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Results: 1 to 20 of 581

1.

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. Epub 2007 Sep 25.

PMID:
17893705
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

Associations between the oxytocin receptor gene (OXTR) and affect, loneliness and intelligence in normal subjects.

Lucht MJ, Barnow S, Sonnenfeld C, Rosenberger A, Grabe HJ, Schroeder W, Völzke H, Freyberger HJ, Herrmann FH, Kroemer H, Rosskopf D.

Prog Neuropsychopharmacol Biol Psychiatry. 2009 Aug 1;33(5):860-6. doi: 10.1016/j.pnpbp.2009.04.004. Epub 2009 Apr 17.

PMID:
19376182
[PubMed - indexed for MEDLINE]
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.

PMID:
19777562
[PubMed - indexed for MEDLINE]
6.

Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study: mediation by socialization skills.

Yirmiya N, Rosenberg C, Levi S, Salomon S, Shulman C, Nemanov L, Dina C, Ebstein RP.

Mol Psychiatry. 2006 May;11(5):488-94.

PMID:
16520824
[PubMed - indexed for MEDLINE]
7.

Molecular genetic studies of the arginine vasopressin 1a receptor (AVPR1a) and the oxytocin receptor (OXTR) in human behaviour: from autism to altruism with some notes in between.

Israel S, Lerer E, Shalev I, Uzefovsky F, Reibold M, Bachner-Melman R, Granot R, Bornstein G, Knafo A, Yirmiya N, Ebstein RP.

Prog Brain Res. 2008;170:435-49. doi: 10.1016/S0079-6123(08)00434-2. Review.

PMID:
18655900
[PubMed - indexed for MEDLINE]
8.

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. Epub 2007 Feb 3.

PMID:
17383819
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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
[PubMed - indexed for MEDLINE]
10.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

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

PMID:
15121991
[PubMed - indexed for MEDLINE]
11.

Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD).

Zhou XL, Giacobini M, Anderlid BM, Anckarsäter H, Omrani D, Gillberg C, Nordenskjöld M, Lindblom A.

Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):351-4.

PMID:
17221838
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

Association between the oxytocin receptor gene and amygdalar volume in healthy adults.

Inoue H, Yamasue H, Tochigi M, Abe O, Liu X, Kawamura Y, Takei K, Suga M, Yamada H, Rogers MA, Aoki S, Sasaki T, Kasai K.

Biol Psychiatry. 2010 Dec 1;68(11):1066-72. doi: 10.1016/j.biopsych.2010.07.019. Epub 2010 Sep 15.

PMID:
20832055
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

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.

PMID:
16080114
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Brief report: the Vineland Adaptive Behavior Scales in young children with autism spectrum disorders at different cognitive levels.

Perry A, Flanagan HE, Dunn Geier J, Freeman NL.

J Autism Dev Disord. 2009 Jul;39(7):1066-78. doi: 10.1007/s10803-009-0704-9. Epub 2009 Feb 21.

PMID:
19234777
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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
[PubMed - indexed for MEDLINE]
19.

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.

Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):628-36. doi: 10.1002/ajmg.b.30655.

PMID:
18205172
[PubMed - indexed for MEDLINE]
20.

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. Epub 2008 Jun 13.

PMID:
18597938
[PubMed - indexed for MEDLINE]

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