Anna Pelet

8.6k total citations · 2 hit papers
63 papers, 4.1k citations indexed

About

Anna Pelet is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Anna Pelet has authored 63 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Surgery, 29 papers in Molecular Biology and 16 papers in Genetics. Recurrent topics in Anna Pelet's work include Congenital gastrointestinal and neural anomalies (34 papers), Metabolism and Genetic Disorders (9 papers) and Congenital Diaphragmatic Hernia Studies (8 papers). Anna Pelet is often cited by papers focused on Congenital gastrointestinal and neural anomalies (34 papers), Metabolism and Genetic Disorders (9 papers) and Congenital Diaphragmatic Hernia Studies (8 papers). Anna Pelet collaborates with scholars based in France, United States and United Kingdom. Anna Pelet's 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 and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Anna Pelet

62 papers receiving 3.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

1994 689 citations Francis Rousseau, Jacky Bonaventure et al. Nature profile →
Mutations of the RET proto-oncogene in Hirschsprung's disease

1994 540 citations Patrick Edery, Stanislas Lyonnet et al. Nature profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anna Pelet France	28	2.0k	1.9k	1.5k	303	293	63	4.1k
Anita Farhi United States	12	280 0.1×	2.3k 1.2×	1.1k 0.7×	198 0.7×	92 0.3×	14	3.5k
Margherita Silengo Italy	29	489 0.2×	2.0k 1.1×	1.7k 1.2×	118 0.4×	617 2.1×	114	3.3k
Andreas Winterpacht Germany	33	232 0.1×	2.5k 1.3×	1.4k 1.0×	252 0.8×	275 0.9×	85	3.7k
Guillermo Antiñolo Spain	30	913 0.5×	2.0k 1.0×	792 0.5×	253 0.8×	204 0.7×	179	3.3k
Margherita Lerone Italy	25	1.3k 0.7×	1.1k 0.6×	827 0.6×	86 0.3×	181 0.6×	101	2.8k
Susan Holder United Kingdom	21	525 0.3×	1.1k 0.6×	1.2k 0.8×	89 0.3×	265 0.9×	43	2.2k
Sigrid Tinschert Germany	31	345 0.2×	1.3k 0.7×	985 0.7×	232 0.8×	157 0.5×	94	3.1k
Salud Borrego Spain	28	1.1k 0.6×	1.8k 0.9×	738 0.5×	172 0.6×	99 0.3×	135	3.0k
Arnold Munnich France	25	410 0.2×	1.9k 1.0×	724 0.5×	310 1.0×	109 0.4×	54	3.2k
Clarisse Baumann France	26	495 0.2×	969 0.5×	853 0.6×	114 0.4×	252 0.9×	73	2.1k

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-authorship network of co-authors of Anna Pelet

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Pelet. A scholar is included among the top collaborators of Anna Pelet based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anna Pelet. Anna Pelet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Castéra, Laurent, Catherine Dehainault, Dorothée Michaux, et al.. (2012). Fine mapping of whole RB1 gene deletions in retinoblastoma patients confirms PCDH8 as a candidate gene for psychomotor delay. European Journal of Human Genetics. 21(4). 460–464. 9 indexed citations

Jannot, Anne‐Sophie, Jeanne Amiel, Anna Pelet, et al.. (2012). Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease. European Journal of Human Genetics. 20(9). 917–920. 8 indexed citations

Basel‐Vanagaite, Lina, Anna Pelet, Zvi Steiner, et al.. (2006). Allele dosage-dependent penetrance of RET proto-oncogene in an Israeli-Arab inbred family segregating Hirschsprung disease. European Journal of Human Genetics. 15(2). 242–245. 10 indexed citations

Castanet, Mireille, Laurence Leenhardt, Juliane Léger, et al.. (2005). Thyroid Hemiagenesis Is a Rare Variant of Thyroid Dysgenesis with a Familial Component but without Pax8 Mutations in a Cohort of 22 Cases. Pediatric Research. 57(6). 908–913. 40 indexed citations

Amiel, Jeanne, Yolanda Espinosa‐Parrilla, Julie Steffann, et al.. (2001). Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures. The American Journal of Human Genetics. 69(6). 1370–1377. 79 indexed citations

Touraine, Renaud, Tania Attié‐Bitach, E. Manceau, et al.. (2000). Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain. The American Journal of Human Genetics. 66(5). 1496–1503. 124 indexed citations

Pelet, Anna, Olivier Geneste, Patrick Edery, et al.. (1998). Various mechanisms cause RET-mediated signaling defects in Hirschsprung's disease.. Journal of Clinical Investigation. 101(6). 1415–1423. 83 indexed citations

Salomon, Rémi, Tania Attié‐Bitach, Anna Pelet, et al.. (1996). Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease. Nature Genetics. 14(3). 345–347. 150 indexed citations

Amiel, Jeanne, Patrick Edery, Anna Pelet, et al.. (1996). [Genetics of Hirschsprung disease].. PubMed. 50(7). 538–41. 2 indexed citations

10.

Attié‐Bitach, Tania, Anna Pelet, Patrick Edery, et al.. (1995). Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease. Human Molecular Genetics. 4(8). 1381–1386. 242 indexed citations

11.

Bonnet, Damien, Anna Pelet, Laurence Legeai‐Mallet, et al.. (1994). A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12. Nature Genetics. 6(4). 405–408. 33 indexed citations

12.

Merrer, Martine Le, Francis Rousseau, Laurence Legeai‐Mallet, et al.. (1994). A gene for achondroplasia–hypochondroplasia maps to chromosome 4p. Nature Genetics. 6(3). 318–321. 89 indexed citations

13.

Rousseau, Francis, Jacky Bonaventure, Laurence Legeai‐Mallet, et al.. (1994). Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature. 371(6494). 252–254. 689 indexed citations breakdown →

14.

Lyonnet, Stanislas, Alessandra Bolino, Anna Pelet, et al.. (1993). A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. Nature Genetics. 4(4). 346–350. 142 indexed citations

15.

Serville, F, Paule Bénit, Pascale Saugier-Véber, et al.. (1993). Prenatal exclusion of X‐linked hydrocephalus‐stenosis of the aqueduct of sylvius sequence using closely linked DNA markers. Prenatal Diagnosis. 13(6). 435–439. 4 indexed citations

16.

Lyonnet, Stanislas, Anna Pelet, F Serville, et al.. (1992). The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52. Genomics. 14(2). 508–510. 21 indexed citations

17.

Feldmann, D, Jean‐Michel Rozet, Anna Pelet, et al.. (1992). Site specific screening for point mutations in ornithine transcarbamylase deficiency.. PubMed. 29(7). 471–5. 9 indexed citations

18.

Pelet, Anna, et al.. (1991). Fatal hyperammonemia resulting from a C-to-T mutation at a MspI site of the ornithine transcarbamylase gene. Human Genetics. 88(2). 153–6. 25 indexed citations

19.

Kaplan, Jeffrey, Anna Pelet, M Guilloud-Bataille, et al.. (1990). [An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia].. PubMed. 37(1). 13–9. 2 indexed citations

20.

Pelet, Anna, Agnès Rötig, Daniel Rabier, et al.. (1990). Carrier detection in a partially dominant X-linked disease: ornithine transcarbamylase deficiency. Human Genetics. 84(2). 167–71. 17 indexed citations

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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