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Human Molecular Genetics|December 10, 2019
Insights into the genetic basis of retinal detachmentThibaud S Boutin, David G Charteris, Aman Chandra, et al.Human Heredity|March 14, 2015
The role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African AmericansYun Ju Sung, Jacob Basson, Nuo Cheng, et al.Human Molecular Genetics|May 22, 2020
Analysis of putative cis-regulatory elements regulating blood pressure variationPriyanka Nandakumar, Dongwon Lee, Thomas J Hoffmann, et al.Nature Genetics|July 14, 2022
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathwaysKyoko Watanabe, Philip R Jansen, Jeanne E Savage, et al.European Journal of Human Genetics : EJHG|January 31, 2018
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locusJoão Fadista, Marie Lund, Line Skotte, et al.Plos Genetics|March 28, 2017
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressureKaren Y He, Heming Wang, Brian E Cade, et al.Journal of Hypertension|February 25, 2017
Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestryPriyanka Nandakumar, Dongwon Lee, Melissa A Richard, et al.Gut|June 30, 2021
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosisJue-Sheng Ong, Jiyuan An, Xikun Han, et al.European Journal of Human Genetics : EJHG|September 29, 2018
Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31Heming Wang, Priyanka Nandakumar, Fasil Tekola-Ayele, et al.Nature Genetics|April 23, 2021
Genetic analyses identify widespread sex-differential participation biasNicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, et al.Pageof 3