Anna Pelet

8.6k citations

63 papers · 4.1k indexed · 2 hit papers · h-index 28

Impact in

Genetics top 1%
- Digestive system and related health
- Connective tissue disorders research
Surgery top 1%
- Congenital gastrointestinal and neural anomalies
- Intestinal Malrotation and Obstruction Disorders
- Congenital Anomalies and Fetal Surgery

Papers in ⓘ

Clinical Biochemistry 9
- Metabolism and Genetic Disorders 9
Surgery 35
- Congenital gastrointestinal and neural anomalies 34
- Congenital Diaphragmatic Hernia Studies 8
- Congenital Anomalies and Fetal Surgery 6
- Intestinal Malrotation and Obstruction Disorders 4

Co-authors: Arnold Münnich (28 shared papers)Stanislas Lyonnet (42 shared papers)Patrick Edery (13 shared papers)Jeanne Amiel (24 shared papers)Tania Attié‐Bitach (12 shared papers)Claire Nihoul‐Feketé (11 shared papers)Laurence Legeai‐Mallet (4 shared papers)P Maroteaux (3 shared papers)
Journals: Nature Genetics (6 papers)European Journal of Human Genetics (5 papers)Human Molecular Genetics (4 papers)Human Genetics (4 papers)Journal of Medical Genetics (4 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Anna Pelet

62 papers receiving 3.9k citations

Hit Papers

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Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia 1994 · 689 citations

Peers

Countries citing papers authored by Anna Pelet

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Anna Pelet Line = papers co-authored together Anna Pelet links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 63 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 Nature ·Francis Rousseau, Jacky Bonaventure, Laurence Legeai‐Mallet, Anna Pelet, Jean‐Michel Rozet, P Maroteaux, Martine Le Merrer, Arnold Münnich Hit paper breakdown →	1994	689
2	Mutations of the RET proto-oncogene in Hirschsprung's disease Nature ·Patrick Edery, Stanislas Lyonnet, Lois M. Mulligan, Anna Pelet, Eleanore Dow, Laurent Abel, Susan Holder, Claire Nihoul‐Feketé, Bruce A.J. Ponder, Arnold Münnich Hit paper breakdown →	1994	540
3	Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome) Nature Genetics ·Patrick Edery, Tania Attié‐Bitach, Jeanne Amiel, Anna Pelet, Charis Eng, Robert M.W. Hofstra, Hélène Martelli, Christelle Bonod‐Bidaud, Arnold Münnich, Stanislas Lyonnet	1996	334
4	Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease Human Molecular Genetics ·Tania Attié‐Bitach, Anna Pelet, Patrick Edery, Charis Eng, Lois M. Mulligan, Jeanne Amiel, Laetitia Boutrand, Chérif Beldjord, Claire Nihoul‐Feketé, Arnold Munnich, Bruce A.J. Ponder, Stanislas Lyonnet	1995	242
5	Segregation at three loci explains familial and population risk in Hirschsprung disease Nature Genetics ·Stacey Gabriel, Rémi Salomon, Anna Pelet, Misha Angrist, Jeanne Amiel, Myriam Fornage, Tania Attié‐Bitach, Jane M. Olson, Robert M.W. Hofstra, Charles H.C.M. Buys, Julie Steffann, Arnold Münnich, Stanislas Lyonnet, Aravinda Chakravarti	2002	190
6	A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus Proceedings of the National Academy of Sciences ·Stacey Bolk, Anna Pelet, Robert M.W. Hofstra, Misha Angrist, Rémi Salomon, David Croaker, Charles H.C.M. Buys, Stanislas Lyonnet, Aravinda Chakravarti	2000	156
7	Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease Human Molecular Genetics ·Tania Attié‐Bitach, Marianne Till, Anna Pelet, Jeanne Amiel, Patrick Edery, Laetitia Boutrand, Arnold Münnich, Stanislas Lyonnet	1995	151
8	Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease Nature Genetics ·Rémi Salomon, Tania Attié‐Bitach, Anna Pelet, Christelle Bonod‐Bidaud, Charis Eng, Jeanne Amiel, Sabine Sarnacki, Olivier Goulet, C. Ricour, Claire Nihoul‐Feketé, Arnold Münnich, Stanislas Lyonnet	1996	150
9	A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10 Nature Genetics ·Stanislas Lyonnet, Alessandra Bolino, Anna Pelet, Laurent Abel, Claire Nihoul‐Feketé, Marie‐Louise Briard, V. Mok-Siu, H Kääriäinen, Giuseppe Martucciello, Margherita Lerone, Aldamaria Puliti, Yin Luo, J. Weissenbach, Marcella Devoto, Arnold Münnich, Giovanni Romeo	1993	142
10	Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain The American Journal of Human Genetics ·Renaud Touraine, Tania Attié‐Bitach, E. Manceau, Eckhard Korsch, Pierre Sarda, Véronique Pingault, Férechté Encha‐Razavi, Anna Pelet, Joëlle Augé, A Nivelon‐Chevallier, A. M. Holschneider, Marc Munnes, Walter Doerfler, Michel Goossens, Arnold Munnich, Michel Vekemans, Stanislas Lyonnet	2000	124
11	Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities Pediatric Research ·France Demaugre, Jean‐Paul Bonnefont, Grant Mitchell, Nam Nguyen-Hoang, Anna Pelet, Marco Rimoldi, Stefano Di Donato, Jean-Marie Saudubray	1988	105
12	A gene for achondroplasia–hypochondroplasia maps to chromosome 4p Nature Genetics ·Martine Le Merrer, Francis Rousseau, Laurence Legeai‐Mallet, Jean-Christophe Landais, Anna Pelet, Jacky Bonaventure, Marek Sanak, Jean Weissenbach, Claude Stoll, Arnold Münnich, P Maroteaux	1994	89
13	Various mechanisms cause RET-mediated signaling defects in Hirschsprung's disease. Journal of Clinical Investigation ·Anna Pelet, Olivier Geneste, Patrick Edery, Andrea Pasini, S Chappuis, T Atti, A Munnich, Gilbert Lenoir, Stanislas Lyonnet, Marc Billaud	1998	83
14	Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures The American Journal of Human Genetics ·Jeanne Amiel, Yolanda Espinosa‐Parrilla, Julie Steffann, Philippe Gosset, Anna Pelet, Marguerite Prieur, Odile Boute, Agnès Choiset, Didier Lacombe, Nicole Philip, Martine Le Merrer, Hajime Tanaka, Marianne Till, Renaud Touraine, Annick Toutain, Michel Vekemans, Arnold Münnich, Stanislas Lyonnet	2001	79
15	Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease. PubMed ·(unknown), Rémi Salomon, Guy Van Camp, Anna Pelet, (unknown), Charis Eng, M Bonduelle, Jeanne Amiel, Claire Nihoul‐Feketé, Patrick J. Willems, Arnold Münnich, Stanislas Lyonnet	1998	65
16	Spectrum ofHLXB9gene mutations in Currarino syndrome and genotype-phenotype correlation Human Mutation ·Célia Cretolle, Anna Pelet, Damien Sanlaville, Michel Zérah, Jeanne Amiel, F Jaubert, Y. Révillon, Lekbir Baala, Arnold Münnich, Claire Nihoul‐Feketé, Stanislas Lyonnet	2008	60
17	Endothelin-3 Gene Mutations in Isolated and Syndromic Hirschsprung Disease European Journal of Human Genetics ·Christelle Bonod‐Bidaud, Rémi Salomon, Guy Van Camp, Anna Pelet, Tania Attié‐Bitach, Charis Eng, M Bonduelle, Jeanne Amiel, Claire Nihoul‐Feketé, Patrick J. Willems, Arnold Münnich, Stanislas Lyonnet	1997	59
18	Epistatic interactions with a common hypomorphicRET allele in syndromic Hirschsprung disease Human Mutation ·Loïc de Pontual, Anna Pelet, Mathieu Clément‐Ziza, Delphine Trochet, Stylianos E. Antonarakis, Tania Attié‐Bitach, Philip L. Beales, Julie Blouin, Florence Dastot‐Le Moal, Hélène Dollfus, Michel Goossens, Nicholas Katsanis, Renaud Touraine, J Feingold, Arnold Münnich, Stanislas Lyonnet, Jeanne Amiel	2007	57
19	Expression of theRET proto-oncogene in human Embryos American Journal of Medical Genetics ·Tania Attié‐Bitach, Marc Abitbol, Marion G�rard, Anne‐Lise Delezoide, Joelle Aug�, Anna Pelet, Jeanne Amiel, Vassilis Pachnis, Arnold Munnich, Stanislas Lyonnet, Michel Vekemans	1998	54
20	Action of the antiepileptic drug, valproic acid, on fatty acid oxidation in isolated rat hepatocytes Biochemical and Biophysical Research Communications ·F. X. Coudé, G Grimber, Anna Pelet, Y. Benoît	1983	54

About Anna Pelet

Anna Pelet is a scholar working on Clinical Biochemistry, Surgery, Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 63 papers that have together received 4.1k indexed citations. Recurring topics across this work include Congenital gastrointestinal and neural anomalies (34 papers), Metabolism and Genetic Disorders (9 papers), Congenital Diaphragmatic Hernia Studies (8 papers), Digestive system and related health (7 papers), Congenital Anomalies and Fetal Surgery (6 papers), Fetal and Pediatric Neurological Disorders (5 papers), Congenital heart defects research (5 papers) and Intestinal Malrotation and Obstruction Disorders (4 papers). The work is most often cited by research in Genetics (1.5k citations), Surgery (2.0k citations), Gastroenterology (232 citations), Clinical Biochemistry (230 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, Laurence Legeai‐Mallet, P Maroteaux, Francis Rousseau and Jacky Bonaventure. Their work appears in journals such as Nature Genetics, European Journal of Human Genetics, Human Molecular Genetics, Human Genetics and Journal of Medical 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.

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