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Science (New York, N.Y.)|December 2, 2021
Genetic and functional evidence links a missense variant in B4GALT1 to lower LDL and fibrinogenMay E Montasser, Cristopher V Van Hout, Lawrence Miloscio, et al.Nature|October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participantsJoshua D Backman, Alexander H Li, Anthony Marcketta, et al.Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.Nature|May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|May 16, 2015
Mendelian Randomization Study of Body Mass Index and Colorectal Cancer RiskAaron P Thrift, Jian Gong, Ulrike Peters, et al.Nature|November 30, 2022
Common and rare variant associations with clonal haematopoiesis phenotypesMichael D Kessler, Amy Damask, Sean O'Keeffe, et al.The New England Journal of Medicine|August 8, 2022
Germline Mutations in CIDEB and Protection against Liver DiseaseNiek Verweij, Mary E Haas, Jonas B Nielsen, et al.Nature Genetics|September 15, 2015
Population genetic differentiation of height and body mass index across EuropeMatthew R Robinson, Gibran Hemani, Carolina Medina-Gomez, et al.Pageof 8