Frédéric Huet

6.6k total citations
120 papers, 2.4k citations indexed

About

Frédéric Huet is a scholar working on Genetics, Surgery and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Frédéric Huet has authored 120 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 26 papers in Surgery and 25 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Frédéric Huet's work include Genomic variations and chromosomal abnormalities (12 papers), Viral gastroenteritis research and epidemiology (12 papers) and Cystic Fibrosis Research Advances (11 papers). Frédéric Huet is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Viral gastroenteritis research and epidemiology (12 papers) and Cystic Fibrosis Research Advances (11 papers). Frédéric Huet collaborates with scholars based in France, Belgium and Switzerland. Frédéric Huet's co-authors include Leif Gothefors, Carlo Giaquinto, Pierre Van Damme, Laurence Faivre, Marie Van der Wielen, Jean‐Bernard Gouyon, Melanie Maxwell, Alice Masurel‐Paulet, Patrick Callier and Pierre Pothier and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Clinical Infectious Diseases.

In The Last Decade

Frédéric Huet

114 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frédéric Huet France 27 588 580 555 425 377 120 2.4k
Andreas Jenke Germany 31 383 0.7× 153 0.3× 604 1.1× 341 0.8× 213 0.6× 75 2.1k
Giuseppe Murdaca Italy 39 263 0.4× 347 0.6× 563 1.0× 578 1.4× 303 0.8× 145 4.4k
Ilan Krause Israel 36 374 0.6× 261 0.5× 289 0.5× 413 1.0× 305 0.8× 104 3.2k
Amita Aggarwal India 36 262 0.4× 251 0.4× 1.0k 1.8× 438 1.0× 362 1.0× 298 5.1k
Eran Israeli Israel 32 1.0k 1.8× 191 0.3× 529 1.0× 1.2k 2.7× 204 0.5× 96 3.5k
Simon Ball United Kingdom 33 897 1.5× 283 0.5× 1.1k 2.0× 425 1.0× 301 0.8× 127 3.8k
Gianfranco Rizzoni Italy 37 367 0.6× 453 0.8× 655 1.2× 197 0.5× 533 1.4× 108 3.7k
Naresh Sachdeva India 31 444 0.8× 335 0.6× 631 1.1× 344 0.8× 200 0.5× 194 3.6k
Reto A. Schuepbach Switzerland 25 182 0.3× 469 0.8× 526 0.9× 361 0.8× 231 0.6× 101 2.8k
Donald C. Dafoe United States 33 222 0.4× 274 0.5× 342 0.6× 407 1.0× 896 2.4× 148 3.8k

Countries citing papers authored by Frédéric Huet

Since Specialization
Citations

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

Fields of papers citing papers by Frédéric Huet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Frédéric Huet. 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 Frédéric Huet. The network helps show where Frédéric Huet may publish in the future.

Co-authorship network of co-authors of Frédéric Huet

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Huet. A scholar is included among the top collaborators of Frédéric Huet 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 Frédéric Huet. Frédéric Huet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Fanton, Annlyse, Karine Astruc, Frédéric Huet, et al.. (2019). Carriage of a Single Strain of Nontoxigenic Corynebacterium diphtheriae bv. Belfanti ( Corynebacterium belfantii ) in Four Patients with Cystic Fibrosis. Journal of Clinical Microbiology. 57(5). 8 indexed citations
2.
Béjot, Yannick, et al.. (2017). Épidémiologie des accidents vasculaires cérébraux en pédiatrie. Soins Pédiatrie/Puériculture. 38(295). 12–13.
3.
Gueneau, Lucie, Laurence Duplomb, Pierre Sarda, et al.. (2013). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. American Journal of Medical Genetics Part A. 164(2). 522–527. 11 indexed citations
4.
Masurel‐Paulet, Alice, Vera M. Kalscheuer, Nicolas Lebrun, et al.. (2013). Expanding the clinical phenotype of patients with a ZDHHC9 mutation. American Journal of Medical Genetics Part A. 164(3). 789–795. 28 indexed citations
5.
Huet, Frédéric, et al.. (2012). Résultats du traitement précoce par hormone de croissance dans les hypopituitarismes de l'enfant. Bulletin de l Académie Nationale de Médecine. 196(1). 117–125. 3 indexed citations
6.
Piard, Juliette, Muriel Holder‐Espinasse, Bernard Aral, et al.. (2011). Systematic search for neutropenia should be part of the first screening in patients with poikiloderma. European Journal of Medical Genetics. 55(1). 8–11. 18 indexed citations
7.
Duez, Jean-Marie, Eliane Siébor, Karine Astruc, et al.. (2010). In VitroSynergistic Activity of Combined Piperacillin and Tobramycin Against Clinical Strains ofAchromobacter xylosoxidans. Journal of Chemotherapy. 22(2). 139–141. 2 indexed citations
8.
Beltrand, Jacques, Najiba Lahlou, Tifenn Le Charpentier, et al.. (2010). Resistance to leptin-replacement therapy in Berardinelli–Seip congenital lipodystrophy: an immunological origin. European Journal of Endocrinology. 162(6). 1083–1091. 46 indexed citations
9.
Masurel‐Paulet, Alice, Eric Haan, Elizabeth M. Thompson, et al.. (2010). Lung disease associated with periventricular nodular heterotopia and an FLNA mutation. European Journal of Medical Genetics. 54(1). 25–28. 47 indexed citations
10.
Martha, B., Delphine Croisier, Annlyse Fanton, et al.. (2009). Factors associated with mucoid transition of Pseudomonas aeruginosa in cystic fibrosis patients. Clinical Microbiology and Infection. 16(6). 617–623. 8 indexed citations
11.
Diene, Gwénaëlle, et al.. (2009). Apnées sévères différées en période néonatale et syndrome de Prader-Willi : à propos de 2 cas. Archives de Pédiatrie. 16(3). 248–251.
12.
Méjean, N., et al.. (2009). The pituitary stalk interruption syndrome: Endocrine features and benefits of growth hormone therapy. Annales d Endocrinologie. 71(2). 102–110. 13 indexed citations
13.
Rötig, Agnès, Alain Fischer, Pascale de Lonlay, et al.. (2008). Tubulopathy and pancytopaenia with normal pancreatic function: A variant of Pearson syndrome. European Journal of Medical Genetics. 52(1). 23–26. 22 indexed citations
14.
Dupuis, Delphine S., Laurence Faivre, Alice Masurel‐Paulet, et al.. (2008). Severe neonatal non‐dystrophic myotonia secondary to a novel mutation of the voltage‐gated sodium channel (SCN4A) gene. American Journal of Medical Genetics Part A. 146A(3). 380–383. 53 indexed citations
15.
Huet, Frédéric & Nathalie Lazaric. (2008). Capacités d’absorption et d’interaction : une étude de la coopération dans les PME françaises. Revue d économie industrielle. 121. 65–84. 7 indexed citations
16.
Giaquinto, Carlo, Pierre Van Damme, Frédéric Huet, et al.. (2007). Clinical Consequences of Rotavirus Acute Gastroenteritis in Europe, 2004–2005: The REVEAL Study. The Journal of Infectious Diseases. 195(s1). S26–S35. 78 indexed citations
17.
Mosca, A.L., Nicole Laurent, Laurent Guibaud, et al.. (2006). Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?. European Journal of Medical Genetics. 50(1). 48–53. 3 indexed citations
18.
Colombani, Marina, Nicole Laurent, Martine Le Merrer, et al.. (2006). A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders. Prenatal Diagnosis. 26(12). 1151–1155. 2 indexed citations
19.
Carel, Jean‐Claude, Frédéric Huet, & Jean‐Louis Chaussain. (2003). Treatment of Growth Hormone Deficiency in Very Young Children. Hormone Research in Paediatrics. 60(Suppl. 1). 10–17. 8 indexed citations
20.
Bernardini, Sergio, et al.. (1997). Effects of cisapride on QTc interval in neonates: Figure 1. Archives of Disease in Childhood Fetal & Neonatal. 77(3). F241–F243. 33 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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