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Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.Nature Communications|May 17, 2019
Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitisJohn A Lees, Bart Ferwerda, Philip H C Kremer, et al.Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.Nature Genetics|November 8, 2011
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseGosia Trynka, Karen A Hunt, Nicholas A Bockett, et al.Plos One|November 1, 2008
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studiesBrendan J Keating, Sam Tischfield, Sarah S Murray, et al.Nature Genetics|August 2, 2016
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencingAlejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, et al.Nature Genetics|March 2, 2010
Multiple common variants for celiac disease influencing immune gene expressionPatrick C A Dubois, Gosia Trynka, Lude Franke, et al.Nature Genetics|October 24, 2007
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants, , Paul R Burton, et al.Nature Genetics|November 25, 2010
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility lociAndre Franke, Dermot P B McGovern, Jeffrey C Barrett, et al.Nature Genetics|August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputationShane McCarthy, Sayantan Das, Warren Kretzschmar, et al.Pageof 19