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Items: 10

1.

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

Auer PL, Johnsen JM, Johnson AD, Logsdon BA, Lange LA, Nalls MA, Zhang G, Franceschini N, Fox K, Lange EM, Rich SS, O'Donnell CJ, Jackson RD, Wallace RB, Chen Z, Graubert TA, Wilson JG, Tang H, Lettre G, Reiner AP, Ganesh SK, Li Y.

Am J Hum Genet. 2012 Nov 2;91(5):794-808. doi: 10.1016/j.ajhg.2012.08.031. Epub 2012 Oct 25.

2.

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.

3.

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
4.

Recent developments in genome and exome-wide analyses of plasma lipids.

Lange LA, Willer CJ, Rich SS.

Curr Opin Lipidol. 2015 Apr;26(2):96-102. doi: 10.1097/MOL.0000000000000159. Review.

PMID:
25692345
5.

Statistical methods for genome-wide and sequencing association studies of complex traits in related samples.

Thornton TA.

Curr Protoc Hum Genet. 2015 Jan 20;84:1.28.1-9. doi: 10.1002/0471142905.hg0128s84. Review.

6.

The role and challenges of exome sequencing in studies of human diseases.

Wang Z, Liu X, Yang BZ, Gelernter J.

Front Genet. 2013 Aug 26;4:160. doi: 10.3389/fgene.2013.00160. Review.

7.

Identifying functional noncoding variants from genome-wide association studies for cardiovascular disease and related traits.

Smith AJ, Humphries SE, Talmud PJ.

Curr Opin Lipidol. 2015 Apr;26(2):120-6. doi: 10.1097/MOL.0000000000000158. Review.

PMID:
25692342
8.

Discovery of rare variants for complex phenotypes.

Kosmicki JA, Churchhouse CL, Rivas MA, Neale BM.

Hum Genet. 2016 Jun;135(6):625-34. doi: 10.1007/s00439-016-1679-1. Epub 2016 May 24. Review.

PMID:
27221085
9.

The Arab genome: Health and wealth.

Zayed H.

Gene. 2016 Nov 5;592(2):239-43. doi: 10.1016/j.gene.2016.07.007. Epub 2016 Jul 5. Review.

PMID:
27393651
10.

Inherited platelet disorders: toward DNA-based diagnosis.

Lentaigne C, Freson K, Laffan MA, Turro E, Ouwehand WH; BRIDGE-BPD Consortium and the ThromboGenomics Consortium.

Blood. 2016 Jun 9;127(23):2814-23. doi: 10.1182/blood-2016-03-378588. Epub 2016 Apr 19. Review.

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