Cornelia M. van Duijn

Author

Also Known As

Aaron Isaacs, Agustin Ruiz, Alex W. Hewitt, Alexander P Reiner, Alina Solomon, Alison Goate, Alison M Dunning, Andrew Hicks, André G Uitterlinden, André G. Uitterlinden

1.9K

Publications

242.3K

Citations

237

H-Index

425

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam Leiden University Medical Center University of Oxford Harvard University

About

Cornelia M. van Duijn is an author at Erasmus MC specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	103	307	53.8K
2	Health Sciences	24	32	4.9K
3	Engineering	8	8	761
4	Management	4	4	125
5	Education	2	2	1.6K

Cornelia M. van Duijn

795

Publications

111K

Citations

161

H-Index

Page 1

	Year	Citations
Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, Science GeneticsDisease Gene IdentificationSocial SciencesMendelian DisorderDj-1 Protein	2003	2.8K
Variant of <i>TREM2</i> Associated with the Risk of Alzheimer's Disease Thorlákur Jónsson, Hreinn Stefánsson, Stacy Steinberg, New England Journal of Medicine	2012	2.5K
Hundreds of variants clustered in genomic loci and biological pathways affect human height Hana Lango Allen, Karol Estrada, Guillaume Lettre, Nature Genome-wide Association StudyGenetic AnalysisAllelic VariantQuantitative GeneticsGenotype-phenotype Association	2010	2K
GenABEL: an R library for genome-wide association analysis Yurii S. Aulchenko, Stephan Ripke, Aaron Isaacs, Bioinformatics	2007	1.9K
Large-scale association analyses identify host factors influencing human gut microbiome composition Alexander Kurilshikov, Carolina Medina‐Gómez, Rodrigo Bacigalupe, Nature Genetics DysbiosisHost-microbe InteractionsLarge-scale AssociationHost FactorsMicrobiota	2021	1.7K
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, Nature Genetics Genome-wide Association StudyOcular DiseaseOphthalmologyGeneticsAge-related Diseases	2015	1.6K
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 Marc Cruts, Ilse Gijselinck, Julie van der Zee, Nature Neurodegenerative DiseasesAlzheimer's DiseaseMendelian DisorderNull MutationsGenetic Disorder	2006	1.5K
Genome-wide association study identifies 74 loci associated with educational attainment Aysu Okbay, Jonathan Beauchamp, Mark Alan Fontana, Nature Genome-wide Association StudyGenotype-phenotype AssociationMedicineGeneticsEducational Attainment	2016	1.5K
The Rotterdam Study: objectives and design update Albert Hofman, Monique M.B. Breteler, Cornelia M. van Duijn, European Journal of Epidemiology	2007	1.4K
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease Valentina Escott‐Price, Céline Bellenguez, Li‐San Wang, PLoS ONE	2014	1.4K

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