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Items: 1 to 20 of 119

1.

Associations between single-nucleotide polymorphism in the FNDC3A and autism spectrum disorder in a Korean population.

Ro M, Park J, Nam M, Bang HJ, Yang JW, Choi KS, Kim SK, Chung JH, Kwack K.

Psychiatry Res. 2013 Sep 30;209(2):246-8. doi: 10.1016/j.psychres.2013.02.028. Epub 2013 Apr 29.

PMID:
23639254
2.

Association with tryptophan hydroxylase 2 gene polymorphisms and autism spectrum disorders in Korean families.

Yang SY, Yoo HJ, Cho IH, Park M, Kim SA.

Neurosci Res. 2012 Aug;73(4):333-6. doi: 10.1016/j.neures.2012.05.012. Epub 2012 Jun 12.

PMID:
22698779
3.

Association between peroxisomal biogenesis factor 7 and autism spectrum disorders in a Korean population.

Ro M, Park J, Nam M, Bang HJ, Yang J, Choi KS, Kim SK, Chung JH, Kwack K.

J Child Neurol. 2012 Oct;27(10):1270-5. Epub 2012 Feb 28.

PMID:
22378669
4.

Association of the catechol-o-methyltransferase gene polymorphisms with Korean autism spectrum disorders.

Yoo HJ, Cho IH, Park M, Yang SY, Kim SA.

J Korean Med Sci. 2013 Sep;28(9):1403-6. doi: 10.3346/jkms.2013.28.9.1403. Epub 2013 Aug 28.

5.

MTHFR 1298A>C is a risk factor for autism spectrum disorder in the Korean population.

Park J, Ro M, Pyun JA, Nam M, Bang HJ, Yang JW, Choi KS, Kim SK, Chung JH, Kwack K.

Psychiatry Res. 2014 Jan 30;215(1):258-9. doi: 10.1016/j.psychres.2013.11.006. Epub 2013 Nov 18. No abstract available.

PMID:
24295761
6.

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. Epub 2010 Jun 3.

PMID:
20523082
7.

Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios.

Cho IH, Yoo HJ, Park M, Lee YS, Kim SA.

Brain Res. 2007 Mar 30;1139:34-41. Epub 2007 Jan 8.

PMID:
17280648
8.

Genetic association analyses of neuregulin 1 gene polymorphism with endopheontype for sociality of Korean autism spectrum disorders family.

Yoo HJ, Woo RS, Cho SC, Kim BN, Kim JW, Shin MS, Park TW, Son JW, Chung US, Park S, Park M, Kim SA.

Psychiatry Res. 2015 Jun 30;227(2-3):366-8. doi: 10.1016/j.psychres.2015.03.015. Epub 2015 Mar 23. Erratum in: Psychiatry Res. 2015 Nov 30;230(1):120.

PMID:
25858800
9.

A detailed association analysis between the tryptophan hydroxylase 2 (TPH2) gene and autism spectrum disorders in a Japanese population.

Egawa J, Watanabe Y, Nunokawa A, Endo T, Kaneko N, Tamura R, Sugiyama T, Someya T.

Psychiatry Res. 2012 Apr 30;196(2-3):320-2. doi: 10.1016/j.psychres.2011.09.001. Epub 2012 Feb 22.

PMID:
22361444
10.

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. Epub 2010 Jan 22.

PMID:
20094064
11.

Further evidence for the role of MET in autism susceptibility.

Thanseem I, Nakamura K, Miyachi T, Toyota T, Yamada S, Tsujii M, Tsuchiya KJ, Anitha A, Iwayama Y, Yamada K, Hattori E, Matsuzaki H, Matsumoto K, Iwata Y, Suzuki K, Suda S, Kawai M, Sugihara G, Takebayashi K, Takei N, Ichikawa H, Sugiyama T, Yoshikawa T, Mori N.

Neurosci Res. 2010 Oct;68(2):137-41. doi: 10.1016/j.neures.2010.06.014. Epub 2010 Jul 6.

PMID:
20615438
12.

Two genetic variants of CD38 in subjects with autism spectrum disorder and controls.

Munesue T, Yokoyama S, Nakamura K, Anitha A, Yamada K, Hayashi K, Asaka T, Liu HX, Jin D, Koizumi K, Islam MS, Huang JJ, Ma WJ, Kim UH, Kim SJ, Park K, Kim D, Kikuchi M, Ono Y, Nakatani H, Suda S, Miyachi T, Hirai H, Salmina A, Pichugina YA, Soumarokov AA, Takei N, Mori N, Tsujii M, Sugiyama T, Yagi K, Yamagishi M, Sasaki T, Yamasue H, Kato N, Hashimoto R, Taniike M, Hayashi Y, Hamada J, Suzuki S, Ooi A, Noda M, Kamiyama Y, Kido MA, Lopatina O, Hashii M, Amina S, Malavasi F, Huang EJ, Zhang J, Shimizu N, Yoshikawa T, Matsushima A, Minabe Y, Higashida H.

Neurosci Res. 2010 Jun;67(2):181-91. doi: 10.1016/j.neures.2010.03.004. Epub 2010 May 1.

PMID:
20435366
13.

Catechol-O-methyltransferase Val158Met polymorphism and risk of autism spectrum disorders.

Guo T, Wang W, Liu B, Chen H, Yang C.

J Int Med Res. 2013 Jun;41(3):725-34. doi: 10.1177/0300060513479871. Epub 2013 Apr 15.

PMID:
23613504
14.

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. Epub 2007 Mar 13.

PMID:
17428563
15.

Association of the FGA and SLC6A4 genes with autistic spectrum disorder in a Korean population.

Ro M, Won S, Kang H, Kim SY, Lee SK, Nam M, Bang HJ, Yang JW, Choi KS, Kim SK, Chung JH, Kwack K.

Neuropsychobiology. 2013;68(4):212-20. doi: 10.1159/000355299. Epub 2013 Nov 1.

PMID:
24192574
16.

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. doi: 10.1002/aur.1353. Epub 2013 Nov 18.

PMID:
24249596
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.

Association study between single nucleotide polymorphisms in promoter region of AVPR1A and Korean autism spectrum disorders.

Yang SY, Cho SC, Yoo HJ, Cho IH, Park M, Kim BN, Kim JW, Shin MS, Park TW, Son JW, Chung US, Kim HW, Yang YH, Kang JO, Kim SA.

Neurosci Lett. 2010 Aug 2;479(3):197-200. doi: 10.1016/j.neulet.2010.05.050. Epub 2010 May 28.

PMID:
20546835
19.

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. Epub 2008 Nov 30.

PMID:
19100789
20.

Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.

Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X.

PLoS One. 2013;8(2):e56639. doi: 10.1371/journal.pone.0056639. Epub 2013 Feb 26.

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