Eric Strengman

29.5k total citations
27 papers, 1.3k citations indexed

About

Eric Strengman is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Eric Strengman has authored 27 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Oncology. Recurrent topics in Eric Strengman's work include Genomic variations and chromosomal abnormalities (7 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Associations and Epidemiology (4 papers). Eric Strengman is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Associations and Epidemiology (4 papers). Eric Strengman collaborates with scholars based in Netherlands, United States and United Kingdom. Eric Strengman's co-authors include Roel A. Ophoff, Cisca Wijmenga, Jacobine E. Buizer‐Voskamp, Simone de Jong, René S. Kahn, Esther Janson, Marco P. Boks, Chiara Sabatti, Steve Horvath and Kristel R. van Eijk and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Eric Strengman

27 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Eric Strengman Netherlands 18 739 518 146 134 120 27 1.3k
Seishi Maeda Japan 20 361 0.5× 156 0.3× 75 0.5× 45 0.3× 133 1.1× 84 1.3k
Jingmin Wang China 22 757 1.0× 400 0.8× 20 0.1× 89 0.7× 88 0.7× 117 1.5k
Yizhou Ye United States 14 349 0.5× 218 0.4× 152 1.0× 56 0.4× 145 1.2× 28 1.0k
Élisabeth André France 16 627 0.8× 202 0.4× 42 0.3× 146 1.1× 195 1.6× 20 1.4k
Amanda L. Lumsden Australia 19 403 0.5× 293 0.6× 123 0.8× 28 0.2× 75 0.6× 42 1.1k
R Giorgi Brazil 15 319 0.4× 165 0.3× 52 0.4× 77 0.6× 52 0.4× 39 816
Toshihiro Uesaka Japan 20 431 0.6× 212 0.4× 252 1.7× 31 0.2× 81 0.7× 45 1.4k
Jian‐Huan Chen China 21 573 0.8× 204 0.4× 15 0.1× 65 0.5× 88 0.7× 71 1.1k
Hui Guo China 18 736 1.0× 502 1.0× 13 0.1× 38 0.3× 108 0.9× 96 1.4k
Tomasz Brudek Denmark 21 478 0.6× 121 0.2× 42 0.3× 162 1.2× 127 1.1× 47 1.5k

Countries citing papers authored by Eric Strengman

Since Specialization
Citations

This map shows the geographic impact of Eric Strengman'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 Eric Strengman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Strengman more than expected).

Fields of papers citing papers by Eric Strengman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric Strengman. 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 Eric Strengman. The network helps show where Eric Strengman may publish in the future.

Co-authorship network of co-authors of Eric Strengman

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Strengman. A scholar is included among the top collaborators of Eric Strengman 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 Eric Strengman. Eric Strengman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Strengman, Eric, et al.. (2019). Amplicon-Based Targeted Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue. Methods in molecular biology. 1908. 1–17. 5 indexed citations
2.
Gómez-Cuadrado, Laura, Milou Tenhagen, Adam Byron, et al.. (2018). E-cadherin loss induces targetable autocrine activation of growth factor signalling in lobular breast cancer. Scientific Reports. 8(1). 15454–15454. 42 indexed citations
3.
Albersen, Monique, Marjolein Bosma, Jurjen J. Luykx, et al.. (2014). Vitamin B-6 vitamers in human plasma and cerebrospinal fluid. American Journal of Clinical Nutrition. 100(2). 587–592. 22 indexed citations
4.
Knol, Wilma, Rob J. van Marum, Paul A. F. Jansen, et al.. (2013). Genetic Variation and the Risk of Haloperidol-Related Parkinsonism in Elderly Patients. Journal of Clinical Psychopharmacology. 33(3). 405–410. 12 indexed citations
5.
Luykx, Jurjen J., Steven C. Bakker, Christiaan H. Vinkers, et al.. (2013). D-Amino Acid Aberrations in Cerebrospinal Fluid and Plasma of Smokers. Neuropsychopharmacology. 38(10). 2019–2026. 17 indexed citations
6.
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
7.
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
8.
Jong, Simone de, Marco P. Boks, Tova F Fuller, et al.. (2012). A Gene Co-Expression Network in Whole Blood of Schizophrenia Patients Is Independent of Antipsychotic-Use and Enriched for Brain-Expressed Genes. PLoS ONE. 7(6). e39498–e39498. 112 indexed citations
9.
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
10.
Luykx, Jurjen J., Marco P. Boks, Elemi Breetvelt, et al.. (2012). BDNF Val66Met homozygosity does not influence plasma BDNF levels in healthy human subjects. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 43. 185–187. 13 indexed citations
11.
Jong, Simone de, Iouri Chepelev, Esther Janson, et al.. (2012). Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. BMC Genomics. 13(1). 458–458. 43 indexed citations
12.
Buizer‐Voskamp, Jacobine E., Jan-Willem Muntjewerff, Eric Strengman, et al.. (2011). Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients. Biological Psychiatry. 70(7). 655–662. 54 indexed citations
13.
Jong, Simone de, Tova F Fuller, Esther Janson, et al.. (2010). Gene expression profiling in C57BL/6J and A/J mouse inbred strains reveals gene networks specific for brain regions independent of genetic background. BMC Genomics. 11(1). 20–20. 16 indexed citations
14.
Muntjewerff, Jan-Willem, Roel A. Ophoff, Jacobine E. Buizer‐Voskamp, Eric Strengman, & Martin den Heijer. (2010). Effects of season of birth and a common MTHFR gene variant on the risk of schizophrenia. European Neuropsychopharmacology. 21(4). 300–305. 17 indexed citations
15.
Réthelyi, János, Steven C. Bakker, Pál Czobor, et al.. (2009). Association study of NRG1, DTNBP1, RGS4, G72/G30, and PIP5K2A with schizophrenia and symptom severity in a Hungarian sample. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(3). 792–801. 44 indexed citations
16.
Vrijenhoek, Terry, Jacobine E. Buizer‐Voskamp, Inge van der Stelt, et al.. (2008). Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients. The American Journal of Human Genetics. 83(4). 504–510. 202 indexed citations
17.
Diosdado, Begoña, Harm van Bakel, Eric Strengman, et al.. (2007). Neutrophil Recruitment and Barrier Impairment in Celiac Disease: A Genomic Study. Clinical Gastroenterology and Hepatology. 5(5). 574–581.e5. 36 indexed citations
18.
Sandkuijl, Lodewijk A., et al.. (2003). Variance‐Component Analysis of Obesity in Type 2 Diabetes Confirms Loci on Chromosomes 1q and 11q. Obesity Research. 11(11). 1290–1294. 13 indexed citations
19.
Wijmenga, Cisca, R. Scott Hansen, Giorgio Gimelli, et al.. (2000). Genetic variation in ICF syndrome: Evidence for genetic heterogeneity. Human Mutation. 16(6). 509–517. 66 indexed citations
20.
Wijmenga, Cisca, Lambert P.W.J. van den Heuvel, Eric Strengman, et al.. (1998). Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping. The American Journal of Human Genetics. 63(3). 803–809. 42 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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