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Nature Communications|March 29, 2022
Genome-wide association studies of metabolites in Finnish men identify disease-relevant lociXianyong Yin, Lap Sum Chan, Debraj Bose, et al.The British Journal of Psychiatry : the Journal of Mental Science|June 24, 2017
Interaction between the FTO gene, body mass index and depression: meta-analysis of 13701 individualsMargarita Rivera, Adam E Locke, Tanguy Corre, et al.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.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|March 11, 2023
Addressing sex-based disparities in solid organ transplantation in the United States - a conference reportDeirdre Sawinski, Jennifer C Lai, Sean Pinney, et al.JAMA Surgery|May 29, 2024
Liver Transplant Costs and Activity After United Network for Organ Sharing Allocation Policy ChangesOla Ahmed, Maria Bernadette Majella Doyle, Marwan S Abouljoud, 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.Pageof 43