Cécile Cazeneuve

3.9k total citations
44 papers, 1.9k citations indexed

About

Cécile Cazeneuve is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Cécile Cazeneuve has authored 44 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 13 papers in Neurology. Recurrent topics in Cécile Cazeneuve's work include Genetic Neurodegenerative Diseases (10 papers), Amyotrophic Lateral Sclerosis Research (8 papers) and Cystic Fibrosis Research Advances (7 papers). Cécile Cazeneuve is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Amyotrophic Lateral Sclerosis Research (8 papers) and Cystic Fibrosis Research Advances (7 papers). Cécile Cazeneuve collaborates with scholars based in France, United States and Armenia. Cécile Cazeneuve's co-authors include Serge Amselem, Éric Leguern, Alexis Brice, Philippe Duquesnoy, Michel Goossens, François Salachas, Stéphanie Millecamps, Vincent Meininger, Danielle Seilhean and Gilles Grateau and has published in prestigious journals such as Journal of Biological Chemistry, Blood and The American Journal of Human Genetics.

In The Last Decade

Cécile Cazeneuve

42 papers receiving 1.8k citations

Peers

Cécile Cazeneuve
Marie‐Claude Babron France
Piraye Oflazer Türkiye
Maria Hoeltzenbein Germany
Kondi Wong United States
Josep Gámez Spain
Shentong Fang Finland
Ian Sutton Australia
Yuichi Kawagashira Japan
Julien Ratelade United States
Huiming Xu China
Marie‐Claude Babron France
Cécile Cazeneuve
Citations per year, relative to Cécile Cazeneuve Cécile Cazeneuve (= 1×) peers Marie‐Claude Babron

Countries citing papers authored by Cécile Cazeneuve

Since Specialization
Citations

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

Fields of papers citing papers by Cécile Cazeneuve

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Cazeneuve

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Cazeneuve. A scholar is included among the top collaborators of Cécile Cazeneuve 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 Cécile Cazeneuve. Cécile Cazeneuve 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.
Sebbag, Laurent, Cécile Cazeneuve, Nathan Mewton, et al.. (2025). Arrhythmogenic Cardiomyopathy Is a New Phenotype Associated With the CACNA1C p.Arg518Cys (R518C) Variant. JACC. Clinical electrophysiology. 11(11). 2509–2512.
2.
Ader, Flavie, Guillaume Jedraszak, Alexandre Janin, et al.. (2024). Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical Genetics. 105(6). 676–682. 4 indexed citations
3.
Janin, Alexandre, Karine Nguyen, Émilie Consolino, et al.. (2022). Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants. Molecular Diagnosis & Therapy. 26(5). 551–560. 7 indexed citations
4.
Janin, Alexandre, et al.. (2021). Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center’s Experience Over 5 Years. Molecular Diagnosis & Therapy. 25(3). 373–385. 14 indexed citations
5.
Bouchghoul, Hanane, D Vauthier, Cécile Cazeneuve, et al.. (2016). Prenatal testing in Huntington disease: after the test, choices recommence. European Journal of Human Genetics. 24(11). 1535–1540. 10 indexed citations
6.
Clot, Fabienne, Anne Rovelet‐Lecrux, Foudil Lamari, et al.. (2014). Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics. 15(2). 95–100. 7 indexed citations
7.
Teyssou, Elisa, Takahiro Takeda, Vincent Lebon, et al.. (2013). Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology. Acta Neuropathologica. 125(4). 511–522. 185 indexed citations
8.
Millecamps, Stéphanie, Séverine Boillée, Isabelle Le Ber, et al.. (2012). Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes. Journal of Medical Genetics. 49(4). 258–263. 129 indexed citations
9.
Millecamps, Stéphanie, Séverine Boillée, E Chabrol, et al.. (2011). Screening of OPTN in French familial amyotrophic lateral sclerosis. Neurobiology of Aging. 32(3). 557.e11–557.e13. 63 indexed citations
10.
Seilhean, Danielle, Cécile Cazeneuve, Stéphanie Millecamps, et al.. (2009). Accumulation of TDP-43 and α-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation. Acta Neuropathologica. 118(4). 561–573. 57 indexed citations
11.
Cazeneuve, Cécile, Salah A. Ibrahim, Maowia M. Mukhtar, et al.. (2009). A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease. Neurogenetics. 10(3). 265–270. 20 indexed citations
12.
Ribrag, Vincent, Serge Koscielny, Olivier Casasnovas, et al.. (2008). Pharmacogenetic study in Hodgkin lymphomas reveals the impact of UGT1A1 polymorphisms on patient prognosis. Blood. 113(14). 3307–3313. 25 indexed citations
13.
Grateau, Gilles, Isabelle Jéru, S. Rouaghe, et al.. (2005). Amyloidosis and Auto-Inflammatory Syndromes. Current Drug Targets - Inflammation & Allergy. 4(1). 57–65. 23 indexed citations
14.
Cazeneuve, Cécile, David Geneviève, Hasmik Hayrapetyan, et al.. (2003). Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations. Arthritis & Rheumatism. 48(8). 2324–2331. 36 indexed citations
15.
Papin, Stéphanie, Cécile Cazeneuve, Philippe Duquesnoy, et al.. (2003). The Tumor Necrosis Factor α-dependent Activation of the Human Mediterranean Fever (MEFV) Promoter Is Mediated by a Synergistic Interaction between C/EBPβ and NFκB p65. Journal of Biological Chemistry. 278(49). 48839–48847. 46 indexed citations
16.
Cazeneuve, Cécile, Stéphanie Papin, Françoise Roudot‐Thoraval, et al.. (2000). Identification of MEFV-Independent Modifying Genetic Factors for Familial Mediterranean Fever. The American Journal of Human Genetics. 67(5). 1136–1143. 155 indexed citations
17.
Cazeneuve, Cécile, Tamara Sarkisian, Christophe Pécheux, et al.. (1999). MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications. The American Journal of Human Genetics. 65(1). 88–97. 203 indexed citations
18.
Danan, Claude, Damien Sternberg, André Van Steirteghem, et al.. (1999). Evaluation of Parental Mitochondrial Inheritance in Neonates Born after Intracytoplasmic Sperm Injection. The American Journal of Human Genetics. 65(2). 463–473. 64 indexed citations
19.
Bienvenu, Thierry, Cécile Cazeneuve, Isabelle Fajac, et al.. (1995). Identification of a Novel Missense Mutation G239R in Exon 6a of the CFTR Gene. Human Heredity. 45(1). 53–54. 1 indexed citations
20.
Bienvenu, Thierry, Virginie Penard‐Lacronique, Michel Raymondjean, et al.. (1995). Three novel sequence variations in the 5? upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defect. Human Genetics. 95(6). 698–702. 20 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marie‐Claude Babron Breakdown of academic impact, for papers by Piraye Oflazer Breakdown of academic impact, for papers by Maria Hoeltzenbein Breakdown of academic impact, for papers by Kondi Wong Breakdown of academic impact, for papers by Josep Gámez Breakdown of academic impact, for papers by Shentong Fang Breakdown of academic impact, for papers by Ian Sutton Breakdown of academic impact, for papers by Yuichi Kawagashira Breakdown of academic impact, for papers by Julien Ratelade Breakdown of academic impact, for papers by Huiming Xu
Rankless by CCL
2026