Articles with public access mandates - Cornelia M van Duijn - Chief Scientist Office, Scottish ExecutiveLearn 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: 49
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
RM Freathy, DO Mook-Kanamori, U Sovio, I Prokopenko, NJ Timpson, ...
Nature genetics 42 (5), 430-435, 2010
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
JC Bis, M Kavousi, N Franceschini, A Isaacs, GR Abecasis, U Schminke, ...
Nature genetics 43 (10), 940-947, 2011
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
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
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 association and functional follow-up reveals new loci for kidney function
C Pattaro, A Köttgen, A Teumer, M Garnaas, CA Böger, C Fuchsberger, ...
PLoS genetics 8 (3), e1002584, 2012
Meta-analysis of genome-wide association studies for extraversion: findings from the genetics of personality consortium
SM Van den Berg, MHM de Moor, KJH Verweij, RF Krueger, M Luciano, ...
Behavior genetics 46, 170-182, 2016
GWAS for executive function and processing speed suggests involvement of the CADM2 gene
CA Ibrahim-Verbaas, J Bressler, S Debette, M Schuur, AV Smith, JC Bis, ...
Molecular psychiatry 21 (2), 189-197, 2016
Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory
SM Van Den Berg, MHM De Moor, M McGue, E Pettersson, A Terracciano, ...
Behavior genetics 44, 295-313, 2014
Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach
FP Velders, M Kuningas, M Kumari, MJ Dekker, AG Uitterlinden, ...
Psychoneuroendocrinology 36 (7), 1053-1061, 2011
Evidence of inbreeding depression on human height
R McQuillan, N Eklund, N Pirastu, M Kuningas, BP McEvoy, T Esko, ...
PLoS genetics 8 (7), e1002655, 2012
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
VJM Verhoeven, PG Hysi, SM Saw, V Vitart, A Mirshahi, JA Guggenheim, ...
Human genetics 131, 1467-1480, 2012
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
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
MF Feitosa, AT Kraja, DI Chasman, YJ Sung, TW Winkler, I Ntalla, X Guo, ...
PloS one 13 (6), e0198166, 2018
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration
M Ansari, PM Mckeigue, C Skerka, C Hayward, I Rudan, V Vitart, ...
Human molecular genetics 22 (23), 4857-4869, 2013
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
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
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
Assessing the genetic overlap between BMI and cognitive function
RE Marioni, J Yang, D Dykiert, R Mõttus, A Campbell, G Davies, ...
Molecular psychiatry 21 (10), 1477-1482, 2016
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
Publication and funding information is determined automatically by a computer program