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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 Medicine|February 23, 2026
Genetic regulation across germline and somatic variation on the Y chromosome contributes to type 2 diabetesGo Sato, Yuji Yamamoto, Kyuto Sonehara, et al.Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in All of UsWenhan Lu, Robert J Carroll, Matthew Solomonson, et al.Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.Gastroenterology|April 30, 2013
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studiesDavid Ellinghaus, Hu Zhang, Sebastian Zeissig, et al.Nature Genetics|March 16, 2010
Genome-wide association identifies multiple ulcerative colitis susceptibility lociDermot P B McGovern, Agnès Gardet, Leif Törkvist, 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.The Journal of Clinical Investigation|September 25, 2014
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathyMichaela Yuen, Sarah A Sandaradura, James J Dowling, 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.Nature Medicine|March 30, 2026
Deleterious coding variation associated with autism is shared across ancestriesMarina Natividad Avila, Seulgi Jung, F Kyle Satterstrom, et al.Pageof 163