M. Fontés

704 total citations
15 papers, 520 citations indexed

About

M. Fontés is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, M. Fontés has authored 15 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in M. Fontés's work include Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (4 papers) and RNA regulation and disease (4 papers). M. Fontés is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (4 papers) and RNA regulation and disease (4 papers). M. Fontés collaborates with scholars based in France, Italy and United States. M. Fontés's co-authors include Laurent Villard, H. Dumon, M Quilici, Renaud Piarroux, F Gambarelli, Carlos Cardoso, Arlette Kpebe, Jamel Chelly, Marc Tardieu and S Dunan and has published in prestigious journals such as Journal of Molecular Biology, Neurology and Journal of Clinical Microbiology.

In The Last Decade

M. Fontés

15 papers receiving 501 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Fontés France	8	246	222	202	129	115	15	520
Charles L. Magness United States	7	177 0.7×	168 0.8×	261 1.3×	153 1.2×	12 0.1×	8	572
Fabiele Baldino Russo Brazil	13	67 0.3×	145 0.7×	212 1.0×	68 0.5×	76 0.7×	25	536
Willem M.R. van den Akker Netherlands	13	145 0.6×	42 0.2×	352 1.7×	82 0.6×	32 0.3×	17	638
Anne-Marie Lossi France	8	154 0.6×	82 0.4×	140 0.7×	44 0.3×	17 0.1×	11	275
Phung Lang Switzerland	12	292 1.2×	68 0.3×	250 1.2×	367 2.8×	20 0.2×	30	664
Amy Slender Australia	8	109 0.4×	166 0.7×	120 0.6×	32 0.2×	16 0.1×	17	384
S. Testoni Italy	13	96 0.4×	39 0.2×	135 0.7×	31 0.2×	51 0.4×	34	501
Tony del Rio United States	11	176 0.7×	69 0.3×	183 0.9×	242 1.9×	7 0.1×	14	533
Cheryl Filippich Australia	13	135 0.5×	165 0.7×	143 0.7×	18 0.1×	36 0.3×	20	527
Amelia H. Osborn Australia	13	15 0.1×	139 0.6×	307 1.5×	140 1.1×	72 0.6×	17	544

Countries citing papers authored by M. Fontés

Since Specialization

Citations

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

Fields of papers citing papers by M. Fontés

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Fontés

This figure shows the co-authorship network connecting the top 25 collaborators of M. Fontés. A scholar is included among the top collaborators of M. 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 M. Fontés. M. 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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15 of 15 papers shown

Villard, Laurent, Arlette Kpebe, Carlos Cardoso, et al.. (2000). Two affected boys in a Rett syndrome family. Neurology. 55(8). 1188–1193. 153 indexed citations

Villard, Laurent, M. Fontés, & Jonathan J. Ewbank. (1999). Characterization of xnp-1, a Caenorhabditis elegans gene similar to the human XNP/ATR-X gene. Gene. 236(1). 13–19. 7 indexed citations

Villard, Laurent, et al.. (1999). Transcript map of the human chromosome Xq11–Xq21 region: localization of 33 novel genes and one pseudogene. Gene. 235(1-2). 43–50. 7 indexed citations

Villard, Laurent, Fatima Abidi, Jérôme Belougne, et al.. (1999). Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome. Journal of Medical Genetics. 36(3). 183–186. 19 indexed citations

Fichera, Marco, Corrado Romano, Lucia Castiglia, et al.. (1998). New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. Online.. PubMed. 12(3). 214–214. 13 indexed citations

Villard, Laurent, Didier Lacombe, & M. Fontés. (1996). A Point Mutation in the XNP Gene,Associated with an ATR-XPhenotype without a-Thalassemia. European Journal of Human Genetics. 4(6). 316–320. 24 indexed citations

Villard, Laurent, E. Passage, Laurence Colleaux, & M. Fontés. (1995). Use of interspersed repetitive sequences-PCR products for cDNA selection. Mammalian Genome. 6(9). 617–622. 4 indexed citations

Gécz, Jozef, et al.. (1994). Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3. Human Molecular Genetics. 3(1). 39–44. 32 indexed citations

Piarroux, Renaud, F Gambarelli, H. Dumon, et al.. (1994). Comparison of PCR with direct examination of bone marrow aspiration, myeloculture, and serology for diagnosis of visceral Leishmaniasis in immunocompromised patients. Journal of Clinical Microbiology. 32(3). 746–749. 149 indexed citations

10.

Clark, Paula A., Tracy Lester, Laurent Villard, M. Fontés, & Christine Kinnon. (1994). Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.. Journal of Medical Genetics. 31(4). 344–345. 4 indexed citations

11.

Piarroux, Renaud, R. Azaiez, Anne-Marie Lossi, et al.. (1993). Isolation and Characterization of a Repetitive DNA Sequence from Leishmania infantum: Development of a Visceral Leishmaniasis Polymerase Chain Reaction. American Journal of Tropical Medicine and Hygiene. 49(3). 364–369. 85 indexed citations

12.

Gécz, Jozef, et al.. (1993). Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcripts. Human Molecular Genetics. 2(9). 1389–1396. 13 indexed citations

13.

Muscatelli, Françoise, Anthony P. Monaco, P.N. Goodfellow, et al.. (1992). Isolation of new probes from Xq12→q13: an example of the screening of reference libraries with <i>Alu-PCR</i> products from radiation hybrids. Cytogenetic and Genome Research. 61(2). 109–113. 1 indexed citations

14.

Moncla, A, et al.. (1991). Physical mapping of the 17p chromosomal region relationship with the charcot marie tooth disease. 58. 2009. 2 indexed citations

15.

Fontés, M., et al.. (1987). There is an α-actin skeletal muscle-specific gene in a salamander (Pleurodeles waltlii). Journal of Molecular Biology. 193(2). 409–412. 7 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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