Chris T. Evelo

32.2k total citations · 2 hit papers
175 papers, 6.9k citations indexed

About

Chris T. Evelo is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Chris T. Evelo has authored 175 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Molecular Biology, 24 papers in Genetics and 21 papers in Physiology. Recurrent topics in Chris T. Evelo's work include Bioinformatics and Genomic Networks (45 papers), Biomedical Text Mining and Ontologies (21 papers) and Glutathione Transferases and Polymorphisms (19 papers). Chris T. Evelo is often cited by papers focused on Bioinformatics and Genomic Networks (45 papers), Biomedical Text Mining and Ontologies (21 papers) and Glutathione Transferases and Polymorphisms (19 papers). Chris T. Evelo collaborates with scholars based in Netherlands, United States and United Kingdom. Chris T. Evelo's co-authors include Alexander R. Pico, Thomas Kelder, Kristina Hanspers, Martijn van Iersel, Martina Kutmon, Bruce R. Conklin, Susan L. Coort, Egon Willighagen, Andra Waagmeester and Anwesha Bohler and has published in prestigious journals such as Nucleic Acids Research, Circulation and SHILAP Revista de lepidopterología.

In The Last Decade

Chris T. Evelo

171 papers receiving 6.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

WikiPathways: connecting communities

2020 507 citations Marvin Martens, Ammar Ammar et al. Nucleic Acids Research profile →
The Chemistry Development Kit (CDK) v2.0: atom typing, depiction, molecular formulas, and substructure searching

2017 366 citations Egon Willighagen, Chris T. Evelo et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chris T. Evelo Netherlands	40	4.0k	765	722	706	694	175	6.9k
Noa Rappaport United States	20	3.4k 0.8×	743 1.0×	468 0.6×	500 0.7×	809 1.2×	34	5.8k
C. George Priya Doss India	41	3.8k 0.9×	916 1.2×	347 0.5×	454 0.6×	573 0.8×	331	6.7k
Tsippi Iny Stein Israel	13	4.1k 1.0×	1.0k 1.3×	677 0.9×	375 0.5×	938 1.4×	13	6.9k
Naomi Rosen Israel	8	3.5k 0.9×	870 1.1×	541 0.7×	307 0.4×	776 1.1×	13	5.9k
Marilyn Safran Israel	25	5.4k 1.3×	1.3k 1.7×	728 1.0×	454 0.6×	1.3k 1.9×	32	8.8k
Ismail Kola Australia	43	4.0k 1.0×	552 0.7×	831 1.2×	649 0.9×	760 1.1×	94	8.1k
Ruth Roberts United Kingdom	45	3.0k 0.7×	826 1.1×	549 0.8×	422 0.6×	376 0.5×	148	6.4k
Alexander R. Pico United States	30	5.7k 1.4×	1.0k 1.4×	510 0.7×	375 0.5×	655 0.9×	57	7.8k
Ferrán Sanz Spain	35	5.1k 1.3×	683 0.9×	1.6k 2.3×	442 0.6×	767 1.1×	187	8.8k
Maureen A. Sartor United States	49	5.1k 1.3×	1.4k 1.8×	350 0.5×	715 1.0×	895 1.3×	169	8.6k

Countries citing papers authored by Chris T. Evelo

Since Specialization

Citations

This map shows the geographic impact of Chris T. Evelo'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 Chris T. Evelo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chris T. Evelo more than expected).

Fields of papers citing papers by Chris T. Evelo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chris T. Evelo. 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 Chris T. Evelo. The network helps show where Chris T. Evelo may publish in the future.

Co-authorship network of co-authors of Chris T. Evelo

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Martens, Helge, Norman D. Rosenblum, Andreas Schedl, et al.. (2025). Molecular pathways of kidney development and their applications to clinical research. Kidney International. 109(2). 287–296.

Ammar, Ammar, Chris T. Evelo, & Egon Willighagen. (2024). FAIR assessment of nanosafety data reusability with community standards. Scientific Data. 11(1). 503–503. 6 indexed citations

Mazurenko, Stanislav, Martin Scheringer, Vítor A. P. Martins dos Santos, et al.. (2024). Making PBPK models more reproducible in practice. Briefings in Bioinformatics. 25(6). 5 indexed citations

Slenter, Denise, et al.. (2023). Extending inherited metabolic disorder diagnostics with biomarker interaction visualizations. Orphanet Journal of Rare Diseases. 18(1). 95–95.

Kutmon, Martina, et al.. (2023). Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome. Orphanet Journal of Rare Diseases. 18(1). 335–335. 1 indexed citations

Martínez‐Martínez, Pilar, et al.. (2023). Interactive neuroinflammation pathways and transcriptomics-based identification of drugs and chemical compounds for schizophrenia. The World Journal of Biological Psychiatry. 25(2). 116–129. 2 indexed citations

Martens, Marvin, Chris T. Evelo, & Egon Willighagen. (2022). Providing Adverse Outcome Pathways from the AOP-Wiki in a Semantic Web Format to Increase Usability and Accessibility of the Content. PubMed. 8(1). 2–13. 14 indexed citations

Bishop, Emma L., Danyang Li, Louisa Jeffery, et al.. (2021). Tolerogenic effects of 1,25-dihydroxyvitamin D on dendritic cells involve induction of fatty acid synthesis. The Journal of Steroid Biochemistry and Molecular Biology. 211. 105891–105891. 15 indexed citations

Ehrhart, Friederike, et al.. (2021). A resource to explore the discovery of rare diseases and their causative genes. Scientific Data. 8(1). 124–124. 15 indexed citations

10.

Ehrhart, Friederike, Annika Jacobsen, Maria Rigau, et al.. (2021). A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration. Scientific Data. 8(1). 10–10. 21 indexed citations

11.

Jin, Han, Pieter Goossens, Péter Juhász, et al.. (2021). Integrative multiomics analysis of human atherosclerosis reveals a serum response factor‐driven network associated with intraplaque hemorrhage. SHILAP Revista de lepidopterología. 11(6). e458–e458. 53 indexed citations

12.

Martens, Marvin, Ammar Ammar, Anders Riutta, et al.. (2020). WikiPathways: connecting communities. Nucleic Acids Research. 49(D1). D613–D621. 507 indexed citations breakdown →

13.

Kolk, Birgitta W. van der, Marianthi Kalafati, Michiel Adriaens, et al.. (2019). Subcutaneous Adipose Tissue and Systemic Inflammation Are Associated With Peripheral but Not Hepatic Insulin Resistance in Humans. Diabetes. 68(12). 2247–2258. 45 indexed citations

14.

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

15.

Ehrhart, Friederike, Henk J. van Kranen, Mark D. Wilkinson, et al.. (2018). MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases. Human Mutation. 39(7). 914–924. 13 indexed citations

16.

Ehrhart, Friederike, Sylvia Roozen, Jef Verbeek, et al.. (2018). Review and gap analysis: molecular pathways leading to fetal alcohol spectrum disorders. Molecular Psychiatry. 24(1). 10–17. 54 indexed citations

17.

Ehrhart, Friederike, et al.. (2018). Prader-Willi syndrome and Angelman syndrome: Visualisation of the molecular pathways for two chromosomal disorders. The World Journal of Biological Psychiatry. 20(9). 670–682. 14 indexed citations

18.

Ehrhart, Friederike, Susan L. Coort, Elisa Cirillo, et al.. (2016). New insights in Rett syndrome using pathway analysis for transcriptomics data. Wiener Medizinische Wochenschrift. 166(11-12). 346–352. 8 indexed citations

19.

Ehrhart, Friederike, Susan L. Coort, Elisa Cirillo, et al.. (2016). Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes. Orphanet Journal of Rare Diseases. 11(1). 158–158. 53 indexed citations

20.

Orhan, Hi̇lmi̇, Chris T. Evelo, & Gönül Şahin. (2005). Erythrocyte antioxidant defense response against cigarette smoking in humans—the glutathione S‐transferase vulnerability. Journal of Biochemical and Molecular Toxicology. 19(4). 226–233. 39 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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