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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. Lee S, et al. Among authors: 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. Am J Hum Genet. 2012. PMID: 22863193 Free PMC article.
SNP set association analysis for familial data.
Schifano ED, Epstein MP, Bielak LF, Jhun MA, Kardia SL, Peyser PA, Lin X. Schifano ED, et al. Among authors: lin x. Genet Epidemiol. 2012 Dec;36(8):797-810. doi: 10.1002/gepi.21676. Epub 2012 Sep 11. Genet Epidemiol. 2012. PMID: 22968922 Free PMC article.
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