Articles with public access mandates - Cornelia M van Duijn - Academy of FinlandLearn 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
Available based on mandate: 53
Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance
H Mei, J Simino, L Li, F Jiang, JC Bis, G Davies, WD Hill, C Xia, ...
Alzheimer's Research & Therapy 16 (1), 14, 2024
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
Transferability of a European-derived Alzheimer Disease Genetic Risk Score across Multi-Ancestry Populations.
A Nicolas, B Grenier-Boley, R Sherva, Y Kim, M Kikuchi, itziar de Rojas, ...
medRxiv, 2023.10. 17.23297061, 2023
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
S Kanoni, SE Graham, Y Wang, I Surakka, S Ramdas, X Zhu, SL Clarke, ...
Genome biology 23 (1), 268, 2022
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
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
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
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
Trans-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, ...
medRxiv, 2021.10. 11.21264235, 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
Association of circulating metabolites in plasma or serum and risk of stroke: meta-analysis from 7 prospective cohorts
D Vojinovic, M Kalaoja, S Trompet, K Fischer, MJ Shipley, S Li, ...
Neurology 96 (8), e1110-e1123, 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
Genome-wide association study identifies 48 common genetic variants associated with handedness
G Cuellar-Partida, JY Tung, N Eriksson, E Albrecht, F Aliev, ...
Nature human behaviour 5 (1), 59-70, 2021
Genetic predisposition to coronary artery disease in type 2 diabetes mellitus
NR Van Zuydam, C Ladenvall, BF Voight, RJ Strawbridge, ...
Circulation: Genomic and Precision Medicine 13 (6), e002769, 2020
A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease
I Prokić, L Lahousse, M de Vries, J Liu, M Kalaoja, JM Vonk, ...
BMC Pulmonary Medicine 20, 1-10, 2020
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
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ...
Molecular psychiatry 25 (8), 1859-1875, 2020
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI
A Couto Alves, NMG De Silva, V Karhunen, U Sovio, S Das, HR Taal, ...
Science Advances 5 (9), eaaw3095, 2019
Exome-derived adiponectin-associated variants implicate obesity and lipid biology
CN Spracklen, T Karaderi, H Yaghootkar, C Schurmann, RS Fine, ...
The American Journal of Human Genetics 105 (1), 15-28, 2019
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
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