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Human Molecular Genetics|August 17, 2005
A comparison of tagging methods and their tagging spaceXiayi Ke, Marcos M Miretti, John Broxholme, et al.Genetic Epidemiology|January 21, 2010
Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control groupJoanna J Zhuang, Krina Zondervan, Fredrik Nyberg, et al.American Journal of Human Genetics|July 1, 2008
Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platformsCarl A Anderson, Fredrik H Pettersson, Jeffrey C Barrett, et al.Nature Protocols|April 25, 2009
Marker selection for genetic case-control association studiesFredrik H Pettersson, Carl A Anderson, Geraldine M Clarke, et al.Nature Reviews. Genetics|April 10, 2008
Genome-wide association studies for complex traits: consensus, uncertainty and challengesMark I McCarthy, Gonçalo R Abecasis, Lon R Cardon, et al.Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 20, 2020
It's in the Bloody Genes!David M EvansAmerican Journal of Medical Genetics|March 29, 2002
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorderErik G Willcutt, Bruce F Pennington, Shelley D Smith, et al.Nature Genetics|November 1, 2005
An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data setsEleftheria Zeggini, William Rayner, Andrew P Morris, et al.American Journal of Medical Genetics|September 5, 2002
Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease geneticsDavid A van Heel, Dermot P B McGovern, Lon R Cardon, et al.Pageof 38