Articles with public access mandates - Cornelia M van Duijn - Government of ItalyLearn more
OverallNIHMRCEuropean CommissionWellcomeZonMwNWONIHRBHFNHMRCSwedish Research CouncilDFGCIHRCancer Research UKBBSRCESRCINSERMAcademy of FinlandCSOBMBFGovernment of ItalySNSFGovernment of SpainFWFARCFWOHelmholtzDHFVersus Arthritis, UKAlzheimers's 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
Not available based on mandate: 1
Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene
A Poleggi, S Van Der Lee, S Capellari, M Puopolo, A Ladogana, ...
Journal of Neurology, Neurosurgery & Psychiatry 89 (12), 1243-1249, 2018
Available based on mandate: 44
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error
AM Musolf, AEG Haarman, RN Luben, JS Ong, K Patasova, RH Trapero, ...
Communications biology 6 (1), 6, 2023
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
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
PJ Hop, RAJ Zwamborn, E Hannon, GL Shireby, MF Nabais, EM Walker, ...
Science translational medicine 14 (633), eabj0264, 2022
Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarization
WJ Young, N Lahrouchi, A Isaacs, TV Duong, L Foco, F Ahmed, JA Brody, ...
medRxiv, 2021.11. 04.21265866, 2021
Genome-Wide Meta-Analysis of Late-Onset Alzheimer’s Disease Using Rare Variant Imputation in 65,602 Subjects Identifies Novel Rare Variant Locus NCK2: The …
AC Naj, G Leonenko, X Jian, B Grenier-Boley, MC Dalmasso, ...
medRxiv, 2021.03. 14.21253553, 2021
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
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
V Lagou, R Mägi, JJ Hottenga, H Grallert, JRB Perry, N Bouatia-Naji, ...
Nature communications 12 (1), 24, 2021
New insights on the genetic etiology of Alzheimer’s and related dementia
C Bellenguez, F Küçükali, I Jansen, V Andrade, S Moreno-Grau, N Amin, ...
MedRxiv, 2020.10. 01.20200659, 2020
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
E Jones, H Hummerich, E Viré, J Uphill, A Dimitriadis, H Speedy, ...
The Lancet Neurology 19 (10), 840-848, 2020
Genome-wide association study identifies risk variants for sporadic Creutzfeldt-Jakob disease in STX6 and GAL3ST1
E Jones, H Hummerich, E Viré, J Uphill, A Dimitriadis, H Speedy, ...
medRxiv, 2020.04. 06.20055376, 2020
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
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
E Evangelou, HR Warren, D Mosen-Ansorena, B Mifsud, R Pazoki, H Gao, ...
Nature genetics 50 (10), 1412-1425, 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
Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, AC Naj, A Boland, ...
BioRxiv, 294629, 2018
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
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
Genome-wide physical activity interactions in adiposity―A meta-analysis of 200,452 adults
M Graff, RA Scott, AE Justice, KL Young, MF Feitosa, L Barata, ...
PLoS genetics 13 (4), e1006528, 2017
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
AE Justice, TW Winkler, MF Feitosa, M Graff, VA Fisher, K Young, L Barata, ...
Nature communications 8 (1), 14977, 2017
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption
N Pirastu, M Kooyman, A Robino, A Van Der Spek, L Navarini, N Amin, ...
Scientific reports 6 (1), 1-6, 2016
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