Articles with public access mandates - Tõnu Esko - US National Institutes of HealthLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallNIHMRCWellcomeEuropean CommissionNIHRBHFSwedish Research CouncilNHMRCCancer Research UKDFGNWOESRCAcademy of FinlandBBSRCSNSFARCCSOCIHRZonMwBMBFVAGovernment of SpainVersus Arthritis, UKGovernment of ItalyAHANSERCDFFUK Research & InnovationFRQSHelmholtzINSERMDoris Duke Charitable FoundationHealth Data Research, UKKnut and Alice Wallenberg FoundationRCNDHFBusiness FinlandGenome CanadaFORTENSFFWFDiabetes UKA*StarJDRFRoyal Society UKFWOKNAWNMRCLeducq Foundation, USAMacArthurNSFCDCTIAction on Hearing Loss, UKDSFTekesSFIBank of Sweden Tercentenary FoundationEPSRCFondazione CariploANRNational Research Foundation, SingaporeDOEDoDHSFSSHRCDNRFHRBTelethonFCTFormasParkinson's UKNordforskBanking Foundation "la Caixa"Marianne and Marcus Wallenberg FoundationAcademy of Medical Sciences, UKAlzheimers's UKMotor Neurone Disease Association, UKNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKMichael J Fox FoundationAutism Speaks Inc, USAAXA Research Fund, FranceSusan G. KomenFAPESPUSDAHHMICCSIDRCCASLeibniz AssociationDNATFCSIRDBTDSTDMTProstate Cancer UKStroke Association, UKWorldwide Cancer Research, UKState of CalifoniaKWFNKFIResearch Grants Council, Hong KongWorld Cancer Researh Fund, UKJules Thorn Trust, UKCarlsberg Foundation DKJSTOICRMinistry of Health, SingaporeCZI
Not available based on mandate: 30
Signatures of negative selection in the genetic architecture of human complex traits
J Zeng, R De Vlaming, Y Wu, MR Robinson, LR Lloyd-Jones, L Yengo, ...
Nature genetics 50 (5), 746-753, 2018
Genetic evidence of assortative mating in humans
MR Robinson, A Kleinman, M Graff, AAE Vinkhuyzen, D Couper, ...
Nature Human Behaviour 1 (1), 0016, 2017
A KATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila
KV Allebrandt, N Amin, B Müller-Myhsok, T Esko, M Teder-Laving, ...
Molecular psychiatry 18 (1), 122-132, 2013
Genotype–covariate interaction effects and the heritability of adult body mass index
MR Robinson, G English, G Moser, LR Lloyd-Jones, MA Triplett, Z Zhu, ...
Nature genetics 49 (8), 1174-1181, 2017
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans
KJ Karczewski, LC Francioli, G Tiao, BB Cummings, J Alföldi, Q Wang, ...
Nature 590 (7846), E53-E53, 2021
Proteome-wide Mendelian randomization identifies causal links between blood proteins and acute pancreatitis
J Bourgault, E Abner, HD Manikpurage, N Pujol-Gualdo, T Laisk, É Gobeil, ...
Gastroenterology 164 (6), 953-965. e3, 2023
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (5), 766-767, 2018
Correction: 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 12 (6), e1006166, 2016
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
Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease
N Whiffin, IM Armean, A Kleinman, JL Marshall, EV Minikel, JK Goodrich, ...
BioRxiv, 561472, 2019
Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure
H Warren, T Edwards, A Vaez, J Keaton, Z Kamali, T Xie, A Ani, ...
Hemani et al. reply
G Hemani, K Shakhbazov, HJ Westra, T Esko, AK Henders, AF McRae, ...
Nature 514 (7520), E5-E6, 2014
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
Characterising the loss-of-function impact of 5’untranslated region variants in whole genome sequence data from 15,708 individuals
N Whiffin, KJ Karczewski, X Zhang, S Chothani, MJ Smith, DG Evans, ...
BioRxiv, 543504, 2019
Genetic associations with subjective well-being also implicate depression and neuroticism
A Okbay, BML Baselmans, JE De Neve, P Turley, MG Nivard, MA Fontana, ...
bioRxiv, 032789, 2015
Genome-wide screen of otosclerosis in population biobanks: 18 loci and shared heritability with skeletal structure
JT Rämö, T Kiiskinen, J Karjalainen, K Krebs, M Kurki, AS Havulinna, ...
medRxiv, 2020.11. 15.20227868, 2020
Identifying tissues implicated in anorexia nervosa using transcriptomic imputation
LM Huckins, A Dobbyn, W McFadden, D Ruderfer, W Wang, E Gamazon, ...
bioRxiv, 265017, 2018
Genetic variants of inducible costimulator are associated with allergic asthma susceptibility
AK Andiappan, S Narayanan, RA Myers, B Lee, MA Nieuwenhuis, ...
Journal of Allergy and Clinical Immunology 135 (2), 556-558. e13, 2015
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
J Flannick, C Fuchsberger, A Mahajan, TM Teslovich, V Agarwala, ...
Scientific data 5 (1), 1-2, 2018
Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein (a) in individuals of European and African ancestries
SM Zekavat, S Ruotsalainen, RE Handsaker, M Alver, J Bloom, T Poterba, ...
Nature communications 11 (1), 1715, 2020
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