Articles with public access mandates - Tõnu Esko - National Institute for Health Research, UKLearn 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: 17
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
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
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
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
Identifying tissues implicated in anorexia nervosa using transcriptomic imputation
LM Huckins, A Dobbyn, W McFadden, D Ruderfer, W Wang, E Gamazon, ...
bioRxiv, 265017, 2018
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
Genome-wide association study of susceptibility to hospitalised respiratory infections
AT Williams, N Shrine, H Naghra-van Gijzel, JC Betts, J Chen, EM Hessel, ...
Wellcome Open Research 6 (290), 290, 2023
Mapping pQTLs of circulating inflammatory proteins identifies drivers of immune-related disease risk and novel therapeutic targets
SCALLOP consortium, JH Zhao, D Stacey, N Eriksson, ...
medRxiv, 2023.03. 24.23287680, 2023
Mapping the aetiological foundations of the heart failure spectrum using human genetics
A Henry, X Mo, C Finan, MD Chaffin, D Speed, H Issa, S Denaxas, ...
medRxiv, 2023.10. 01.23296379, 2023
Genome-wide association analysis reveals insights into the molecular aetiology underlying dilated cardiomyopathy
SL Zheng, A Henry, D Cannie, M Lee, D Miller, KA McGurk, I Bond, X Xu, ...
medRxiv, 2023.09. 28.23295408, 2023
Genome-wide study identifies association between HLA-B* 55: 01 and penicillin allergy
K Krebs, J Bovijn, M Lepamets, JC Censin, T Jürgenson, D Särg, Y Luo, ...
bioRxiv, 2020.02. 27.967497, 2020
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
P Surendran, EV Feofanova, N Lahrouchi, I Ntalla, S Karthikeyan, J Cook, ...
Nature genetics 53 (5), 762-762, 2021
Tuuli Jürgenson, Dage Särg, 6 Erik Abner, Triin Laisk, Yang Luo, 7, 8, 9, 10, 11 Line Skotte, 12 Frank Geller, 12 Bjarke Feenstra, 12 Wei Wang, 13 Adam Auton, 13 23andMe …
S Raychaudhuri, T Esko, A Metspalu, S Laur, DM Roden, WQ Wei, ...
The American Journal of Human Genetics 107, 612-621, 2020
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics …
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
bioRxiv, 040493, 2016
Population genetic differentiation of height and body mass index across Europe
PM Visscher
Nature Genetics 47 (11), 2015
Available based on mandate: 124
The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans
GTEx Consortium, KG Ardlie, DS Deluca, AV Segrè, TJ Sullivan, ...
Science 348 (6235), 648-660, 2015
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature genetics 47 (10), 1121-1130, 2015
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
JJ Lee, R Wedow, A Okbay, E Kong, O Maghzian, M Zacher, ...
Nature genetics 50 (8), 1112-1121, 2018
Publication and funding information is determined automatically by a computer program