Corinne Collet

4.4k total citations
125 papers, 2.1k citations indexed

About

Corinne Collet is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Corinne Collet has authored 125 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 48 papers in Molecular Biology and 19 papers in Oncology. Recurrent topics in Corinne Collet's work include Craniofacial Disorders and Treatments (27 papers), Cleft Lip and Palate Research (24 papers) and Connective tissue disorders research (17 papers). Corinne Collet is often cited by papers focused on Craniofacial Disorders and Treatments (27 papers), Cleft Lip and Palate Research (24 papers) and Connective tissue disorders research (17 papers). Corinne Collet collaborates with scholars based in France, United States and Switzerland. Corinne Collet's co-authors include Marie‐Christine de Vernejoul, Valérie Geoffroy, Jean‐Marie Launay, Jean Laplanche, Jacques Callebert, Federico Di Rocco, Francine Côté, Éric Arnaud, Luc Maroteaux and Martine Cohen‐Solal and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Corinne Collet

117 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Corinne Collet France	26	817	538	335	273	215	125	2.1k
Francesca Marini Italy	28	1.1k 1.3×	322 0.6×	784 2.3×	255 0.9×	91 0.4×	113	2.7k
Marie‐Christine de Vernejoul France	30	1.3k 1.6×	517 1.0×	636 1.9×	298 1.1×	170 0.8×	80	2.9k
Alan C. Dalkin United States	29	883 1.1×	689 1.3×	226 0.7×	126 0.5×	98 0.5×	66	2.9k
R. Clay Bunn United States	28	1.2k 1.5×	288 0.5×	434 1.3×	312 1.1×	77 0.4×	46	2.6k
Dionisios Chrysis Greece	23	748 0.9×	447 0.8×	171 0.5×	180 0.7×	66 0.3×	65	1.8k
Jui‐Cheng Hsieh United States	24	910 1.1×	926 1.7×	246 0.7×	146 0.5×	641 3.0×	34	3.2k
Toshio Tsushima Japan	33	1.2k 1.5×	498 0.9×	584 1.7×	351 1.3×	207 1.0×	119	3.7k
Michio Suda Japan	20	1.0k 1.3×	450 0.8×	416 1.2×	326 1.2×	658 3.1×	36	3.3k
Rachel A. Davey Australia	26	1.2k 1.5×	554 1.0×	467 1.4×	135 0.5×	52 0.2×	61	2.5k
Kathryn M. Thrailkill United States	36	1.5k 1.8×	582 1.1×	539 1.6×	445 1.6×	123 0.6×	75	3.5k

Countries citing papers authored by Corinne Collet

Since Specialization

Citations

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

Fields of papers citing papers by Corinne Collet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Collet

This figure shows the co-authorship network connecting the top 25 collaborators of Corinne Collet. A scholar is included among the top collaborators of Corinne Collet 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 Corinne Collet. Corinne Collet 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

Obadia, Mickaël Alexandre, Corinne Collet, France Woimant, et al.. (2025). Relative exchangeable copper: A highly specific and sensitive biomarker for Wilson disease diagnosis. JHEP Reports. 7(10). 101537–101537.

Dubourg, Christèle, et al.. (2024). Novel variant in LRP6 associated with unusual and severe clinical presentation: Case report. Clinical Genetics. 105(6). 666–670.

Hennocq, Quentin, Corinne Collet, Jeanne Amiel, et al.. (2024). AI-based diagnosis and phenotype – Genotype correlations in syndromic craniosynostoses. Journal of Cranio-Maxillofacial Surgery. 52(10). 1172–1187. 7 indexed citations

Rocco, Federico Di, Massimiliano Rossi, Alexandru Szathmári, et al.. (2023). Clinical interest of molecular study in cases of isolated midline craniosynostosis. European Journal of Human Genetics. 31(6). 621–628. 7 indexed citations

Fabre, Stéphanie, Guillaume Mabilleau, Aude Couturier, et al.. (2023). Lrp5 p. Val667Met Variant Compromises Bone Mineral Density and Matrix Properties in Osteoporosis. JBMR Plus. 7(6). e10741–e10741. 4 indexed citations

Merle, Blandine, Corinne Collet, Olivier Borel, et al.. (2023). Dysregulation of MicroRNAs in Adult Osteogenesis Imperfecta: The miROI Study. Journal of Bone and Mineral Research. 38(11). 1665–1678. 4 indexed citations

Collet, Corinne, Isabelle Gennero, Sanaa Eddiry, et al.. (2022). Diagnostic yield of bone fragility gene panel sequencing in children and young adults referred for idiopathic primary osteoporosis at a single regional reference centre. Bone Reports. 16. 101176–101176. 11 indexed citations

Orcel, Philippe, et al.. (2021). More severe phenotype of early‐onset osteoporosis associated with recessive form ofLRP5and combination withDKK1orWNT3A. Molecular Genetics & Genomic Medicine. 9(6). e1681–e1681. 11 indexed citations

Woimant, France, et al.. (2020). A novel deep intronic variant in ATP7B in five unrelated families affected by Wilson disease. Molecular Genetics & Genomic Medicine. 8(10). e1428–e1428. 9 indexed citations

10.

Morice, Anne, Raphaël Cornette, Amerigo Giudice, et al.. (2020). Early mandibular morphological differences in patients with FGFR2 and FGFR3-related syndromic craniosynostoses: A 3D comparative study. Bone. 141. 115600–115600. 12 indexed citations

11.

Michot, Caroline, Geneviève Baujat, S. Baron, et al.. (2019). Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review. Clinical Genetics. 96(4). 309–316. 31 indexed citations

12.

Collet, Corinne, et al.. (2018). High genetic carrier frequency of Wilson’s disease in France: discrepancies with clinical prevalence. BMC Medical Genetics. 19(1). 143–143. 47 indexed citations

13.

Brischoux‐Boucher, Elise, Aurélien Trimouille, Geneviève Baujat, et al.. (2018). IL11RA‐related Crouzon‐like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences. Clinical Genetics. 94(3-4). 373–380. 26 indexed citations

14.

Funck‐Brentano, Thomas, Corinne Collet, Amélie E. Coudert, & Martine Cohen‐Solal. (2018). Les ostéopétroses. Revue du Rhumatisme Monographies. 86(1). 26–30. 1 indexed citations

15.

Nampoothiri, Sheela, Ayşe Özden, Björn Fischer‐Zirnsak, et al.. (2018). Sclerosing bone dysplasias with hallmarks of dysosteosclerosis in four patients carrying mutations in SLC29A3 and TCIRG1. Bone. 120. 495–503. 16 indexed citations

16.

Funck‐Brentano, Thomas, Agnès Ostertag, Françoise Debiais, et al.. (2016). Identification of a p.Arg708Gln variant in COL1A2 in atypical femoral fractures. Joint Bone Spine. 84(6). 715–718. 14 indexed citations

17.

Hénaff, Carole Le, Aurélie Hatton, Denis Tondelier, et al.. (2016). Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosis. Human Molecular Genetics. 25(7). 1281–1293. 12 indexed citations

18.

Loupy, Alexandre, Suresh Krishna Ramakrishnan, Bharath Wootla, et al.. (2012). PTH-independent regulation of blood calcium concentration by the calcium-sensing receptor. Journal of Clinical Investigation. 122(9). 3355–3367. 149 indexed citations

19.

Banas, Sophie M., Stéphane Doly, Katia Boutourlinsky, et al.. (2011). Deconstructing antiobesity compound action: requirement of serotonin 5-HT2B receptors for dexfenfluramine anorectic effects.. HAL (Le Centre pour la Communication Scientifique Directe). 29 indexed citations

20.

Leroyer, R., et al.. (1997). A propos d’une intoxication par l’éthylène glycol. Journal de Pharmacie Clinique. 16(3). 177–182. 1 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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