Maité Cabes

694 total citations
10 papers, 139 citations indexed

About

Maité Cabes is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Maité Cabes has authored 10 papers receiving a total of 139 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Maité Cabes's work include Chronic Lymphocytic Leukemia Research (6 papers), Glycosylation and Glycoproteins Research (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). Maité Cabes is often cited by papers focused on Chronic Lymphocytic Leukemia Research (6 papers), Glycosylation and Glycoproteins Research (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). Maité Cabes collaborates with scholars based in United Kingdom, Belgium and Sweden. Maité Cabes's co-authors include Toby A. Eyre, Anna Schuh, Ruth Clifford, Andrew Wotherspoon, Elizabeth J. Soilleux, Niamh Appleby, Hélène Dreau, José I. Martı́n-Subero, Niko Popitsch and Mats Ehinger and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and BMC Cancer.

In The Last Decade

Maité Cabes

8 papers receiving 137 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maité Cabes United Kingdom 5 100 96 47 41 39 10 139
Pauline Robbe United Kingdom 5 91 0.9× 88 0.9× 25 0.5× 34 0.8× 42 1.1× 14 137
Grégory Lazarian France 5 176 1.8× 136 1.4× 54 1.1× 34 0.8× 70 1.8× 17 203
Iryna Kryachok Ukraine 8 127 1.3× 123 1.3× 64 1.4× 35 0.9× 70 1.8× 23 197
Sean D. Reiff United States 7 135 1.4× 102 1.1× 33 0.7× 45 1.1× 32 0.8× 13 163
Alexander Jethwa Germany 6 127 1.3× 82 0.9× 45 1.0× 72 1.8× 57 1.5× 8 183
Annalisa D’Avola United Kingdom 8 91 0.9× 67 0.7× 21 0.4× 65 1.6× 69 1.8× 13 159
Barbara Mankel Germany 6 36 0.4× 76 0.8× 72 1.5× 43 1.0× 18 0.5× 12 131
Miguel Quijada‐Álamo Spain 9 124 1.2× 68 0.7× 67 1.4× 80 2.0× 66 1.7× 17 191
Jennifer A. Arzt United States 4 65 0.7× 58 0.6× 52 1.1× 64 1.6× 27 0.7× 5 151
C-M Wendtner Germany 5 84 0.8× 57 0.6× 16 0.3× 64 1.6× 31 0.8× 5 148

Countries citing papers authored by Maité Cabes

Since Specialization
Citations

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

Fields of papers citing papers by Maité Cabes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maité Cabes

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

All Works

10 of 10 papers shown
1.
2.
Klintman, Jenny, Niamh Appleby, Basile Stamatopoulos, et al.. (2020). Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia. Blood. 137(20). 2800–2816. 59 indexed citations
3.
4.
Lomas, Oliver, Sarah Gooding, Karthik Ramasamy, et al.. (2019). Clinical-Grade Whole Genome Sequencing Reproduces FISH Cytogenetics and Provides Actionable Data in Newly Diagnosed Myeloma - a Pilot Study from the UK 100,000 Genomes Project. Blood. 134(Supplement_1). 3062–3062. 2 indexed citations
5.
Stamatopoulos, Basile, Pavlos Antoniou, Dimitris Vavoulis, et al.. (2016). Characterization of Recurrent Mutations in Patient with a Richter Syndrome By Targeted Next Generation Sequencing. Blood. 128(22). 3200–3200. 2 indexed citations
6.
7.
Eyre, Toby A., Ruth Clifford, Adrian Bloor, et al.. (2015). SINGLE ARM NCRI FEASIBILITY PHASE II STUDY OF CHOP IN COMBINATION WITH OFATUMUMAB IN INDUCTION AND MAINTENANCE FOR PATIENTS WITH NEWLY DIAGNOSED RICHTER'S SYNDROME. Haematologica. 100. 109–109. 2 indexed citations
8.
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Robbe, Pauline, Adele Timbs, Adam Burns, et al.. (2013). COMPREHENSIVE GENOME-WIDE ANALYSIS OF CLL SAMPLES FROM UK 1ST LINE AND RELAPSED/REFRACTORY CLINICAL TRIALS. Haematologica. 98. 241–241.
10.
Ait‐Tahar, Kamel, Amanda P. Liggins, Graham P. Collins, et al.. (2010). CD4-positive T-helper cell responses to the PASD1 protein in patients with diffuse large B-cell lymphoma. Haematologica. 96(1). 78–86. 12 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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2026