Summary Statistics - HUNT
Summary Statistics
A selection of publications with shared summary statistics can be found here.
2024
Moksnes MR et al. A genome-wide association study provides insights into the genetic etiology of 57 essential and non-essential trace elements in humans. Commun Biol. 2024 Apr 9;7(1):432.
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2022
Moksnes, M.R., Graham, S.E., Wu, KH. et al. Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT. Commun Biol 5, 591 (2022).
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2021
Marta R Moksnes, Helge Røsjø, Anne Richmond, Magnus N Lyngbakken, Sarah E Graham, Ailin Falkmo Hansen, Brooke N Wolford, Sarah A Gagliano Taliun, Jonathon LeFaive, Humaira Rasheed, Laurent F Thomas, Wei Zhou, Nay Aung, Ida Surakka, Nicholas J Douville, Archie Campbell, David J Porteous, Steffen E Petersen, Patricia B Munroe, Paul Welsh, Naveed Sattar, George Davey Smith, Lars G Fritsche, Jonas B Nielsen, Bjørn Olav Åsvold, Kristian Hveem, Caroline Hayward, Cristen J Willer, Ben M Brumpton, Torbjørn Omland, Genome-wide association study of cardiac troponin I in the general population, Human Molecular Genetics, Volume 30, Issue 21, 1 November 2021, Pages 2027–2039
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2020
Zhou, W., Brumpton, B., Kabil, O. et al. GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. Nat Commun 11, 3981 (2020).
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Surakka, I., Fritsche, L.G., Zhou, W. et al. MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk. Nat Commun 11, 4093 (2020).
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Nielsen, J.B., Rom, O., Surakka, I. et al. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Nat Commun 11, 6417 (2020).
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2019
Graham, S.E., Nielsen, J.B., Zawistowski, M. et al. Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Nat Commun 10, 1847 (2019).
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2018
Nielsen, J.B., Thorolfsdottir, R.B., Fritsche, L.G. et al. Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. Nat Genet 50, 1234–1239 (2018).