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Genome Research|October 28, 2005
Calibrating a coalescent simulation of human genome sequence variationStephen F Schaffner, Catherine Foo, Stacey Gabriel, et al.Science (New York, N.Y.)|November 8, 2008
Genetic mapping in human diseaseDavid Altshuler, Mark J Daly, Eric S LanderNature Genetics|August 6, 2002
Human genome sequence variation and the influence of gene history, mutation and recombinationDavid E Reich, Stephen F Schaffner, Mark J Daly, et al.Genetic Epidemiology|March 19, 2008
Estimation of the multiple testing burden for genomewide association studies of nearly all common variantsItsik Pe'er, Roman Yelensky, David Altshuler, et al.Plos Genetics|August 18, 2010
Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traitsAyellet V Segrè, , , et al.Nature Genetics|August 29, 2006
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degenerationJulian Maller, Sarah George, Shaun Purcell, et al.Nature Genetics|May 23, 2006
Evaluating and improving power in whole-genome association studies using fixed marker setsItsik Pe'er, Paul I W de Bakker, Julian Maller, et al.European Journal of Human Genetics : EJHG|September 10, 2015
Phenotypic extremes in rare variant study designsGina M Peloso, Daniel J Rader, Stacey Gabriel, et al.American Journal of Human Genetics|April 17, 2004
Methods for high-density admixture mapping of disease genesNick Patterson, Neil Hattangadi, Barton Lane, et al.Plos Genetics|September 15, 2010
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain functionSoumya Raychaudhuri, Joshua M Korn, Steven A McCarroll, et al.Pageof 119