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Journal of Autoimmunity|August 11, 2015
Understanding inflammatory bowel disease via immunogeneticsKatrina M de Lange, Jeffrey C BarrettHuman Molecular Genetics|September 1, 2010
Synthetic associations in the context of genome-wide association scan signalsGisela Orozco, Jeffrey C Barrett, Eleftheria ZegginiNature Reviews. Genetics|September 16, 2015
Using human genetics to make new medicinesJeffrey C Barrett, Ian Dunham, Ewan BirneyGenetic 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.European Journal of Human Genetics : EJHG|March 3, 2011
Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference setsLuke Jostins, Katherine I Morley, Jeffrey C BarrettPlos One|November 9, 2013
Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experimentsLuke Jostins, Adam P Levine, Jeffrey C BarrettNature 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.American 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.Genome Research|October 28, 2005
Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variantsRobert Lawrence, David M Evans, Andrew P Morris, et al.Pageof 19