Chantal Desmaze
Impact in
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- Sarcoma Diagnosis and Treatment
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- Lymphoma Diagnosis and Treatment
Papers in
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- DNA Repair Mechanisms 13
- CRISPR and Genetic Engineering 4
- Congenital heart defects research 4
- Physiology 12
- Telomeres, Telomerase, and Senescence 10
- Co-authors
- Jessica Zucman‐Rossi (15 shared papers)Alain Aurias (18 shared papers)Olivier Delattre (17 shared papers)Thomas Melot (9 shared papers)Martine Peter (5 shared papers)Béatrice Plougastel-Douglas (6 shared papers)Gilles Thomas (11 shared papers)Guy A. Rouleau (8 shared papers)
- Journals
- Human Molecular Genetics (6 papers)Human Genetics (3 papers)Cytogenetic and Genome Research (3 papers)Oncotarget (2 papers)Cellular and Molecular Life Sciences (2 papers)
- Partner nations
- FranceUnited StatesCanada
In The Last Decade
Chantal Desmaze
41 papers receiving 4.4k citations
Chantal Desmaze's Hit Papers
Peers
Comparison fields: 5 of 105
- Pulmonary and Respiratory Medicine 2.1k
- Pathology and Forensic Medicine 743
- Cancer Research 597
- Rheumatology 573
- Molecular Biology 2.6k
Countries citing papers authored by Chantal Desmaze
This map shows the geographic impact of Chantal Desmaze'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 Chantal Desmaze with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chantal Desmaze more than expected).
Fields of papers citing papers by Chantal Desmaze
This network shows the impact of papers produced by Chantal Desmaze. 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 Chantal Desmaze. The network helps show where Chantal Desmaze may publish in the future.
Co-authors
The 25 scholars most cited alongside Chantal Desmaze, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours Hit paper breakdown → | 1992 | 1443 |
| 2 | Cloning and characterization of hOGG1 , a human homolog of the OGG1 gene of Saccharomyces cerevisiae Hit paper breakdown → | 1997 | 525 |
| 3 | 1993 | 438 | |
| 4 | 1993 | 395 | |
| 5 | 2004 | 255 | |
| 6 | 1992 | 238 | |
| 7 | 1995 | 165 | |
| 8 | 2006 | 140 | |
| 9 | 1995 | 94 | |
| 10 | 1995 | 58 | |
| 11 | 1997 | 57 | |
| 12 | 1994 | 57 | |
| 13 | 2003 | 53 | |
| 14 | 1993 | 53 | |
| 15 | 1993 | 49 | |
| 16 | 2004 | 48 | |
| 17 | 1993 | 47 | |
| 18 | 1992 | 45 | |
| 19 | Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases. | 1993 | 45 |
| 20 | 2011 | 35 |
About Chantal Desmaze
Chantal Desmaze is a scholar working on Molecular Biology, Physiology, Pulmonary and Respiratory Medicine, Genetics and Neurology, having authored 43 papers that have together received 4.5k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (13 papers), Telomeres, Telomerase, and Senescence (10 papers), Sarcoma Diagnosis and Treatment (7 papers), Chromosomal and Genetic Variations (6 papers), Neurofibromatosis and Schwannoma Cases (6 papers), CRISPR and Genetic Engineering (4 papers), Congenital heart defects research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (2.1k citations), Pathology and Forensic Medicine (743 citations), Cancer Research (597 citations), Rheumatology (573 citations) and Molecular Biology (2.6k citations). Chantal Desmaze has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Jessica Zucman‐Rossi, Alain Aurias, Olivier Delattre, Thomas Melot, Martine Peter, Béatrice Plougastel-Douglas, Gilles Thomas, Guy A. Rouleau, Pieter de Jong and Heinrich Kovar. Their work appears in journals such as Human Molecular Genetics, Human Genetics, Cytogenetic and Genome Research, Oncotarget and Cellular and Molecular Life Sciences.
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.