Franck Bourdeaut
Impact in
Papers in
- Co-authors
- Olivier Delattre (47 shared papers)Julien Masliah‐Planchon (30 shared papers)Gaëlle Pierron (29 shared papers)Michael Christoph Frühwald (6 shared papers)Ivan Bièche (4 shared papers)Laurence Brugières (16 shared papers)Jean‐Marc Guinebretière (2 shared papers)Susan N Chi (5 shared papers)
- Journals
- Neuro-Oncology (22 papers)Pediatric Blood & Cancer (18 papers)Acta Neuropathologica (10 papers)Acta Neuropathologica Communications (8 papers)European Journal of Human Genetics (7 papers)
- Partner nations
- FranceGermanyUnited States
In The Last Decade
Franck Bourdeaut
199 papers receiving 8.9k citations
Franck Bourdeaut's Hit Papers
Peers
Comparison fields: 5 of 110
- Genetics 3.1k
- Neurology 889
- Cancer Research 544
- Molecular Biology 2.4k
- Pulmonary and Respiratory Medicine 1k
Countries citing papers authored by Franck Bourdeaut
This map shows the geographic impact of Franck Bourdeaut'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 Franck Bourdeaut with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Franck Bourdeaut more than expected).
Fields of papers citing papers by Franck Bourdeaut
This network shows the impact of papers produced by Franck Bourdeaut. 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 Franck Bourdeaut. The network helps show where Franck Bourdeaut may publish in the future.
Co-authors
The 25 scholars most cited alongside Franck Bourdeaut, 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 212 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas Hit paper breakdown → | 2012 | 808 |
| 2 | Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition Hit paper breakdown → | 2014 | 624 |
| 3 | 2003 | 315 | |
| 4 | 2015 | 305 | |
| 5 | 2004 | 270 | |
| 6 | 2014 | 250 | |
| 7 | 2014 | 247 | |
| 8 | 2020 | 241 | |
| 9 | 2016 | 180 | |
| 10 | 2017 | 176 | |
| 11 | 2011 | 171 | |
| 12 | 2014 | 162 | |
| 13 | 2019 | 161 | |
| 14 | 2017 | 156 | |
| 15 | 2017 | 149 | |
| 16 | 2013 | 138 | |
| 17 | 2019 | 138 | |
| 18 | 2010 | 135 | |
| 19 | 2017 | 132 | |
| 20 | 2019 | 125 |
About Franck Bourdeaut
Franck Bourdeaut is a scholar working on Genetics, Neurology, Molecular Biology, Cancer Research and Pulmonary and Respiratory Medicine, having authored 212 papers that have together received 9.1k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (79 papers), Chromatin Remodeling and Cancer (49 papers), Neuroblastoma Research and Treatments (18 papers), Sarcoma Diagnosis and Treatment (14 papers), Genetic factors in colorectal cancer (13 papers), Cancer Genomics and Diagnostics (11 papers), BRCA gene mutations in cancer (10 papers) and Hedgehog Signaling Pathway Studies (10 papers). The work is most often cited by research in Genetics (3.1k citations), Neurology (889 citations), Cancer Research (544 citations), Molecular Biology (2.4k citations) and Pulmonary and Respiratory Medicine (1k citations). Franck Bourdeaut has collaborated with scholars based in France, Germany and United States. Frequent co-authors include Olivier Delattre, Julien Masliah‐Planchon, Gaëlle Pierron, Michael Christoph Frühwald, Ivan Bièche, Laurence Brugières, Jean‐Marc Guinebretière, Susan N Chi, Isabelle Janoueix‐Lerosey and Jean Marie Michon. Their work appears in journals such as Neuro-Oncology, Pediatric Blood & Cancer, Acta Neuropathologica, Acta Neuropathologica Communications and European Journal of Human Genetics.
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.