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Items: 1 to 20 of 166

1.

beta2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort.

Cheslack-Postava K, Fallin MD, Avramopoulos D, Connors SL, Zimmerman AW, Eberhart CG, Newschaffer CJ.

Mol Psychiatry. 2007 Mar;12(3):283-91. Epub 2007 Jan 2.

PMID:
17199132
2.

HLA-DR4 as a risk allele for autism acting in mothers of probands possibly during pregnancy.

Johnson WG, Buyske S, Mars AE, Sreenath M, Stenroos ES, Williams TA, Stein R, Lambert GH.

Arch Pediatr Adolesc Med. 2009 Jun;163(6):542-6. doi: 10.1001/archpediatrics.2009.74.

PMID:
19487610
3.

Possible association between the androgen receptor gene and autism spectrum disorder.

Henningsson S, Jonsson L, Ljunggren E, Westberg L, Gillberg C, Råstam M, Anckarsäter H, Nygren G, Landén M, Thuresson K, Betancur C, Leboyer M, Gillberg C, Eriksson E, Melke J.

Psychoneuroendocrinology. 2009 Jun;34(5):752-61. doi: 10.1016/j.psyneuen.2008.12.007. Epub 2009 Jan 23.

4.

Association of codon 16 and codon 27 beta 2-adrenergic receptor gene polymorphisms with obesity: a meta-analysis.

Jalba MS, Rhoads GG, Demissie K.

Obesity (Silver Spring). 2008 Sep;16(9):2096-106.

PMID:
19186333
5.

Association of beta-adrenoceptor polymorphisms with cardiac autonomic modulation in Japanese males.

Matsunaga T, Yasuda K, Adachi T, Gu N, Yamamura T, Moritani T, Tsujimoto G, Tsuda K.

Am Heart J. 2007 Oct;154(4):759-66.

PMID:
17893006
6.

Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence.

Chu X, Dong Y, Shen M, Sun L, Dong C, Wang Y, Wang B, Zhang K, Hua Q, Xu S, Huang W.

BMC Med Genet. 2009 Mar 13;10:26. doi: 10.1186/1471-2350-10-26.

7.

Polymorphic variants of the beta2-adrenergic receptor (ADRB2) gene and ADRB2-related propanolol-induced dyslipidemia in the Colombian population.

Isaza C, Henao J, Ramirez E, Cuesta F, Cacabelos R.

Methods Find Exp Clin Pharmacol. 2005 May;27(4):237-44.

PMID:
16082424
8.

Associations of beta2-adrenergic receptor genotypes and haplotypes with wheezing illness in Taiwanese schoolchildren.

Lee YL, Wang ST, Tsai CH, Guo YL.

Allergy. 2009 Oct;64(10):1451-7. doi: 10.1111/j.1398-9995.2009.02020.x. Epub 2009 Feb 25.

PMID:
19254291
9.

Association of beta-1 and beta-2 adrenergic receptor gene polymorphisms with myocardial infarction.

Yilmaz A, Kaya MG, Merdanoglu U, Ergun MA, Cengel A, Menevse S.

J Clin Lab Anal. 2009;23(4):237-43. doi: 10.1002/jcla.20327.

PMID:
19623647
11.

Evaluation of FOXP2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Pietila J, Goedken RJ, Folstein SE, Sheffield VC.

Am J Med Genet. 2002 Jul 8;114(5):566-9.

PMID:
12116195
12.

Beta2-adrenergic receptor gene polymorphisms and risk of ischemic stroke.

Stanzione R, Di Angelantonio E, Evangelista A, Barbato D, Marchitti S, Zanda B, Pirisi A, Quarta G, Volpe M, Rubattu S.

Am J Hypertens. 2007 Jun;20(6):657-62.

PMID:
17531924
13.

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
14.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.

Wassink TH, Piven J, Vieland VJ, Jenkins L, Frantz R, Bartlett CW, Goedken R, Childress D, Spence MA, Smith M, Sheffield VC.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):36-44.

PMID:
15892143
15.

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.

16.

Linkage and association of the glutamate receptor 6 gene with autism.

Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T; Paris Autism Research International Sibpair (PARIS) Study.

Mol Psychiatry. 2002;7(3):302-10.

17.
18.

Family-based and population study of a functional promoter-region monoamine oxidase A polymorphism in autism: possible association with IQ.

Yirmiya N, Pilowsky T, Tidhar S, Nemanov L, Altmark L, Ebstein RP.

Am J Med Genet. 2002 Apr 8;114(3):284-7.

PMID:
11920849
19.

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
20.

Family-based association study between autism and glutamate receptor 6 gene in Chinese Han trios.

Shuang M, Liu J, Jia MX, Yang JZ, Wu SP, Gong XH, Ling YS, Ruan Y, Yang XL, Zhang D.

Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):48-50.

PMID:
15389769

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