F. Tomé

719 total citations
15 papers, 584 citations indexed

About

F. Tomé is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, F. Tomé has authored 15 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 3 papers in Physiology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in F. Tomé's work include Muscle Physiology and Disorders (10 papers), Mitochondrial Function and Pathology (5 papers) and Telomeres, Telomerase, and Senescence (2 papers). F. Tomé is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Mitochondrial Function and Pathology (5 papers) and Telomeres, Telomerase, and Senescence (2 papers). F. Tomé collaborates with scholars based in France, Finland and Sweden. F. Tomé's co-authors include Michel Fardeau, Eva Engvall, Dominique Récan, Philippe Chafey, Hélène Gilgenkrantz, Anders Paetau, Tero Kivelä, Pirkko Santavuori, Hannu Somer and Matti Haltia and has published in prestigious journals such as Cell, Journal of Clinical Investigation and The Journal of Cell Biology.

In The Last Decade

F. Tomé

14 papers receiving 577 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Tomé France	11	507	99	95	85	83	15	584
Tiziana Mongini Italy	14	399 0.8×	117 1.2×	56 0.6×	141 1.7×	111 1.3×	46	595
Flavia Blàsevich Italy	14	412 0.8×	72 0.7×	44 0.5×	65 0.8×	92 1.1×	31	525
J.Rafael M. Gorospe United States	7	429 0.8×	70 0.7×	51 0.5×	62 0.7×	161 1.9×	8	497
U. L. Fairbrother United Kingdom	7	625 1.2×	86 0.9×	270 2.8×	141 1.7×	148 1.8×	10	817
J. Philpot United Kingdom	13	622 1.2×	138 1.4×	25 0.3×	114 1.3×	118 1.4×	15	696
L. Feng United Kingdom	13	674 1.3×	254 2.6×	69 0.7×	107 1.3×	67 0.8×	19	795
Alexandre Briguet Switzerland	11	539 1.1×	59 0.6×	54 0.6×	120 1.4×	142 1.7×	13	658
Andrée Rouche France	12	462 0.9×	128 1.3×	76 0.8×	189 2.2×	32 0.4×	18	599
Kowashi Yoshioka Japan	13	406 0.8×	74 0.7×	31 0.3×	83 1.0×	115 1.4×	20	449
Kimi Watanabe Japan	11	333 0.7×	47 0.5×	34 0.4×	51 0.6×	84 1.0×	27	428

Countries citing papers authored by F. Tomé

Since Specialization

Citations

This map shows the geographic impact of F. 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. 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. Tomé more than expected).

Fields of papers citing papers by F. Tomé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Tomé

This figure shows the co-authorship network connecting the top 25 collaborators of F. Tomé. A scholar is included among the top collaborators of F. 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. Tomé. F. Tomé 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

Tomé, F.. (1999). The Saga of Congenital Muscular Dystrophy. Neuropediatrics. 30(2). 55–65. 34 indexed citations

Vilquin, Jean‐Thomas, B. Guérette, Jack Puymirat, et al.. (1999). Myoblast transplantations lead to the expression of the laminin α2 chain in normal and dystrophic (dy/dy) mouse muscles. Gene Therapy. 6(5). 792–800. 24 indexed citations

Haltia, Matti, Ilmo Leivo, Hannu Somer, et al.. (1997). Muscle—eye—brain disease: A neuropathological study. Annals of Neurology. 41(2). 173–180. 122 indexed citations

Pini, Antonella, Luciano Merlini, F. Tomé, M. Chevallay, & Giuseppe Gobbi. (1996). Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families. Brain and Development. 18(4). 316–322. 49 indexed citations

Vilquin, Jean‐Thomas, Ikuo Kinoshita, Brigitte Roy, et al.. (1996). Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantation.. The Journal of Cell Biology. 133(1). 185–197. 37 indexed citations

Pini, Antonella, Luciano Merlini, F. Tomé, M. Chevallay, & G. Gobbi. (1996). Merosin-negative congenital muscular dystrophy, cortical dysplasia and epilepsy: An association to investigate. Neuromuscular Disorders. 6(2). S17–S17. 1 indexed citations

Matsumura, Kiichiro, F. Tomé, H. Barry Collin, et al.. (1994). Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy. Neuromuscular Disorders. 4(2). 115–120. 30 indexed citations

Philippe, Christophe, M. Chery, Hélène Gilgenkrantz, et al.. (1994). Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X‐chromosome inactivation. American Journal of Medical Genetics. 52(2). 198–206. 32 indexed citations

Askanas, Valerie, et al.. (1993). Prion protein is strongly immunolocalized at the postsynaptic domain of human normal neuromuscular junctions. Neuroscience Letters. 159(1-2). 111–114. 40 indexed citations

10.

Récan, Dominique, Philippe Chafey, France Leturcq, et al.. (1992). Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?. Journal of Clinical Investigation. 89(2). 712–716. 46 indexed citations

11.

Gilgenkrantz, Hélène, Ghislaine Hamard, Philippe Chafey, et al.. (1990). Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies. Cell. 63(6). 1239–1248. 141 indexed citations

12.

Hentati, Fayçal, F. Tomé, Koussay Dellagi, et al.. (1990). Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy. Neurology. 40(12). 1903–1903. 24 indexed citations

13.

Gayraud, M., F. Tomé, S. Herson, et al.. (1989). [Histopathologic aspects of polymyositis and dermatomyositis. Correlation with the clinical course. Study of 57 cases].. PubMed. 140(6). 445–8. 2 indexed citations

14.

Fardeau, Michel, et al.. (1978). [Role of electron microscopy in peripheral nerve pathology (author's transl)].. PubMed. 26(6). 283–91. 1 indexed citations

15.

Gambetti, P., et al.. (1965). [CHRONIC MENINGO-ENCEPHALITIS OF INFANCY, EPITHELOID CELLS AND SUB-INTIMAL CALCIFICATIONS].. PubMed. 19. 38–58. 1 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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