Mathilde Gay‐Bellile
Impact in
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- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
Papers in
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- Congenital heart defects research 3
- DNA Repair Mechanisms 2
- Wnt/β-catenin signaling in development and cancer 2
- PI3K/AKT/mTOR signaling in cancer 2
- Genetics 9
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Philippe Vago (9 shared papers)Andréï Tchirkov (9 shared papers)Maud Privat (11 shared papers)Yves‐Jean Bignon (10 shared papers)Éléonore Eymard-Pierre (8 shared papers)Laëtitia Gouas (6 shared papers)Yannick Bidet (10 shared papers)Céline Pebrel‐Richard (6 shared papers)
In The Last Decade
Mathilde Gay‐Bellile
22 papers receiving 197 citations
Peers
Comparison fields: 5 of 43
- Aging 5
- Genetics 70
- Physiology 42
- Cancer Research 23
- Biotechnology 12
Countries citing papers authored by Mathilde Gay‐Bellile
This map shows the geographic impact of Mathilde Gay‐Bellile'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 Mathilde Gay‐Bellile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mathilde Gay‐Bellile more than expected).
Fields of papers citing papers by Mathilde Gay‐Bellile
This network shows the impact of papers produced by Mathilde Gay‐Bellile. 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 Mathilde Gay‐Bellile. The network helps show where Mathilde Gay‐Bellile may publish in the future.
Co-authors
The 25 scholars most cited alongside Mathilde Gay‐Bellile, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 37 | |
| 2 | 2013 | 30 | |
| 3 | 2014 | 20 | |
| 4 | 2016 | 20 | |
| 5 | 2016 | 15 | |
| 6 | 2018 | 14 | |
| 7 | 2020 | 9 | |
| 8 | 2014 | 9 | |
| 9 | 2020 | 8 | |
| 10 | 2023 | 7 | |
| 11 | 2015 | 7 | |
| 12 | 2019 | 6 | |
| 13 | 2016 | 5 | |
| 14 | 2019 | 5 | |
| 15 | 2016 | 5 | |
| 16 | 2020 | 3 | |
| 17 | 2023 | 3 | |
| 18 | 2023 | 3 | |
| 19 | 2014 | 2 | |
| 20 | 2025 | 1 |
About Mathilde Gay‐Bellile
Mathilde Gay‐Bellile is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Oncology and Physiology, having authored 22 papers that have together received 211 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic factors in colorectal cancer (4 papers), Congenital heart defects research (3 papers), Telomeres, Telomerase, and Senescence (3 papers), DNA Repair Mechanisms (2 papers), Wnt/β-catenin signaling in development and cancer (2 papers) and PI3K/AKT/mTOR signaling in cancer (2 papers). The work is most often cited by research in Aging (5 citations), Genetics (70 citations), Physiology (42 citations), Cancer Research (23 citations) and Biotechnology (12 citations). Mathilde Gay‐Bellile has collaborated with scholars based in France, Canada and Greece. Frequent co-authors include Philippe Vago, Andréï Tchirkov, Maud Privat, Yves‐Jean Bignon, Éléonore Eymard-Pierre, Laëtitia Gouas, Yannick Bidet, Céline Pebrel‐Richard, Carole Goumy and Lauren Véronèse. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, Clinical Genetics, Oncotarget, Genes and Gene.
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.