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Nature Genetics|August 6, 2002
Human genome sequence variation and the influence of gene history, mutation and recombinationDavid E Reich, Stephen F Schaffner, Mark J Daly, et al.The Pharmacogenomics Journal|August 4, 2026
Large-scale analysis demonstrates the influence of CYP2C19 genotype on specific SSRI side effectsChris Eijsbouts, Yunxuan Jiang, James R Ashenhurst, et al.Nature Communications|June 2, 2022
Genome-wide association analysis and replication in 810,625 individuals with varicose veinsWaheed-Ul-Rahman Ahmed, Sam Kleeman, Michael Ng, et al.Bioinformatics (Oxford, England)|April 4, 2019
HLA*LA-HLA typing from linearly projected graph alignmentsAlexander T Dilthey, Alexander J Mentzer, Raphael Carapito, et al.Plos Genetics|April 24, 2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseaseLoukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, et al.Nature Genetics|April 23, 2021
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severityJanie F Shelton, Anjali J Shastri, Chelsea Ye, et al.Nature Communications|January 20, 2026
Preventing premature deaths through polygenic risk scoresMelisa Chuong, Deborah Thompson, Michael E Weale, et al.Translational Psychiatry|August 18, 2025
Multivariate genome-wide association analysis of dyslexia and quantitative reading skill improves gene discoveryHayley S Mountford, Else Eising, Pierre Fontanillas, et al.Nature|November 7, 2012
An integrated map of genetic variation from 1,092 human genomes, Goncalo R Abecasis, Adam Auton, et al.Human Molecular Genetics|May 14, 2021
Estimating heritability and its enrichment in tissue-specific gene sets in admixed populationsYang Luo, Xinyi Li, Xin Wang, et al.Pageof 17