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Nature Communications|March 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestriesAndrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.Nature Communications|June 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethalityAsmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, et al.Annals of the Rheumatic Diseases|April 26, 2022
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subsetSaedis Saevarsdottir, Lilja Stefansdottir, Patrick Sulem, et al.Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.Nature|July 3, 2009
Common variants conferring risk of schizophreniaHreinn Stefansson, Roel A Ophoff, Stacy Steinberg, et al.Nature Genetics|January 20, 2009
Sequence variants at the TERT-CLPTM1L locus associate with many cancer typesThorunn Rafnar, Patrick Sulem, Simon N Stacey, et al.Nature Genetics|September 28, 2011
A germline variant in the TP53 polyadenylation signal confers cancer susceptibilitySimon N Stacey, Patrick Sulem, Aslaug Jonasdottir, et al.Nature Genetics|July 13, 2010
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysmSolveig Gretarsdottir, Annette F Baas, Gudmar Thorleifsson, et al.Nature|September 19, 2014
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarcheJohn Rb Perry, Felix Day, Cathy E Elks, et al.Pageof 12