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
Prediction of male-pattern baldness from genotypes
F Liu, MA Hamer, S Heilmann, C Herold, S Moebus, A Hofman, ...
European Journal of Human Genetics 24 (6), 895-902, 2016
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness
G Cuellar-Partida, H Springelkamp, SEM Lucas, S Yazar, AW Hewitt, ...
Human molecular genetics 24 (17), 5060-5068, 2015
Metabolic Age Based on the BBMRI-NL 1H-NMR Metabolomics Repository as Biomarker of Age-related Disease
EB Van Den Akker, S Trompet, JJH Barkey Wolf, M Beekman, ...
Circulation: Genomic and Precision Medicine 13 (5), 541-547, 2020
Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes
EM Reinthaler, B Dejanovic, D Lal, M Semtner, Y Merkler, A Reinhold, ...
Annals of neurology 77 (6), 972-986, 2015
Risk scores of common genetic variants for lipid levels influence atherosclerosis and incident coronary heart disease
A Isaacs, SM Willems, D Bos, A Dehghan, A Hofman, MA Ikram, ...
Arteriosclerosis, thrombosis, and vascular biology 33 (9), 2233-2239, 2013
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
H Currant, P Hysi, TW Fitzgerald, P Gharahkhani, PWM Bonnemaijer, ...
PLoS genetics 17 (5), e1009497, 2021
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels
A Tin, Y Li, JA Brody, T Nutile, AY Chu, JE Huffman, Q Yang, MH Chen, ...
Nature communications 9 (1), 4228, 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
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
EM Van Leeuwen, LC Karssen, J Deelen, A Isaacs, C Medina-Gomez, ...
Nature communications 6 (1), 6065, 2015
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
A Mendelian randomization study of metabolite profiles, fasting glucose, and type 2 diabetes
J Liu, JB Van Klinken, S Semiz, KW Van Dijk, A Verhoeven, T Hankemeier, ...
Diabetes 66 (11), 2915-2926, 2017
Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
IE Jansen, SJ van der Lee, D Gomez-Fonseca, I De Rojas, MC Dalmasso, ...
Acta neuropathologica 144 (5), 821-842, 2022
Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine
GLJ Onderwater, L Ligthart, M Bot, A Demirkan, J Fu, CJH van der Kallen, ...
Neurology 92 (16), e1899-e1911, 2019
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects
A Mishra, G Chauhan, MH Violleau, D Vojinovic, X Jian, JC Bis, S Li, ...
Brain 142 (4), 1009-1023, 2019
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
BP Prins, TJ Mead, JA Brody, G Sveinbjornsson, I Ntalla, NA Bihlmeyer, ...
Genome biology 19, 1-17, 2018
Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans
E Olfson, NL Saccone, EO Johnson, LS Chen, R Culverhouse, K Doheny, ...
Molecular psychiatry 21 (5), 601-607, 2016
Haplotype reference consortium panel: Practical implications of imputations with large reference panels
AI Iglesias, SJ Van Der Lee, PWM Bonnemaijer, R Höhn, A Nag, ...
Human mutation 38 (8), 1025-1032, 2017
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
Interplay of metabolome and gut microbiome in individuals with major depressive disorder vs control individuals
N Amin, J Liu, B Bonnechere, S MahmoudianDehkordi, M Arnold, R Batra, ...
JAMA psychiatry 80 (6), 597-609, 2023
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
EM van Leeuwen, A Sabo, JC Bis, JE Huffman, A Manichaikul, AV Smith, ...
Journal of medical genetics 53 (7), 441-449, 2016
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