Articles with public access mandates - Cornelia M van Duijn - National Natural Science Foundation of ChinaLearn more
OverallNIHMRCEuropean CommissionWellcomeZonMwNWONIHRBHFNHMRCSwedish Research CouncilDFGCIHRCancer Research UKBBSRCESRCINSERMAcademy of FinlandCSOBMBFGovernment of ItalySNSFGovernment of SpainFWFARCFWOHelmholtzDHFAlzheimers's UKVersus Arthritis, UKVAAHADFFRCNDMTANRLeducq Foundation, USADoDKNAWFORTEKnut and Alice Wallenberg FoundationJDRFHHMIDiabetes UKNSFDoris Duke Charitable FoundationUK Research & InnovationFRQSMacArthurA*StarFondazione CariploNMRCGenome CanadaNSERCNSFCDNRFBanking Foundation "la Caixa"Parkinson's UKDSFMotor Neurone Disease Association, UKDCTIHealth Data Research, UKRoyal Society UKSFIEPSRCAXA Research Fund, FranceMarianne and Marcus Wallenberg FoundationBank of Sweden Tercentenary FoundationAction on Hearing Loss, UKMultiple Sclerosis Society, UKNational Research Foundation, SingaporeDOEHSFCASTekesTelethonFCTResearch Grants Council, Hong KongAutism Speaks Inc, USAWorld Cancer Researh Fund, UKUSDAFNRSSSHRCDBTFormasKWFBusiness FinlandAIRC Foundation for Cancer Research in ItalyJSTNordforskSusan G. KomenNASAUSEDCCSIDRCDNATFCSIRDSTAHRCProstate Cancer UKStroke Association, UKMSFHRState of CalifoniaMultiple Sclerosis Society of CanadaInnovation Fund DenmarkMichael J Fox FoundationRWJFOICRGovernment of ArgentinaBELSPOMinistry of Health, Singapore
Available based on mandate: 8
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
A common haplotype lowers PU. 1 expression in myeloid cells and delays onset of Alzheimer's disease
K Huang, E Marcora, AA Pimenova, AF Di Narzo, M Kapoor, SC Jin, ...
Nature neuroscience 20 (8), 1052-1061, 2017
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium
Q Fan, X Guo, JWL Tideman, KM Williams, S Yazar, SM Hosseini, ...
Scientific reports 6 (1), 25853, 2016
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
PG Hysi, AM Valdes, F Liu, NA Furlotte, DM Evans, V Bataille, A Visconti, ...
Nature genetics 50 (5), 652-656, 2018
Multiancestry genome-wide association study of lipid levels incorporating gene-alcohol interactions
PS De Vries, MR Brown, AR Bentley, YJ Sung, TW Winkler, I Ntalla, ...
American journal of epidemiology 188 (6), 1033-1054, 2019
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair
F Liu, Y Chen, G Zhu, PG Hysi, S Wu, K Adhikari, K Breslin, E Pośpiech, ...
Human Molecular Genetics 27 (3), 559-575, 2018
Genetic mechanisms of 184 neuro-related proteins in human plasma
L Repetto, J Chen, Z Yang, R Zhai, PRHJ Timmers, T Li, EL Twait, ...
MedRxIv, 2023
Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders
L Repetto, J Chen, Z Yang, R Zhai, PRHJ Timmers, T Li, EL Twait, ...
Research square, 2023
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