F.M.S. Tomé

71 papers receiving 4.3k citations

F.M.S. Tomé's Hit Papers

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy 1998 · 590 citations
5900+10+20Years since publication100200300400500

Peers

F.M.S. Tomé
Comparison fields: 5 of 98
  • Cellular and Molecular Neuroscience 1.4k
  • Immunology and Allergy 347
  • Molecular Biology 3.7k
  • Cell Biology 864
  • Genetics 512
Replace Yoshihide Sunada with:
Yoshihide Sunada Japan
Eijiro Ozawa Japan
Silvia Torelli United Kingdom
Lucía Morandi Italy
Fumiaki Saito Japan
Yuko Miyagoe‐Suzuki Japan
Mariz Vainzof Brazil
Beril Talim Türkiye
Yoh‐suke Mukouyama United States
Reginald E. Bittner Austria
F.M.S. Tomé relative to Yoshihide Sunada Japan Yoshihide Sunada's profile →
Citations per field
00.5×1.6×
Yoshihide Sunada · 1×
Citations per year

Countries citing papers authored by F.M.S. Tomé

Since Specialization
Citations

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

Fields of papers citing papers by F.M.S. Tomé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
Hit paper breakdown →
1998590
2
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy
Hit paper breakdown →
1995509
3 1994381
4
Congenital muscular dystrophy with merosin deficiency.
1994349
5 1991230
6 1992200
7 1996141
8 1998123
9 1995112
10 199797
11 199796
12 199378
13 199175
14 199772
15
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.
199671
16 199363
17 199862
18 199360
19 199657
20 198653

About F.M.S. Tomé

F.M.S. Tomé is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology, Genetics and Cardiology and Cardiovascular Medicine, having authored 72 papers that have together received 4.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (48 papers), Genetic Neurodegenerative Diseases (25 papers), Cardiomyopathy and Myosin Studies (8 papers), Neurogenetic and Muscular Disorders Research (7 papers), Biotin and Related Studies (6 papers), Neurological diseases and metabolism (6 papers), Adipose Tissue and Metabolism (6 papers) and RNA regulation and disease (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.4k citations), Immunology and Allergy (347 citations), Molecular Biology (3.7k citations), Cell Biology (864 citations) and Genetics (512 citations). F.M.S. Tomé has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Michel Fardeau, Kevin P. Campbell, A. Leclerc, Jean‐Claude Kaplan, J. Beckmann, Pascale Guicheney, H. Barry Collin, Haluk Topaloğlu, France Leturcq and Karl Tryggvason. Their work appears in journals such as Neuromuscular Disorders, Neurology, FEBS Letters, Biology of the Cell and Brain.

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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