Christophe Béroud
Impact in
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
- Cancer, Hypoxia, and Metabolism
- Oncology top 1%
- Cancer-related Molecular Pathways
Papers in
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- Muscle Physiology and Disorders 12
- RNA Research and Splicing 10
- Epigenetics and DNA Methylation 10
- RNA modifications and cancer 10
- RNA and protein synthesis mechanisms 9
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- Cancer Genomics and Diagnostics 24
- Co-authors
- Thierry Soussi (10 shared papers)Dalil Hamroun (17 shared papers)Mireille Claustres (15 shared papers)Gwenaëlle Collod‐Béroud (14 shared papers)Jean‐Pierre Desvignes (14 shared papers)Cathérine Boileau (14 shared papers)Chikashi Ishioka (3 shared papers)David Salgado (14 shared papers)
- Journals
- Human Mutation (31 papers)Nucleic Acids Research (10 papers)Neuromuscular Disorders (9 papers)Genes Chromosomes and Cancer (2 papers)BMC Bioinformatics (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Christophe Béroud
115 papers receiving 7.2k citations
Christophe Béroud's Hit Papers
Peers
Comparison fields: 5 of 127
- Cancer Research 1.2k
- Oncology 1.5k
- Molecular Biology 3.7k
- Genetics 1.4k
- Genetics 449
Countries citing papers authored by Christophe Béroud
This map shows the geographic impact of Christophe Béroud'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 Christophe Béroud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christophe Béroud more than expected).
Fields of papers citing papers by Christophe Béroud
This network shows the impact of papers produced by Christophe Béroud. 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 Christophe Béroud. The network helps show where Christophe Béroud may publish in the future.
Co-authors
The 25 scholars most cited alongside Christophe Béroud, 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 117 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Human Splicing Finder: an online bioinformatics tool to predict splicing signals Hit paper breakdown → | 2009 | 1881 |
| 2 | Assessing TP53 status in human tumours to evaluate clinical outcome Hit paper breakdown → | 2001 | 514 |
| 3 | 1996 | 328 | |
| 4 | 2014 | 211 | |
| 5 | 2004 | 166 | |
| 6 | 1996 | 164 | |
| 7 | 2006 | 155 | |
| 8 | 2018 | 140 | |
| 9 | 1998 | 128 | |
| 10 | 2003 | 127 | |
| 11 | 2014 | 120 | |
| 12 | 2005 | 118 | |
| 13 | 2002 | 114 | |
| 14 | 2011 | 107 | |
| 15 | 1998 | 105 | |
| 16 | 2000 | 105 | |
| 17 | 2006 | 102 | |
| 18 | Candidate genetic modifiers of individual susceptibility to renal cell carcinoma: a study of polymorphic human xenobiotic-metabolizing enzymes. | 1999 | 100 |
| 19 | Retinal hemangioblastoma in von Hippel-Lindau disease: a clinical and molecular study. | 2002 | 97 |
| 20 | 2006 | 96 |
About Christophe Béroud
Christophe Béroud is a scholar working on Molecular Biology, Cancer Research, Genetics, Oncology and Pathology and Forensic Medicine, having authored 117 papers that have together received 7.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (24 papers), Genomics and Rare Diseases (18 papers), Cancer-related Molecular Pathways (14 papers), Muscle Physiology and Disorders (12 papers), RNA Research and Splicing (10 papers), Epigenetics and DNA Methylation (10 papers), RNA modifications and cancer (10 papers) and RNA and protein synthesis mechanisms (9 papers). The work is most often cited by research in Cancer Research (1.2k citations), Oncology (1.5k citations), Molecular Biology (3.7k citations), Genetics (1.4k citations) and Genetics (449 citations). Christophe Béroud has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Thierry Soussi, Dalil Hamroun, Mireille Claustres, Gwenaëlle Collod‐Béroud, Jean‐Pierre Desvignes, Cathérine Boileau, Chikashi Ishioka, David Salgado, Nicolas Lévy and Martin Krahn. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Neuromuscular Disorders, Genes Chromosomes and Cancer and BMC Bioinformatics.
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.