Articles with public access mandates - Cornelia M van Duijn - Netherlands Organisation for Health Research and DevelopmentLearn more
NoteFor this mandate, articles should be available from specific locations.
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
Available based on mandate: 179
Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression
DA Van Der Plaat, JM Vonk, N Terzikhan, K de Jong, M De Vries, ...
Human molecular genetics 28 (15), 2477-2485, 2019
Determining possible shared genetic architecture between myopia and primary open-angle glaucoma
AI Iglesias, JS Ong, AP Khawaja, P Gharahkhani, MS Tedja, ...
Investigative ophthalmology & visual science 60 (8), 3142-3149, 2019
Gray matter heritability in family‐based and population‐based studies using voxel‐based morphometry
SJ van der Lee, GV Roshchupkin, HHH Adams, H Schmidt, E Hofer, ...
Human brain mapping 38 (5), 2408-2423, 2017
Genetic loci for serum lipid fractions and intracerebral hemorrhage
S Akoudad, MA Ikram, MLP Portegies, HH Adams, D Bos, A Hofman, ...
Atherosclerosis 246, 287-292, 2016
Circulating metabolites modulated by diet are associated with depression
A van der Spek, ID Stewart, B Kühnel, M Pietzner, T Alshehri, F Gauß, ...
Molecular Psychiatry 28 (9), 3874-3887, 2023
MIND diet lowers risk of open-angle glaucoma: the Rotterdam Study
JE Vergroesen, TOE De Crom, CM Van Duijn, T Voortman, CCW Klaver, ...
European Journal of Nutrition 62 (1), 477-487, 2023
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
A Mishra, C Duplaa, D Vojinovic, H Suzuki, M Sargurupremraj, NR Zilhão, ...
Brain 145 (6), 1992-2007, 2022
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological …
LM Reus, IE Jansen, MO Mol, F van Ruissen, J van Rooij, NM van Schoor, ...
Translational psychiatry 11 (1), 451, 2021
Heritability and genome-wide associations studies of cerebral blood flow in the general population
MA Ikram, HI Zonneveld, G Roshchupkin, AV Smith, OH Franco, ...
Journal of Cerebral Blood Flow & Metabolism 38 (9), 1598-1608, 2018
A genome-wide linkage study for chronic obstructive pulmonary disease in a Dutch genetic isolate identifies novel rare candidate variants
I Nedeljkovic, N Terzikhan, JM Vonk, DA Van der Plaat, L Lahousse, ...
Frontiers in genetics 9, 133, 2018
Common variants at 2q11. 2, 8q21. 3, and 11q13. 2 are associated with major mood disorders
X Xiao, L Wang, C Wang, TF Yuan, D Zhou, F Zheng, L Li, ...
Translational psychiatry 7 (12), 1273, 2017
Genetic determinants of unruptured intracranial aneurysms in the general population
A Peymani, HHH Adams, LGM Cremers, G Krestin, A Hofman, ...
Stroke 46 (10), 2961-2964, 2015
Serum fatty acid chain length associates with prevalent symptomatic end-stage osteoarthritis, independent of BMI
J Meessen, F Saberi-Hosnijeh, N Bomer, W den Hollander, ...
Scientific Reports 10 (1), 15459, 2020
The Well-Known Gene HHIP and Novel Gene MECR Are Implicated in Small Airway Obstruction
DA Van Der Plaat, K de Jong, L Lahousse, A Faiz, JM Vonk, ...
American Journal of Respiratory and Critical Care Medicine 194 (10), 1299-1302, 2016
The dystrophin gene and cognitive function in the general population
D Vojinovic, HHH Adams, SJ Van Der Lee, CA Ibrahim-Verbaas, ...
European Journal of Human Genetics 23 (6), 837-843, 2015
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
C Medina-Gomez, BH Mullin, A Chesi, V Prijatelj, JP Kemp, ...
Communications biology 6 (1), 691, 2023
Genome-wide association study of change in fasting glucose over time in 13,807 non-diabetic European ancestry individuals
CT Liu, J Merino, D Rybin, D DiCorpo, KS Benke, JL Bragg-Gresham, ...
Scientific reports 9 (1), 9439, 2019
A potential role for the STXBP5-AS1 gene in adult ADHD symptoms
A Arias-Vásquez, AJ Groffen, S Spijker, KG Ouwens, M Klein, D Vojinovic, ...
Behavior genetics 49, 270-285, 2019
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology
AA Seyerle, CM Sitlani, R Noordam, SM Gogarten, J Li, X Li, DS Evans, ...
The pharmacogenomics journal 18 (2), 215-226, 2018
Exome-wide meta-analysis identifies rare 3′-UTR variant in ERCC1/CD3EAP associated with symptoms of sleep apnea
A Van der Spek, AI Luik, D Kocevska, C Liu, RWW Brouwer, ...
Frontiers in Genetics 8, 151, 2017
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