Claude Denis

408 total citations
9 papers, 301 citations indexed

About

Claude Denis is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Claude Denis has authored 9 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Claude Denis's work include Chronic Lymphocytic Leukemia Research (4 papers), Acute Myeloid Leukemia Research (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). Claude Denis is often cited by papers focused on Chronic Lymphocytic Leukemia Research (4 papers), Acute Myeloid Leukemia Research (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). Claude Denis collaborates with scholars based in France and Belgium. Claude Denis's co-authors include Claude Preudhomme, Christophe Roumier, Richard Garand, Nicole Dastugue, Jean Pierre Kerckaert, Elizabeth Macintyre, Pierre Fenaux, Jean Luc Laı̈, Alain Cosson and F Bauters and has published in prestigious journals such as Blood, Gene and Aquaculture.

In The Last Decade

Claude Denis

9 papers receiving 295 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claude Denis France 7 188 178 83 41 40 9 301
L C Chan Hong Kong 7 194 1.0× 221 1.2× 101 1.2× 31 0.8× 32 0.8× 10 399
Janet D. Rowley United States 8 173 0.9× 160 0.9× 63 0.8× 27 0.7× 44 1.1× 9 325
Fiona Watkins United Kingdom 6 246 1.3× 180 1.0× 117 1.4× 38 0.9× 38 0.9× 8 379
D Falzetti Italy 10 114 0.6× 113 0.6× 87 1.0× 75 1.8× 46 1.1× 21 297
Konstantin Petropoulos Germany 5 142 0.8× 194 1.1× 66 0.8× 19 0.5× 28 0.7× 8 275
Marie‐José Gregoire France 8 169 0.9× 140 0.8× 130 1.6× 18 0.4× 39 1.0× 10 357
Carola Reindl Germany 7 275 1.5× 164 0.9× 160 1.9× 25 0.6× 38 0.9× 8 359
Derek Bouman Canada 8 129 0.7× 229 1.3× 64 0.8× 33 0.8× 71 1.8× 9 377
N Smadja France 9 332 1.8× 243 1.4× 124 1.5× 33 0.8× 104 2.6× 17 440
Scott VanWier United States 4 209 1.1× 167 0.9× 49 0.6× 42 1.0× 72 1.8× 4 275

Countries citing papers authored by Claude Denis

Since Specialization
Citations

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

Fields of papers citing papers by Claude Denis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claude Denis

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

All Works

9 of 9 papers shown
2.
Preudhomme, Claude, Christophe Roumier, Richard Garand, et al.. (2000). High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21. Blood. 96(8). 2862–2869. 187 indexed citations
3.
Preudhomme, Claude, Christophe Roumier, Richard Garand, et al.. (2000). High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21. Blood. 96(8). 2862–2869. 12 indexed citations
4.
Galiègue‐Zouitina, Sylvie, Sabine Quief, Marie‐Paule Hildebrand, et al.. (1999). Nonrandom fusion of LPlastinLCP1 and LAZ3BCL6 genes by t(3;13)(q27;q14) chromosome translocation in two cases of B‐cell non‐Hodgkin lymphoma. Genes Chromosomes and Cancer. 26(2). 97–105. 3 indexed citations
5.
Quief, Sabine, et al.. (1999). Nonrandom fusion ofL-Plastin(LCP1) andLAZ3(BCL6) genes by t(3;13)(q27;q14) chromosome translocation in two cases of B-cell non-Hodgkin lymphoma. Genes Chromosomes and Cancer. 26(2). 97–105. 26 indexed citations
6.
Roumier, Christophe, et al.. (1997). Genomic Structure and Assignment of theRhoH/TTFSmall GTPase Gene (ARHH) to 4p13 byin SituHybridization. Genomics. 43(1). 89–94. 28 indexed citations
7.
Galiègue‐Zouitina, Sylvie, et al.. (1994). Molecular cloning of a t(11; 14)(q13;q32) translocation breakpoint centromeric to the BCLI‐MTC. Genes Chromosomes and Cancer. 11(4). 246–255. 16 indexed citations
8.
Denis, Claude, et al.. (1992). Effect of recombinant trout growth hormone on rainbow trout at growth-inhibiting temperatures. Aquaculture. 100(1-3). 322–323. 1 indexed citations
9.
Loppes, Roland & Claude Denis. (1983). Chloroplast and nuclear DNA fragments from Chlamydomonas promoting high frequency transformation of yeast. Current Genetics. 7(6). 473–480. 13 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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