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Glutathione pathway gene variation and risk of autism spectrum disorders.

Bowers K, Li Q, Bressler J, Avramopoulos D, Newschaffer C, Fallin MD.

J Neurodev Disord. 2011 Jun;3(2):132-43. doi: 10.1007/s11689-011-9077-4. Epub 2011 Mar 5.


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, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.


The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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


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 1;35(6):1512-7. doi: 10.1016/j.pnpbp.2011.04.010. Epub 2011 May 5.


Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.

Wermter AK, Kamp-Becker I, Hesse P, Schulte-Körne G, Strauch K, Remschmidt H.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):629-39. doi: 10.1002/ajmg.b.31032.


SNP-SNP interactions in breast cancer susceptibility.

Onay VU, Briollais L, Knight JA, Shi E, Wang Y, Wells S, Li H, Rajendram I, Andrulis IL, Ozcelik H.

BMC Cancer. 2006 May 3;6:114.


Genetic variant of glutathione peroxidase 1 in autism.

Ming X, Johnson WG, Stenroos ES, Mars A, Lambert GH, Buyske S.

Brain Dev. 2010 Feb;32(2):105-9. doi: 10.1016/j.braindev.2008.12.017. Epub 2009 Feb 4.


Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism.

Correia CT, Coutinho AM, Sequeira AF, Sousa IG, Lourenço Venda L, Almeida JP, Abreu RL, Lobo C, Miguel TS, Conroy J, Cochrane L, Gallagher L, Gill M, Ennis S, Oliveira GG, Vicente AM.

Genes Brain Behav. 2010 Oct;9(7):841-8. doi: 10.1111/j.1601-183X.2010.00627.x. Epub 2010 Aug 19.


Genetic polymorphisms in DNA base-excision repair genes ADPRT, XRCC1, and APE1 and the risk of squamous cell carcinoma of the head and neck.

Li C, Hu Z, Lu J, Liu Z, Wang LE, El-Naggar AK, Sturgis EM, Spitz MR, Wei Q.

Cancer. 2007 Aug 15;110(4):867-75.


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.


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.


Association and interaction of the IL4R, IL4, and IL13 loci with type 1 diabetes among Filipinos.

Bugawan TL, Mirel DB, Valdes AM, Panelo A, Pozzilli P, Erlich HA.

Am J Hum Genet. 2003 Jun;72(6):1505-14. Epub 2003 May 13.


No association between common variants in glyoxalase 1 and autism spectrum disorders.

Rehnström K, Ylisaukko-Oja T, Vanhala R, von Wendt L, Peltonen L, Hovatta I.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):124-7.


Improved use of SNP information to detect the role of genes.

Jannot AS, Essioux L, Reese MG, Clerget-Darpoux F.

Genet Epidemiol. 2003 Sep;25(2):158-67.


Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes.

Wu X, Gu J, Grossman HB, Amos CI, Etzel C, Huang M, Zhang Q, Millikan RE, Lerner S, Dinney CP, Spitz MR.

Am J Hum Genet. 2006 Mar;78(3):464-79. Epub 2006 Jan 31.


Colorectal adenoma risk is modified by the interplay between polymorphisms in arachidonic acid pathway genes and fish consumption.

Siezen CL, van Leeuwen AI, Kram NR, Luken ME, van Kranen HJ, Kampman E.

Carcinogenesis. 2005 Feb;26(2):449-57. Epub 2004 Nov 18.


High density SNP association study of a major autism linkage region on chromosome 17.

Stone JL, Merriman B, Cantor RM, Geschwind DH, Nelson SF.

Hum Mol Genet. 2007 Mar 15;16(6):704-15. Epub 2007 Mar 21.


Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study.

Holliday KL, Nicholl BI, Macfarlane GJ, Thomson W, Davies KA, McBeth J.

Ann Rheum Dis. 2010 Mar;69(3):556-60. doi: 10.1136/ard.2009.116137. Epub 2009 Aug 31.


Immune function genes CD99L2, JARID2 and TPO show association with autism spectrum disorder.

Ramos PS, Sajuthi S, Langefeld CD, Walker SJ.

Mol Autism. 2012 Jun 9;3(1):4. doi: 10.1186/2040-2392-3-4.


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, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.

Ann Hum Genet. 2006 May;70(Pt 3):281-92.

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