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Biorxiv : the Preprint Server for Biology|November 24, 2025
Comprehensive gene heritability estimation reveals the genetic architecture of rare coding variants underlying complex traitsZhengtong Liu, Boyang Fu, Moonseong Jeong, et al.Nature Communications|June 5, 2025
Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditionsAngela Wei, Richard Border, Boyang Fu, et al.Perspectives on Psychological Science : a Journal of the Association for Psychological Science|January 27, 2015
Candidate gene-environment interaction research: reflections and recommendationsDanielle M Dick, Arpana Agrawal, Matthew C Keller, et al.Nature Communications|May 6, 2024
Genetic influence on within-person longitudinal change in anthropometric traits in the UK BiobankKathryn E Kemper, Julia Sidorenko, Huanwei Wang, et al.Nature Communications|February 17, 2021
Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individualsKathryn E Kemper, Loic Yengo, Zhili Zheng, et al.Science (New York, N.Y.)|November 17, 2022
Cross-trait assortative mating is widespread and inflates genetic correlation estimatesRichard Border, Georgios Athanasiadis, Alfonso Buil, et al.American Journal of Human Genetics|May 13, 2023
Declining autozygosity over time: An exploration in over 1 million individuals from three diverse cohortsSarah M C Colbert, Frank R Wendt, Gita A Pathak, et al.BMC Proceedings|March 1, 2012
Mutational load analysis of unrelated individualsDaniel P Howrigan, Matthew A Simonson, Helen M Kamens, et al.Nature Genetics|November 21, 2023
Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorderAndrew Dahl, Michael Thompson, Ulzee An, et al.Nature Genetics|February 21, 2012
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPsS Hong Lee, Teresa R DeCandia, Stephan Ripke, et al.Pageof 14