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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.Annals of Surgery|September 10, 2021
Optimal Timing of Administration of Direct-acting Antivirals for Patients With Hepatitis C-associated Hepatocellular Carcinoma Undergoing Liver TransplantationMichael K Turgeon, Shimul A Shah, Aaron M Delman, 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.Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.Pageof 34