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Items: 1 to 20 of 30

1.

Common and rare variants in multifactorial susceptibility to common diseases.

Bodmer W, Bonilla C.

Nat Genet. 2008 Jun;40(6):695-701. doi: 10.1038/ng.f.136. Review.

2.

Identifying rare variants associated with complex traits via sequencing.

Li B, Liu DJ, Leal SM.

Curr Protoc Hum Genet. 2013 Jul;Chapter 1:Unit 1.26. doi: 10.1002/0471142905.hg0126s78. Review.

3.

In search of low-frequency and rare variants affecting complex traits.

Panoutsopoulou K, Tachmazidou I, Zeggini E.

Hum Mol Genet. 2013 Oct 15;22(R1):R16-21. doi: 10.1093/hmg/ddt376. Epub 2013 Aug 6. Review.

4.

Genome-wide association studies for common diseases and complex traits.

Hirschhorn JN, Daly MJ.

Nat Rev Genet. 2005 Feb;6(2):95-108. Review.

PMID:
15716906
5.

[Progress in genetic association study for multifactorial diseases].

Yamamoto K.

Nihon Rinsho. 2009 Jun;67(6):1063-7. Review. Japanese.

PMID:
19507493
6.

Linkage analysis in the next-generation sequencing era.

Bailey-Wilson JE, Wilson AF.

Hum Hered. 2011;72(4):228-36. doi: 10.1159/000334381. Epub 2011 Dec 23. Review.

7.

Emerging trends in the search for genetic variants predisposing to human obesity.

Swarbrick MM, Vaisse C.

Curr Opin Clin Nutr Metab Care. 2003 Jul;6(4):369-75. Review.

PMID:
12806208
8.

Finding genes that underlie complex traits.

Glazier AM, Nadeau JH, Aitman TJ.

Science. 2002 Dec 20;298(5602):2345-9. Review.

PMID:
12493905
9.

Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.

Fearnhead NS, Winney B, Bodmer WF.

Cell Cycle. 2005 Apr;4(4):521-5. Epub 2005 Apr 7. Review.

PMID:
15753653
10.

Common and rare alleles as causes of complex phenotypes.

Polychronakos C.

Curr Atheroscler Rep. 2008 Jun;10(3):194-200. Review.

PMID:
18489846
11.

Genome-wide association studies: results from the first few years and potential implications for clinical medicine.

Hirschhorn JN, Gajdos ZK.

Annu Rev Med. 2011;62:11-24. doi: 10.1146/annurev.med.091708.162036. Review.

PMID:
21226609
12.

Height matters-from monogenic disorders to normal variation.

Durand C, Rappold GA.

Nat Rev Endocrinol. 2013 Mar;9(3):171-7. doi: 10.1038/nrendo.2012.251. Epub 2013 Jan 22. Review.

PMID:
23337954
13.

Estimation and partition of heritability in human populations using whole-genome analysis methods.

Vinkhuyzen AA, Wray NR, Yang J, Goddard ME, Visscher PM.

Annu Rev Genet. 2013;47:75-95. doi: 10.1146/annurev-genet-111212-133258. Epub 2013 Aug 22. Review.

14.

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

Visscher PM, Goddard ME, Derks EM, Wray NR.

Mol Psychiatry. 2012 May;17(5):474-85. doi: 10.1038/mp.2011.65. Epub 2011 Jun 14. Review.

PMID:
21670730
15.

Genetic susceptibility to autoimmune thyroid disease: past, present, and future.

Tomer Y.

Thyroid. 2010 Jul;20(7):715-25. doi: 10.1089/thy.2010.1644. Review.

16.

Type 2 diabetes: new genes, new understanding.

Prokopenko I, McCarthy MI, Lindgren CM.

Trends Genet. 2008 Dec;24(12):613-21. doi: 10.1016/j.tig.2008.09.004. Epub 2008 Oct 25. Review.

PMID:
18952314
17.

Genetics of rheumatoid arthritis: an impressionist perspective.

Jacob N, Jacob CO.

Rheum Dis Clin North Am. 2012 May;38(2):243-57. doi: 10.1016/j.rdc.2012.05.001. Epub 2012 Jun 22. Review.

PMID:
22819082
18.

Strategic approaches to unraveling genetic causes of cardiovascular diseases.

Marian AJ, Belmont J.

Circ Res. 2011 May 13;108(10):1252-69. doi: 10.1161/CIRCRESAHA.110.236067. Review.

19.

Genetics of the autoimmune polyglandular syndrome type 3 variant.

Dittmar M, Kahaly GJ.

Thyroid. 2010 Jul;20(7):737-43. doi: 10.1089/thy.2010.1639. Review.

PMID:
20578896
20.

Unraveling new therapeutic targets of coronary artery disease by genetic approaches.

Lee SE, Kim HS.

Circ J. 2015;79(1):8-14. doi: 10.1253/circj.CJ-14-0985. Epub 2014 Dec 12. Review.

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