Thierry Billette
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
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- RNA modifications and cancer
- RNA Research and Splicing
- Muscle Physiology and Disorders
Papers in
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- Fetal and Pediatric Neurological Disorders 2
- Prenatal Screening and Diagnostics 2
- Co-authors
- Cathérine Garel (1 shared paper)Jérôme Massardier (1 shared paper)Mona Massoud (1 shared paper)Christelle Rougeot (1 shared paper)N. Varene (1 shared paper)A. Bénézit (1 shared paper)Jean‐Marie Jouannic (1 shared paper)P. Gaucherand (1 shared paper)
In The Last Decade
Thierry Billette
7 papers receiving 410 citations
Peers
Comparison fields: 5 of 37
- Genetics 306
- Molecular Biology 276
- Pediatrics, Perinatology and Child Health 46
- Cellular and Molecular Neuroscience 40
- Surgery 87
Countries citing papers authored by Thierry Billette
This map shows the geographic impact of Thierry Billette'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 Thierry Billette with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thierry Billette more than expected).
Fields of papers citing papers by Thierry Billette
This network shows the impact of papers produced by Thierry Billette. 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 Thierry Billette. The network helps show where Thierry Billette may publish in the future.
Co-authors
The 25 scholars most cited alongside Thierry Billette, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1990 | 330 | |
| 2 | 2013 | 41 | |
| 3 | 2016 | 28 | |
| 4 | 2020 | 16 | |
| 5 | 2021 | 13 | |
| 6 | 2009 | 2 | |
| 7 | Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU | 2018 | 1 |
About Thierry Billette
Thierry Billette is a scholar working on Pediatrics, Perinatology and Child Health, Nephrology, Genetics, Genetics and Physiology, having authored 7 papers that have together received 431 indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Ion channel regulation and function (1 paper), Tuberous Sclerosis Complex Research (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Genetics (306 citations), Molecular Biology (276 citations), Pediatrics, Perinatology and Child Health (46 citations), Cellular and Molecular Neuroscience (40 citations) and Surgery (87 citations). Thierry Billette has collaborated with scholars based in France, Italy and Canada. Frequent co-authors include Cathérine Garel, Jérôme Massardier, Mona Massoud, Christelle Rougeot, N. Varene, A. Bénézit, Jean‐Marie Jouannic, P. Gaucherand, Vincent Desportes and Guibaud Laurent. Their work appears in journals such as Neurology, Nature, Ultrasound in Obstetrics and Gynecology, Brain 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.