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Results: 6

Related Articles by Review for PubMed (Select 22863193)

1.

Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.

Lee S, Emond MJ, Bamshad MJ, Barnes KC, Rieder MJ, Nickerson DA; NHLBI GO Exome Sequencing Project—ESP Lung Project Team, Christiani DC, Wurfel MM, Lin X.

Am J Hum Genet. 2012 Aug 10;91(2):224-37. doi: 10.1016/j.ajhg.2012.06.007. Epub 2012 Aug 2.

2.

Molecular genetic studies of complex phenotypes.

Marian AJ.

Transl Res. 2012 Feb;159(2):64-79. doi: 10.1016/j.trsl.2011.08.001. Epub 2011 Aug 31. Review.

3.

Exome versus transcriptome sequencing in identifying coding region variants.

Ku CS, Wu M, Cooper DN, Naidoo N, Pawitan Y, Pang B, Iacopetta B, Soong R.

Expert Rev Mol Diagn. 2012 Apr;12(3):241-51. doi: 10.1586/erm.12.10. Review.

PMID:
22468815
4.

Statistical power and significance testing in large-scale genetic studies.

Sham PC, Purcell SM.

Nat Rev Genet. 2014 May;15(5):335-46. doi: 10.1038/nrg3706. Review.

PMID:
24739678
5.

Exome sequencing and complex disease: practical aspects of rare variant association studies.

Do R, Kathiresan S, Abecasis GR.

Hum Mol Genet. 2012 Oct 15;21(R1):R1-9. Epub 2012 Sep 13. Review.

6.

Whole exome sequencing of intracranial aneurysm.

Foroud T; FIA Study Investigators.

Stroke. 2013 Jun;44(6 Suppl 1):S26-8. doi: 10.1161/STROKEAHA.113.001174. Review. No abstract available.

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