158 related articles for article (PubMed ID: 19035560)
21. 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
Teratology; 2000 Dec; 62(6):393-405. PubMed ID: 11091361
[TBL] [Abstract][Full Text] [Related]
22. Glutamate receptor 6 gene (GluR6 or GRIK2) polymorphisms in the Indian population: a genetic association study on autism spectrum disorder.
Dutta S; Das S; Guhathakurta S; Sen B; Sinha S; Chatterjee A; Ghosh S; Ahmed S; Ghosh S; Usha R
Cell Mol Neurobiol; 2007 Dec; 27(8):1035-47. PubMed ID: 17712621
[TBL] [Abstract][Full Text] [Related]
23. No association between single nucleotide polymorphisms in DLX6 and Piccolo genes at 7q21-q22 and autism.
Nabi R; Zhong H; Serajee FJ; Huq AH
Am J Med Genet B Neuropsychiatr Genet; 2003 May; 119B(1):98-101. PubMed ID: 12707945
[TBL] [Abstract][Full Text] [Related]
24. Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects.
Carayol J; Sacco R; Tores F; Rousseau F; Lewin P; Hager J; Persico AM
Biol Psychiatry; 2011 Nov; 70(9):880-7. PubMed ID: 21757185
[TBL] [Abstract][Full Text] [Related]
25. Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal.
Guhathakurta S; Sinha S; Ghosh S; Chatterjee A; Ahmed S; Gangopadhyay PK; Usha R
Brain Res; 2008 Nov; 1240():12-21. PubMed ID: 18804097
[TBL] [Abstract][Full Text] [Related]
26. Lack of evidence for an association between WNT2 and RELN polymorphisms and autism.
Li J; Nguyen L; Gleason C; Lotspeich L; Spiker D; Risch N; Myers RM
Am J Med Genet B Neuropsychiatr Genet; 2004 Apr; 126B(1):51-7. PubMed ID: 15048648
[TBL] [Abstract][Full Text] [Related]
27. Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
Wassink TH; Piven J; Vieland VJ; Jenkins L; Frantz R; Bartlett CW; Goedken R; Childress D; Spence MA; Smith M; Sheffield VC
Am J Med Genet B Neuropsychiatr Genet; 2005 Jul; 136B(1):36-44. PubMed ID: 15892143
[TBL] [Abstract][Full Text] [Related]
28. Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.
Chien YL; Wu YY; Chiu YN; Liu SK; Tsai WC; Lin PI; Chen CH; Gau SS; Chien WH
Prog Neuropsychopharmacol Biol Psychiatry; 2011 Aug; 35(6):1512-7. PubMed ID: 21575668
[TBL] [Abstract][Full Text] [Related]
29. Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
Dutta S; Sinha S; Ghosh S; Chatterjee A; Ahmed S; Usha R
Neurosci Lett; 2008 Aug; 441(1):56-60. PubMed ID: 18597938
[TBL] [Abstract][Full Text] [Related]
30. A Novel Stratification Method in Linkage Studies to Address Inter- and Intra-Family Heterogeneity in Autism.
Talebizadeh Z; Arking DE; Hu VW
PLoS One; 2013; 8(6):e67569. PubMed ID: 23840741
[TBL] [Abstract][Full Text] [Related]
31. Association of GABRG3, GABRB3, HTR2A gene variants with autism spectrum disorder.
Coskunpinar EM; Tur S; Cevher Binici N; Yazan Songür C
Gene; 2023 Jun; 870():147399. PubMed ID: 37019319
[TBL] [Abstract][Full Text] [Related]
32. A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.
Hettinger JA; Liu X; Schwartz CE; Michaelis RC; Holden JJ
Am J Med Genet B Neuropsychiatr Genet; 2008 Jul; 147B(5):628-36. PubMed ID: 18205172
[TBL] [Abstract][Full Text] [Related]
33. Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.
Benayed R; Choi J; Matteson PG; Gharani N; Kamdar S; Brzustowicz LM; Millonig JH
Biol Psychiatry; 2009 Nov; 66(10):911-7. PubMed ID: 19615670
[TBL] [Abstract][Full Text] [Related]
34. Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
Ylisaukko-oja T; Alarcón M; Cantor RM; Auranen M; Vanhala R; Kempas E; von Wendt L; Järvelä I; Geschwind DH; Peltonen L
Ann Neurol; 2006 Jan; 59(1):145-55. PubMed ID: 16288458
[TBL] [Abstract][Full Text] [Related]
35. Family-based association study between GRIK2 polymorphisms and autism spectrum disorders in the Korean trios.
Kim SA; Kim JH; Park M; Cho IH; Yoo HJ
Neurosci Res; 2007 Jul; 58(3):332-5. PubMed ID: 17428563
[TBL] [Abstract][Full Text] [Related]
36. A genomewide 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; Ylisaukko-Oja T; Sinsheimer JS; Peltonen L; Järvelä I
Am J Hum Genet; 2002 Oct; 71(4):777-90. PubMed ID: 12192642
[TBL] [Abstract][Full Text] [Related]
37. Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios.
Cho IH; Yoo HJ; Park M; Lee YS; Kim SA
Brain Res; 2007 Mar; 1139():34-41. PubMed ID: 17280648
[TBL] [Abstract][Full Text] [Related]
38. A genome-wide scan for common alleles affecting risk for autism.
Anney R; Klei L; Pinto D; Regan R; Conroy J; Magalhaes TR; Correia C; Abrahams BS; Sykes N; Pagnamenta AT; Almeida J; Bacchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bölte S; Bolton PF; Bourgeron T; Brennan S; Brian J; Carson AR; Casallo G; Casey J; Chu SH; Cochrane L; Corsello C; Crawford EL; Crossett A; Dawson G; de Jonge M; Delorme R; Drmic I; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Goldberg J; Green J; Guter SJ; Hakonarson H; Heron EA; Hill M; Holt R; Howe JL; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Korvatska O; Kustanovich V; Lajonchere CM; Lamb JA; Laskawiec M; Leboyer M; Le Couteur A; Leventhal BL; Lionel AC; Liu XQ; Lord C; Lotspeich L; Lund SC; Maestrini E; Mahoney W; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Melhem NM; Merikangas A; Migita O; Minshew NJ; Mirza GK; Munson J; Nelson SF; Noakes C; Noor A; Nygren G; Oliveira G; Papanikolaou K; Parr JR; Parrini B; Paton T; Pickles A; Piven J; Posey DJ; Poustka A; Poustka F; Prasad A; Ragoussis J; Renshaw K; Rickaby J; Roberts W; Roeder K; Roge B; Rutter ML; Bierut LJ; Rice JP; Salt J; Sansom K; Sato D; Segurado R; Senman L; Shah N; Sheffield VC; Soorya L; Sousa I; Stoppioni V; Strawbridge C; Tancredi R; Tansey K; Thiruvahindrapduram B; Thompson AP; Thomson S; Tryfon A; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Wallace S; Wang K; Wang Z; Wassink TH; Wing K; Wittemeyer K; Wood S; Yaspan BL; Zurawiecki D; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Gallagher L; Geschwind DH; Gill M; Haines JL; Miller J; Monaco AP; Nurnberger JI; Paterson AD; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vicente AM; Vieland VJ; Wijsman EM; Devlin B; Ennis S; Hallmayer J
Hum Mol Genet; 2010 Oct; 19(20):4072-82. PubMed ID: 20663923
[TBL] [Abstract][Full Text] [Related]
39. 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 JL; Lam AY; Organ EL; Folstein SE; Haines JL; Sutcliffe JS
Mol Psychiatry; 2003 Jun; 8(6):624-34, 570. PubMed ID: 12851639
[TBL] [Abstract][Full Text] [Related]
40. High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.
Strom SP; Stone JL; Ten Bosch JR; Merriman B; Cantor RM; Geschwind DH; Nelson SF
Mol Psychiatry; 2010 Oct; 15(10):996-1005. PubMed ID: 19455149
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
