C. Cazeneuve

1.6k citations
25 papers · 1.3k · h-index 13

Impact in

  • Neurology top 5%
    • Amyotrophic Lateral Sclerosis Research
    • Neurological diseases and metabolism
  • Genetics top 5%
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders

Papers in

C. Cazeneuve

25 papers receiving 1.2k citations

Peers

C. Cazeneuve
Comparison fields: 5 of 69
  • Neurology 331
  • Genetics 184
  • Psychiatry and Mental health 232
  • Clinical Biochemistry 79
  • Neurology 93
Replace S. S. Schochet with:
S. S. Schochet United States
Keiji Kurita Japan
Paulo José Lorenzoni Brazil
Aleksandra Nadaj-Pakleza France
Juan Manuel Politei Argentina
Stephanie L. Austin United States
Paola Cudia Italy
Jung‐Joon Sung South Korea
Kelley J. Murphy United States
S. Lane Rutledge United States
C. Cazeneuve relative to S. S. Schochet United States S. S. Schochet's profile →
Citations per field
00.5×5×10×15×17.5×
S. S. Schochet · 1×
Citations per year

Countries citing papers authored by C. Cazeneuve

Since Specialization
Citations

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

Fields of papers citing papers by C. Cazeneuve

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside C. Cazeneuve, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with C. Cazeneuve Line = papers co-authored together C. Cazeneuve links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2008308
2 2010251
3
CFTR gene mutations in adults with disseminated bronchiectasis.
1997126
4 2009119
5
Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial Mediterranean fever.
200092
6 199487
7 200074
8 200552
9 200540
10 199825
11 200624
12 202221
13 201018
14
Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: A large European study [3]
200112
15 201112
16 200011
17 202010
18 20049
19
Conventional mutations are associated with a different phenotype than polyglutamine expansions in spinocerebellar ataxias
20096
20
[French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Familial Mediterranean fever].
19993

About C. Cazeneuve

C. Cazeneuve is a scholar working on Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry, Neurology and Genetics, having authored 25 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), Inflammasome and immune disorders (6 papers), Cystic Fibrosis Research Advances (4 papers), Metabolism and Genetic Disorders (3 papers), Tracheal and airway disorders (2 papers), Neurological diseases and metabolism (2 papers), Mitochondrial Function and Pathology (2 papers) and Gout, Hyperuricemia, Uric Acid (2 papers). The work is most often cited by research in Neurology (331 citations), Genetics (184 citations), Psychiatry and Mental health (232 citations), Clinical Biochemistry (79 citations) and Neurology (93 citations). C. Cazeneuve has collaborated with scholars based in France and Italy. Frequent co-authors include Serge Amselem, Gilles Grateau, Boris Keren, Wassila Carpentier, Oriane Trouillard, Agnès Gautier, Stéphanie Baulac, Rima Nabbout, Delphine Bouteiller and Alexis A. Arzimanoglou. Their work appears in journals such as Journal of Medical Genetics, British Journal of Clinical Pharmacology, Parkinsonism & Related Disorders, Neurology and Annals of Human Genetics.

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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