Articles with public access mandates - Tõnu Esko - Genome CanadaLearn 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: 11
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
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2
RG Walters, S Jacquemont, A Valsesia, AJ de Smith, D Martinet, ...
Nature 463 (7281), 671-675, 2010
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11. 2 locus
S Jacquemont, A Reymond, F Zufferey, L Harewood, RG Walters, ...
Nature 478 (7367), 97-102, 2011
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
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
Resource profile and user guide of the Polygenic Index Repository
J Becker, CAP Burik, G Goldman, N Wang, H Jayashankar, M Bennett, ...
Nature human behaviour 5 (12), 1744-1758, 2021
Genome-wide association study reveals first locus for anorexia nervosa and metabolic correlations
L Duncan, Z Yilmaz, R Walters, J Goldstein, V Anttila, B Bulik-Sullivan, ...
The American journal of psychiatry 174 (9), 850, 2017
Testing the role of predicted gene knockouts in human anthropometric trait variation
S Lessard, AK Manning, C Low-Kam, PL Auer, A Giri, M Graff, ...
Human Molecular Genetics 25 (10), 2082-2092, 2016
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases
G Butler-Laporte, J Farjoun, T Nakanishi, T Lu, E Abner, Y Chen, ...
Communications Biology 6 (1), 1113, 2023
HLA allele-calling using whole-exome sequencing identifies 129 novel associations in 11 autoimmune diseases: a multi-ancestry analysis in the UK Biobank
G Butler-Laporte, J Farjoun, T Nakanishi, T Lu, E Abner, Y Chen, ...
medRxiv, 2023.01. 15.23284570, 2023
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