A Tullio-Pelet

564 total citations
9 papers, 369 citations indexed

About

A Tullio-Pelet is a scholar working on Surgery, Gastroenterology and Molecular Biology. According to data from OpenAlex, A Tullio-Pelet has authored 9 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Surgery, 5 papers in Gastroenterology and 2 papers in Molecular Biology. Recurrent topics in A Tullio-Pelet's work include Gastroesophageal reflux and treatments (5 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Congenital Anomalies and Fetal Surgery (2 papers). A Tullio-Pelet is often cited by papers focused on Gastroesophageal reflux and treatments (5 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Congenital Anomalies and Fetal Surgery (2 papers). A Tullio-Pelet collaborates with scholars based in France, Italy and Canada. A Tullio-Pelet's co-authors include Stanislas Lyonnet, S. Hadj‐Rabia, Marc Nicolino, Claude Mugnier, Martine Bégeot, Marc‐Henri De Laet, Danielle Naville, Fawzi Bakiri, Laurence Cattolico and Jean-Louis Chaussain and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

A Tullio-Pelet

9 papers receiving 356 citations

Peers

A Tullio-Pelet

MB

SURGE

GASTR

GENET

Fawzi Bakiri Algeria

Mariateresa Falco Italy

Mingyang Deng China

Essam A. R. Ismail Kuwait

Sara Bertok Slovenia

Andrew Lane United States

J.-M. Vanderwinden Belgium

Modlin Im United States

Sezer Acar Türkiye

C B Lamers Netherlands

Fawzi Bakiri Algeria

A Tullio-Pelet

152 ×0.9

MB

94 ×0.6

SURGE

82 ×0.7

GASTR

49 ×0.8

GENET

26 ×0.5

GENET

Citations per year, relative to A Tullio-Pelet A Tullio-Pelet (= 1×) peers Fawzi Bakiri

Countries citing papers authored by A Tullio-Pelet

Since Specialization

Citations

This map shows the geographic impact of A Tullio-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 A Tullio-Pelet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Tullio-Pelet more than expected).

Fields of papers citing papers by A Tullio-Pelet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A Tullio-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 A Tullio-Pelet. The network helps show where A Tullio-Pelet may publish in the future.

Co-authorship network of co-authors of A Tullio-Pelet

This figure shows the co-authorship network connecting the top 25 collaborators of A Tullio-Pelet. A scholar is included among the top collaborators of A Tullio-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 A Tullio-Pelet. A Tullio-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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9 of 9 papers shown

1.

Amiel, Jeanne, Guillermo Antiñolo, Salud Borrego, et al.. (2006). Higher prevalence of Hirschsprung disease in China explained by a common RET mutation. 2 indexed citations

2.

Nardo, Giovanni Di, A Tullio-Pelet, Vito Annese, et al.. (2005). Idiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the locus. Digestive and Liver Disease. 37(5). 312–315. 13 indexed citations

3.

Roman, Sabine, et al.. (2005). Triple-A Syndrome: A Rare Etiology of Adult Achalasia. Digestive Diseases and Sciences. 50(3). 440–442. 4 indexed citations

4.

Barat, Pascal, et al.. (2004). Phenotypic heterogeneity in AAAS gene mutation. Acta Paediatrica. 93(9). 1257–1259. 4 indexed citations

5.

Barat, Pascal, et al.. (2004). Phenotypic heterogeneity in AAAS gene mutation. Acta Paediatrica. 93(9). 1257–1259. 12 indexed citations

6.

Roubergue, Anne, Emmanuelle Apartis, Marie Vidailhet, et al.. (2003). Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation. Movement Disorders. 19(3). 344–346. 9 indexed citations

7.

Goizet, Cyril, Bogdan Catargi, F Tison, et al.. (2002). Progressive bulbospinal amyotrophy in Triple A syndrome with AAAS gene mutation. Neurology. 58(6). 962–965. 47 indexed citations

8.

Sandrini, Fabiano, Constantine Farmakidis, Lawrence S. Kirschner, et al.. (2001). Spectrum of Mutations of theAAASGene in Allgrove Syndrome: Lack of Mutations in Six Kindreds with Isolated Resistance to Corticotropin. The Journal of Clinical Endocrinology & Metabolism. 86(11). 5433–5437. 52 indexed citations

9.

Tullio-Pelet, A, Rémi Salomon, S. Hadj‐Rabia, et al.. (2000). Mutant WD-repeat protein in triple-A syndrome. Nature Genetics. 26(3). 332–335. 226 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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