXA1/HOXB1 and autism
-
Gallagher L, Hawi Z, Kearney G, Fitzgerald M, Gill M (2004). No association between allelic variants of HOXA1/HOXB1 and autism. Am J Med Genet 124:64-67.
-
(2004)
Am J Med Genet
, vol.124
, pp. 64-67
-
-
Gallagher, L.1
Hawi, Z.2
Kearney, G.3
Fitzgerald, M.4
Gill, M.5
-
14
-
-
25844487226
-
Diseases of unstable repeat expansion: Mechanisms and common principles
-
Gatchel JR, Zoghbi HY (2005). Diseases of unstable repeat expansion: mechanisms and common principles. Nat Rev Genet 6:743-755.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 743-755
-
-
Gatchel, J.R.1
Zoghbi, H.Y.2
-
15
-
-
0037487188
-
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder
-
Gauthier J, Joober R, Mouron L, Laurent S, Fuchs M, De Kimpe V, et al. (2003). Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. Am J Med Genet 118:172-175.
-
(2003)
Am J Med Genet
, vol.118
, pp. 172-175
-
-
Gauthier, J.1
Joober, R.2
Mouron, L.3
Laurent, S.4
Fuchs, M.5
De Kimpe, V.6
-
16
-
-
3142523276
-
Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder
-
Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH (2004). Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder. Mol Psychiatry 9:474-484.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 474-484
-
-
Gharani, N.1
Benayed, R.2
Mancuso, V.3
Brzustowicz, L.M.4
Millonig, J.H.5
-
17
-
-
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. (2004). Association between the FOXP2 gene and autistic disorder in Chinese population. Am J Med Genet 127:113-116.
-
(2004)
Am J Med Genet
, vol.127
, pp. 113-116
-
-
Gong, X.1
Jia, M.2
Ruan, Y.3
Shuang, M.4
Liu, J.5
Wu, S.6
-
18
-
-
2342506529
-
Cerebellum development and schizophrenia: An association study of the human homeogene Engrailed 2
-
Gourion D, Leroy S, Bourdel MC, Goldberger C, Poirier MF, Olie JP, et al. (2004). Cerebellum development and schizophrenia: an association study of the human homeogene Engrailed 2. Psychiatry Res 126:93-98.
-
(2004)
Psychiatry Res
, vol.126
, pp. 93-98
-
-
Gourion, D.1
Leroy, S.2
Bourdel, M.C.3
Goldberger, C.4
Poirier, M.F.5
Olie, J.P.6
-
19
-
-
27844568628
-
Analysis of four DLX homeobox genes in autistic probands
-
Hamilton SP, Woo JM, Carlson EJ, Ghanem N, Ekker M, Rubenstein JL (2005). Analysis of four DLX homeobox genes in autistic probands. BMC Genet 6:52.
-
(2005)
BMC Genet
, vol.6
, pp. 52
-
-
Hamilton, S.P.1
Woo, J.M.2
Carlson, E.J.3
Ghanem, N.4
Ekker, M.5
Rubenstein, J.L.6
-
20
-
-
0033667613
-
Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders
-
Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR, Rodier PM (2000). Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders. Teratology 62:393-405.
-
(2000)
Teratology
, vol.62
, pp. 393-405
-
-
Ingram, J.L.1
Stodgell, C.J.2
Hyman, S.L.3
Figlewicz, D.A.4
Weitkamp, L.R.5
Rodier, P.M.6
-
21
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
International Molecular Genetic Study of Autism Consortium IMGSAC
-
International Molecular Genetic Study of Autism Consortium (IMGSAC) (2001). A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 69:570-581.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 570-581
-
-
-
22
-
-
0030069671
-
Engrailed, Wnt and Pax genes regulate midbrain-hindbrain development
-
Joyner AL (1996). Engrailed, Wnt and Pax genes regulate midbrain-hindbrain development. Trends Genet 12:15-20.
-
(1996)
Trends Genet
, vol.12
, pp. 15-20
-
-
Joyner, A.L.1
-
23
-
-
0029983147
-
Trinucleotide repeats and long homopeptides in genes and proteins associated with nervous system disease and development
-
Karlin S, Burge C (1996). Trinucleotide repeats and long homopeptides in genes and proteins associated with nervous system disease and development. Proc Natl Acad Sci U S A 93:1560-1555.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 1560-1555
-
-
Karlin, S.1
Burge, C.2
-
24
-
-
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 (2001). A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413:519-523.
-
(2001)
Nature
, vol.413
, pp. 519-523
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Vargha-Khadem, F.4
Monaco, A.P.5
-
25
-
-
14644415479
-
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
-
Li H, Yamagata T, Mori M, Momoi MY (2005). Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients. Brain Dev 27:207-210.
-
(2005)
Brain Dev
, vol.27
, pp. 207-210
-
-
Li, H.1
Yamagata, T.2
Mori, M.3
Momoi, M.Y.4
-
26
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord C, Rutter M, LeCouteur A (1994). Autism diagnostic interview-revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 24: 659-685.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
LeCouteur, A.3
-
27
-
-
21044445447
-
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
-
MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, et al. (2005). Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet 76:1074-1080.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1074-1080
-
-
MacDermot, K.D.1
Bonora, E.2
Sykes, N.3
Coupe, A.M.4
Lai, C.S.5
Vernes, S.C.6
-
29
-
-
34247327707
-
HOXA1 gene variants influence head growth rates in humans
-
Muscarella LA, Guarnieri V, Sacco R, Militemi R, Bravaccio C, Trillo S, et al. (2007). HOXA1 gene variants influence head growth rates in humans. Am J Med Genet 144:388-390.
-
(2007)
Am J Med Genet
, vol.144
, pp. 388-390
-
-
Muscarella, L.A.1
Guarnieri, V.2
Sacco, R.3
Militemi, R.4
Bravaccio, C.5
Trillo, S.6
-
30
-
-
18344368187
-
-
Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, et al.; International Molecular Genetic Study of Autism Consortium (2002). FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet 70:1318-1327.
-
Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, et al.; International Molecular Genetic Study of Autism Consortium (2002). FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet 70:1318-1327.
-
-
-
-
31
-
-
0028134880
-
Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics initiative
-
Numberger JI Jr, Blehar MC, Kaufmann CA, York-Cooler C, Simpson SG, Harkavy-Friedman J, et al. (1994). Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics initiative. Arch Gen Psychiatry 51:849-859.
-
(1994)
Arch Gen Psychiatry
, vol.51
, pp. 849-859
-
-
Numberger Jr, J.I.1
Blehar, M.C.2
Kaufmann, C.A.3
York-Cooler, C.4
Simpson, S.G.5
Harkavy-Friedman, J.6
-
32
-
-
33847272589
-
Enhanced autophagic cell death in expanded polyhistidine variants of HOXA1 reduces PBX1-coupled transcriptional activity and inhibits neuronal differentiation
-
Paraguison RC, Higaki K, Yamamoto K, Matsumoto H, Sasaki T, Kato N, et al. (2007). Enhanced autophagic cell death in expanded polyhistidine variants of HOXA1 reduces PBX1-coupled transcriptional activity and inhibits neuronal differentiation. J Neurosci Res 85:479-487.
-
(2007)
J Neurosci Res
, vol.85
, pp. 479-487
-
-
Paraguison, R.C.1
Higaki, K.2
Yamamoto, K.3
Matsumoto, H.4
Sasaki, T.5
Kato, N.6
-
33
-
-
0036796883
-
Developmental functions of the Distal-less/Dlx homeobox genes
-
Panganiban G, Rubenstein JL (2002). Developmental functions of the Distal-less/Dlx homeobox genes. Development 129:4371-4386.
-
(2002)
Development
, vol.129
, pp. 4371-4386
-
-
Panganiban, G.1
Rubenstein, J.L.2
-
34
-
-
0029169674
-
Association study with two markers of a human homeogene in infantile autism
-
Petit E, Herault J, Martineau J, Perrot A, Barthelemy C, Hameury L, et al. (1995). Association study with two markers of a human homeogene in infantile autism. J Med Genet 32:269-274.
-
(1995)
J Med Genet
, vol.32
, pp. 269-274
-
-
Petit, E.1
Herault, J.2
Martineau, J.3
Perrot, A.4
Barthelemy, C.5
Hameury, L.6
-
35
-
-
34547657628
-
Investigation of the behavioural phenotype of parents of autistic children through the new FAQ self-report
-
Piana H, Fortin C, Noulhiane M, Golse B, Robel L (2007). Investigation of the behavioural phenotype of parents of autistic children through the new FAQ self-report. L'Encéphale 33:285-292.
-
(2007)
L'Encéphale
, vol.33
, pp. 285-292
-
-
Piana, H.1
Fortin, C.2
Noulhiane, M.3
Golse, B.4
Robel, L.5
-
36
-
-
33748992010
-
The genetics of mental retardation
-
Raymond FL, Tarpey P (2006). The genetics of mental retardation. Hum Mol Genet 15:R110-R116.
-
(2006)
Hum Mol Genet
, vol.15
-
-
Raymond, F.L.1
Tarpey, P.2
-
37
-
-
57149144688
-
Molecular genetics of autism
-
Hollander E, editor, New York: Marcel Dekker Press; pp
-
Reichert JG, Kilifarski M, Bespalova I, Ramoz N, Buxbaum JD (2003.) Molecular genetics of autism. In: Hollander E, editor. Autism spectrum disorders. New York: Marcel Dekker Press; pp. 133-151.
-
(2003)
Autism spectrum disorders
, pp. 133-151
-
-
Reichert, J.G.1
Kilifarski, M.2
Bespalova, I.3
Ramoz, N.4
Buxbaum, J.D.5
-
38
-
-
33744458952
-
Molecular genetic studies of schizophrenia
-
Riley B, Kendler KS (2006). Molecular genetic studies of schizophrenia. Eur J Hum Genet 14:669-680.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 669-680
-
-
Riley, B.1
Kendler, K.S.2
-
39
-
-
33749253516
-
Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations
-
Sanjuán J, Tolosa A, Gonzalez JC, Aguilar EJ, Perez-Tur J, Najera C, et al. (2006). Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations. Psychiatr Genet 16:67-72.
-
(2006)
Psychiatr Genet
, vol.16
, pp. 67-72
-
-
Sanjuán, J.1
Tolosa, A.2
Gonzalez, J.C.3
Aguilar, E.J.4
Perez-Tur, J.5
Najera, C.6
-
40
-
-
0345107244
-
The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): One gene leads to many phenotypes
-
Sherr EH (2003). The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes. Curr Opin Pediatr 15:567-571.
-
(2003)
Curr Opin Pediatr
, vol.15
, pp. 567-571
-
-
Sherr, E.H.1
-
41
-
-
22144496080
-
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
-
Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA, et al. (2005). Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. Proc Natl Acad Sci U S A 102:9643-9648.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 9643-9648
-
-
Shu, W.1
Cho, J.Y.2
Jiang, Y.3
Zhang, M.4
Weisz, D.5
Elder, G.A.6
-
42
-
-
0031574072
-
The ClustaIX windows interface: Flexible strategies for multiple sequence alignment aided by quality analysis tools
-
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997). The ClustaIX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 25: 4876-4882.
-
(1997)
Nucleic Acids Res
, vol.25
, pp. 4876-4882
-
-
Thompson, J.D.1
Gibson, T.J.2
Plewniak, F.3
Jeanmougin, F.4
Higgins, D.G.5
-
43
-
-
27144541072
-
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
-
Tischfield MA, Bosley TM, Salih MA, Alorainy IA, Sener EC, Nester MJ, et al. (2005). Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nat Genet 37: 1035-1037.
-
(2005)
Nat Genet
, vol.37
, pp. 1035-1037
-
-
Tischfield, M.A.1
Bosley, T.M.2
Salih, M.A.3
Alorainy, I.A.4
Sener, E.C.5
Nester, M.J.6
-
44
-
-
0037043075
-
Evaluation of FOXP2 as an autism susceptibility gene
-
Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, et al. (2002). Evaluation of FOXP2 as an autism susceptibility gene. Am J Med Genet 114:566-569.
-
(2002)
Am J Med Genet
, vol.114
, 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
|