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Freerk van Dijk
Freerk van Dijk
Programmer at University Medical Center Groningen
Verified email at umcg.nl
Title
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Cited by
Year
Cohort Profile: LifeLines, a three-generation cohort study and biobank
S Scholtens, N Smidt, MA Swertz, SJL Bakker, A Dotinga, JM Vonk, ...
International journal of epidemiology 44 (4), 1172-1180, 2015
8462015
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Nature genetics 46 (8), 818-825, 2014
7062014
Disease variants alter transcription factor levels and methylation of their binding sites
MJ Bonder, R Luijk, DV Zhernakova, M Moed, P Deelen, M Vermaat, ...
Nature genetics 49 (1), 131-138, 2017
4462017
Identification of context-dependent expression quantitative trait loci in whole blood
DV Zhernakova, P Deelen, M Vermaat, M Van Iterson, M Van Galen, ...
Nature genetics 49 (1), 139-145, 2017
4422017
Genetic and environmental influences interact with age and sex in shaping the human methylome
J Van Dongen, MG Nivard, G Willemsen, JJ Hottenga, Q Helmer, ...
Nature communications 7 (1), 11115, 2016
3482016
The Genome of the Netherlands: design, and project goals
DI Boomsma, C Wijmenga, EP Slagboom, MA Swertz, LC Karssen, ...
European journal of human genetics 22 (2), 221-227, 2014
3232014
DNA methylation analysis identifies loci for blood pressure regulation
MA Richard, T Huan, S Ligthart, R Gondalia, MA Jhun, JA Brody, MR Irvin, ...
The American Journal of Human Genetics 101 (6), 888-902, 2017
1712017
Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19
A Duarri, J Jezierska, M Fokkens, M Meijer, HJ Schelhaas, ...
Annals of neurology 72 (6), 870-880, 2012
1532012
Characteristics of de novo structural changes in the human genome
WP Kloosterman, LC Francioli, F Hormozdiari, T Marschall, JY Hehir-Kwa, ...
Genome research 25 (6), 792-801, 2015
1512015
Improving phenotypic prediction by combining genetic and epigenetic associations
S Shah, MJ Bonder, RE Marioni, Z Zhu, AF McRae, A Zhernakova, ...
The American Journal of Human Genetics 97 (1), 75-85, 2015
1482015
Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’
P Deelen, A Menelaou, EM Van Leeuwen, A Kanterakis, F Van Dijk, ...
European Journal of Human Genetics 22 (11), 1321-1326, 2014
1212014
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants
JY Hehir-Kwa, T Marschall, WP Kloosterman, LC Francioli, JA Baaijens, ...
Nature communications 7 (1), 1-10, 2016
1042016
Population-specific genotype imputations using minimac or IMPUTE2
EM Van Leeuwen, A Kanterakis, P Deelen, MV Kattenberg, PE Slagboom, ...
Nature protocols 10 (9), 1285-1296, 2015
972015
CoNVaDING: single exon variation detection in targeted NGS data
LF Johansson, F van Dijk, EN de Boer, KK van Dijk‐Bos, JDH Jongbloed, ...
Human mutation 37 (5), 457-464, 2016
952016
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs
I Ricaño-Ponce, DV Zhernakova, P Deelen, O Luo, X Li, A Isaacs, ...
Journal of autoimmunity 68, 62-74, 2016
812016
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
V Iotchkova, J Huang, JA Morris, D Jain, C Barbieri, K Walter, JL Min, ...
Nature genetics 48 (11), 1303-1312, 2016
802016
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency
A Kiezun, SL Pulit, LC Francioli, F van Dijk, M Swertz, DI Boomsma, ...
PLoS genetics 9 (2), e1003301, 2013
722013
Epigenome-wide association study of attention-deficit/hyperactivity disorder symptoms in adults
J van Dongen, NR Zilhão, K Sugden, BT Heijmans, P AC’t Hoen, ...
Biological psychiatry 86 (8), 599-607, 2019
602019
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
512015
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly
A Kim, C Savary, C Dubourg, W Carré, C Mouden, H Hamdi-Roze, ...
Brain 142 (1), 35-49, 2019
472019
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