N. Ravisé

810 total citations
30 papers, 585 citations indexed

About

N. Ravisé is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, N. Ravisé has authored 30 papers receiving a total of 585 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cellular and Molecular Neuroscience, 13 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in N. Ravisé's work include Hereditary Neurological Disorders (15 papers), Neurological diseases and metabolism (6 papers) and Genetic Neurodegenerative Diseases (6 papers). N. Ravisé is often cited by papers focused on Hereditary Neurological Disorders (15 papers), Neurological diseases and metabolism (6 papers) and Genetic Neurodegenerative Diseases (6 papers). N. Ravisé collaborates with scholars based in France, United Kingdom and United States. N. Ravisé's co-authors include Alexis Brice, Éric Leguern, P. Bouché, Merle Ruberg, P. Couillin, Judith Lopes, E. Le Guern, J. Weissenbach, J Boué and Yves Agid and has published in prestigious journals such as Nature Genetics, Neurology and Annals of the New York Academy of Sciences.

In The Last Decade

N. Ravisé

30 papers receiving 564 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N. Ravisé France 14 345 298 136 111 95 30 585
Eric J. Meershoek Netherlands 10 252 0.7× 160 0.5× 86 0.6× 101 0.9× 100 1.1× 11 434
Memnune Yüksel Apak Türkiye 11 213 0.6× 215 0.7× 69 0.5× 93 0.8× 140 1.5× 20 549
Panos Ioannou Australia 15 239 0.7× 478 1.6× 50 0.4× 123 1.1× 17 0.2× 26 632
Yasuhide Hayashi Japan 9 288 0.8× 374 1.3× 140 1.0× 47 0.4× 114 1.2× 9 741
Jennifer N. Partlow United States 13 119 0.3× 432 1.4× 32 0.2× 209 1.9× 52 0.5× 14 640
Dong-Hui Chen United States 9 277 0.8× 370 1.2× 127 0.9× 83 0.7× 39 0.4× 10 579
Anna-Elina Lehesjoki Finland 10 92 0.3× 395 1.3× 67 0.5× 197 1.8× 33 0.3× 10 768
Éléonore Eymard-Pierre France 16 180 0.5× 685 2.3× 272 2.0× 146 1.3× 184 1.9× 38 1.1k
Rachel Flomen United Kingdom 12 77 0.2× 370 1.2× 45 0.3× 180 1.6× 20 0.2× 17 583
Liesbeth M. Bleeker-Wagemakers Netherlands 10 51 0.1× 415 1.4× 36 0.3× 205 1.8× 92 1.0× 12 557

Countries citing papers authored by N. Ravisé

Since Specialization
Citations

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

Fields of papers citing papers by N. Ravisé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Ravisé

This figure shows the co-authorship network connecting the top 25 collaborators of N. Ravisé. A scholar is included among the top collaborators of N. Ravisé 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 N. Ravisé. N. Ravisé 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.
Chojnowski, Alexandre, N. Ravisé, Corinne Bachelin, et al.. (2007). Silencing of the Charcot–Marie–Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells. Neurobiology of Disease. 26(2). 323–331. 10 indexed citations
2.
Azzedine, Hamid, N. Ravisé, Christophe Verny, et al.. (2006). Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations. Neurology. 67(4). 602–606. 76 indexed citations
3.
Ravisé, N., O. Dubourg, Sandrine Tardieu, et al.. (2003). Rapid detection of 17p11.2 rearrangements by FISH without cell culture (direct FISH, DFISH): A prospective study of 130 patients with inherited peripheral neuropathies. American Journal of Medical Genetics Part A. 118A(1). 43–48. 4 indexed citations
4.
Coullin, Philippe, C. Philippe, N. Ravisé, & Alain Bernheim. (1999). Simultaneous Fluorescence In-situ Hybridization (FISH) and R-Banding By Primed In-situ Labelling (PRINS). Chromosome Research. 7(3). 241–242. 8 indexed citations
5.
Guilbot, A., N. Ravisé, T. Hammadouche, et al.. (1999). The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33. Annals of the New York Academy of Sciences. 883(1). 56–59. 7 indexed citations
6.
Ravisé, N., Ahmed Bouhouche, Philippe Coullin, et al.. (1999). Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31–q33: exclusion of candidate genes including EGR1. European Journal of Human Genetics. 7(8). 849–859. 8 indexed citations
7.
Guilbot, A., N. Ravisé, T. Hammadouche, et al.. (1999). The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33. Annals of the New York Academy of Sciences. 883(1). 453–456. 4 indexed citations
8.
Lopes, Judith, N. Ravisé, A. Vandenberghe, et al.. (1998). Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Human Molecular Genetics. 7(1). 141–148. 66 indexed citations
9.
Ravisé, N., Judith Lopes, N. Abbas, et al.. (1996). A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2?. Human Molecular Genetics. 5(1). 103–106. 27 indexed citations
10.
Benomar, Ali, Giovanni Stévanin, Géraldine Cancel‐Tassin, et al.. (1995). The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1. Nature Genetics. 10(1). 84–88. 126 indexed citations
11.
Leguern, Éric, Riadh Gouider, Judith Lopes, et al.. (1995). Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. Human Molecular Genetics. 4(9). 1673–1674. 15 indexed citations
12.
Guern, E. Le, Alain Vignal, Cécile Fizames, et al.. (1994). Assignment of 112 Microsatellite Markers to 23 Chromosome 11 Subregions Delineated by Somatic Hybrids: Comparison with the Genetic Map. Genomics. 21(2). 379–387. 19 indexed citations
13.
Guern, E. Le, Michel Gugenheim, Riadh Gouider, et al.. (1994). Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP). Cytogenetic and Genome Research. 65(4). 261–264. 37 indexed citations
14.
Guern, E. Le, N. Ravisé, Michel Gugenheim, et al.. (1994). Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11–Xq21 microsatellites in a new large family: Three new markers are closely linked to the gene. Neuromuscular Disorders. 4(5-6). 463–469. 8 indexed citations
15.
Couillin, P., Rosella Mollicone, Anne Gibaud, et al.. (1991). Chromosome 11q localization of one of the three expected genes for the human α-3-fucosyltransferases, by somatic hybridization. Cytogenetic and Genome Research. 56(2). 108–111. 23 indexed citations
16.
Guern, E. Le, P. Couillin, I. Oberlé, N. Ravisé, & J Boué. (1990). More precise localization of the gene for Hunter syndrome. Genomics. 7(3). 358–362. 16 indexed citations
17.
Mornet, Étienne, J Boué, P. Couillin, et al.. (1989). Early prenatal diagnosis of 21‐hydroxylase deficiency using amniotic fluid 17‐hydroxyprogesterone determination and DNA probes. Prenatal Diagnosis. 9(7). 457–466. 7 indexed citations
18.
Couillin, P., Isabelle Henry, N. Ravisé, et al.. (1989). Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Human Genetics. 82(2). 171–178. 18 indexed citations
19.
Boué, A, et al.. (1977). HLA markers in parents of triploid conceptuses.. PubMed. 25(9). 647–50. 6 indexed citations
20.
Ravisé, N., et al.. (1976). [Indirect hemagglutination test for detection of antibodies to cytomegalovirus in blood collected on blotting paper (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 24(8). 575–9. 4 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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