N. Ravisé

810 citations

30 papers · 585 indexed · h-index 14

Cellular and Molecular Neuroscience top 5%
Molecular Biology
Neurology top 10%
Genetics
Neurology top 10%

Co-authors: Alexis Brice Éric Leguern P. Bouché Merle Ruberg P. Couillin Judith Lopes E. Le Guern J. Weissenbach
Topics: Hereditary Neurological Disorders (15 papers)Neurological diseases and metabolism (6 papers)Genetic Neurodegenerative Diseases (6 papers)
Cited by: Cellular and Molecular Neuroscience Neurology
Journals: Nature Genetics Neurology Annals of the New York Academy of Sciences
Partner nations: France United Kingdom United States

In The Last Decade

N. Ravisé

30 papers receiving 564 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Silencing of the Charcot–Marie–Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells 2007 ·Neurobiology of Disease ·Alexandre Chojnowski,N. Ravisé,Corinne Bachelin,Christel Depienne,Merle Ruberg,Bernard Brugg,Jocelyn Laporte,Anne Baron‐Van Evercooren,Eric Leguern	10
2	Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations 2006 ·Neurology ·Hamid Azzedine,N. Ravisé,Christophe Verny,A.A.W.M. Gabreëls‐Festen,Martin Lammens,(unknown),Jean‐Michel Vallat,(unknown),Jan Senderek,Sonia Nouioua,Tarik Hamadouche,Ahmed Bouhouche,A. Guilbot,Claudia Stendel,Merle Ruberg,Alexis Brice,Nazha Birouk,O. Dubourg,Mériem Tazir,Éric Leguern	76
3	Rapid detection of 17p11.2 rearrangements by FISH without cell culture (direct FISH, DFISH): A prospective study of 130 patients with inherited peripheral neuropathies 2003 ·American Journal of Medical Genetics Part A ·N. Ravisé,O. Dubourg,Sandrine Tardieu,(unknown),(unknown),Philippe Coullin,Merle Ruberg,Martin Catala,(unknown),Alexis Brice,Éric Leguern	4
4	Simultaneous Fluorescence In-situ Hybridization (FISH) and R-Banding By Primed In-situ Labelling (PRINS) 1999 ·Chromosome Research ·Philippe Coullin,C. Philippe,N. Ravisé,Alain Bernheim	8
5	The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33 1999 ·Annals of the New York Academy of Sciences ·A. Guilbot,(unknown),N. Ravisé,T. Hammadouche,Ahmed Bouhouche,Thierry Maisonobe,(unknown),Alexis Brice,Éric Leguern	7
6	Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31–q33: exclusion of candidate genes including EGR1 1999 ·European Journal of Human Genetics ·(unknown),N. Ravisé,Ahmed Bouhouche,Philippe Coullin,Nazha Birouk,Thierry Maisonobe,Thierry Küntzer,Christophe Vial,Djamel Grid,Alexis Brice,Éric Leguern	8
7	The Autosomal Recessive Form of CMT Disease Linked to 5q31‐q33 1999 ·Annals of the New York Academy of Sciences ·A. Guilbot,(unknown),N. Ravisé,T. Hammadouche,Ahmed Bouhouche,Thierry Maisonobe,(unknown),Alexis Brice,Éric Leguern	4
8	Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination 1998 ·Human Molecular Genetics ·Judith Lopes,N. Ravisé,A. Vandenberghe,Francesc Palau,Victor Ionâşescu,M. Mayer,Nicolas Lévy,Nicholas Wood,Nobutada Tachi,P. Bouché,Philippe Latour,Merle Ruberg,Alexis Brice,(unknown)	66
9	A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2? 1996 ·Human Molecular Genetics ·(unknown),(unknown),N. Ravisé,Judith Lopes,(unknown),(unknown),N. Abbas,P. Bouché,Y. Agid,Alexis Brice	27
10	The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1 1995 ·Nature Genetics ·Ali Benomar,(unknown),Giovanni Stévanin,Géraldine Cancel‐Tassin,Éric Leguern,Gilles David,H. Ouhabi,Jean‐Jacques Martin,Alexandra Dürr,(unknown),N. Ravisé,(unknown),Christiane Penet,Nicole Van Regemorter,J. Weissenbach,M. Yahyaoui,T. Chkili,Yves Agid,Christine Van Broeckhoven,Alexis Brice	126
11	Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases 1995 ·Human Molecular Genetics ·Éric Leguern,Riadh Gouider,Judith Lopes,N. Abbas,Michel Gugenheim,Sandrine Tardieu,N. Ravisé,J.-M. Léger,Jean‐Michel Vallat,P. Bouché,Yves Agid,Alexis Brice	15
12	Assignment of 112 Microsatellite Markers to 23 Chromosome 11 Subregions Delineated by Somatic Hybrids: Comparison with the Genetic Map 1994 ·Genomics ·(unknown),E. Le Guern,Alain Vignal,Cécile Fizames,N. Ravisé,(unknown),(unknown),(unknown),Claudine Junien,Veronica van Heyningen,J. Weissenbach	19
13	Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP) 1994 ·Cytogenetic and Genome Research ·E. Le Guern,(unknown),Michel Gugenheim,Riadh Gouider,(unknown),N. Ravisé,Pierre‐Marie Gonnaud,(unknown),P. Bouché,G Chazot,Y. Agid,A. Vandenberghe,Alexis Brice	37
14	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 1994 ·Neuromuscular Disorders ·E. Le Guern,N. Ravisé,Michel Gugenheim,Alain Vignal,Christiane Penet,P. Bouché,Jean Weissenbach,Yves Agid,Alexis Brice	8
15	Chromosome 11q localization of one of the three expected genes for the human α-3-fucosyltransferases, by somatic hybridization 1991 ·Cytogenetic and Genome Research ·P. Couillin,Rosella Mollicone,(unknown),Anne Gibaud,N. Ravisé,J Feingold,Rafaël Oriol	23
16	More precise localization of the gene for Hunter syndrome 1990 ·Genomics ·E. Le Guern,P. Couillin,I. Oberlé,N. Ravisé,J Boué	16
17	Early prenatal diagnosis of 21‐hydroxylase deficiency using amniotic fluid 17‐hydroxyprogesterone determination and DNA probes 1989 ·Prenatal Diagnosis ·(unknown),Étienne Mornet,J Boué,P. Couillin,J.F. Oury,N. Ravisé,(unknown),A Boué	7
18	Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13 1989 ·Human Genetics ·P. Couillin,(unknown),Isabelle Henry,N. Ravisé,(unknown),Marc Jeanpierre,F. Barichard,Philippe Métézeau,Jean‐Jacques Candelier,William H. Lewis,Veronica van Heyningen,Claudine Junien	18
19	HLA markers in parents of triploid conceptuses. 1977 ·PubMed ·(unknown),A Boué,J Boué,N. Ravisé,N Feingold,J Hors	6
20	[Indirect hemagglutination test for detection of antibodies to cytomegalovirus in blood collected on blotting paper (author's transl)]. 1976 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·(unknown),(unknown),N. Ravisé,M Coulon,A Boué	4

About N. Ravisé

N. Ravisé is a scholar working on Cellular and Molecular Neuroscience, Neurology and Pediatrics, Perinatology and Child Health, having authored 30 papers that have together received 585 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (15 papers), Neurological diseases and metabolism (6 papers) and Genetic Neurodegenerative Diseases (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (345 citations), Neurology (95 citations) and Neurology (136 citations). N. Ravisé has collaborated with scholars based in France, United Kingdom and United States. Frequent 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. Their work appears in journals such as Nature Genetics, Neurology and Annals of the New York Academy of Sciences.

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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