490 related articles for article (PubMed ID: 25531569)
21. Networks of neuronal genes affected by common and rare variants in autism spectrum disorders.
Ben-David E; Shifman S
PLoS Genet; 2012; 8(3):e1002556. PubMed ID: 22412387
[TBL] [Abstract][Full Text] [Related]
22. Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder.
Uddin M; Tammimies K; Pellecchia G; Alipanahi B; Hu P; Wang Z; Pinto D; Lau L; Nalpathamkalam T; Marshall CR; Blencowe BJ; Frey BJ; Merico D; Yuen RK; Scherer SW
Nat Genet; 2014 Jul; 46(7):742-7. PubMed ID: 24859339
[TBL] [Abstract][Full Text] [Related]
23. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
O'Roak BJ; Deriziotis P; Lee C; Vives L; Schwartz JJ; Girirajan S; Karakoc E; Mackenzie AP; Ng SB; Baker C; Rieder MJ; Nickerson DA; Bernier R; Fisher SE; Shendure J; Eichler EE
Nat Genet; 2011 Jun; 43(6):585-9. PubMed ID: 21572417
[TBL] [Abstract][Full Text] [Related]
24. The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.
Steinberg J; Webber C
Am J Hum Genet; 2013 Nov; 93(5):825-39. PubMed ID: 24207117
[TBL] [Abstract][Full Text] [Related]
25. Genetically meaningful phenotypic subgroups in autism spectrum disorders.
Veatch OJ; Veenstra-Vanderweele J; Potter M; Pericak-Vance MA; Haines JL
Genes Brain Behav; 2014 Mar; 13(3):276-85. PubMed ID: 24373520
[TBL] [Abstract][Full Text] [Related]
26. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
[TBL] [Abstract][Full Text] [Related]
27. De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.
Babbs C; Lloyd D; Pagnamenta AT; Twigg SR; Green J; McGowan SJ; Mirza G; Naples R; Sharma VP; Volpi EV; Buckle VJ; Wall SA; Knight SJ; ; Parr JR; Wilkie AO
J Med Genet; 2014 Nov; 51(11):737-47. PubMed ID: 25228304
[TBL] [Abstract][Full Text] [Related]
28. Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes.
Bruining H; de Sonneville L; Swaab H; de Jonge M; Kas M; van Engeland H; Vorstman J
PLoS One; 2010 May; 5(5):e10887. PubMed ID: 20526357
[TBL] [Abstract][Full Text] [Related]
29. Sex differences in autism spectrum disorders.
Werling DM; Geschwind DH
Curr Opin Neurol; 2013 Apr; 26(2):146-53. PubMed ID: 23406909
[TBL] [Abstract][Full Text] [Related]
30. [Autism spectrum disorder and genes for synaptic proteins].
Shishido E
Brain Nerve; 2012 Jan; 64(1):65-70. PubMed ID: 22223503
[TBL] [Abstract][Full Text] [Related]
31. Commentary for special issue of Autism research on mouse models in ASD: a clinical perspective.
Minshew N; McFadden K
Autism Res; 2011 Feb; 4(1):1-4. PubMed ID: 21328567
[No Abstract] [Full Text] [Related]
32. Three hypotheses for developmental defects that may underlie some forms of autism spectrum disorder.
Rubenstein JL
Curr Opin Neurol; 2010 Apr; 23(2):118-23. PubMed ID: 20087182
[TBL] [Abstract][Full Text] [Related]
33. Intellectual disability is associated with increased runs of homozygosity in simplex autism.
Gamsiz ED; Viscidi EW; Frederick AM; Nagpal S; Sanders SJ; Murtha MT; Schmidt M; ; Triche EW; Geschwind DH; State MW; Istrail S; Cook EH; Devlin B; Morrow EM
Am J Hum Genet; 2013 Jul; 93(1):103-9. PubMed ID: 23830515
[TBL] [Abstract][Full Text] [Related]
34. Connecting genes to brain in the autism spectrum disorders.
Abrahams BS; Geschwind DH
Arch Neurol; 2010 Apr; 67(4):395-9. PubMed ID: 20385903
[TBL] [Abstract][Full Text] [Related]
35. Autism genetics.
Persico AM; Napolioni V
Behav Brain Res; 2013 Aug; 251():95-112. PubMed ID: 23769996
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.
Robinson EB; Samocha KE; Kosmicki JA; McGrath L; Neale BM; Perlis RH; Daly MJ
Proc Natl Acad Sci U S A; 2014 Oct; 111(42):15161-5. PubMed ID: 25288738
[TBL] [Abstract][Full Text] [Related]
38. Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD).
Kantojärvi K; Kotala I; Rehnström K; Ylisaukko-Oja T; Vanhala R; von Wendt TN; von Wendt L; Järvelä I
Autism Res; 2011 Jun; 4(3):228-33. PubMed ID: 21384559
[TBL] [Abstract][Full Text] [Related]
39. A framework for the interpretation of de novo mutation in human disease.
Samocha KE; Robinson EB; Sanders SJ; Stevens C; Sabo A; McGrath LM; Kosmicki JA; Rehnström K; Mallick S; Kirby A; Wall DP; MacArthur DG; Gabriel SB; DePristo M; Purcell SM; Palotie A; Boerwinkle E; Buxbaum JD; Cook EH; Gibbs RA; Schellenberg GD; Sutcliffe JS; Devlin B; Roeder K; Neale BM; Daly MJ
Nat Genet; 2014 Sep; 46(9):944-50. PubMed ID: 25086666
[TBL] [Abstract][Full Text] [Related]
40. Evidence for interaction between markers in GABA(A) receptor subunit genes in an Argentinean autism spectrum disorder population.
Sesarini CV; Costa L; Naymark M; Grañana N; Cajal AR; García Coto M; Pallia RC; Argibay PF
Autism Res; 2014 Feb; 7(1):162-6. PubMed ID: 24249596
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
