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Nature Neuroscience|November 8, 2016
Ultra-rare disruptive and damaging mutations influence educational attainment in the general populationAndrea Ganna, Giulio Genovese, Daniel P Howrigan, et al.
Nature Methods|June 23, 2014
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomicsAlicia Lundby, Elizabeth J Rossin, Annette B Steffensen, et al.
Nature Genetics|December 25, 2012
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretionJeroen R Huyghe, Anne U Jackson, Marie P Fogarty, et al.
Nature Neuroscience|August 6, 2013
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disordersGeorg Stoll, Olli P H Pietiläinen, Bastian Linder, et al.
Annals of Neurology|January 26, 2007
A second major histocompatibility complex susceptibility locus for multiple sclerosisTai Wai Yeo, Philip L De Jager, Simon G Gregory, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2009
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases, John D Rioux, Philippe Goyette, et al.
Plos Genetics|September 27, 2013
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitisMélissa Beaudoin, Philippe Goyette, Gabrielle Boucher, et al.
Nature Communications|September 5, 2014
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B allelesJacqueline I Goldstein, L Fredrik Jarskog, Chris Hilliard, et al.
Medrxiv : the Preprint Server for Health Sciences|November 25, 2020
Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancerSeyedeh M Zekavat, Shu-Hong Lin, Alexander G Bick, et al.
Nature Communications|April 20, 2023
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patientsYiming Wu, Kyle Gettler, Meltem Ece Kars, et al.
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