Stéphanie Tomé

915 total citations
17 papers, 591 citations indexed

About

Stéphanie Tomé is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine. According to data from OpenAlex, Stéphanie Tomé has authored 17 papers receiving a total of 591 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Stéphanie Tomé's work include Genetic Neurodegenerative Diseases (14 papers), Mitochondrial Function and Pathology (8 papers) and DNA Repair Mechanisms (7 papers). Stéphanie Tomé is often cited by papers focused on Genetic Neurodegenerative Diseases (14 papers), Mitochondrial Function and Pathology (8 papers) and DNA Repair Mechanisms (7 papers). Stéphanie Tomé collaborates with scholars based in France, United Kingdom and United States. Stéphanie Tomé's co-authors include Geneviève Gourdon, Christopher E. Pearson, David Chitayat, Arturo López Castel, Jodie P. Simard, Glenn E. Morris, Charles A. Thornton, Ian Holt, Masayuki Nakamori and Meghan M. Slean and has published in prestigious journals such as International Journal of Molecular Sciences, Human Molecular Genetics and Nature Structural & Molecular Biology.

In The Last Decade

Stéphanie Tomé

16 papers receiving 587 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Stéphanie Tomé 534 416 93 91 53 17 591
Jodie P. Simard 444 0.8× 306 0.7× 69 0.7× 47 0.5× 63 1.2× 8 484
Arturo López Castel 688 1.3× 450 1.1× 125 1.3× 76 0.8× 31 0.6× 19 751
Edith Lopez 579 1.1× 506 1.2× 76 0.8× 147 1.6× 39 0.7× 8 681
Sherman Ku 314 0.6× 168 0.4× 53 0.6× 19 0.2× 13 0.2× 8 337
Beatriz Llamusí 590 1.1× 455 1.1× 18 0.2× 76 0.8× 24 0.5× 33 691
Song‐Ro Yoon 347 0.6× 194 0.5× 132 1.4× 52 0.6× 11 0.2× 9 447
Kerin Gibbons 361 0.7× 298 0.7× 123 1.3× 145 1.6× 7 0.1× 6 491
Jihae Shin 463 0.9× 255 0.6× 43 0.5× 34 0.4× 5 0.1× 13 511
Jill S. Napierala 519 1.0× 431 1.0× 84 0.9× 78 0.9× 4 0.1× 31 572
Sergio Arias 229 0.4× 94 0.2× 107 1.2× 48 0.5× 15 0.3× 33 414

Countries citing papers authored by Stéphanie Tomé

Since Specialization
Citations

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

Fields of papers citing papers by Stéphanie Tomé

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Tomé

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

All Works

17 of 17 papers shown
1.
Benarroch, Louise, Pierre‐Yves Boëlle, Nobuyuki Eura, et al.. (2025). Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion Disorders. Genomics Proteomics & Bioinformatics.
2.
Tsai, Yu‐Chih, Cheryl Heiner, Tanya Stojkovic, et al.. (2022). Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read Sequencing. Journal of Molecular Diagnostics. 24(11). 1143–1154. 13 indexed citations
3.
Tomé, Stéphanie, et al.. (2022). Overview of the Complex Relationship between Epigenetics Markers, CTG Repeat Instability and Symptoms in Myotonic Dystrophy Type 1. International Journal of Molecular Sciences. 23(7). 3477–3477. 7 indexed citations
4.
Mangin, Antoine, Yu‐Chih Tsai, Mathilde Nizon, et al.. (2021). Robust Detection of Somatic Mosaicism and Repeat Interruptions by Long-Read Targeted Sequencing in Myotonic Dystrophy Type 1. International Journal of Molecular Sciences. 22(5). 2616–2616. 28 indexed citations
5.
Tomé, Stéphanie & Geneviève Gourdon. (2020). DM1 Phenotype Variability and Triplet Repeat Instability: Challenges in the Development of New Therapies. International Journal of Molecular Sciences. 21(2). 457–457. 26 indexed citations
6.
Scrudato, Mirella Lo, Karine Poulard, Stéphanie Tomé, et al.. (2019). Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 Mice. Molecular Therapy. 27(8). 1372–1388. 42 indexed citations
7.
Tomé, Stéphanie & Geneviève Gourdon. (2019). Fast Assays to Detect Interruptions in CTG.CAG Repeat Expansions. Methods in molecular biology. 2056. 11–23. 4 indexed citations
8.
Scrudato, Mirella Lo, Karine Poulard, Stéphanie Tomé, et al.. (2019). O.32Genome editing of expanded CTG repeats within the human DMPK gene reduces nuclear RNA foci in muscle of DM1 mice. Neuromuscular Disorders. 29. S125–S125. 2 indexed citations
9.
Tomé, Stéphanie, Céline Dogan, Alexis Bertrand, et al.. (2018). Unusual association of a unique CAG interruption in 5′ of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism. Human Mutation. 39(7). 970–982. 27 indexed citations
10.
Tomé, Stéphanie, Annie Nicole, Mário Gomes‐Pereira, & Geneviève Gourdon. (2014). Non-Radioactive Detection of Trinucleotide Repeat Size Variability. PLoS Currents. 6. 8 indexed citations
11.
Tomé, Stéphanie, Jodie P. Simard, Randell T. Libby, et al.. (2013). Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age. Human Molecular Genetics. 23(6). 1606–1618. 41 indexed citations
12.
Tomé, Stéphanie, Kevin Manley, Jodie P. Simard, et al.. (2013). MSH3 Polymorphisms and Protein Levels Affect CAG Repeat Instability in Huntington's Disease Mice. PLoS Genetics. 9(2). e1003280–e1003280. 109 indexed citations
13.
Tomé, Stéphanie, Jodie P. Simard, Meghan M. Slean, et al.. (2012). Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues. DNA repair. 12(1). 46–52. 28 indexed citations
14.
Holt, Ian, Le Thanh Lam, Stéphanie Tomé, et al.. (2011). The mouse mismatch repair protein, MSH3, is a nucleoplasmic protein that aggregates into denser nuclear bodies under conditions of stress. Journal of Cellular Biochemistry. 112(6). 1612–1621. 9 indexed citations
15.
Castel, Arturo López, Masayuki Nakamori, Stéphanie Tomé, et al.. (2010). Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues. Human Molecular Genetics. 20(1). 1–15. 115 indexed citations
16.
Cleary, John D., Stéphanie Tomé, Arturo López Castel, et al.. (2010). Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus. Nature Structural & Molecular Biology. 17(9). 1079–1087. 55 indexed citations
17.
Tomé, Stéphanie, Ian Holt, Winfried Edelmann, et al.. (2009). MSH2 ATPase Domain Mutation Affects CTG•CAG Repeat Instability in Transgenic Mice. PLoS Genetics. 5(5). e1000482–e1000482. 77 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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