Michel Fontés

1.0k total citations
17 papers, 418 citations indexed

About

Michel Fontés is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Michel Fontés has authored 17 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 3 papers in Cell Biology. Recurrent topics in Michel Fontés's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA regulation and disease (3 papers). Michel Fontés is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA regulation and disease (3 papers). Michel Fontés collaborates with scholars based in France, United Kingdom and Australia. Michel Fontés's co-authors include Laurent Villard, Jozef Gécz, Stéphane Burtey, Roland Perasso, H. Dumon, Claude Moraine, M Quilici, Renaud Piarroux, Stanislas Bataille and Claude Houdayer and has published in prestigious journals such as Journal of Virology, Biochemical and Biophysical Research Communications and American Journal of Kidney Diseases.

In The Last Decade

Michel Fontés

16 papers receiving 411 citations

Peers

Countries citing papers authored by Michel Fontés

Since Specialization

Citations

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

Fields of papers citing papers by Michel Fontés

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michel Fontés

This figure shows the co-authorship network connecting the top 25 collaborators of Michel Fontés. A scholar is included among the top collaborators of Michel Fontés 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 Michel Fontés. Michel Fontés is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Association of PKD2 (Polycystin 2) Mutations With Left-Right Laterality Defects 2011 ·American Journal of Kidney Diseases ·Stanislas Bataille, Nathalie Demoulin, Olivier Devuyst, Marie‐Pierre Audrézet, Karin Dahan, M. Godin, Michel Fontés, Yves Pirson, Stéphane Burtey	34
2	High Resolution Melt analysis for mutation screening in PKD1 and PKD2 2011 ·BMC Nephrology ·Stanislas Bataille, Yvon Berland, Michel Fontés, Stéphane Burtey	18
3	Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley–Lowry syndrome 2004 ·European Journal of Human Genetics ·Fatima Abidi, Carlos Cardoso, Anne-Marie Lossi, R. Brian Lowry, D. Depétris, Marie‐Geneviève Mattéi, Herbert A. Lubs, Roger E. Stevenson, Michel Fontés, Albert E. Chudley, Charles E. Schwartz	37
4	Aspects cliniques et bases moléculaires du syndrome d‘α‐thalassémie associée à un retard mental 2003 ·Hématologie ·Carlos Cardoso, Catherine Badens, Marie‐Geneviève Mattéi, Michel Fontés	2
5	Spectrum of MECP2 Mutations in Rett Syndrome 2002 ·Genetic Testing ·Thierry Bienvenu, Laurent Villard, Nicolás de Roux, Violaine Bourdon, Michel Fontés, Chérif Beldjord, Marc Tardieu, Philippe Jonveaux, Jamel Chelly	14
6	Alpha-thalassemia/mental retardation syndrome, X-Linked (ATR-X, MIM #301040, ATR-X/XNP/XH2 gene MIM #300032) 2002 ·European Journal of Human Genetics ·Laurent Villard, Michel Fontés	21
7	PrP Expression and Replication by Schwann Cells: Implications in Prion Spreading 2002 ·Journal of Virology ·Jérôme Follet, (unknown), (unknown), (unknown), Sylvain Lehmann, Jean‐Paul Chauvin, (unknown), (unknown), Jacques Grassi, Michel Fontés, Jean-Yves Cesbron	61
8	Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]? 2000 ·American Journal of Medical Genetics ·Sylvain Briault, Laurent Villard, Ute C. Rogner, Johannes Coy, Sylvie Odent, Josette Lucas, E. Passage, Danping Zhu, Antony E. Shrimpton, Marcus Pembrey, Marianne Till, (unknown), (unknown), Michel Fontés, Annemarie Poustka, Claude Moraine	18
9	Linkage of X-linked myopathy with excessive autophagy (XMEA) to Xq28 2000 ·European Journal of Human Genetics ·Laurent Villard, Vincent des Portes, Nicolas Lévy, Jean‐Pierre Louboutin, Dominique Récan, M Coquet, B. Chabrol, Dominique Figarella‐Branger, Jamel Chelly, Jean‐François Pellissier, Michel Fontés	22
10	Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome 2000 ·American Journal of Medical Genetics ·L. Ṽillard, Michel Fontés, Lesley C. Adès, Jozef Gécz	3
11	Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia. 1996 ·PubMed ·Laurent Villard, Annick Toutain, (unknown), Jozef Gécz, Claude Houdayer, Claude Moraine, Michel Fontés	49
12	Construction of a YAC contig spanning the Xq13.3 subband 1995 ·Genomics ·Laurent Villard, Jozef Gécz, Laurence Colleaux, Anne-Marie Lossi, Jamel Chelly, Yumiko Ishikawa-Brush, Anthony P. Monaco, Michel Fontés	16
13	Phylogenetic relationships between Old World Leishmania strains revealed by analysis of a repetitive DNA sequence 1995 ·Molecular and Biochemical Parasitology ·Renaud Piarroux, Michel Fontés, Roland Perasso, (unknown), (unknown), H. Dumon, M Quilici	58
14	Assignment of a polycomb-like chromobox gene (CBX2) to human chromosome 17q25 1995 ·Genomics ·Jozef Gécz, Stephen J. Gaunt, E. Passage, Robert D. Burton, (unknown), Jonathan Pearce, Michel Fontés	19
15	Localization of a Potassium Channel Gene (KCNE1) to 21q22.1-q22.2 by in Situ Hybridization and Somatic Cell Hybridization 1993 ·Genomics ·Christophe Chevillard, Bernard Attali, Florian Lesage, Michel Fontés, Jacques Barhanin, Michel Lazdunski, Marie‐Geneviève Mattéi	24
16	Presence in invertebrate genomes of sequences characterized by the repetition of the triplet CCPurine 1990 ·Biochemical and Biophysical Research Communications ·Norbert Bakalara, (unknown), (unknown), (unknown), Michel Fontés	0
17	Muscle dedifferentiation and contractile protein synthesis during post-traumatic regeneration by Owenia fusiformis (polychaete annelid) 1983 ·Cell Differentiation ·Michel Fontés, (unknown), (unknown), (unknown)	22

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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