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Nature Genetics|May 12, 2009
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetesJeffrey C Barrett, David G Clayton, Patrick Concannon, et al.Nature|September 28, 2018
Common genetic variants contribute to risk of rare severe neurodevelopmental disordersMari E K Niemi, Hilary C Martin, Daniel L Rice, et al.Nature Genetics|July 1, 2008
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseJeffrey C Barrett, Sarah Hansoul, Dan L Nicolae, et al.Human Molecular Genetics|February 27, 2009
Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' diseaseOliver J Brand, Jeffrey C Barrett, Matthew J Simmonds, et al.Nature Genetics|March 17, 2015
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migrationJames Curtis, Yang Luo, Helen L Zenner, et al.Nature Genetics|September 11, 2012
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosisJimmy Z Liu, Mohamed A Almarri, Daniel J Gaffney, et al.Nature|November 20, 2024
Examining the role of common variants in rare neurodevelopmental conditionsQin Qin Huang, Emilie M Wigdor, Daniel S Malawsky, et al.Nature Genetics|June 27, 2017
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disabilityTarjinder Singh, James T R Walters, Mandy Johnstone, et al.Gastroenterology|October 11, 2019
HLA-DQA1*05 Carriage Associated With Development of Anti-Drug Antibodies to Infliximab and Adalimumab in Patients With Crohn's DiseaseAleksejs Sazonovs, Nicholas A Kennedy, Loukas Moutsianas, et al.Plos Genetics|August 20, 2011
Pervasive sharing of genetic effects in autoimmune diseaseChris Cotsapas, Benjamin F Voight, Elizabeth Rossin, et al.Pageof 19