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Available based on mandate: 14
An expanded genome-wide association study of type 2 diabetes in Europeans
RA Scott, LJ Scott, R Mägi, L Marullo, KJ Gaulton, M Kaakinen, ...
Diabetes 66 (11), 2888-2902, 2017
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
L Folkersen, S Gustafsson, Q Wang, DH Hansen, ÅK Hedman, A Schork, ...
Nature metabolism 2 (10), 1135-1148, 2020
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
AE Justice, TW Winkler, MF Feitosa, M Graff, VA Fisher, K Young, L Barata, ...
Nature communications 8 (1), 14977, 2017
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
V Lagou, R Mägi, JJ Hottenga, H Grallert, JRB Perry, N Bouatia-Naji, ...
Nature communications 12 (1), 24, 2021
Multiancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions
PS De Vries, MR Brown, AR Bentley, YJ Sung, TW Winkler, I Ntalla, ...
American journal of epidemiology 188 (6), 1033-1054, 2019
Genetic and In Vitro Inhibition of PCSK9 and Calcific Aortic Valve Stenosis
N Perrot, V Valerio, D Moschetta, SM Boekholdt, C Dina, HY Chen, ...
Basic to Translational Science 5 (7), 649-661, 2020
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
N Trpchevska, MB Freidin, L Broer, BC Oosterloo, S Yao, Y Zhou, B Vona, ...
The American Journal of Human Genetics 109 (6), 1077-1091, 2022
Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study
M Nethander, E Coward, E Reimann, L Grahnemo, ME Gabrielsen, ...
Cell Reports Medicine 3 (10), 2022
Genomic evaluation of circulating proteins for drug target characterisation and precision medicine
L Folkersen, S Gustafsson, Q Wang, DH Hansen, ÅK Hedman, A Schork, ...
BioRxiv, 2020.04. 03.023804, 2020
The genomics of heart failure: design and rationale of the HERMES consortium
RT Lumbers, S Shah, H Lin, T Czuba, A Henry, DI Swerdlow, A Mälarstig, ...
ESC heart failure 8 (6), 5531-5541, 2021
Mapping genetic determinants of 184 circulating proteins in 26,494 individuals to connect proteins and diseases
E Macdonald-Dunlop, L Klarić, L Folkersen, PRHJ Timmers, S Gustafsson, ...
MedRxiv, 2021.08. 03.21261494, 2021
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19
L Klaric, JS Gisby, A Papadaki, MD Muckian, E Macdonald-Dunlop, ...
MedRxiv, 2021
Genetic predisposition to coronary artery disease in type 2 diabetes mellitus
NR Van Zuydam, C Ladenvall, BF Voight, RJ Strawbridge, ...
Circulation: Genomic and Precision Medicine 13 (6), e002769, 2020
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