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
Genome-wide analyses of borderline personality features
GH Lubke, C Laurin, N Amin, JJ Hottenga, G Willemsen, ...
Molecular psychiatry 19 (8), 923-929, 2014
Predicting stroke through genetic risk functions: the CHARGE Risk Score Project
CA Ibrahim-Verbaas, M Fornage, JC Bis, SH Choi, BM Psaty, JB Meigs, ...
Stroke 45 (2), 403-412, 2014
Blood-based metabolic signatures in Alzheimer's disease
FA de Leeuw, CFW Peeters, MI Kester, AC Harms, EA Struys, ...
Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring 8, 196-207, 2017
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck
M Li, R Rothwell, M Vermaat, M Wachsmuth, R Schröder, JFJ Laros, ...
Genome research 26 (4), 417-426, 2016
Heritability of the shape of subcortical brain structures in the general population
GV Roshchupkin, BA Gutman, MW Vernooij, N Jahanshad, NG Martin, ...
Nature communications 7 (1), 13738, 2016
Multilocus genetic risk score associates with ischemic stroke in case–control and prospective cohort studies
R Malik, S Bevan, MA Nalls, EG Holliday, WJ Devan, YC Cheng, ...
Stroke 45 (2), 394-402, 2014
Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses
A Demirkan, P Henneman, A Verhoeven, H Dharuri, N Amin, ...
PLoS genetics 11 (1), e1004835, 2015
An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis
J Liu, E Carnero-Montoro, J van Dongen, S Lent, I Nedeljkovic, S Ligthart, ...
Nature communications 10 (1), 2581, 2019
Genetic analysis for a shared biological basis between migraine and coronary artery disease
BS Winsvold, CP Nelson, R Malik, P Gormley, V Anttila, J Vander Heiden, ...
Neurology: Genetics 1 (1), e10, 2015
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with …
D Stambolian, R Wojciechowski, K Oexle, M Pirastu, X Li, LJ Raffel, ...
Human molecular genetics 22 (13), 2754-2764, 2013
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve …
AI Iglesias, H Springelkamp, H van der Linde, LA Severijnen, N Amin, ...
Human molecular genetics 23 (5), 1320-1332, 2014
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
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
The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders
H Chang, N Hoshina, C Zhang, Y Ma, H Cao, Y Wang, DD Wu, SE Bergen, ...
Molecular psychiatry 23 (2), 400-412, 2018
Common DNA variants predict tall stature in Europeans
F Liu, AEJ Hendriks, A Ralf, AM Boot, E Benyi, L Sävendahl, BA Oostra, ...
Human genetics 133, 587-597, 2014
Trans-ethnic meta-analysis of white blood cell phenotypes
MF Keller, AP Reiner, Y Okada, FJA van Rooij, AD Johnson, MH Chen, ...
Human molecular genetics 23 (25), 6944-6960, 2014
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes
N Pervjakova, GH Moen, MC Borges, T Ferreira, JP Cook, C Allard, ...
Human Molecular Genetics 31 (19), 3377-3391, 2022
Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia
FM de Vrij, CG Bouwkamp, N Gunhanlar, G Shpak, B Lendemeijer, ...
Molecular psychiatry 24 (5), 757-771, 2019
Integration of epidemiologic, pharmacologic, genetic and gut microbiome data in a drug–metabolite atlas
J Liu, L Lahousse, MG Nivard, M Bot, L Chen, JB van Klinken, CS Thesing, ...
Nature medicine 26 (1), 110-117, 2020
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci
CL Simpson, R Wojciechowski, K Oexle, F Murgia, L Portas, X Li, ...
PloS one 9 (9), e107110, 2014
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