Saevarsdottir S. et al. Multi-omics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. Read me file (1 KB). Summary data (1 GB). Seronegative (1 GB). Seropositive (1 GB).
Mikaelsdottir EK, et al. Genetic variants associated with platelet count are predictive of human disease and physiological markers. Read me file (1 KB), PRS weights Iceland (5 MB), PRS weights UKB (5 MB), Meta (980 MB).
Dowsett J. et al. Eleven Genomic Loci Affect Plasma Levels of Chronic Inflammation Marker Soluble Urokinase-type Plasminogen Activator Receptor. Communications Biology, 2021. Read me file (1 KB). Summary data (900 MB).
Juliusdottir, T., et al. Distinction between the effects of parental and fetal genomes on fetal growth. Read me file (1 KB). Birthlength.gz (570 MB), Birthweight.gz (620 MB), Birthweight_offspring_mothers.gz (610 MB), Birthweight_offspring_fathers.gz (620 MB), Poinderal_index.gz (620 MB).
Bell S, et al. A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis. Read me file (2 KB). Ferritin (450 MB), serum iron (450 MB), TIBC (450 MB), TSAT (450 MB).
Olafsdottir, T. et al. Loss-of-Function Variants in the Tumor Suppressor Gene PTPN14 confer increased Cancer Risk. Summary data (200 KB)
Gisladottir, R., et al. Sequence variants in TAAR5 and other loci affect human odor perception and naming. Summary data (8 GB).
Olafsdottir T, et al. Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank. Summary data (700 MB).
Oskarsson, et al. Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis. Summary data (700 MB).
Saevarsdottir, et al. FLT3 stop mutation raises FLT3 ligand and autoimmune thyroid disease risk. Summary data (850 MB).
Olafsdottir T.A., et al, Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis. Summary data (570 MB).
Liyanarachchi, et al. Assessing thyroid cancer risk using polygenic risk scores. Summary data (13 MB).
Norland, K. et al. Sequence variants with large effects on cardiac electrophysiology and disease. Summary data (47 GB).
Styrkarsdottir, U et al. GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Summary data.
Bjornsdottir, G. et al. A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. Summary data.