M. Fontés

684 citations
15 papers · 595 · h-index 8

Impact in

  • Genetics top 10%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
  • Parasitology top 10%

Papers in

    • Genetics and Neurodevelopmental Disorders 8
    • Animal Genetics and Reproduction 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
    • RNA regulation and disease 4
    • RNA modifications and cancer 3
    • CRISPR and Genetic Engineering 1

M. Fontés

14 papers receiving 558 citations

Peers

M. Fontés
Comparison fields: 5 of 61
  • Genetics 296
  • Parasitology 58
  • Public Health, Environmental and Occupational Health 232
  • Cognitive Neuroscience 108
  • Epidemiology 123
Replace Anne-Marie Lossi with:
Anne-Marie Lossi France
Willem M.R. van den Akker Netherlands
Cheryl Filippich Australia
Phung Lang Switzerland
Fabiele Baldino Russo Brazil
Daniel Williamson United States
S. Testoni Italy
Tony del Rio United States
Jennifer Daily United States
C.L. Wilcox United States
M. Fontés relative to Anne-Marie Lossi France Anne-Marie Lossi's profile →
Citations per field
00.5×2×3×4×4.9×
Anne-Marie Lossi · 1×
Citations per year

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-authors

The 25 scholars most cited alongside M. Fontés, 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 M. Fontés Line = papers co-authored together M. Fontés links everyone, so they are left out of the graph.

All Works

15 of 15 papers shown
#Work
1 2000168
2 1994155
3 199390
4 199954
5 199438
6 199630
7
New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. Online.
199814
8 199313
9 19998
10 19878
11 19997
12 19944
13 19954
14
Physical mapping of the 17p chromosomal region relationship with the charcot marie tooth disease
19912
15 20080

About M. Fontés

M. Fontés is a scholar working on Genetics, Molecular Biology, Aging, Cellular and Molecular Neuroscience and Public Health, Environmental and Occupational Health, having authored 15 papers that have together received 595 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), RNA regulation and disease (4 papers), RNA modifications and cancer (3 papers), Animal Genetics and Reproduction (2 papers), Research on Leishmaniasis Studies (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), CRISPR and Genetic Engineering (1 paper) and T-cell and Retrovirus Studies (1 paper). The work is most often cited by research in Genetics (296 citations), Parasitology (58 citations), Public Health, Environmental and Occupational Health (232 citations), Cognitive Neuroscience (108 citations) and Epidemiology (123 citations). M. Fontés has collaborated with scholars based in France, Italy and Spain. Frequent co-authors include Laurent Villard, Carlos Cardoso, F Gambarelli, H. Dumon, Renaud Piarroux, Michel Quilici, Jamel Chelly, Arlette Kpebe, Marc Tardieu and S Dunan. Their work appears in journals such as Human Molecular Genetics, Gene, Journal of Molecular Biology, Journal of Clinical Microbiology and The American Journal 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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