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Nature Communications|July 17, 2021
Discovery and prioritization of variants and genes for kidney function in >1.2 million individualsKira J Stanzick, Yong Li, Pascal Schlosser, et al.Nature Communications|October 24, 2020
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture riskIda Surakka, Lars G Fritsche, Wei Zhou, et al.Circulation. Genomic and Precision Medicine|June 19, 2019
Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic DissectionBrooke N Wolford, Whitney E Hornsby, Dongchuan Guo, et al.Diabetes|August 6, 2008
Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genesKyle J Gaulton, Cristen J Willer, Yun Li, et al.Nature Genetics|March 18, 2014
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction riskOddgeir L Holmen, He Zhang, Yanbo Fan, et al.Diabetes|August 29, 2006
Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in FinnsLori L Bonnycastle, Cristen J Willer, Karen N Conneely, et al.Communications Biology|April 9, 2024
A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humansMarta R Moksnes, Ailin F Hansen, Brooke N Wolford, et al.Human Molecular Genetics|July 17, 2014
Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African AmericansMengmeng Du, Paul L Auer, Shuo Jiao, et al.Diabetes|December 29, 2006
Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genesCristen J Willer, Lori L Bonnycastle, Karen N Conneely, et al.Cell Genomics|February 13, 2023
The HUNT study: A population-based cohort for genetic researchBen M Brumpton, Sarah Graham, Ida Surakka, et al.Pageof 20