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Nature Genetics|April 15, 2014
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31Unnur Styrkarsdottir, Gudmar Thorleifsson, Hafdis T Helgadottir, et al.Nature Communications|January 22, 2020
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesisThorunn A Olafsdottir, Fannar Theodors, Kristbjorg Bjarnadottir, et al.Communications Biology|April 25, 2020
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesisGudjon R Oskarsson, Asmundur Oddsson, Magnus K Magnusson, et al.Human Molecular Genetics|November 27, 2018
Sequence variants associating with urinary biomarkersStefania Benonisdottir, Ragnar P Kristjansson, Asmundur Oddsson, et al.Nature Genetics|September 17, 2013
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degenerationHannes Helgason, Patrick Sulem, Maheswara R Duvvari, et al.Plos Genetics|March 9, 2017
A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthmaDirk Smith, Hannes Helgason, Patrick Sulem, et al.Nature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.The New England Journal of Medicine|November 8, 2023
Actionable Genotypes and Their Association with Life Span in IcelandBrynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir, et al.Nature Genetics|January 16, 2019
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitisRagnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, et al.Pageof 12