Pierre Billuart
Impact in
- Developmental Neuroscience top 1%
- Neurogenesis and neuroplasticity mechanisms
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- Neuroscience and Neuropharmacology Research
Papers in
- Genetics 40
- Genetics and Neurodevelopmental Disorders 39
- Genomic variations and chromosomal abnormalities 6
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- Ubiquitin and proteasome pathways 9
- RNA modifications and cancer 6
- Epigenetics and DNA Methylation 6
- Co-authors
- Axel Kahn (6 shared papers)Chérif Beldjord (6 shared papers)Jamel Chelly (12 shared papers)Claire-Angélique Renard (1 shared paper)Marie‐Annick Buendia (1 shared paper)Christine Perret (1 shared paper)Monique Fabrè (1 shared paper)Jamel Chelly (1 shared paper)
- Journals
- Journal of Neuroscience (6 papers)Human Molecular Genetics (6 papers)European Journal of Human Genetics (3 papers)Molecular Psychiatry (2 papers)Human Mutation (2 papers)
- Partner nations
- FranceItalyUnited States
In The Last Decade
Pierre Billuart
65 papers receiving 3.9k citations
Pierre Billuart's Hit Papers
Peers
Comparison fields: 5 of 105
- Developmental Neuroscience 481
- Cellular and Molecular Neuroscience 905
- Cell Biology 788
- Genetics 1.2k
- Molecular Biology 2.3k
Countries citing papers authored by Pierre Billuart
This map shows the geographic impact of Pierre Billuart'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 Pierre Billuart with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pierre Billuart more than expected).
Fields of papers citing papers by Pierre Billuart
This network shows the impact of papers produced by Pierre Billuart. 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 Pierre Billuart. The network helps show where Pierre Billuart may publish in the future.
Co-authors
The 25 scholars most cited alongside Pierre Billuart, 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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas Hit paper breakdown → | 1998 | 969 |
| 2 | A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome Hit paper breakdown → | 1998 | 632 |
| 3 | 1998 | 420 | |
| 4 | 2001 | 181 | |
| 5 | 2007 | 114 | |
| 6 | 2010 | 101 | |
| 7 | 2003 | 86 | |
| 8 | 2021 | 84 | |
| 9 | 2019 | 81 | |
| 10 | 2009 | 77 | |
| 11 | 2005 | 73 | |
| 12 | 2011 | 56 | |
| 13 | 2001 | 55 | |
| 14 | 2011 | 55 | |
| 15 | 2015 | 52 | |
| 16 | 1997 | 49 | |
| 17 | 2009 | 42 | |
| 18 | 2017 | 39 | |
| 19 | 2019 | 36 | |
| 20 | 2017 | 36 |
About Pierre Billuart
Pierre Billuart is a scholar working on Genetics, Molecular Biology, Developmental Neuroscience, Cellular and Molecular Neuroscience and Cell Biology, having authored 65 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (39 papers), Ubiquitin and proteasome pathways (9 papers), Neuroscience and Neuropharmacology Research (8 papers), Neurogenesis and neuroplasticity mechanisms (7 papers), Cellular transport and secretion (7 papers), Genomic variations and chromosomal abnormalities (6 papers), RNA modifications and cancer (6 papers) and Epigenetics and DNA Methylation (6 papers). The work is most often cited by research in Developmental Neuroscience (481 citations), Cellular and Molecular Neuroscience (905 citations), Cell Biology (788 citations), Genetics (1.2k citations) and Molecular Biology (2.3k citations). Pierre Billuart has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Axel Kahn, Chérif Beldjord, Jamel Chelly, Claire-Angélique Renard, Marie‐Annick Buendia, Christine Perret, Monique Fabrè, Jamel Chelly, Olivier Soubrane and Béatrice Romagnolo. Their work appears in journals such as Journal of Neuroscience, Human Molecular Genetics, European Journal of Human Genetics, Molecular Psychiatry and Human Mutation.
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.