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Items: 1 to 20 of 308

1.

Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population.

Liu X, Kawamura Y, Shimada T, Otowa T, Koishi S, Sugiyama T, Nishida H, Hashimoto O, Nakagami R, Tochigi M, Umekage T, Kano Y, Miyagawa T, Kato N, Tokunaga K, Sasaki T.

J Hum Genet. 2010 Mar;55(3):137-41. doi: 10.1038/jhg.2009.140.

PMID:
20094064
2.

Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population.

Wu S, Jia M, Ruan Y, Liu J, Guo Y, Shuang M, Gong X, Zhang Y, Yang X, Zhang D.

Biol Psychiatry. 2005 Jul 1;58(1):74-7.

PMID:
15992526
3.

Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.

Lerer E, Levi S, Salomon S, Darvasi A, Yirmiya N, Ebstein RP.

Mol Psychiatry. 2008 Oct;13(10):980-8.

PMID:
17893705
4.

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-K├Ârne 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.

PMID:
19777562
5.
6.

Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patients.

Kato C, Tochigi M, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T.

Psychiatr Genet. 2008 Jun;18(3):133-6. doi: 10.1097/YPG.0b013e3282fb0064.

PMID:
18496211
7.

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism.

Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH Jr.

Neurosci Lett. 2007 Apr 24;417(1):6-9.

8.

Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean.

Yoo HJ, Lee SK, Park M, Cho IH, Hyun SH, Lee JC, Yang SY, Kim SA.

Neurosci Res. 2009 Mar;63(3):172-6. doi: 10.1016/j.neures.2008.11.007.

PMID:
19100789
9.

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.

PMID:
18804097
10.

Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population.

Yang P, Shu BC, Hallmayer JF, Lung FW.

Neuropsychobiology. 2010;62(2):104-15. doi: 10.1159/000315441.

PMID:
20523082
11.

Association of the neuropilin-2 (NRP2) gene polymorphisms with autism in Chinese Han population.

Wu S, Yue W, Jia M, Ruan Y, Lu T, Gong X, Shuang M, Liu J, Yang X, Zhang D.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):492-5.

PMID:
17427189
12.

No association between the ryanodine receptor 3 gene and autism in a Japanese population.

Tochigi M, Kato C, Ohashi J, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T.

Psychiatry Clin Neurosci. 2008 Jun;62(3):341-4. doi: 10.1111/j.1440-1819.2008.01802.x.

13.

Role of STAT4 polymorphisms in systemic lupus erythematosus in a Japanese population: a case-control association study of the STAT1-STAT4 region.

Kawasaki A, Ito I, Hikami K, Ohashi J, Hayashi T, Goto D, Matsumoto I, Ito S, Tsutsumi A, Koga M, Arinami T, Graham RR, Hom G, Takasaki Y, Hashimoto H, Behrens TW, Sumida T, Tsuchiya N.

Arthritis Res Ther. 2008;10(5):R113. doi: 10.1186/ar2516.

14.

Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.

Kim KS, Kim GS, Hwang JY, Lee HJ, Park MH, Kim KJ, Jung J, Cha HS, Shin HD, Kang JH, Park EK, Kim TH, Hong JM, Koh JM, Oh B, Kimm K, Kim SY, Lee JY.

BMC Med Genet. 2007 Nov 26;8:70.

15.

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.

Li X, Hu Z, He Y, Xiong Z, Long Z, Peng Y, Bu F, Ling J, Xun G, Mo X, Pan Q, Zhao J, Xia K.

Psychiatr Genet. 2010 Jun;20(3):113-7. doi: 10.1097/YPG.0b013e32833a216f.

PMID:
20414140
16.

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 15;441(1):56-60. doi: 10.1016/j.neulet.2008.06.022.

PMID:
18597938
17.

Association of the growth hormone receptor gene polymorphisms with mandibular height in a Korean population.

Kang EH, Yamaguchi T, Tajima A, Nakajima T, Tomoyasu Y, Watanabe M, Yamaguchi M, Park SB, Maki K, Inoue I.

Arch Oral Biol. 2009 Jun;54(6):556-62. doi: 10.1016/j.archoralbio.2009.03.002.

PMID:
19344888
19.

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
20.

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.

PMID:
17428563
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