Articles with public access mandates - Cornelia M van Duijn - Fondazione CariploLearn 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: 10
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
J Wessel, AY Chu, SM Willems, S Wang, H Yaghootkar, JA Brody, ...
Nature communications 6 (1), 5897, 2015
Low-frequency and rare-coding variation contributes to multiple sclerosis risk
M Mitrovič, NA Patsopoulos, AH Beecham, T Dankowski, A Goris, ...
Cell 175 (6), 1679-1687. e7, 2018
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
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
M Simcoe, A Valdes, F Liu, NA Furlotte, DM Evans, G Hemani, SM Ring, ...
Science Advances 7 (11), eabd1239, 2021
Association Analysis of Bitter Receptor Genes in Five Isolated Populations Identifies a Significant Correlation between TAS2R43 Variants and Coffee Liking
N Pirastu, M Kooyman, M Traglia, A Robino, SM Willems, G Pistis, ...
PloS one 9 (3), e92065, 2014
Modulation of genetic associations with serum urate levels by body-mass-index in humans
JE Huffman, E Albrecht, A Teumer, M Mangino, K Kapur, T Johnson, ...
PloS one 10 (3), e0119752, 2015
Common variants in Mendelian kidney disease genes and their association with renal function
A Parsa, C Fuchsberger, A Koettgen, CM O’Seaghdha, C Pattaro, ...
Journal of the American Society of Nephrology 24 (12), 2105-2117, 2013
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings
N Pirastu, M Kooyman, M Traglia, A Robino, SM Willems, G Pistis, N Amin, ...
Reviews in Endocrine and Metabolic Disorders 17, 209-219, 2016
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking
N Pirastu, M Kooyman, M Traglia, A Robino, SM Willems, G Pistis, N Amin, ...
European Journal of Human Genetics 23 (12), 1717-1722, 2015
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