Anna Pelet
Impact in
Papers in
- Surgery 36
- Congenital gastrointestinal and neural anomalies 35
- Congenital Diaphragmatic Hernia Studies 7
- Congenital Anomalies and Fetal Surgery 6
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- Congenital heart defects research 5
- Co-authors
- Arnold Münnich (28 shared papers)Stanislas Lyonnet (43 shared papers)Patrick Edery (14 shared papers)Jeanne Amiel (25 shared papers)Tania Attié‐Bitach (11 shared papers)Claire Nihoul‐Feketé (11 shared papers)Martine Le Merrer (5 shared papers)Laurence Legeai‐Mallet (4 shared papers)
- Journals
- Nature Genetics (6 papers)European Journal of Human Genetics (5 papers)Human Molecular Genetics (4 papers)Journal of Medical Genetics (4 papers)Human Genetics (4 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Anna Pelet
63 papers receiving 4.2k citations
Anna Pelet's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 1.5k
- Surgery 2.1k
- Gastroenterology 208
- Clinical Biochemistry 259
- Molecular Biology 1.9k
Countries citing papers authored by Anna Pelet
This map shows the geographic impact of Anna Pelet'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 Anna Pelet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Pelet more than expected).
Fields of papers citing papers by Anna Pelet
This network shows the impact of papers produced by Anna Pelet. 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 Anna Pelet. The network helps show where Anna Pelet may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Pelet, 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 | Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia Hit paper breakdown → | 1994 | 759 |
| 2 | Mutations of the RET proto-oncogene in Hirschsprung's disease Hit paper breakdown → | 1994 | 604 |
| 3 | 1996 | 363 | |
| 4 | 1995 | 265 | |
| 5 | 2002 | 210 | |
| 6 | 1995 | 169 | |
| 7 | 2000 | 166 | |
| 8 | 1996 | 159 | |
| 9 | 1993 | 154 | |
| 10 | 2000 | 138 | |
| 11 | 1988 | 118 | |
| 12 | 1994 | 98 | |
| 13 | 1998 | 89 | |
| 14 | 2001 | 80 | |
| 15 | Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease. | 1998 | 73 |
| 16 | 1997 | 69 | |
| 17 | 2008 | 65 | |
| 18 | 2007 | 60 | |
| 19 | 1983 | 60 | |
| 20 | 1998 | 57 |
About Anna Pelet
Anna Pelet is a scholar working on Surgery, Molecular Biology, Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 65 papers that have together received 4.4k indexed citations. Recurring topics across this work include Congenital gastrointestinal and neural anomalies (35 papers), Metabolism and Genetic Disorders (10 papers), Congenital Diaphragmatic Hernia Studies (7 papers), Digestive system and related health (6 papers), Congenital Anomalies and Fetal Surgery (6 papers), Congenital heart defects research (5 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (1.5k citations), Surgery (2.1k citations), Gastroenterology (208 citations), Clinical Biochemistry (259 citations) and Molecular Biology (1.9k citations). Anna Pelet has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Arnold Münnich, Stanislas Lyonnet, Patrick Edery, Jeanne Amiel, Tania Attié‐Bitach, Claire Nihoul‐Feketé, Martine Le Merrer, Laurence Legeai‐Mallet, Francis Rousseau and Jacky Bonaventure. Their work appears in journals such as Nature Genetics, European Journal of Human Genetics, Human Molecular Genetics, Journal of Medical Genetics and 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.