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Nature Genetics|October 26, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without auraGyda Bjornsdottir, Mona A Chalmer, Lilja Stefansdottir, et al.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|November 26, 2020
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian womenValgerdur Steinthorsdottir, Ralph McGinnis, Nicholas O Williams, 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 14, 2023
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditionsNilufer Rahmioglu, Sally Mortlock, Marzieh Ghiasi, et al.Nature|April 9, 2025
Translational genomics of osteoarthritis in 1,962,069 individualsKonstantinos Hatzikotoulas, Lorraine Southam, Lilja Stefansdottir, et al.Nature Communications|November 2, 2019
Associations of autozygosity with a broad range of human phenotypesDavid W Clark, Yukinori Okada, Kristjan H S Moore, et al.Pageof 6