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Nature|October 12, 2018
The UK Biobank resource with deep phenotyping and genomic dataClare Bycroft, Colin Freeman, Desislava Petkova, et al.Nature Communications|January 23, 2015
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility lociRegina C Betz, Lynn Petukhova, Stephan Ripke, et al.European Journal of Human Genetics : EJHG|January 27, 2011
The effect of genome-wide association scan quality control on imputation outcome for common variantsLorraine Southam, Kalliope Panoutsopoulou, N William Rayner, et al.Nature Genetics|September 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK BiobankSheila M Gaynor, Tyler Joseph, Xiaodong Bai, et al.Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.Plos Genetics|February 6, 2014
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysmsMitja I Kurki, Emília Ilona Gaál, Johannes Kettunen, et al.Genome Research|March 13, 2013
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomesStephen B Montgomery, David L Goode, Erika Kvikstad, et al.Nature Communications|March 14, 2026
Humans with function-disrupting variants in the myostatin gene (MSTN) have increased skeletal muscle mass and strength, and less adiposityJoseph L Herman, Peter Dornbos, Karl Landheer, et al.Communications Biology|June 6, 2022
Population-scale analysis of common and rare genetic variation associated with hearing loss in adultsKavita Praveen, Lee Dobbyn, Lauren Gurski, et al.Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.Pageof 11