F.M.S. Tomé

6.1k total citations · 2 hit papers
72 papers, 4.4k citations indexed

About

F.M.S. Tomé is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, F.M.S. Tomé has authored 72 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 29 papers in Cellular and Molecular Neuroscience and 13 papers in Cell Biology. Recurrent topics in F.M.S. Tomé's work include Muscle Physiology and Disorders (49 papers), Genetic Neurodegenerative Diseases (25 papers) and Cardiomyopathy and Myosin Studies (8 papers). F.M.S. Tomé is often cited by papers focused on Muscle Physiology and Disorders (49 papers), Genetic Neurodegenerative Diseases (25 papers) and Cardiomyopathy and Myosin Studies (8 papers). F.M.S. Tomé collaborates with scholars based in France, United States and United Kingdom. F.M.S. Tomé's co-authors include Michel Fardeau, Kevin P. Campbell, A. Leclerc, Jean‐Claude Kaplan, Pascale Guicheney, J. Beckmann, H. Barry Collin, Haluk Topaloğlu, France Leturcq and Corinne Cruaud and has published in prestigious journals such as Nature, Cell and Journal of Clinical Investigation.

In The Last Decade

F.M.S. Tomé

71 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1998 583 citations F.M.S. Tomé, Michel Fardeau et al. profile →
Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

1995 506 citations Haluk Topaloğlu, F.M.S. Tomé et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F.M.S. Tomé France	32	3.9k	1.5k	921	707	607	72	4.4k
Eijiro Ozawa Japan	31	4.1k 1.1×	1.1k 0.7×	1.1k 1.2×	943 1.3×	385 0.6×	99	4.7k
Yoshihide Sunada Japan	39	3.9k 1.0×	973 0.6×	1.0k 1.1×	630 0.9×	371 0.6×	144	5.2k
Silvia Torelli United Kingdom	29	4.0k 1.0×	737 0.5×	512 0.6×	796 1.1×	595 1.0×	80	4.4k
Mariz Vainzof Brazil	38	4.2k 1.1×	1.4k 0.9×	855 0.9×	1.3k 1.9×	923 1.5×	189	4.8k
Beril Talim Türkiye	31	3.0k 0.8×	580 0.4×	609 0.7×	492 0.7×	487 0.8×	138	4.0k
Fumiaki Saito Japan	22	2.3k 0.6×	864 0.6×	644 0.7×	215 0.3×	159 0.3×	54	3.0k
France Leturcq France	35	3.4k 0.9×	890 0.6×	547 0.6×	947 1.3×	639 1.1×	130	4.0k
Yoh‐suke Mukouyama United States	35	2.7k 0.7×	1.0k 0.7×	900 1.0×	247 0.3×	317 0.5×	73	4.5k
Reginald E. Bittner Austria	34	2.1k 0.5×	417 0.3×	657 0.7×	509 0.7×	411 0.7×	82	3.5k
Yuko Miyagoe‐Suzuki Japan	36	3.6k 0.9×	430 0.3×	509 0.6×	284 0.4×	929 1.5×	70	4.4k

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-authorship network of co-authors of F.M.S. Tomé

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Hoeltzenbein, Maria & F.M.S. Tomé. (2001). Oppenheim's Myatonia Congenita. Neuropediatrics. 32(2). 57–61. 1 indexed citations

Moghadaszadeh, Behzad, Isabelle Desguerre, Haluk Topaloğlu, et al.. (1998). Identification of a New Locus for a Peculiar Form of Congenital Muscular Dystrophy with Early Rigidity of the Spine, on Chromosome 1p35-36. The American Journal of Human Genetics. 62(6). 1439–1445. 62 indexed citations

Khurana, Tejvir S., Linda A. Specht, Alan H. Beggs, et al.. (1997). The Concomitant Use of Dystrophin and Utrophin/Dystrophin Related Protein Antibodies to Reduce Misdiagnosis of Duchenne/Becker Muscular Dystrophy. Biochemical and Biophysical Research Communications. 241(2). 232–235. 1 indexed citations

Fardeau, Michel & F.M.S. Tomé. (1997). Oculopharyngeal muscular dystrophy in France. Neuromuscular Disorders. 7. S30–S33. 11 indexed citations

Uyama, Eiichiro, F.M.S. Tomé, Danielle Château, et al.. (1997). Oculopharyngeal muscular dystrophy in Japan. Neuromuscular Disorders. 7. S41–S49. 13 indexed citations

Jung, Daniel, France Leturcq, Yoshihide Sunada, et al.. (1996). Absence of γ‐sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12. FEBS Letters. 381(1-2). 15–20. 46 indexed citations

Fardeau, Michel, B. Eymard, C. Mignard, et al.. (1996). Chromosome 15-linked limb-girdle muscular dystrophy: Clinical phenotypes in Reunion Island and French metropolitan communities. Neuromuscular Disorders. 6(6). 447–453. 57 indexed citations

Jeanpierre, Marc, Alain Carrié, Fédérica Piccolo, et al.. (1996). From adhalinopathies to alpha-sarcoglycanopathies: An overview. Neuromuscular Disorders. 6(6). 463–465. 13 indexed citations

Sewry, Caroline A., M. Chevallay, & F.M.S. Tomé. (1995). Expression of laminin subunits in human fetal skeletal muscle. The Histochemical Journal. 27(7). 497–504. 1 indexed citations

10.

Khurana, Tejvir S., R A Prendergast, Hala S. Alameddine, et al.. (1995). Absence of extraocular muscle pathology in Duchenne's muscular dystrophy: role for calcium homeostasis in extraocular muscle sparing.. The Journal of Experimental Medicine. 182(2). 467–475. 112 indexed citations

11.

Sewry, Caroline A., M. Chevallay, & F.M.S. Tomé. (1995). Expression of laminin subunits in human fetal skeletal muscle.. PubMed. 27(7). 497–504. 33 indexed citations

12.

Matsumura, Kiichiro, Arthur H.M. Burghes, Marina Mora, et al.. (1994). Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.. Journal of Clinical Investigation. 93(1). 99–105. 45 indexed citations

13.

Tomé, F.M.S., Kiichiro Matsumura, M. Chevallay, Kevin P. Campbell, & Michel Fardeau. (1994). Expression of dystrophin-associated glycoproteins during human fetal muscle development: A preliminary immunocytochemical study. Neuromuscular Disorders. 4(4). 343–348. 40 indexed citations

14.

Fardeau, Michel & F.M.S. Tomé. (1994). Ultrastructure of muscle and neuromuscular junction: an historical survey of the early french contributions. Biology of the Cell. 80(2-3). 115–117. 2 indexed citations

15.

Matsumura, Kiichiro, F.M.S. Tomé, Victor Ionâşescu, et al.. (1993). Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.. Journal of Clinical Investigation. 92(2). 866–871. 60 indexed citations

16.

Cartaud, Annie, Marie‐Aline Ludosky, F.M.S. Tomé, et al.. (1992). Localization of dystrophin and dystrophin-related protein at the electromotor synapse and neuromuscular junction in Torpedo marmorata. Neuroscience. 48(4). 995–1003. 32 indexed citations

17.

Matsumura, Kiichiro, F.M.S. Tomé, H. Barry Collin, et al.. (1992). Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature. 359(6393). 320–322. 200 indexed citations

18.

Tomé, F.M.S., et al.. (1989). Nuclear inclusions in innervated cultured muscle fibers from patients with oculopharyngeal muscular dystrophy. Neurology. 39(7). 926–926. 21 indexed citations

19.

Eymard, B., F.M.S. Tomé, Pascal Brunet, & M Fardeau. (1986). [Marfan's disease and familial neuropathy with sausage-shaped swelling. A case of fortuitous association].. PubMed. 142(8-9). 703–5. 2 indexed citations

20.

Pons, F., Jocelyne Léger, M. Chevallay, et al.. (1986). Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles. Journal of the Neurological Sciences. 76(2-3). 151–163. 53 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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