Jeroen van Rooij - Concepedia

Author

Jeroen van Rooij

Also Known As

A.G. Uitterlinden, Abbe Ullgren, Anne Tybjærg-Hansen, Boer, Cindy G., Chambert, Kimberly, Cornelia M. van Duijn, H. Eka D. Suchiman, Henne Holstege, Irene Nooren, J G J van Rooij

192

Publications

10K

Citations

H-Index

106

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam Amsterdam Neuroscience Leiden University Medical Center University Medical Center Groningen

About

Jeroen van Rooij is an author at Erasmus MC specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	22	2.4K
2	Public Health	6	6	879
3	Engineering	3	3	181
4	Health Sciences	2	2	34
5	Natural Sciences	1	1	24

Jeroen van Rooij

Publications

7.7K

Citations

H-Index

Page 1

	Year	Citations
New insights into the genetic etiology of Alzheimer’s disease and related dementias Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Nature Genetics	2022	2.3K
Disease variants alter transcription factor levels and methylation of their binding sites Marc Jan Bonder, René Luijk, Daria V. Zhernakova, Nature Genetics Epigenetic ChangeGeneticsDna MethylationEpigenomicsDisease Gene Identification	2016	544
Identification of context-dependent expression quantitative trait loci in whole blood Daria V. Zhernakova, Patrick Deelen, Martijn Vermaat, Nature Genetics Genome-wide Association StudyAllelic VariantQuantitative GeneticsGenotype-phenotype AssociationMedicine	2016	502
Quantifying prion disease penetrance using large population control cohorts Eric Vallabh Minikel, Sonia M. Vallabh, Monkol Lek, Science Translational Medicine	2016	448
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease Laurie Robak, Iris E. Jansen, Jeroen van Rooij, Brain GeneticsGenetic EpidemiologyVariant BurdenDisease Gene IdentificationGenome-wide Association Study	2017	440
Genetic and environmental influences interact with age and sex in shaping the human methylome Jenny van Dongen, Michel G. Nivard, Gonneke Willemsen, Nature Communications	2016	410
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits Eleonora Porcu, Sina Rüeger, Kaido Lepik, Nature Communications	2019	330
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease Henne Holstege, Marc Hulsman, Camille Charbonnier, Nature Genetics	2022	206
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations Sonia Shah, Marc Jan Bonder, Riccardo E. Marioni, The American Journal of Human Genetics	2015	154
MicroRNA signatures in peripheral blood mononuclear cells of chronic heart failure patients Christine Voellenkle, Jeroen van Rooij, Claudia Cappuzzello, Physiological Genomics Microrna SignaturesCardiomyopathyHeart FailureCardiac ReprogrammingMirna Signature	2010	137

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