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Items: 1 to 20 of 102

1.

Examination of association of genes in the serotonin system to autism.

Anderson BM, Schnetz-Boutaud NC, Bartlett J, Wotawa AM, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Neurogenetics. 2009 Jul;10(3):209-16. doi: 10.1007/s10048-009-0171-7. Epub 2009 Jan 28.

2.

Examination of association to autism of common genetic variationin genes related to dopamine.

Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Autism Res. 2008 Dec;1(6):364-9. doi: 10.1002/aur.55.

3.

Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels.

Coutinho AM, Sousa I, Martins M, Correia C, Morgadinho T, Bento C, Marques C, Ataíde A, Miguel TS, Moore JH, Oliveira G, Vicente AM.

Hum Genet. 2007 Apr;121(2):243-56. Epub 2007 Jan 3.

PMID:
17203304
4.

Association of tryptophan 2,3 dioxygenase gene polymorphism with autism.

Nabi R, Serajee FJ, Chugani DC, Zhong H, Huq AH.

Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):63-8.

PMID:
14755447
5.

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79. Epub 2005 Jul 1.

6.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
7.

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.

8.

Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.

Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1116-25. doi: 10.1002/ajmg.b.30733.

9.

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.

10.

Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes.

Napolioni V, Lombardi F, Sacco R, Curatolo P, Manzi B, Alessandrelli R, Militerni R, Bravaccio C, Lenti C, Saccani M, Schneider C, Melmed R, Pascucci T, Puglisi-Allegra S, Reichelt KL, Rousseau F, Lewin P, Persico AM.

Eur J Hum Genet. 2011 Mar;19(3):353-9. doi: 10.1038/ejhg.2010.180. Epub 2010 Nov 24.

11.

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism.

Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Sasaki T, Kato N.

Int J Neuropsychopharmacol. 2009 Feb;12(1):1-10. doi: 10.1017/S1461145708009127. Epub 2008 Jul 30. Erratum in: Int J Neuropsychopharmacol. 2009 Apr;12(3):439. Sasaki, Tsukasa [added].

PMID:
18664314
12.

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. doi: 10.1038/mp.2009.41. Epub 2009 May 19.

13.

[Evidence for association and epistasis between the genetic markers SLC6A4 and HTR2A in autism etiology].

Valencia AV, Páez AL, Sampedro ME, Ávila C, Cardona JC, Mesa C, Galvis L, Carrizosa J, Camargo M, Ruiz A, Cornejo W, Bedoya G.

Biomedica. 2012 Oct-Dec;32(4):585-601. doi: 10.1590/S0120-41572012000400014. Spanish.

14.

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder.

Betancur C, Corbex M, Spielewoy C, Philippe A, Laplanche JL, Launay JM, Gillberg C, Mouren-Siméoni MC, Hamon M, Giros B, Nosten-Bertrand M, Leboyer M.

Mol Psychiatry. 2002;7(1):67-71.

15.

Examination of tetrahydrobiopterin pathway genes in autism.

Schnetz-Boutaud NC, Anderson BM, Brown KD, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.

Genes Brain Behav. 2009 Nov;8(8):753-7. doi: 10.1111/j.1601-183X.2009.00521.x. Epub 2009 Jul 14.

16.

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 13;1240:12-21. doi: 10.1016/j.brainres.2008.08.063. Epub 2008 Sep 4.

PMID:
18804097
17.

The association analysis of RELN and GRM8 genes with autistic spectrum disorder in Chinese Han population.

Li H, Li Y, Shao J, Li R, Qin Y, Xie C, Zhao Z.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):194-200.

PMID:
17955477
18.

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
19.

Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.

Qin J, Jia M, Wang L, Lu T, Ruan Y, Liu J, Guo Y, Zhang J, Yang X, Yue W, Zhang D.

BMC Med Genet. 2009 Jun 30;10:61. doi: 10.1186/1471-2350-10-61.

20.

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.

PMID:
17722011

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