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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
GB Ehret, T Ferreira, DI Chasman, AU Jackson, EM Schmidt, T Johnson, ...
Nature genetics 48 (10), 1171-1184, 2016
Mandates: US National Institutes of Health, Versus Arthritis, UK, British Heart …
The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study
TW Winkler, AE Justice, M Graff, L Barata, MF Feitosa, S Chu, ...
PLoS genetics 11 (10), e1005378, 2015
Mandates: Swiss National Science Foundation, US National Institutes of Health, US …
Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations
MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ...
Cell 182 (5), 1198-1213. e14, 2020
Mandates: US National Institutes of Health, US Department of Veterans Affairs …
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ...
Nature genetics 47 (12), 1415-1425, 2015
Mandates: US National Institutes of Health, German Research Foundation, Danish Council …
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
Mandates: US National Institutes of Health, American Heart Association, National …
Improved polygenic prediction by Bayesian multiple regression on summary statistics
LR Lloyd-Jones, J Zeng, J Sidorenko, L Yengo, G Moser, KE Kemper, ...
Nature communications 10 (1), 5086, 2019
Mandates: US National Institutes of Health, Australian Research Council, National …
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
FR Day, KS Ruth, DJ Thompson, KL Lunetta, N Pervjakova, DI Chasman, ...
Nature genetics 47 (11), 1294-1303, 2015
Mandates: US National Institutes of Health, Cancer Research UK, UK Medical Research …
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
Mandates: US National Institutes of Health, American Heart Association, German …
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
medrxiv, 2022.03. 03.22271360, 2022
Mandates: Business Finland
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
A Okbay, Y Wu, N Wang, H Jayashankar, M Bennett, SM Nehzati, ...
Nature genetics 54 (4), 437-449, 2022
Mandates: US National Institutes of Health, Australian Research Council, National …
Seventy-five genetic loci influencing the human red blood cell
P Van Der Harst, W Zhang, I Mateo Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369-375, 2012
Mandates: US National Institutes of Health, Austrian Science Fund, British Heart …
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci
D Ellinghaus, E Ellinghaus, RP Nair, PE Stuart, T Esko, A Metspalu, ...
The American Journal of Human Genetics 90 (4), 636-647, 2012
Mandates: US National Institutes of Health
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
L Stolk, JRB Perry, DI Chasman, C He, M Mangino, P Sulem, M Barbalic, ...
Nature genetics 44 (3), 260-268, 2012
Mandates: US National Institutes of Health, Dunhill Medical Trust, UK
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
Mandates: Swiss National Science Foundation, US Department of Defense, US National …
The impact of low-frequency and rare variants on lipid levels
I Surakka, M Horikoshi, R Mägi, AP Sarin, A Mahajan, V Lagou, L Marullo, ...
Nature genetics 47 (6), 589-597, 2015
Mandates: Academy of Finland, British Heart Foundation, UK Medical Research Council …
Biomarker profiling by nuclear magnetic resonance spectroscopy for the prediction of all-cause mortality: an observational study of 17,345 persons
K Fischer, J Kettunen, P Würtz, T Haller, AS Havulinna, AJ Kangas, ...
PLoS medicine 11 (2), e1001606, 2014
Mandates: UK Medical Research Council, Wellcome Trust
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
N Kato, M Loh, F Takeuchi, N Verweij, X Wang, W Zhang, TN Kelly, ...
Nature genetics 47 (11), 1282-1293, 2015
Mandates: US National Institutes of Health, John D. and Catherine T. MacArthur …
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants
LC Tsoi, PE Stuart, C Tian, JE Gudjonsson, S Das, M Zawistowski, ...
Nature communications 8 (1), 15382, 2017
Mandates: US National Institutes of Health, US Department of Veterans Affairs, German …
A genome-wide association study of anorexia nervosa
V Boraska, CS Franklin, JAB Floyd, LM Thornton, LM Huckins, L Southam, ...
Molecular psychiatry 19 (10), 1085-1094, 2014
Mandates: US National Institutes of Health, Austrian Science Fund, Swedish Council for …
Effect of predicted protein-truncating genetic variants on the human transcriptome
MA Rivas, M Pirinen, DF Conrad, M Lek, EK Tsang, KJ Karczewski, ...
Science 348 (6235), 666-669, 2015
Mandates: Swiss National Science Foundation, US National Institutes of Health, Natural …
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