Frédéric Bilan
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment
Papers in
- Genetics 31
- Genetics and Neurodevelopmental Disorders 15
- Genomics and Rare Diseases 10
- Congenital Ear and Nasal Anomalies 10
- Genomic variations and chromosomal abnormalities 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Epilepsy research and treatment 5
- Co-authors
- Alain Kitzis (15 shared papers)Caroline Norez (5 shared papers)Frédéric Becq (5 shared papers)Vincent Thoreau (5 shared papers)Brigitte Gilbert‐Dussardier (12 shared papers)Patricia Melin‐Heschel (3 shared papers)Marine Legendre (4 shared papers)Radu Harbuz (3 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)The American Journal of Human Genetics (4 papers)Journal of Molecular Diagnostics (4 papers)European Journal of Medical Genetics (3 papers)Orphanet Journal of Rare Diseases (3 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Frédéric Bilan
54 papers receiving 1.4k citations
Frédéric Bilan's Hit Papers
Peers
Comparison fields: 5 of 86
- Genetics 617
- Genetics 158
- Psychiatry and Mental health 173
- Developmental Neuroscience 30
- Pediatrics, Perinatology and Child Health 77
Countries citing papers authored by Frédéric Bilan
This map shows the geographic impact of Frédéric Bilan'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 Frédéric Bilan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frédéric Bilan more than expected).
Fields of papers citing papers by Frédéric Bilan
This network shows the impact of papers produced by Frédéric Bilan. 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 Frédéric Bilan. The network helps show where Frédéric Bilan may publish in the future.
Co-authors
The 25 scholars most cited alongside Frédéric Bilan, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 160 | |
| 2 | 2010 | 112 | |
| 3 | 2013 | 95 | |
| 4 | 2021 | 95 | |
| 5 | 2015 | 88 | |
| 6 | 2017 | 57 | |
| 7 | 2004 | 49 | |
| 8 | 2015 | 49 | |
| 9 | 2012 | 43 | |
| 10 | 2018 | 42 | |
| 11 | 2019 | 41 | |
| 12 | 2013 | 40 | |
| 13 | 2004 | 37 | |
| 14 | 2004 | 36 | |
| 15 | 2021 | 36 | |
| 16 | 2017 | 29 | |
| 17 | 2020 | 29 | |
| 18 | 2020 | 26 | |
| 19 | PFMG2025–integrating genomic medicine into the national healthcare system in France Hit paper breakdown → | 2025 | 26 |
| 20 | 2021 | 25 |
About Frédéric Bilan
Frédéric Bilan is a scholar working on Genetics, Genetics, Psychiatry and Mental health, Cell Biology and Pulmonary and Respiratory Medicine, having authored 57 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomics and Rare Diseases (10 papers), Congenital Ear and Nasal Anomalies (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Epilepsy research and treatment (5 papers), Cystic Fibrosis Research Advances (5 papers), Cellular transport and secretion (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (617 citations), Genetics (158 citations), Psychiatry and Mental health (173 citations), Developmental Neuroscience (30 citations) and Pediatrics, Perinatology and Child Health (77 citations). Frédéric Bilan has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Alain Kitzis, Caroline Norez, Frédéric Becq, Vincent Thoreau, Brigitte Gilbert‐Dussardier, Patricia Melin‐Heschel, Marine Legendre, Radu Harbuz, François Guilhot and Nicolas Bourmeyster. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Journal of Molecular Diagnostics, European Journal of Medical Genetics and Orphanet Journal of Rare Diseases.
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.