Cédric Le Maréchal

3.7k total citations
76 papers, 2.1k citations indexed

About

Cédric Le Maréchal is a scholar working on Hematology, Surgery and Oncology. According to data from OpenAlex, Cédric Le Maréchal has authored 76 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Hematology, 21 papers in Surgery and 18 papers in Oncology. Recurrent topics in Cédric Le Maréchal's work include Pancreatitis Pathology and Treatment (19 papers), Blood groups and transfusion (15 papers) and Erythrocyte Function and Pathophysiology (14 papers). Cédric Le Maréchal is often cited by papers focused on Pancreatitis Pathology and Treatment (19 papers), Blood groups and transfusion (15 papers) and Erythrocyte Function and Pathophysiology (14 papers). Cédric Le Maréchal collaborates with scholars based in France, United States and United Kingdom. Cédric Le Maréchal's co-authors include Claude Férec, Jian‐Min Chen, Odile Raguénès, Emmanuelle Masson, Marie‐Pierre Audrézet, Philippe Ruszniewski, I. Quéré, Yann Fichou, Virginie Scotet and Philippe Lévy and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

In The Last Decade

Cédric Le Maréchal

72 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cédric Le Maréchal France 28 927 778 396 390 356 76 2.1k
Richard F. Olsson Sweden 26 630 0.7× 274 0.4× 94 0.2× 692 1.8× 284 0.8× 55 1.8k
Lisa Ma United States 23 130 0.1× 567 0.7× 207 0.5× 623 1.6× 126 0.4× 40 2.1k
Eugene Y. Koh United States 18 266 0.3× 509 0.7× 75 0.2× 232 0.6× 110 0.3× 68 1.8k
MC Berndt Australia 20 430 0.5× 138 0.2× 197 0.5× 942 2.4× 252 0.7× 35 1.7k
David A. Wilcox United States 24 154 0.2× 258 0.3× 185 0.5× 932 2.4× 434 1.2× 48 1.8k
Mitsuru Hara Japan 22 337 0.4× 288 0.4× 339 0.9× 44 0.1× 160 0.4× 70 1.6k
Tamotsu Miyazaki Japan 19 598 0.6× 137 0.2× 266 0.7× 315 0.8× 70 0.2× 88 1.5k
Elizabeth A. Traxler United States 10 116 0.1× 210 0.3× 177 0.4× 424 1.1× 200 0.6× 15 1.2k
Kazumi Suzukawa Japan 24 117 0.1× 233 0.3× 108 0.3× 606 1.6× 120 0.3× 75 1.6k
Yin Luo Italy 17 1.0k 1.1× 564 0.7× 99 0.3× 174 0.4× 629 1.8× 33 2.9k

Countries citing papers authored by Cédric Le Maréchal

Since Specialization
Citations

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

Fields of papers citing papers by Cédric Le Maréchal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cédric Le Maréchal. 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 Cédric Le Maréchal. The network helps show where Cédric Le Maréchal may publish in the future.

Co-authorship network of co-authors of Cédric Le Maréchal

This figure shows the co-authorship network connecting the top 25 collaborators of Cédric Le Maréchal. A scholar is included among the top collaborators of Cédric Le Maréchal 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 Cédric Le Maréchal. Cédric Le Maréchal 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.
Uguen, Kévin, Sylvia Redon, Karen Rouault, et al.. (2024). An unusual diagnosis of alpha‐mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation. American Journal of Medical Genetics Part A. 194(5). e63532–e63532.
2.
Maréchal, Cédric Le, et al.. (2019). Characterization of GJB2 cis-regulatory elements in the DFNB1 locus. Human Genetics. 138(11-12). 1275–1286. 10 indexed citations
3.
Leclère, J, et al.. (2017). GJB2 mutations: Genotypic and phenotypic correlation in a cohort of 690 hearing-impaired patients, toward a new mutation?. International Journal of Pediatric Otorhinolaryngology. 102. 80–85. 11 indexed citations
4.
Uguen, Arnaud, Matthieu Talagas, Sebastian Costa, et al.. (2015). NRAS Q61R , BRAF V600E immunohistochemistry: a concomitant tool for mutation screening in melanomas. Diagnostic Pathology. 10(1). 121–121. 28 indexed citations
5.
Uguen, Arnaud, Camille Laurent, Blandine Boisselier, et al.. (2015). Severe hydrocephalus caused by diffuse leptomeningeal and neurocutaneous melanocytosis of antenatal onset: a clinical, pathologic, and molecular study of 2 cases. Human Pathology. 46(8). 1189–1196. 9 indexed citations
6.
Guéguen, Paul, Karen Rouault, Jian‐Min Chen, et al.. (2013). A Missense Mutation in the Alpha-Actinin 1 Gene (ACTN1) Is the Cause of Autosomal Dominant Macrothrombocytopenia in a Large French Family. PLoS ONE. 8(9). e74728–e74728. 34 indexed citations
7.
Saliou, Philippe, Gérald Le Gac, Paul Guéguen, et al.. (2013). Evidence for the High Importance of Co-Morbid Factors in HFE C282Y/H63D Patients Cared by Phlebotomies: Results from an Observational Prospective Study. PLoS ONE. 8(12). e81128–e81128. 5 indexed citations
8.
Chen, Jian‐Min, Yann Fichou, Isabelle Dupont, et al.. (2012). Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms. Transfusion. 53(1). 206–210. 8 indexed citations
9.
Fichou, Yann, Jian‐Min Chen, Cédric Le Maréchal, et al.. (2012). Weak D caused by a founder deletion in the RHD gene. Transfusion. 52(11). 2348–2355. 26 indexed citations
10.
Masson, Emmanuelle, Cédric Le Maréchal, Richard Delcenserie, Jian‐Min Chen, & Claude Férec. (2008). Hereditary pancreatitis caused by a double gain-of-function trypsinogen mutation. Human Genetics. 123(5). 521–529. 34 indexed citations
11.
Verny, Christophe, Patrizia Amati‐Bonneau, Franck Letournel, et al.. (2008). Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis. Diabetes & Metabolism. 34(6). 620–626. 22 indexed citations
12.
Király, Orsolya, Arnaud Boulling, Heiko Witt, et al.. (2007). Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis. Human Mutation. 28(5). 469–476. 66 indexed citations
13.
Masson, Emmanuelle, Cédric Le Maréchal, Giriraj R. Chandak, et al.. (2007). Trypsinogen Copy Number Mutations in Patients With Idiopathic Chronic Pancreatitis. Clinical Gastroenterology and Hepatology. 6(1). 82–88. 54 indexed citations
14.
Maréchal, Cédric Le, Caroline Bénech, B Cavelier, et al.. (2007). Identification of 12 novel RHD alleles in western France by denaturing high‐performance liquid chromatography analysis. Transfusion. 47(5). 858–863. 36 indexed citations
15.
Masson, Emmanuelle, Cédric Le Maréchal, Philippe Lévy, et al.. (2007). Co-inheritance of a novel deletion of the entire SPINK1 gene with a CFTR missense mutation (L997F) in a family with chronic pancreatitis. Molecular Genetics and Metabolism. 92(1-2). 168–175. 21 indexed citations
16.
Maréchal, Cédric Le, Emmanuelle Masson, Jian‐Min Chen, et al.. (2006). Hereditary pancreatitis caused by triplication of the trypsinogen locus. Nature Genetics. 38(12). 1372–1374. 140 indexed citations
17.
Férec, Claude, Cédric Le Maréchal, M.‐P. Audrézet, et al.. (2004). Analysis of genomic CFTR DNA. Journal of Cystic Fibrosis. 3. 7–10. 7 indexed citations
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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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