Showing results (4991-5000 of 7,440) with videos related to
Sort By:
Pageof 744
Nature Genetics|February 7, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke, , Céline Bellenguez, et al.Nature Genetics|March 13, 2012
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephronHélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, et al.Nature Genetics|March 13, 2012
Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expressionJohannes Schödel, Chiara Bardella, Lina K Sciesielski, et al.Nature Genetics|August 2, 2011
Common variation at 10p12.31 near MLLT10 influences meningioma riskSara E Dobbins, Peter Broderick, Beatrice Melin, et al.Nature Genetics|August 2, 2011
Analysis of the coding genome of diffuse large B-cell lymphomaLaura Pasqualucci, Vladimir Trifonov, Giulia Fabbri, et al.Nature Genetics|August 16, 2011
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduriaJennifer L Sloan, Jennifer J Johnston, Irini Manoli, et al.Nature Genetics|August 16, 2011
A genome-wide association study identifies two new risk loci for Graves' diseaseXun Chu, Chun-Ming Pan, Shuang-Xia Zhao, et al.Nature Genetics|July 22, 2011
Analyses of X-linked and autosomal genetic variation in population-scale whole genome sequencingSrikanth Gottipati, Leonardo Arbiza, Adam Siepel, et al.Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.Nature Genetics|December 7, 2010
CEP152 is a genome maintenance protein disrupted in Seckel syndromeErsan Kalay, Gökhan Yigit, Yakup Aslan, et al.Pageof 744