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Results: 1 to 20 of 56

Related Articles by Review for PubMed (Select 20395971)

1.

Mendelian disorders and multifactorial traits: the big divide or one for all?

Antonarakis SE, Chakravarti A, Cohen JC, Hardy J.

Nat Rev Genet. 2010 May;11(5):380-4. doi: 10.1038/nrg2793.

PMID:
20395971
2.

Common disorders are quantitative traits.

Plomin R, Haworth CM, Davis OS.

Nat Rev Genet. 2009 Dec;10(12):872-8. doi: 10.1038/nrg2670. Epub 2009 Oct 27. Review.

PMID:
19859063
3.

Resolving the variable genome and epigenome in human disease.

Knight JC.

J Intern Med. 2012 Apr;271(4):379-91. doi: 10.1111/j.1365-2796.2011.02508.x. Review.

4.

Genome-wide epigenetic data facilitate understanding of disease susceptibility association studies.

Hardison RC.

J Biol Chem. 2012 Sep 7;287(37):30932-40. doi: 10.1074/jbc.R112.352427. Epub 2012 Sep 5. Review.

5.

Genome-wide association studies: a new window into immune-mediated diseases.

Xavier RJ, Rioux JD.

Nat Rev Immunol. 2008 Aug;8(8):631-43. doi: 10.1038/nri2361. Review.

6.

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.

7.

Progress and promise of genome-wide association studies for human complex trait genetics.

Stranger BE, Stahl EA, Raj T.

Genetics. 2011 Feb;187(2):367-83. doi: 10.1534/genetics.110.120907. Epub 2010 Nov 29. Review.

8.

Whole-genome and whole-exome sequencing in neurological diseases.

Foo JN, Liu JJ, Tan EK.

Nat Rev Neurol. 2012 Sep;8(9):508-17. doi: 10.1038/nrneurol.2012.148. Epub 2012 Jul 31. Review.

PMID:
22847385
9.

Genetic mapping in human disease.

Altshuler D, Daly MJ, Lander ES.

Science. 2008 Nov 7;322(5903):881-8. doi: 10.1126/science.1156409. Review.

10.

Uncovering the roles of rare variants in common disease through whole-genome sequencing.

Cirulli ET, Goldstein DB.

Nat Rev Genet. 2010 Jun;11(6):415-25. doi: 10.1038/nrg2779. Review.

PMID:
20479773
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.

The genome-wide association study--a new era for common polygenic disorders.

Roberts R, Wells GA, Stewart AF, Dandona S, Chen L.

J Cardiovasc Transl Res. 2010 Jun;3(3):173-82. doi: 10.1007/s12265-010-9178-6. Epub 2010 Mar 27. Review.

PMID:
20560037
13.

Beyond Mendel: an evolving view of human genetic disease transmission.

Badano JL, Katsanis N.

Nat Rev Genet. 2002 Oct;3(10):779-89. Review.

PMID:
12360236
14.

Genome-wide association studies and infectious disease.

Bowcock AM.

Crit Rev Immunol. 2010;30(3):305-9. Review.

PMID:
20370638
15.

Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X.

Ku CS, Cooper DN, Wu M, Roukos DH, Pawitan Y, Soong R, Iacopetta B.

Mod Pathol. 2012 Aug;25(8):1055-68. doi: 10.1038/modpathol.2012.62. Epub 2012 Apr 20. Review.

16.

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
17.

Modifier genes in Mendelian disorders: the example of cystic fibrosis.

Cutting GR.

Ann N Y Acad Sci. 2010 Dec;1214:57-69. doi: 10.1111/j.1749-6632.2010.05879.x. Review.

18.

Rare-variant genome-wide association studies: a new frontier in genetic analysis of complex traits.

Wagner MJ.

Pharmacogenomics. 2013 Mar;14(4):413-24. doi: 10.2217/pgs.13.36. Review.

PMID:
23438888
19.

Common variants in polygenic schizophrenia.

Glessner JT, Hakonarson H.

Genome Biol. 2009;10(9):236. doi: 10.1186/gb-2009-10-9-236. Epub 2009 Sep 29. Review.

20.

[Genome-wide association study on complex diseases: study design and genetic markers].

Yan WL.

Yi Chuan. 2008 Apr;30(4):400-6. Review. Chinese.

PMID:
18424408
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