Lars Eijssen

2.9k total citations
50 papers, 954 citations indexed

About

Lars Eijssen is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Lars Eijssen has authored 50 papers receiving a total of 954 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 8 papers in Cancer Research and 7 papers in Genetics. Recurrent topics in Lars Eijssen's work include Bioinformatics and Genomic Networks (8 papers), Gene expression and cancer classification (6 papers) and Epigenetics and DNA Methylation (6 papers). Lars Eijssen is often cited by papers focused on Bioinformatics and Genomic Networks (8 papers), Gene expression and cancer classification (6 papers) and Epigenetics and DNA Methylation (6 papers). Lars Eijssen collaborates with scholars based in Netherlands, United Kingdom and United States. Lars Eijssen's co-authors include Chris T. Evelo, Michiel Adriaens, Stan Gaj, Martina Kutmon, Magali Jaillard, Laurence de Nijs, Susan L. Coort, Philip J. de Groot, Michael Müller and Bart P. F. Rutten and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Lars Eijssen

47 papers receiving 940 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lars Eijssen Netherlands 20 423 143 126 121 100 50 954
Luiz Alexandre Viana Magno Brazil 17 480 1.1× 235 1.6× 57 0.5× 77 0.6× 71 0.7× 41 1.3k
Rene Cortese United States 18 383 0.9× 77 0.5× 93 0.7× 83 0.7× 47 0.5× 39 853
Xue Zhang China 18 446 1.1× 40 0.3× 72 0.6× 115 1.0× 73 0.7× 107 1.2k
Glenn A. Doyle United States 19 722 1.7× 182 1.3× 65 0.5× 306 2.5× 120 1.2× 50 1.4k
Manisha Gupte United States 20 393 0.9× 107 0.7× 82 0.7× 45 0.4× 63 0.6× 28 1.5k
Khalid A. Fakhro Qatar 19 672 1.6× 488 3.4× 87 0.7× 88 0.7× 85 0.8× 67 1.5k
Radka Kaneva Bulgaria 20 595 1.4× 274 1.9× 37 0.3× 260 2.1× 53 0.5× 130 1.4k
Katrin Frauenknecht Germany 22 451 1.1× 115 0.8× 59 0.5× 75 0.6× 34 0.3× 57 1.2k
Yang Lü China 19 319 0.8× 61 0.4× 92 0.7× 62 0.5× 42 0.4× 68 943

Countries citing papers authored by Lars Eijssen

Since Specialization
Citations

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

Fields of papers citing papers by Lars Eijssen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lars Eijssen

This figure shows the co-authorship network connecting the top 25 collaborators of Lars Eijssen. A scholar is included among the top collaborators of Lars Eijssen 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 Lars Eijssen. Lars Eijssen 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.
Eijssen, Lars, et al.. (2025). The inconclusive superiority debate of allogeneic versus autologous MSCs in treating patients with HFrEF: a systematic review and meta-analysis of RCTs. Stem Cell Research & Therapy. 16(1). 175–175. 1 indexed citations
2.
Koetsier, J.C., Jonathan Mélius, Martina Kutmon, et al.. (2024). A novel insight into neurological disorders through HDAC6 protein–protein interactions. Scientific Reports. 14(1). 14666–14666. 8 indexed citations
3.
Koetsier, J.C., Ana Rita Gomes, Maria Margarida Diogo, et al.. (2024). Involvement of extracellular vesicle microRNA clusters in developing healthy and Rett syndrome brain organoids. Cellular and Molecular Life Sciences. 81(1). 410–410. 3 indexed citations
4.
Kutmon, Martina, Theo G. M. F. Gorgels, Chris T. Evelo, et al.. (2022). A systematically derived overview of the non-ubiquitous pathways and genes that define the molecular and genetic signature of the healthy trabecular meshwork. Genomics. 114(2). 110280–110280. 1 indexed citations
5.
Cavill, Rachel, Annelien Duits, Sebastian Köhler, et al.. (2022). Machine learning-based prediction of cognitive outcomes in de novo Parkinson’s disease. npj Parkinson s Disease. 8(1). 150–150. 25 indexed citations
6.
Mohren, Ronny, Berta Cillero‐Pastor, Zhao‐Qing Shen, et al.. (2020). Comparative proteomic analysis of human mesenchymal stromal cell behavior on calcium phosphate ceramics with different osteoinductive potential. Materials Today Bio. 7. 100066–100066. 20 indexed citations
7.
Ehrhart, Friederike, Susan L. Coort, Lars Eijssen, et al.. (2019). Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes. The World Journal of Biological Psychiatry. 21(10). 712–725. 20 indexed citations
8.
Eijssen, Lars, Martina Kutmon, Martin Hewison, et al.. (2019). A bioinformatics workflow to decipher transcriptomic data from vitamin D studies. The Journal of Steroid Biochemistry and Molecular Biology. 189. 28–35. 4 indexed citations
9.
Cirillo, Elisa, Martina Kutmon, Manuel A. González Hernández, et al.. (2018). From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results. PLoS ONE. 13(4). e0193515–e0193515. 34 indexed citations
10.
Cirillo, Elisa, Samar Tareen, Amjad Ali, et al.. (2018). Biological Pathways Leading From ANGPTL8 to Diabetes Mellitus–A Co-expression Network Based Analysis. Frontiers in Physiology. 9. 1841–1841. 6 indexed citations
11.
Eijssen, Lars, Michiel Adriaens, Tim J. M. Welting, et al.. (2017). PRC1 Prevents Replication Stress during Chondrogenic Transit Amplification. Epigenomes. 1(3). 22–22. 1 indexed citations
12.
Cirillo, Elisa, Samar Tareen, Amjad Ali, et al.. (2017). Visualizing the regulatory role of Angiopoietin-like protein 8 (ANGPTL8) in glucose and lipid metabolic pathways. Genomics. 109(5-6). 408–418. 25 indexed citations
13.
Adriaens, Michiel, Peggy Prickaerts, Michelle Chan‐Seng‐Yue, et al.. (2016). Quantitative analysis of ChIP-seq data uncovers dynamic and sustained H3K4me3 and H3K27me3 modulation in cancer cells under hypoxia. Epigenetics & Chromatin. 9(1). 48–48. 20 indexed citations
14.
Nelissen, E. C. M., John C.M. Dumoulin, Florence Busato, et al.. (2014). Altered gene expression in human placentas after IVF/ICSI. Human Reproduction. 29(12). 2821–2831. 53 indexed citations
15.
Adriaens, Michiel, et al.. (2012). Molecular Pathways Involved in Prostate Carcinogenesis: Insights from Public Microarray Datasets. PLoS ONE. 7(11). e49831–e49831. 15 indexed citations
16.
Adriaens, Michiel, Magali Jaillard, Lars Eijssen, Claus Mayer, & Chris T. Evelo. (2012). An evaluation of two-channel ChIP-on-chip and DNA methylation microarray normalization strategies. BMC Genomics. 13(1). 42–42. 17 indexed citations
17.
Kelder, Thomas, Lars Eijssen, Robert Kleemann, et al.. (2011). Exploring pathway interactions in insulin resistant mouse liver. BMC Systems Biology. 5(1). 127–127. 13 indexed citations
18.
Eijssen, Lars, B.J.C. van den Bosch, Nicolas Vignier, et al.. (2007). Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice. Genomics. 91(1). 52–60. 11 indexed citations
19.
Eijssen, Lars, Patrick Lindsey, Ralf Peeters, et al.. (2007). A novel stepwise analysis procedure of genome‐wide expression profiles identifies transcript signatures of thiamine genes as classifiers of mitochondrial mutants. Yeast. 25(2). 129–140. 1 indexed citations
20.
Gerards, Mike, Lars Eijssen, Alexandra T.M. Hendrickx, et al.. (2006). Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients. Genetics in Medicine. 8(10). 620–627. 28 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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