Pascal Chambon
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Genomics and Chromatin Dynamics
- Developmental Biology and Gene Regulation
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 4
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Welcome W. Bender (2 shared papers)Pierre Spierer (2 shared papers)David S. Hogness (2 shared papers)Anne Spierer (1 shared paper)Thierry Frébourg (10 shared papers)Thomas Lecompte (1 shared paper)Céline Bonnet (2 shared papers)Christophe Philippe (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Clinical Genetics (2 papers)Acta Neuropathologica Communications (2 papers)Journal of Molecular Biology (2 papers)Clinical Chemistry (2 papers)
- Partner nations
- FranceUnited StatesSwitzerland
In The Last Decade
Pascal Chambon
33 papers receiving 1.2k citations
Pascal Chambon's Hit Papers
Peers
Comparison fields: 5 of 77
- Genetics 396
- Molecular Biology 462
- Cellular and Molecular Neuroscience 95
- Hematology 71
- Pediatrics, Perinatology and Child Health 60
Countries citing papers authored by Pascal Chambon
This map shows the geographic impact of Pascal Chambon'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 Pascal Chambon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pascal Chambon more than expected).
Fields of papers citing papers by Pascal Chambon
This network shows the impact of papers produced by Pascal Chambon. 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 Pascal Chambon. The network helps show where Pascal Chambon may publish in the future.
Co-authors
The 25 scholars most cited alongside Pascal Chambon, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Chromosomal walking and jumping to isolate DNA from the Ace and rosy loci and the bithorax complex in Drosophila melanogaster Hit paper breakdown → | 1983 | 538 |
| 2 | 2017 | 129 | |
| 3 | 2008 | 86 | |
| 4 | 1983 | 85 | |
| 5 | 2017 | 45 | |
| 6 | 2015 | 41 | |
| 7 | 2020 | 36 | |
| 8 | 2018 | 35 | |
| 9 | 2020 | 35 | |
| 10 | 2016 | 31 | |
| 11 | PFMG2025–integrating genomic medicine into the national healthcare system in France Hit paper breakdown → | 2025 | 26 |
| 12 | 2013 | 25 | |
| 13 | 2014 | 23 | |
| 14 | 2020 | 23 | |
| 15 | 2016 | 20 | |
| 16 | 2025 | 20 | |
| 17 | 2014 | 16 | |
| 18 | 2019 | 16 | |
| 19 | 2021 | 16 | |
| 20 | 2020 | 13 |
About Pascal Chambon
Pascal Chambon is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cognitive Neuroscience and Oncology, having authored 33 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Chromatin Dynamics (2 papers), Autism Spectrum Disorder Research (2 papers), Chromosomal and Genetic Variations (2 papers) and Molecular Biology Techniques and Applications (1 paper). The work is most often cited by research in Genetics (396 citations), Molecular Biology (462 citations), Cellular and Molecular Neuroscience (95 citations), Hematology (71 citations) and Pediatrics, Perinatology and Child Health (60 citations). Pascal Chambon has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Welcome W. Bender, Pierre Spierer, David S. Hogness, Anne Spierer, Thierry Frébourg, Thomas Lecompte, Céline Bonnet, Christophe Philippe, Pierre Bordigoni and Marie‐José Gregoire. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Acta Neuropathologica Communications, Journal of Molecular Biology and Clinical Chemistry.
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.