Articles with public access mandates - Tõnu Esko - US Department of DefenseLearn 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
Available based on mandate: 3
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
The genetic architecture of depression in individuals of East Asian ancestry: a genome-wide association study
O Giannakopoulou, K Lin, X Meng, MH Su, PH Kuo, RE Peterson, ...
JAMA psychiatry 78 (11), 1258-1269, 2021
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
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