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Items: 1 to 20 of 87

1.

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.

Chung RH, Ma D, Wang K, Hedges DJ, Jaworski JM, Gilbert JR, Cuccaro ML, Wright HH, Abramson RK, Konidari I, Whitehead PL, Schellenberg GD, Hakonarson H, Haines JL, Pericak-Vance MA, Martin ER.

Mol Autism. 2011 Nov 4;2(1):18. doi: 10.1186/2040-2392-2-18.

2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
3.

Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.

Liu X, Shimada T, Otowa T, Wu YY, Kawamura Y, Tochigi M, Iwata Y, Umekage T, Toyota T, Maekawa M, Iwayama Y, Suzuki K, Kakiuchi C, Kuwabara H, Kano Y, Nishida H, Sugiyama T, Kato N, Chen CH, Mori N, Yamada K, Yoshikawa T, Kasai K, Tokunaga K, Sasaki T, Gau SS.

Autism Res. 2016 Mar;9(3):340-9. doi: 10.1002/aur.1536. Epub 2015 Aug 28.

PMID:
26314684
4.

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium.

Mol Autism. 2017 May 22;8:21. doi: 10.1186/s13229-017-0137-9. eCollection 2017.

5.

Genome-wide association study of autistic-like traits in a general population study of young adults.

Jones RM, Cadby G, Melton PE, Abraham LJ, Whitehouse AJ, Moses EK.

Front Hum Neurosci. 2013 Oct 11;7:658. doi: 10.3389/fnhum.2013.00658. eCollection 2013.

6.

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.

Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum JD.

Autism Res. 2011 Aug;4(4):293-6. doi: 10.1002/aur.195. Epub 2011 Apr 12.

PMID:
21491612
7.

2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.

Liu X, Malenfant P, Reesor C, Lee A, Hudson ML, Harvard C, Qiao Y, Persico AM, Cohen IL, Chudley AE, Forster-Gibson C, Rajcan-Separovic E, Lewis ME, Holden JJ.

Eur J Hum Genet. 2011 Dec;19(12):1264-70. doi: 10.1038/ejhg.2011.112. Epub 2011 Jul 13.

8.

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.

Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, Gauthier J, Crosbie J, Pagnamenta AT, Munson J, Estes AM, Fiebig A, Franke A, Schreiber S, Stewart AF, Roberts R, McPherson R, Guter SJ, Cook EH Jr, Dawson G, Schellenberg GD, Battaglia A, Maestrini E; Autism Genome Project Consortium, Jeng L, Hutchison T, Rajcan-Separovic E, Chudley AE, Lewis SM, Liu X, Holden JJ, Fernandez B, Zwaigenbaum L, Bryson SE, Roberts W, Szatmari P, Gallagher L, Stratton MR, Gecz J, Brady AF, Schwartz CE, Schachar RJ, Monaco AP, Rouleau GA, Hui CC, Lucy Raymond F, Scherer SW, Vincent JB.

Sci Transl Med. 2010 Sep 15;2(49):49ra68. doi: 10.1126/scitranslmed.3001267.

9.

Sex-specific association of a common variant of the XG gene with autism spectrum disorders.

Chang SC, Pauls DL, Lange C, Sasanfar R, Santangelo SL.

Am J Med Genet B Neuropsychiatr Genet. 2013 Oct;162B(7):742-50. doi: 10.1002/ajmg.b.32165.

PMID:
24132906
10.

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. doi: 10.1002/aur.187. Epub 2011 Feb 22.

PMID:
21384559
11.

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families.

Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H.

Autism Res. 2010 Apr;3(2):47-52. doi: 10.1002/aur.119.

PMID:
20437600
12.

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 1;70(9):880-7. doi: 10.1016/j.biopsych.2011.05.020. Epub 2011 Jul 14.

PMID:
21757185
13.

Chronic periodontitis genome-wide association studies: gene-centric and gene set enrichment analyses.

Rhodin K, Divaris K, North KE, Barros SP, Moss K, Beck JD, Offenbacher S.

J Dent Res. 2014 Sep;93(9):882-90. doi: 10.1177/0022034514544506. Epub 2014 Jul 23.

14.

Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.

Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E, Lindenbaum P, Benajjou A, Fontaine K, Vazart C, Gesnouin P, Brooks P, Hager J.

BMC Med Genet. 2007 Dec 6;8:74.

15.

Analysis of X chromosome inactivation in autism spectrum disorders.

Gong X, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsäter H, Rastam M, Gillberg IC, Gillberg C, Moreno-De-Luca D, Carone S, Nummela I, Rossi M, Battaglia A; International Molecular Genetic Study of Autism Consortium (IMGSAC), Jarvela I, Maestrini E, Bourgeron T.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):830-5. doi: 10.1002/ajmg.b.30688.

16.

A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families.

Wang YT, Sung PY, Lin PL, Yu YW, Chung RH.

BMC Genomics. 2015 May 15;16:381. doi: 10.1186/s12864-015-1620-3.

17.

Allowing for sex differences increases power in a GWAS of multiplex Autism families.

Lu AT, Cantor RM.

Mol Psychiatry. 2012 Feb;17(2):215-22. doi: 10.1038/mp.2010.127. Epub 2010 Dec 14.

PMID:
21151189
18.

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.

Hutcheson HB, Olson LM, Bradford Y, Folstein SE, Santangelo SL, Sutcliffe JS, Haines JL.

BMC Med Genet. 2004 May 5;5:12.

19.

Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.

Vojinovic D, Brison N, Ahmad S, Noens I, Pappa I, Karssen LC, Tiemeier H, van Duijn CM, Peeters H, Amin N.

Eur J Hum Genet. 2017 May 17. doi: 10.1038/ejhg.2017.82. [Epub ahead of print]

PMID:
28513607
20.

SNP-based pathway enrichment analysis for genome-wide association studies.

Weng L, Macciardi F, Subramanian A, Guffanti G, Potkin SG, Yu Z, Xie X.

BMC Bioinformatics. 2011 Apr 15;12:99. doi: 10.1186/1471-2105-12-99.

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