-
1
-
-
0036138102
-
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
-
Alarcon M, Cantor RM, Liu J, Gilliam TC, Geschwind DH 2002.Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am J Hum Genet, 70: 60-71.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 60-71
-
-
Alarcon, M.1
Cantor, R.M.2
Liu, J.3
Gilliam, T.C.4
Geschwind, D.H.5
-
2
-
-
23744471663
-
Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs
-
Alarcon M, Yonan AL, Gilliam TC, Cantor RM, Geschwind DH 2005. Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs. Mol Psychiatry, 10: 747-757.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 747-757
-
-
Alarcon, M.1
Yonan, A.L.2
Gilliam, T.C.3
Cantor, R.M.4
Geschwind, D.H.5
-
3
-
-
0004235298
-
-
American Psychiatric Association (APA), Washington, DC: American Psychiatric Association
-
American Psychiatric Association (APA) 1994. Diagnostic and Statistical Manual of Mental Disorders. Washington, DC: American Psychiatric Association.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
4
-
-
0032729834
-
Genetic studies of autistic disorder and chromosome 7
-
Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S et al. 1999. Genetic studies of autistic disorder and chromosome 7. Genomics, 61: 227-236.
-
(1999)
Genomics
, vol.61
, pp. 227-236
-
-
Ashley-Koch, A.1
Wolpert, C.M.2
Menold, M.M.3
Zaeem, L.4
Basu, S.5
-
5
-
-
33645728981
-
An analysis paradigm for investigating multi-locus effects in complex disease: Examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder
-
Ashley-Koch AE, Me H, Gasworks J, Ma DQ, Ritchie MD et al. 2006. An analysis paradigm for investigating multi-locus effects in complex disease: Examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder. Ann Hum Genet, 70: 281-292.
-
(2006)
Ann Hum Genet
, vol.70
, pp. 281-292
-
-
Ashley-Koch, A.E.1
Me, H.2
Gasworks, J.3
Ma, D.Q.4
Ritchie, M.D.5
-
6
-
-
34250557053
-
Die autistischen psychopathen im kindesalter
-
Asperger H 1944. Die autistischen psychopathen im kindesalter. Arch Psychiatr Nervenkr, 117: 76-136.
-
(1944)
Arch Psychiatr Nervenkr
, vol.117
, pp. 76-136
-
-
Asperger, H.1
-
7
-
-
0036780698
-
A genome-wide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E et al. 2002. A genome-wide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27. Am J Hum Genet, 71: 777-790.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
Ayers, K.4
Kempas, E.5
-
8
-
-
0036150925
-
Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7
-
Badner JA, Gershon ES 2002. Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7. Mol Psychiatry, 7: 56-66.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 56-66
-
-
Badner, J.A.1
Gershon, E.S.2
-
9
-
-
0031824657
-
Autism and tuberous sclerosis complex:Prevalence and clinical features
-
Baker P, Piven J, Sato Y 1998. Autism and tuberous sclerosis complex:prevalence and clinical features. J Autism Dev Disord, 28:279-285.
-
(1998)
J Autism Dev Disord
, vol.28
, pp. 279-285
-
-
Baker, P.1
Piven, J.2
Sato, Y.3
-
10
-
-
0037395936
-
Autism and phenylketonuria
-
Baieli S, Pavone L, Meli C, Fiumara A, Coleman M 2003. Autism and phenylketonuria. J Autism Dev Disord, 33: 201-204.
-
(2003)
J Autism Dev Disord
, vol.33
, pp. 201-204
-
-
Baieli, S.1
Pavone, L.2
Meli, C.3
Fiumara, A.4
Coleman, M.5
-
11
-
-
0029872978
-
Autism: Towards and integration of clinical, genetic, neuropsychological, and neurobiological perspectives
-
Bailey A, Phillips W, Rutter M 1996. Autism: Towards and integration of clinical, genetic, neuropsychological, and neurobiological perspectives. J Child Psychol Psychiatr, 37(1): 89-126.
-
(1996)
J Child Psychol Psychiatr
, vol.37
, Issue.1
, pp. 89-126
-
-
Bailey, A.1
Phillips, W.2
Rutter, M.3
-
12
-
-
0032453821
-
Autism: The phenotype in relatives
-
Bailey A, Palferman S, Heavey L, Le Couteur A 1998. Autism: the phenotype in relatives. J Autism Dev Disord, 28: 369-392
-
(1998)
J Autism Dev Disord
, vol.28
, pp. 369-392
-
-
Bailey, A.1
Palferman, S.2
Heavey, L.3
le Couteur, A.4
-
13
-
-
0033573212
-
An autosomal genomic screen for autism. Collaborative linkage study of autism
-
Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL et al. 1999. An autosomal genomic screen for autism. Collaborative linkage study of autism. Am Med Genet, 88: 609-615.
-
(1999)
Am Med Genet
, vol.88
, pp. 609-615
-
-
Barrett, S.1
Beck, J.C.2
Bernier, R.3
Bisson, E.4
Braun, T.A.5
Casavant, T.L.6
-
14
-
-
14644395605
-
Neuroanatomic observations of the brain in autism: A review and future directions
-
Bauman ML, Kemper TL 2005. Neuroanatomic observations of the brain in autism: a review and future directions. Int J Dev Neurosci, 23: 183-187.
-
(2005)
Int J Dev Neurosci
, vol.23
, pp. 183-187
-
-
Bauman, M.L.1
Kemper, T.L.2
-
15
-
-
85047695651
-
Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder
-
Betancur C, Corbex M, Spielewoy C, Phillipe A, Laplanche J-L et al. 2002. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder. Mol Psychiatry, 7: 67-71.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 67-71
-
-
Betancur, C.1
Corbex, M.2
Spielewoy, C.3
Phillipe, A.4
Laplanche, J.-L.5
-
16
-
-
0035844999
-
Construction of a physical map of an autism susceptibility region in 7q32.3-q33
-
Beyer KS, Klauck SM, Wiemann S, Poustka A 2001. Construction of a physical map of an autism susceptibility region in 7q32.3-q33. Gene, 272: 85-91.
-
(2001)
Gene
, vol.272
, pp. 85-91
-
-
Beyer, K.S.1
Klauck, S.M.2
Wiemann, S.3
Poustka, A.4
-
17
-
-
4944257708
-
Genetics of specific language impairments
-
Bonneau D, Verny C, Uzé J 2004.Genetics of specific language impairments. Arch Pediatr, 11(10): 1213-1236.
-
(2004)
Arch Pediatr
, vol.11
, Issue.10
, pp. 1213-1236
-
-
Bonneau, D.1
Verny, C.2
Uzé, J.3
-
18
-
-
85047698938
-
Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region
-
Bonora E, Bacchelli E, Levy ER, Blasi F, Marlow A et al. 2002. Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. Mol Psychiatry, 7: 289-301.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 289-301
-
-
Bonora, E.1
Bacchelli, E.2
Levy, E.R.3
Blasi, F.4
Marlow, A.5
-
19
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J et al. 2001. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet, 68: 1514-1520.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
-
20
-
-
85047700330
-
Association between a GABRB3 polymorphism and autism
-
Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M et al. 2002. Association between a GABRB3 polymorphism and autism. Mol Psychiatry, 7: 311-316.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 311-316
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Greenberg, D.A.4
Kilifarski, M.5
-
21
-
-
1542284674
-
Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19
-
Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E et al. 2004. Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19. Mol Psychiatry, 9: 144-150.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 144-150
-
-
Buxbaum, J.D.1
Silverman, J.2
Keddache, M.3
Smith, C.J.4
Hollander, E.5
-
22
-
-
33750962208
-
A genetic variant that disrupts MET transcription is associated with autism
-
Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Brvaccio C et al 2006. A genetic variant that disrupts MET transcription is associated with autism. Proc Natl Acad Sci USA, 103:16834-168339.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 16834-168339
-
-
Campbell, D.B.1
Sutcliffe, J.S.2
Ebert, P.J.3
Militerni, R.4
Brvaccio, C.5
-
23
-
-
18944365556
-
Replication of autism linkage: Fine-mapping peak at 17q21
-
Cantor R.M, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL et al. 2005. Replication of autism linkage: fine-mapping peak at 17q21. Am J Hum Genet, 76: 1050-1056.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1050-1056
-
-
Cantor, R.M.1
Kono, N.2
Duvall, J.A.3
Alvarez-Retuerto, A.4
Stone, J.L.5
-
24
-
-
0024320628
-
A Chinese classic phenylketonuria manifested as autism
-
Chen CH, Hsiao KJ 1989. A Chinese classic phenylketonuria manifested as autism. Br J Psychiatry, 155: 251-253
-
(1989)
Br J Psychiatry
, vol.155
, pp. 251-253
-
-
Chen, C.H.1
Hsiao, K.J.2
-
25
-
-
3543136466
-
Disorderassociated mutations lead to functional inactivation of neuroligins
-
Chih B, Afridi SK, Clark L, Scheiffele P 2004. Disorderassociated mutations lead to functional inactivation of neuroligins. Hum Mol Genet, 13: 1471-1477.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1471-1477
-
-
Chih, B.1
Afridi, S.K.2
Clark, L.3
Scheiffele, P.4
-
26
-
-
44349186162
-
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
-
Christian SL, Brune CW, Sudi J, Kumar RA, Liu S et al. 2008. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry, 63: 1111-1117.
-
(2008)
Biol Psychiatry
, vol.63
, pp. 1111-1117
-
-
Christian, S.L.1
Brune, C.W.2
Sudi, J.3
Kumar, R.A.4
Liu, S.5
-
27
-
-
34250849699
-
MECP.2 coding sequence and 39UTR variation in 172 unrelated autistic patients
-
Coutinho AM, Oliveira G, Katz C, et al 2007 MECP.2 coding sequence and 39UTR variation in 172 unrelated autistic patients. Am J Med Genet B Neuropsychiatr Genet, 144B: 475-83.
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144 B
, pp. 475-483
-
-
Coutinho, A.M.1
Oliveira, G.2
Katz, C.3
-
28
-
-
33846867244
-
Neurexin-neuroligin signaling in synapse development
-
Craig AM, Kang Y 2007. Neurexin-neuroligin signaling in synapse development. Curr Opin Neurobiol, 17: 43-52.
-
(2007)
Curr Opin Neurobiol
, vol.17
, pp. 43-52
-
-
Craig, A.M.1
Kang, Y.2
-
29
-
-
23044490896
-
An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder
-
Curran S, Roberts S, Thomas S, Veltman M, Browne J et al. 2005. An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet, 137: 25-28.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.137
, pp. 25-28
-
-
Curran, S.1
Roberts, S.2
Thomas, S.3
Veltman, M.4
Browne, J.5
-
30
-
-
33744805839
-
Pervasive developmental disorders in Prader-Willi syndrome: The Leuven experience in 59 subjects and controls
-
Descheemaeker MJ, Govers V, Vermeulen P, Fryns JP 2006. Pervasive developmental disorders in Prader-Willi syndrome: The Leuven experience in 59 subjects and controls. Am J Med Genet A, 140:1136-1142.
-
(2006)
Am J Med Genet A
, vol.140
, pp. 1136-1142
-
-
Descheemaeker, M.J.1
Govers, V.2
Vermeulen, P.3
Fryns, J.P.4
-
31
-
-
34247507349
-
A quantitative trait locus analysis of social responsiveness in multiplex autism families
-
Duvall JA, Lu A, Cantor RM, Todd RD, Constantino JN, Geschwind DH 2007. A quantitative trait locus analysis of social responsiveness in multiplex autism families. Am J Psychiatry, 164: 656-662.
-
(2007)
Am J Psychiatry
, vol.164
, pp. 656-662
-
-
Duvall, J.A.1
Lu, A.2
Cantor, R.M.3
Todd, R.D.4
Constantino, J.N.5
Geschwind, D.H.6
-
32
-
-
0345192350
-
DLX-1, DLX-2 and DLX-5 expression define distinct stages of basal forebrain differentiation
-
Eisenstat DD, Liu JK, Mione M, Zhong W, Yu G et al. 1999. DLX-1, DLX-2 and DLX-5 expression define distinct stages of basal forebrain differentiation. J Comp Neurol, 414: 217-237.
-
(1999)
J Comp Neurol
, vol.414
, pp. 217-237
-
-
Eisenstat, D.D.1
Liu, J.K.2
Mione, M.3
Zhong, W.4
Yu, G.5
-
33
-
-
33750079257
-
High frequency of neurexin 1 beta signal peptide structural variants in patients with autism
-
Feng J, Schoer R, Yan J 2006. High frequency of neurexin 1 beta signal peptide structural variants in patients with autism. Neurosci Lett, 409: 10-13.
-
(2006)
Neurosci Lett
, vol.409
, pp. 10-13
-
-
Feng, J.1
Schoer, R.2
Yan, J.3
-
34
-
-
0038571125
-
Deciphering the genetic basis of speech and language disorders
-
Fisher SE, Lai CS, Monaco AP 2003. Deciphering the genetic basis of speech and language disorders. Annu Rev Neurosci, 26: 57-80.
-
(2003)
Annu Rev Neurosci
, vol.26
, pp. 57-80
-
-
Fisher, S.E.1
Lai, C.S.2
Monaco, A.P.3
-
35
-
-
0017530988
-
Infantile autism: A genetic study of 21 twin pairs
-
Folstein S, Rutter M 1977. Infantile autism: A genetic study of 21 twin pairs. J Child Psychol Psychiatry, 18: 297-321.
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
36
-
-
0036348597
-
Epidemiological trends in rates of autism
-
Fombonne E 2002. Epidemiological trends in rates of autism. Mol Psychiatry, 7: S4-S6.
-
(2002)
Mol Psychiatry
, vol.7
-
-
Fombonne, E.1
-
37
-
-
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(5): 474-84.
-
(2004)
Mol Psychiatry
, vol.9
, Issue.5
, pp. 474-484
-
-
Gharani, N.1
Benayed, R.2
Mancuso, V.3
Brzustowicz, L.M.4
Millonig, J.H.5
-
40
-
-
0035317648
-
Suppressed GABAergic inhibition as a common factor in suspected etiologies of autism
-
Hussman JP 2001. Suppressed GABAergic inhibition as a common factor in suspected etiologies of autism. J Autism Dev Disord, 31: 247-248.
-
(2001)
J Autism Dev Disord
, vol.31
, pp. 247-248
-
-
Hussman, J.P.1
-
41
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium (IMGSAC)
-
International Molecular Genetic Study of Autism Consortium (IMGSAC) 1998. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet, 7: 571-578.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
42
-
-
0034883367
-
A genome-wide 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) 2001a. A genome-wide 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
-
-
-
43
-
-
0035871209
-
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium (IMGSAC)
-
International Molecular Genetic Study of Autism Consortium (IMGSAC) 2001b. Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Hum Mol Genet, 10: 973-982.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 973-982
-
-
-
44
-
-
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 et al. 2003. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet, 34: 27-29.
-
(2003)
Nat Genet
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Rastam, M.4
Colineaux, C.5
-
45
-
-
0000984981
-
Autistic disturbances of affective contact
-
Kanner, L 1943. Autistic disturbances of affective contact. Nervous Child, 2: 217-250.
-
(1943)
Nervous Child
, vol.2
, pp. 217-250
-
-
Kanner, L.1
-
47
-
-
38749084216
-
Disruption of neurexin 1 associated with autism spectrum disorder
-
Kim HG, Kishikawa S, Higgins AW 2008. Disruption of neurexin 1 associated with autism spectrum disorder. Am J Hum Genet, 82: 199-207.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 199-207
-
-
Kim, H.G.1
Kishikawa, S.2
Higgins, A.W.3
-
48
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism
-
Klauck SM, Poustka F, Benner A, Lesch KP, Poustka A 1997. Serotonin transporter (5-HTT) gene variants associated with autism? Hum Mol Genet, 6: 2233-2238.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.P.4
Poustka, A.5
-
49
-
-
0021208967
-
Infantile autism and Duchenne muscular dystrophy
-
Komoto J, Usui S, Otsuki S, Terao A 1984. Infantile autism and Duchenne muscular dystrophy. J Autism Dev Disord, 14: 191-195.
-
(1984)
J Autism Dev Disord
, vol.14
, pp. 191-195
-
-
Komoto, J.1
Usui, S.2
Otsuki, S.3
Terao, A.4
-
50
-
-
13444269226
-
Analysis of IMGSAC autism susceptibility loci: Evidence for sex limited and parent of origin specific effects
-
Lamb JA, Barnby G, Bonora E, Sykes N, Bacchelli E et al. 2005. Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. J Med Genet, 42: 132-137.
-
(2005)
J Med Genet
, vol.42
, pp. 132-137
-
-
Lamb, J.A.1
Barnby, G.2
Bonora, E.3
Sykes, N.4
Bacchelli, E.5
-
51
-
-
12144291350
-
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
-
Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A et al. 2004. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. Am J Hum Genet, 74: 552-557.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 552-557
-
-
Laumonnier, F.1
Bonnet-Brilhault, F.2
Gomot, M.3
Blanc, R.4
David, A.5
-
52
-
-
42649125261
-
Familial deletion within NLGN4 associated with autism and Tourette syndrome
-
Lawson-Yuen A, Saldivar JS, Sommer S, Picker J 2008. Familial deletion within NLGN4 associated with autism and Tourette syndrome. Eur J Hum Genet, 16: 614-618.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 614-618
-
-
Lawson-Yuen, A.1
Saldivar, J.S.2
Sommer, S.3
Picker, J.4
-
53
-
-
1842591879
-
Lack of evidence for an association between WNT2 and RELN polymorphisms and autism
-
Li J, Nguyen L, Gleason C, Lotspeich L, Spiker D et al. 2004. Lack of evidence for an association between WNT2 and RELN polymorphisms and autism. Am J Med Genet, 126: 51-57.
-
(2004)
Am J Med Genet
, vol.126
, pp. 51-57
-
-
Li, J.1
Nguyen, L.2
Gleason, C.3
Lotspeich, L.4
Spiker, D.5
-
54
-
-
20444379578
-
Arcuate nucleus transcriptome profiling identifies ankyrin repeat and suppressor of cytokine signalling box-containing protein 4 as a gene regulated by fasting in central nervous system feeding circuits
-
Li JY, Kuick R, Thompson RC, Misek DE, Lai YM et al. 2005. Arcuate nucleus transcriptome profiling identifies ankyrin repeat and suppressor of cytokine signalling box-containing protein 4 as a gene regulated by fasting in central nervous system feeding circuits. J Neuroendocrinol, 17: 394-404.
-
(2005)
J Neuroendocrinol
, vol.17
, pp. 394-404
-
-
Li, J.Y.1
Kuick, R.2
Thompson, R.C.3
Misek, D.E.4
Lai, Y.M.5
-
55
-
-
0034920299
-
A genome-wide screen for autism susceptibility loci
-
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P et al. 2001. A genome-wide screen for autism susceptibility loci. Am J Hum Genet, 69: 327-340.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
Parano, E.4
Pavone, P.5
-
56
-
-
23944444250
-
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism
-
Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE et al. 2005. Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism. Am J Hum Genet, 77: 377-388.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 377-388
-
-
Ma, D.Q.1
Whitehead, P.L.2
Menold, M.M.3
Martin, E.R.4
Ashley-koch, A.E.5
-
57
-
-
21044445447
-
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
-
MacDermot KD, Bonora E, Sykes N et al. 2005. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet, 76(6): 1074-1080.
-
(2005)
Am J Hum Genet
, vol.76
, Issue.6
, pp. 1074-1080
-
-
Macdermot, K.D.1
Bonora, E.2
Sykes, N.3
-
58
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall CR, Noor A, Vincent JB et al 2008. Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet, 82: 477-488.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
-
59
-
-
0034615152
-
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
-
Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL et al. 2000. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. Am J Med Genet, 96: 43-48.
-
(2000)
Am J Med Genet
, vol.96
, pp. 43-48
-
-
Martin, E.R.1
Menold, M.M.2
Wolpert, C.M.3
Bass, M.P.4
Donnelly, S.L.5
-
60
-
-
7644221741
-
A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism
-
McCauley JL, Olson LM, Delahanty R, Delahanty R, Amin T et al. 2004. A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism. Am J Med Genet B Neuropsychiatr Genet, 131: 51-59.
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.131
, pp. 51-59
-
-
McCauley, J.L.1
Olson, L.M.2
Delahanty, R.3
Delahanty, R.4
Amin, T.5
-
61
-
-
24144452995
-
Genome-wide and ordered-subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates
-
McCauley JL, Li, C, Jiang L, Olson LM, Crockett G et al. 2005. Genome-wide and ordered-subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med Genet, 6: 1.
-
(2005)
BMC Med Genet
, vol.6
, pp. 1
-
-
McCauley, J.L.1
Li, C.2
Jiang, L.3
Olson, L.M.4
Crockett, G.5
-
62
-
-
0026593322
-
Phenylketonuria: An underlying etiology of autistic syndrome. A case report
-
Miladi N, Larnaout A, Kaabachi N, Helayem M, Ben Hamida M 1992. Phenylketonuria: An underlying etiology of autistic syndrome. A case report. J Child Neurol, 7: 22-23.
-
(1992)
J Child Neurol
, vol.7
, pp. 22-23
-
-
Miladi, N.1
Larnaout, A.2
Kaabachi, N.3
Helayem, M.4
Ben Hamida, M.5
-
63
-
-
23744485061
-
Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression
-
Molloy CA, Keddache M, Martin LJ 2005. Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression. Mol Psychiatry, 10: 741-746.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 741-746
-
-
Molloy, C.A.1
Keddache, M.2
Martin, L.J.3
-
64
-
-
0025300371
-
Autistic disorder in Sotos syndrome: A case report
-
Morrow JD, Whitman BY, Accardo PJ 1990. Autistic disorder in Sotos syndrome: A case report. Eur J Pediatr, 149: 567-569.
-
(1990)
Eur J Pediatr
, vol.149
, pp. 567-569
-
-
Morrow, J.D.1
Whitman, B.Y.2
Accardo, P.J.3
-
66
-
-
0036889590
-
Molecular genetics of speech and language disorders
-
Newbury DF, Monaco AP 2002. Molecular genetics of speech and language disorders. Curr Opin Pediatr, 14(6): 696-701.
-
(2002)
Curr Opin Pediatr
, vol.14
, Issue.6
, pp. 696-701
-
-
Newbury, D.F.1
Monaco, A.P.2
-
67
-
-
0041847015
-
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism
-
Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley J et al. 2003. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Mol. Psychiatry, 8: 624-634, 570.
-
(2003)
Mol. Psychiatry
, vol.8
, pp. 624-634
-
-
Nurmi, E.L.1
Amin, T.2
Olson, L.M.3
Jacobs, M.M.4
McCauley, J.5
-
68
-
-
0038692088
-
Association of specific language impairment (SLI) to the region of 7q31
-
O'Brien EK, Zhang X, Nishimura C, Tomblin JB, Murray JC 2003. Association of specific language impairment (SLI) to the region of 7q31. Am J Hum Genet, 72: 1536-1543.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1536-1543
-
-
O'Brien, E.K.1
Zhang, X.2
Nishimura, C.3
Tomblin, J.B.4
Murray, J.C.5
-
69
-
-
0036717789
-
Is there more to GABA than synaptic inhibition?
-
Owens DF, Kriegstein AR 2002. Is there more to GABA than synaptic inhibition? Nat Rev Neurosci, 3: 715-727.
-
(2002)
Nat Rev Neurosci
, vol.3
, pp. 715-727
-
-
Owens, D.F.1
Kriegstein, A.R.2
-
70
-
-
0032879174
-
Autism and autistic behaviour in Jobert Syndrome
-
Ozonoff S, Williams BJ, Gale S, Miller JN 1999.Autism and autistic behaviour in Jobert Syndrome. J Child Neurol, 14: 636-641.
-
(1999)
J Child Neurol
, vol.14
, pp. 636-641
-
-
Ozonoff, S.1
Williams, B.J.2
Gale, S.3
Miller, J.N.4
-
71
-
-
17744393442
-
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
-
Persico AM, D'Agruma L, Maiorano N, Totaro A, Militerni R et al. 2001. Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder. Mol Psychiatry, 6: 150-159.
-
(2001)
Mol Psychiatry
, vol.6
, pp. 150-159
-
-
Persico, A.M.1
D'agruma, L.2
Maiorano, N.3
Totaro, A.4
Militerni, R.5
-
72
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
Philippe A, Martinez M, Guilloud-Bataill M, Gillberg C, Rastam M et al. 1999. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet, 8: 805-812.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataill, M.3
Gillberg, C.4
Rastam, M.5
-
73
-
-
0033799275
-
Communication genes clustered on 7q31
-
Ramsay M 2000. Communication genes clustered on 7q31. Mol Med Today, 6(10): 380-381.
-
(2000)
Mol Med Today
, vol.6
, Issue.10
, pp. 380-381
-
-
Ramsay, M.1
-
74
-
-
0031893613
-
Neurobiology of autism
-
Rapin I, Katzman R 1998. Neurobiology of autism. Ann Neurol, 43: 7-14.
-
(1998)
Ann Neurol
, vol.43
, pp. 7-14
-
-
Rapin, I.1
Katzman, R.2
-
75
-
-
0035151993
-
Autistic disorders in Down syndrome: Background factors and clinical correlates
-
Rasmussen P, Borjesson O, Wentz E, Gillberg C 2001. Autistic disorders in Down syndrome: background factors and clinical correlates. Dev Med Child Neurol, 43: 750-754.
-
(2001)
Dev Med Child Neurol
, vol.43
, pp. 750-754
-
-
Rasmussen, P.1
Borjesson, O.2
Wentz, E.3
Gillberg, C.4
-
76
-
-
24144501508
-
Cytogenetic abnormalities and fragile X syndrome in Autism spectrum disorder
-
Reddy KS 2005. Cytogenetic abnormalities and fragile X syndrome in Autism spectrum disorder. BMC Medical Genetics, 6: 3.
-
(2005)
BMC Medical Genetics
, vol.6
, pp. 3
-
-
Reddy, K.S.1
-
77
-
-
0035960009
-
The reelin pathways modulates the structure and function of retinal synaptic circuitry
-
Rice DS, Nusinowitz S, Azimi AM, Martinez A, Soriano E, Curran T 2001. The reelin pathways modulates the structure and function of retinal synaptic circuitry. Neuron, 31: 929-941.
-
(2001)
Neuron
, vol.31
, pp. 929-941
-
-
Rice, D.S.1
Nusinowitz, S.2
Azimi, A.M.3
Martinez, A.4
Soriano, E.5
Curran, T.6
-
78
-
-
0021912631
-
Autism associated with Williams syndrome
-
Reiss AL, Feinstein C, Rosenbaum KN, Borengasser-Caruso MA, Goldsmith BM. 1985. Autism associated with Williams syndrome. J Pediatr, 106: 247-249.
-
(1985)
J Pediatr
, vol.106
, pp. 247-249
-
-
Reiss, A.L.1
Feinstein, C.2
Rosenbaum, K.N.3
Borengasser-caruso, M.A.4
Goldsmith, B.M.5
-
79
-
-
0033362024
-
Genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, Nassim N, Hinds D et al. 1999. Genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet, 65: 493-507.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nassim, N.4
Hinds, D.5
-
80
-
-
0035675794
-
The behavioral phenotype in fragile X: Symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders
-
Rogers SJ, Wehner DE, Hagerman R 2001. The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J Dev Behav Pediatr, 22: 409-417.
-
(2001)
J Dev Behav Pediatr
, vol.22
, pp. 409-417
-
-
Rogers, S.J.1
Wehner, D.E.2
Hagerman, R.3
-
81
-
-
33750349024
-
Evidence for multiple loci from a genome scan of autism kindreds
-
Schellenberg GD, Dawson G, Sung YJ 2006. Evidence for multiple loci from a genome scan of autism kindreds. Mol Psychiatry, 11: 1049-60.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 1049-1060
-
-
Schellenberg, G.D.1
Dawson, G.2
Sung, Y.J.3
-
82
-
-
37649026213
-
Genomic screen and follow-up analysis for autistic disorder
-
Shao, Y, Wolpert C.M, Raiford KL, Menold MM, Donnelly SL et al. 2002a. Genomic screen and follow-up analysis for autistic disorder. Am J Med Genet, 114: 99-105.
-
(2002)
Am J Med Genet
, vol.114
, pp. 99-105
-
-
Shao, Y.1
Wolpert, C.M.2
Raiford, K.L.3
Menold, M.M.4
Donnelly, S.L.5
-
83
-
-
18344374001
-
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
-
Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA et al. 2002b. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. Am J Hum Genet, 70: 1058-1061.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1058-1061
-
-
Shao, Y.1
Raiford, K.L.2
Wolpert, C.M.3
Cope, H.A.4
Ravan, S.A.5
-
84
-
-
0037371673
-
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
-
Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM et al. 2003. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. Am J Hum Genet, 72: 539-548.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 539-548
-
-
Shao, Y.1
Cuccaro, M.L.2
Hauser, E.R.3
Raiford, K.L.4
Menold, M.M.5
-
85
-
-
3042847437
-
MECP2 structural and 39-UTR variants in schizophrenia, autism and other psychiatric diseases: A possible association with autism
-
Shibayama A, Cook EH Jr, Feng J 2004. MECP2 structural and 39-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism. Am J Med Genet B Neuropsychiatr Genet, 128B: 50-53.
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.128 B
, pp. 50-53
-
-
Shibayama, A.1
Cook Jr., E.H.2
Feng, J.3
-
86
-
-
0029916624
-
Autism in Angelman syndrome: A populationbased study
-
Steffenburg S, Gillberg CL, Steffenburg U, Kyllerman M 1996. Autism in Angelman syndrome: a populationbased study. Pediatr Neurol, 14: 131-136.
-
(1996)
Pediatr Neurol
, vol.14
, pp. 131-136
-
-
Steffenburg, S.1
Gillberg, C.L.2
Steffenburg, U.3
Kyllerman, M.4
-
87
-
-
0037317655
-
Genetics of childhood disorders: XLVII. Autism, part 6: Duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism
-
Sutcliffe JS, Nurmi EL, Lombroso PJ. 2003. Genetics of childhood disorders: XLVII. Autism, part 6: Duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism. J Am Acad Child Adolesc Psychiatry, 42: 253-256.
-
(2003)
J Am Acad Child Adolesc Psychiatry
, vol.42
, pp. 253-256
-
-
Sutcliffe, J.S.1
Nurmi, E.L.2
Lombroso, P.J.3
-
88
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Szatmari P, Paterson AD, Zwaigenbaum L 2007. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet, 39: 319-328.
-
(2007)
Nat Genet
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
-
89
-
-
32844464123
-
A heterogeneity-based genome search meta-analysis for autism-spectrum disorders
-
Trikalinos TA, Karvouni A, Zintzaras E, Ylisaukko-oja T, Peltonen L et al. 2006. A heterogeneity-based genome search meta-analysis for autism-spectrum disorders. Mol Psychiatry, 11: 29-36.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 29-36
-
-
Trikalinos, T.A.1
Karvouni, A.2
Zintzaras, E.3
Ylisaukko-Oja, T.4
Peltonen, L.5
-
90
-
-
4644285329
-
Molecular genetics of autism spectrum disorder
-
Veenstra-VanderWeels J, Cook Jr EH 2004. Molecular genetics of autism spectrum disorder. Mol Psychiatry, 9: 819-831.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 819-831
-
-
Veenstra-Vanderweels, J.1
Cook, E.H.2
-
91
-
-
32844460507
-
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
-
Vorstman JA, Staal WG, van Daalen E, van Engeland H, Hochstenbach PF, Franke L 2006. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol Psychiatry, 11: 18-28.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 18-28
-
-
Vorstman, J.A.1
Staal, W.G.2
van Daalen, E.3
van Engeland, H.4
Hochstenbach, P.F.5
Franke, L.6
-
92
-
-
0034865096
-
No mutations in the coding region of the Rett syndrome gene MeCP2 in 59 autistic patients
-
Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthelemy C et al. 2001. No mutations in the coding region of the Rett syndrome gene MeCP2 in 59 autistic patients. Eur J Hum Genet, 9: 556-558.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 556-558
-
-
Vourc'h, P.1
Bienvenu, T.2
Beldjord, C.3
Chelly, J.4
Barthelemy, C.5
-
93
-
-
0345376666
-
Abnormal serotonergic development in a mouse model for the Smith-Lemli-Opitz syndrome: Implications for autism
-
Waage-Baudet H, Lauder JM, Dehart DB 2003. Abnormal serotonergic development in a mouse model for the Smith-Lemli-Opitz syndrome: implications for autism. Int J Dev Neurosci, 21: 451-459.
-
(2003)
Int J Dev Neurosci
, vol.21
, pp. 451-459
-
-
Waage-Baudet, H.1
Lauder, J.M.2
Dehart, D.B.3
-
94
-
-
45149117520
-
Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population
-
Wang L, Jia M, Yue W 2008. Association of the ENGRAILED 2 (EN2) gene with autism in Chinese Han population. Am J Med Genet B Neuropsychiatr Genet, 147B(4): 434-438.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, Issue.4
, pp. 434-438
-
-
Wang, L.1
Jia, M.2
Yue, W.3
-
95
-
-
0035827826
-
Evidence supporting WNT2 as an autism susceptibility gene
-
Wassink T, Piven J, Vieland V, Huang J, Swiderski R et al. 2001. Evidence supporting WNT2 as an autism susceptibility gene. Am J Med Genet (Neuropsychiatr Genet), 105: 406-413.
-
(2001)
Am J Med Genet (Neuropsychiatr Genet)
, vol.105
, pp. 406-413
-
-
Wassink, T.1
Piven, J.2
Vieland, V.3
Huang, J.4
Swiderski, R.5
-
96
-
-
34247096911
-
MeCP2 gene mutation analysis in autistic boys with developmental regression
-
Xi CY, Ma HW, Lu Y, Zhao YJ, Hua TY, Zhao Y, Ji YH 2007. MeCP2 gene mutation analysis in autistic boys with developmental regression. Psychiatr Genet, 17: 113-116.
-
(2007)
Psychiatr Genet
, vol.17
, pp. 113-116
-
-
Xi, C.Y.1
Ma, H.W.2
Lu, Y.3
Zhao, Y.J.4
Hua, T.Y.5
Zhao, Y.6
Ji, Y.H.7
-
97
-
-
20144389549
-
Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients
-
Yan, J, Oliveira G, Coutinho A, Yang C, Fen, J et al. 2005. Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients. Mol Psychiatry, 10: 329-332.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 329-332
-
-
Yan, J.1
Oliveira, G.2
Coutinho, A.3
Yang, C.4
Fen, J.5
-
98
-
-
44349193331
-
Neurexin 1alpha structural variants associated with autism
-
Yan J, Noltner K, Feng J 2008. Neurexin 1alpha structural variants associated with autism. Neurosci Lett, 438:368-370.
-
(2008)
Neurosci Lett
, vol.438
, pp. 368-370
-
-
Yan, J.1
Noltner, K.2
Feng, J.3
-
99
-
-
45549104943
-
Association of the homeobox transcription factor gene ENGRAILED 2 with autistic disorder in Chinese children
-
Yang P, Lung FW, Jong YJ, Hsieh HY, Liang CL, Juo SH 2008. Association of the homeobox transcription factor gene ENGRAILED 2 with autistic disorder in Chinese children. Neuropsychobiology, 57: 3-8.
-
(2008)
Neuropsychobiology
, vol.57
, pp. 3-8
-
-
Yang, P.1
Lung, F.W.2
Jong, Y.J.3
Hsieh, H.Y.4
Liang, C.L.5
Juo, S.H.6
-
100
-
-
0037218690
-
Prevalence of autism in a US metropolitan area
-
Yeargin-Allsopp M, Rice C, Karapurkar T, Arbella S, Feinsilver T et al. 2003. Prevalence of autism in a US metropolitan area. JAMA, 289: 49-55.
-
(2003)
JAMA
, vol.289
, pp. 49-55
-
-
Yeargin-Allsopp, M.1
Rice, C.2
Karapurkar, T.3
Arbella, S.4
Feinsilver, T.5
-
101
-
-
0035826536
-
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
-
Yirmiya N, Pilowsky T, Nemanov L, Arbella S, Feinsilver T et al. 2001. Evidence for an association with the serotonin transporter promoter region polymorphism and autism. Am J Med Genet, 105: 381-386.
-
(2001)
Am J Med Genet
, vol.105
, pp. 381-386
-
-
Yirmiya, N.1
Pilowsky, T.2
Nemanov, L.3
Arbella, S.4
Feinsilver, T.5
-
103
-
-
0142059641
-
A genome-wide screen of 345 families for autism-susceptibility loci
-
Yonan AL, Alarcon M, Cheng R, Magnusson PK, Spence SJ et al. 2003. A genome-wide screen of 345 families for autism-susceptibility loci. Am J Hum Genet, 73: 886-897.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.4
Spence, S.J.5
-
104
-
-
41849126341
-
The diagnosis of autism in a female: Could it be Rett syndrome?
-
Young DJ, Bebbington A, Anderson A, ravine D, Ellaway C et al. 2008. The diagnosis of autism in a female: could it be Rett syndrome? Eur J Pediatr, 167: 661-669.
-
(2008)
Eur J Pediatr
, vol.167
, pp. 661-669
-
-
Young, D.J.1
Bebbington, A.2
Anderson, A.3
Ravine, D.4
Ellaway, C.5
-
105
-
-
18444371140
-
Presence of large deletions in kindreds with autism
-
Yu CE, Dawson G, Munson J 2002. Presence of large deletions in kindreds with autism. Am J Hum Genet, 71: 100-115.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 100-115
-
-
Yu, C.E.1
Dawson, G.2
Munson, J.3
-
106
-
-
0041819548
-
Study of MECP2 gene in Rett syndrome variants and autistic girls
-
Zappella M, Meloni I, Longo I, Canitano R, Hayek G et al.2003. Study of MECP2 gene in Rett syndrome variants and autistic girls. Am J Med Genet B Neuropsychiatr Genet, 119B: 102-107.
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.119 B
, pp. 102-107
-
-
Zappella, M.1
Meloni, I.2
Longo, I.3
Canitano, R.4
Hayek, G.5
-
107
-
-
0036428852
-
Reelin gene alleles and susceptibility to autism spectrum disorders
-
Zhang H, Liu X, Zhang C, Munod E, Macciardo F et al. 2002. Reelin gene alleles and susceptibility to autism spectrum disorders. Mol Psychiatry, 7: 1012-1017.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 1012-1017
-
-
Zhang, H.1
Liu, X.2
Zhang, C.3
Munod, E.4
Macciardo, F.5
|