Freerk van Dijk - Concepedia

Author

Freerk van Dijk

Also Known As

Androniki Menelaou, Dasha V. Zhernakova, Dijk, Freerk, Dijk, Freerk Van, F DIJK, F Dijk, F van Dijk, F. Dijk, F. Van Dijk, F. van Dijk

118

Publications

5.6K

Citations

H-Index

Concepts

All Affiliations

University of Groningen University Medical Center Groningen University Medical Center Utrecht Erasmus MC Leiden University Medical Center

About

Freerk van Dijk is an author at University of Groningen specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	18	2.4K
2	Public Health	6	6	1.5K
3	Engineering	4	4	180
4	Anatomy	2	2	26
5	Social Sciences	1	1	25

Freerk van Dijk

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
Cohort Profile: LifeLines, a three-generation cohort study and biobank Salome Scholtens, Nynke Smidt, Morris A. Swertz, International Journal of Epidemiology Life AssessmentAgingGenetic EpidemiologyDatabasesHealth Studies	2014	846
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
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
The Genome of the Netherlands: design, and project goals Dorret I. Boomsma, Cisca Wijmenga, P. Eline Slagboom, European Journal of Human Genetics	2013	276
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
Mutations in potassium channel <i>kcnd3</i> cause spinocerebellar ataxia type 19 Anna Duarri, Justyna Jezierska, Michiel R. Fokkens, Annals of Neurology	2012	134
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants Jayne Y. Hehir‐Kwa, Tobias Marschall, Wigard P. Kloosterman, Nature Communications	2016	113
Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’ Patrick Deelen, Androniki Menelaou, Alexandros Kanterakis, European Journal of Human Genetics	2014	110

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