Jane Merlevede

706 total citations
7 papers, 163 citations indexed

About

Jane Merlevede is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Jane Merlevede has authored 7 papers receiving a total of 163 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Cancer Research and 3 papers in Genetics. Recurrent topics in Jane Merlevede's work include Glioma Diagnosis and Treatment (3 papers), Cancer Genomics and Diagnostics (2 papers) and Bioinformatics and Genomic Networks (2 papers). Jane Merlevede is often cited by papers focused on Glioma Diagnosis and Treatment (3 papers), Cancer Genomics and Diagnostics (2 papers) and Bioinformatics and Genomic Networks (2 papers). Jane Merlevede collaborates with scholars based in France, Kazakhstan and Germany. Jane Merlevede's co-authors include Stéphanie Puget, Thomas Kergrohen, David Castel, E. Barret, Jacques Grill, Marie‐Anne Debily, Pascale Varlet, Cathy Philippe, Martin Sill and Christian Sainte‐Rose and has published in prestigious journals such as Bioinformatics, Oncogene and Clinical Cancer Research.

In The Last Decade

Jane Merlevede

6 papers receiving 161 citations

Peers

Jane Merlevede
Andrea Franson United States
Lihong Long United States
Kyle Wierzbicki United States
Amanda L. Rynearson United States
Elke Pfaff Germany
Andrea Franson United States
Jane Merlevede
Citations per year, relative to Jane Merlevede Jane Merlevede (= 1×) peers Andrea Franson

Countries citing papers authored by Jane Merlevede

Since Specialization
Citations

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

Fields of papers citing papers by Jane Merlevede

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jane Merlevede

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

All Works

7 of 7 papers shown
1.
Guerrini‐Rousseau, Léa, Jane Merlevede, Felipe Andreiuolo, et al.. (2024). Glioma oncogenesis in the Constitutional mismatch repair deficiency (CMMRD) syndrome. Neuro-Oncology Advances. 6(1). vdae120–vdae120.
2.
Merlevede, Jane, et al.. (2022). BIODICA: a computational environment for Independent Component Analysis of omics data. Bioinformatics. 38(10). 2963–2964. 5 indexed citations
3.
Merlevede, Jane, et al.. (2020). Systems Biology Analysis for Ewing Sarcoma. Methods in molecular biology. 2226. 303–333. 1 indexed citations
4.
Barret, E., Gwénaël Le Teuff, Jane Merlevede, et al.. (2019). TP53 Pathway Alterations Drive Radioresistance in Diffuse Intrinsic Pontine Gliomas (DIPG). Clinical Cancer Research. 25(22). 6788–6800. 62 indexed citations
5.
Barret, E., Jane Merlevede, Thomas Kergrohen, et al.. (2019). A kinome-wide shRNA screen uncovers vaccinia-related kinase 3 (VRK3) as an essential gene for diffuse intrinsic pontine glioma survival. Oncogene. 38(38). 6479–6490. 11 indexed citations
6.
Castel, David, Cathy Philippe, Thomas Kergrohen, et al.. (2018). Transcriptomic and epigenetic profiling of ‘diffuse midline gliomas, H3 K27M-mutant’ discriminate two subgroups based on the type of histone H3 mutated and not supratentorial or infratentorial location. Acta Neuropathologica Communications. 6(1). 117–117. 83 indexed citations
7.
Merlevede, Jane, Felipe Andreiuolo, Marie-Anne Debily, et al.. (2018). HGG-42. GLIOMA ONCOGENESIS IN CONSTITUTIONNAL MISMATCH REPAIR DEFICIENCY (CMMRD) SYNDROME: A CLINICO-PATHOLOGICAL AND MOLECULAR STUDY IN 15 PATIENTS. Neuro-Oncology. 20(suppl_2). i97–i98. 1 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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