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Items: 1 to 20 of 94

1.

Problems of reporting genetic associations with complex outcomes.

Colhoun HM, McKeigue PM, Davey Smith G.

Lancet. 2003 Mar 8;361(9360):865-72. Review.

PMID:
12642066
2.

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease.

Lohmueller KE, Pearce CL, Pike M, Lander ES, Hirschhorn JN.

Nat Genet. 2003 Feb;33(2):177-82. Epub 2003 Jan 13.

PMID:
12524541
3.

A1166C genetic variation of the angiotensin II type I receptor gene and susceptibility to coronary heart disease: collaborative of 53 studies with 20,435 cases and 23,674 controls.

Xu M, Sham P, Ye Z, Lindpaintner K, He L.

Atherosclerosis. 2010 Nov;213(1):191-9. doi: 10.1016/j.atherosclerosis.2010.07.046. Epub 2010 Aug 4.

PMID:
20732682
4.

Quantitative assessment of the effect of angiotensinogen gene polymorphisms on the risk of coronary heart disease.

Xu MQ, Ye Z, Hu FB, He L.

Circulation. 2007 Sep 18;116(12):1356-66. Epub 2007 Sep 10.

5.

Analyses of associations with asthma in four asthma population samples from Canada and Australia.

Daley D, Lemire M, Akhabir L, Chan-Yeung M, He JQ, McDonald T, Sandford A, Stefanowicz D, Tripp B, Zamar D, Bosse Y, Ferretti V, Montpetit A, Tessier MC, Becker A, Kozyrskyj AL, Beilby J, McCaskie PA, Musk B, Warrington N, James A, Laprise C, Palmer LJ, Paré PD, Hudson TJ.

Hum Genet. 2009 May;125(4):445-59. doi: 10.1007/s00439-009-0643-8. Epub 2009 Feb 27.

PMID:
19247692
6.

Associations of ACE I/D, AGT M235T gene polymorphisms with pregnancy induced hypertension in Chinese population: a meta-analysis.

Zhu M, Zhang J, Nie S, Yan W.

J Assist Reprod Genet. 2012 Sep;29(9):921-32. doi: 10.1007/s10815-012-9800-4. Epub 2012 May 30.

7.
8.

Case-control studies in the genomic era: a clinician's guide.

Healy DG.

Lancet Neurol. 2006 Aug;5(8):701-7. Review.

PMID:
16857576
9.

Genetic association studies in ischaemic stroke: replication failure and prospects.

Pruissen DM, Kappelle LJ, Rosendaal FR, Algra A.

Cerebrovasc Dis. 2009;27(3):290-4. doi: 10.1159/000199467. Epub 2009 Feb 6. Review.

10.

Design considerations for genetic linkage and association studies.

Nsengimana J, Bishop DT.

Methods Mol Biol. 2012;850:237-62. doi: 10.1007/978-1-61779-555-8_13.

PMID:
22307702
11.

Using step-wise linear regression to detect "functional" sequence variants: application to simulated data.

Mitchell BD, Hsueh WC, Schneider JL, Blangero J.

Genet Epidemiol. 2001;21 Suppl 1:S353-7.

PMID:
11793697
12.
13.

Population genomics in Sardinia: a novel approach to hunt for genomic combinations underlying complex traits and diseases.

Siniscalco M, Robledo R, Bender PK, Carcassi C, Contu L, Beck JC.

Cytogenet Cell Genet. 1999;86(2):148-52. Erratum in: Cytogenet Cell Genet 1999;87(3-4):296.

PMID:
10545707
15.
16.

Genetic variants of the monocyte chemoattractant protein-1 gene and its receptor CCR2 and risk of coronary artery disease: a meta-analysis.

Wang Y, Zhang W, Li S, Song W, Chen J, Hui R.

Atherosclerosis. 2011 Nov;219(1):224-30. doi: 10.1016/j.atherosclerosis.2011.07.116. Epub 2011 Aug 4.

PMID:
21868018
17.

ABCA1 rs4149313 polymorphism and susceptibility to coronary heart disease: a meta-analysis.

Fan SL, Li X, Chen SJ, Qi GX.

Ann Hum Genet. 2014 Jul;78(4):264-76. doi: 10.1111/ahg.12068.

18.

Bias: a review of current understanding.

Adebiyi AO.

Afr J Med Med Sci. 2010 Sep;39(3):241-8. Review.

PMID:
21416795
19.
20.

Genetic variation of the ATP-binding cassette transporter A1 and susceptibility to coronary heart disease.

Jiang Z, Zhou R, Xu C, Feng G, Zhou Y.

Mol Genet Metab. 2011 May;103(1):81-8. doi: 10.1016/j.ymgme.2011.01.005. Epub 2011 Jan 22.

PMID:
21300560
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