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American Journal of Human Genetics|June 16, 2026
Genome-wide analysis implicates inner ear development in Ménière diseaseZhuozheng Shi, Ravi Mandla, Jingjing Li, et al.Genome Biology and Evolution|November 7, 2023
Genetic Analysis of Mingrelians Reveals Long-Term Continuity of Populations in Western Georgia (Caucasus)Theodore G Schurr, Ramaz Shengelia, Michel Shamoon-Pour, et al.Bioinformatics (Oxford, England)|June 5, 2014
SMaSH: a benchmarking toolkit for human genome variant callingAmeet Talwalkar, Jesse Liptrap, Julie Newcomb, et al.European Journal of Human Genetics : EJHG|February 12, 2020
The genetic history of FranceAude Saint Pierre, Joanna Giemza, Isabel Alves, et al.Plos Genetics|January 19, 2023
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohortDaniel Hui, Shadi Mehrabi, Alexandra E Quimby, et al.European Journal of Human Genetics : EJHG|March 13, 2020
Correction: The genetic history of FranceAude Saint Pierre, Joanna Giemza, Isabel Alves, et al.Elife|March 22, 2019
Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studiesMashaal Sohail, Robert M Maier, Andrea Ganna, et al.HGG Advances|June 11, 2025
Meta-analysis of uveal melanoma genome-wide association studies identifies novel risk loci and population effect size heterogeneityGeorgia Mies, Noah L Tsao, Alexandre Houy, et al.Elife|June 5, 2019
Genetic diversity of CHC22 clathrin impacts its function in glucose metabolismMatteo Fumagalli, Stephane M Camus, Yoan Diekmann, et al.Journal of Human Genetics|December 2, 2011
Exome sequencing can detect pathogenic mosaic mutations present at low allele frequenciesAlistair T Pagnamenta, Stefano Lise, Victoria Harrison, et al.Pageof 11