Kristel R. van Eijk

6.1k total citations
23 papers, 783 citations indexed

About

Kristel R. van Eijk is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Kristel R. van Eijk has authored 23 papers receiving a total of 783 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Kristel R. van Eijk's work include Genetic Associations and Epidemiology (7 papers), Genetic Syndromes and Imprinting (4 papers) and Epigenetics and DNA Methylation (4 papers). Kristel R. van Eijk is often cited by papers focused on Genetic Associations and Epidemiology (7 papers), Genetic Syndromes and Imprinting (4 papers) and Epigenetics and DNA Methylation (4 papers). Kristel R. van Eijk collaborates with scholars based in Netherlands, United States and United Kingdom. Kristel R. van Eijk's co-authors include René S. Kahn, Marco P. Boks, Roel A. Ophoff, Jan H. Veldink, Flip Mulder, Leonard H. van den Berg, Eric Strengman, Simone de Jong, Lude Franke and Clara C. Elbers and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Scientific Reports.

In The Last Decade

Kristel R. van Eijk

22 papers receiving 773 citations

Peers

Kristel R. van Eijk

GENET

PMH

NEURO

Yoav Kohn Israel

Sally L. Ricketts United Kingdom

Derek Spieler Germany

Elisa De Grandis Italy

Erik Boot Netherlands

Zia Choudhry Canada

Pingxing Xie Canada

Tamar Green United States

Elizabeth A. Lovejoy United Kingdom

Vivek Appadurai United States

Yoav Kohn Israel

Kristel R. van Eijk

332 ×0.9

402 ×1.5

GENET

231 ×1.7

PMH

71 ×0.8

NEURO

156 ×2.1

Citations per year, relative to Kristel R. van Eijk Kristel R. van Eijk (= 1×) peers Yoav Kohn

Countries citing papers authored by Kristel R. van Eijk

Since Specialization

Citations

This map shows the geographic impact of Kristel R. van Eijk's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kristel R. van Eijk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristel R. van Eijk more than expected).

Fields of papers citing papers by Kristel R. van Eijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kristel R. van Eijk. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kristel R. van Eijk. The network helps show where Kristel R. van Eijk may publish in the future.

Co-authorship network of co-authors of Kristel R. van Eijk

This figure shows the co-authorship network connecting the top 25 collaborators of Kristel R. van Eijk. A scholar is included among the top collaborators of Kristel R. van Eijk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kristel R. van Eijk. Kristel R. van Eijk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lin, Bochao, Jentien M. Vermeulen, Koen Bolhuis, et al.. (2023). Associations between genetic liabilities to smoking behavior and schizophrenia symptoms in patients with a psychotic disorder, their siblings and healthy controls. Psychiatry Research. 323. 115143–115143.

Paquin, Vincent, Lotta-Katrin Pries, Margreet ten Have, et al.. (2022). Age- and sex-specific associations between risk scores for schizophrenia and self-reported health in the general population. Social Psychiatry and Psychiatric Epidemiology. 58(1). 43–52. 2 indexed citations

Marchi, Mattia, Willemijn van Gastel, Chris D. Schubart, et al.. (2022). Childhood maltreatment mediates the effect of the genetic background on psychosis risk in young adults. Translational Psychiatry. 12(1). 219–219. 7 indexed citations

Schick, Anita, Ruud van Winkel, Bochao Lin, et al.. (2022). Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study. Psychological Medicine. 53(7). 2798–2807. 7 indexed citations

Hop, Paul J., Ramona A. J. Zwamborn, Eilís Hannon, et al.. (2020). Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies. NAR Genomics and Bioinformatics. 2(4). lqaa105–lqaa105. 15 indexed citations

Pazoki, Raha, Bochao Lin, Kristel R. van Eijk, et al.. (2020). Phenome-wide and genome-wide analyses of quality of life in schizophrenia. BJPsych Open. 7(1). e13–e13. 6 indexed citations

Wadman, Renske I., Marc Jansen, Ewout J. N. Groen, et al.. (2020). Analysis of FUS , PFN2, TDP-43 , and PLS3 as potential disease severity modifiers in spinal muscular atrophy. Neurology Genetics. 6(1). e386–e386. 13 indexed citations

Tan, Harold H G, Henk‐Jan Westeneng, Hannelore K. van der Burgh, et al.. (2020). The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis. Annals of Neurology. 88(4). 796–806. 23 indexed citations

Dekker, Annelot M., Frank P. Diekstra, Sara L. Pulit, et al.. (2019). Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis. Scientific Reports. 9(1). 5931–5931. 11 indexed citations

10.

Eijk, Ruben P. A. van, Marinus J.C. Eijkemans, Stavros Nikolakopoulos, et al.. (2019). Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?. The Pharmacogenomics Journal. 20(2). 220–226. 14 indexed citations

11.

Hiemstra, Marieke, Stefanie A. Nelemans, Susan Branje, et al.. (2018). Genetic vulnerability to schizophrenia is associated with cannabis use patterns during adolescence. Drug and Alcohol Dependence. 190. 143–150. 23 indexed citations

12.

Rheenen, Wouter van, Frank P. Diekstra, Oliver Harschnitz, et al.. (2018). Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study. PLoS ONE. 13(6). e0198874–e0198874. 38 indexed citations

13.

Vink, Matthijs, Max de Leeuw, Jurjen J. Luykx, et al.. (2015). DRD2 Schizophrenia-Risk Allele Is Associated With Impaired Striatal Functioning in Unaffected Siblings of Schizophrenia Patients. Schizophrenia Bulletin. 42(3). 843–850. 21 indexed citations

14.

Eijk, Kristel R. van, Simone de Jong, Eric Strengman, et al.. (2014). Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood. European Journal of Human Genetics. 23(8). 1106–1110. 40 indexed citations

15.

Plongthongkum, Nongluk, Kristel R. van Eijk, Simone de Jong, et al.. (2014). Characterization of Genome-Methylome Interactions in 22 Nuclear Pedigrees. PLoS ONE. 9(7). e99313–e99313. 12 indexed citations

16.

Vinkers, Christiaan H., Willemijn A. van Gastel, Kristel R. van Eijk, et al.. (2013). The effect of childhood maltreatment and cannabis use on adult psychotic symptoms is modified by the COMT Val158Met polymorphism. Schizophrenia Research. 150(1). 303–311. 54 indexed citations

17.

Buizer‐Voskamp, Jacobine E., Hylke M. Blauw, Marco P. Boks, et al.. (2013). Increased paternal age and the influence on burden of genomic copy number variation in the general population. Human Genetics. 132(4). 443–450. 29 indexed citations

18.

Eijk, Kristel R. van, Simone de Jong, Marco P. Boks, et al.. (2012). Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. BMC Genomics. 13(1). 636–636. 162 indexed citations

19.

Jong, Simone de, Kristel R. van Eijk, Eric Strengman, et al.. (2012). Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes. European Journal of Human Genetics. 20(9). 1004–1008. 50 indexed citations

20.

Luykx, Jurjen J., Christiaan H. Vinkers, Steven C. Bakker, et al.. (2012). A Common Variant in ERBB4 Regulates GABA Concentrations in Human Cerebrospinal Fluid. Neuropsychopharmacology. 37(9). 2088–2092. 15 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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