Tomoko Lee

769 total citations
43 papers, 400 citations indexed

About

Tomoko Lee is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Tomoko Lee has authored 43 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Surgery. Recurrent topics in Tomoko Lee's work include Muscle Physiology and Disorders (24 papers), RNA Research and Splicing (11 papers) and RNA modifications and cancer (8 papers). Tomoko Lee is often cited by papers focused on Muscle Physiology and Disorders (24 papers), RNA Research and Splicing (11 papers) and RNA modifications and cancer (8 papers). Tomoko Lee collaborates with scholars based in Japan, Vietnam and China. Tomoko Lee's co-authors include Yasuhiro Takeshima, Masafumi Matsuo, Hiroyuki Awano, Mariko Yagi, Kazumoto Iijima, Atsushi Nishida, Atsuko Takeuchi, Masaaki Matsumoto, Ery Kus Dwianingsih and Rusdy Ghazali Malueka and has published in prestigious journals such as The American Journal of Cardiology, Gene and Clinica Chimica Acta.

In The Last Decade

Tomoko Lee

39 papers receiving 381 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tomoko Lee Japan 14 317 74 61 56 51 43 400
Yo Okizuka Japan 10 307 1.0× 69 0.9× 28 0.5× 75 1.3× 66 1.3× 18 363
Sara Scapolan Italy 10 271 0.9× 57 0.8× 70 1.1× 34 0.6× 49 1.0× 11 348
Ulrike Grieben Germany 10 239 0.8× 54 0.7× 56 0.9× 49 0.9× 57 1.1× 14 348
Sabrina Lucchiari Italy 15 221 0.7× 89 1.2× 35 0.6× 29 0.5× 130 2.5× 30 473
Daniela Piga Italy 9 289 0.9× 19 0.3× 79 1.3× 28 0.5× 14 0.3× 21 401
Anna Marcé‐Grau Spain 10 139 0.4× 26 0.4× 52 0.9× 12 0.2× 48 0.9× 19 284
Heiko Brennenstuhl Germany 11 180 0.6× 10 0.1× 99 1.6× 16 0.3× 74 1.5× 25 315
Magdalena Pajdowska Poland 11 316 1.0× 15 0.2× 209 3.4× 16 0.3× 76 1.5× 22 422
Hideaki Ohtsubo Japan 10 192 0.6× 11 0.1× 40 0.7× 16 0.3× 20 0.4× 14 305

Countries citing papers authored by Tomoko Lee

Since Specialization
Citations

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

Fields of papers citing papers by Tomoko Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomoko Lee

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

All Works

20 of 20 papers shown
1.
Takeshima, Yasuhiro, Tomoko Lee, & Hideki Shimomura. (2025). Development and future prospects of exon-skipping therapy for Duchenne muscular dystrophy. Brain and Development. 47(5). 104457–104457.
2.
Awano, Hiroyuki, Tetsushi Yamamoto, Tomoko Lee, et al.. (2024). Longitudinal data of serum creatine kinase levels and motor, pulmonary, and cardiac functions in 337 patients with Duchenne muscular dystrophy. Muscle & Nerve. 69(5). 604–612. 2 indexed citations
3.
Shimomura, Hideki, et al.. (2023). A Pediatric Case of COLQ-Related Congenital Myasthenic Syndrome with Marked Fatigue. Children. 10(5). 769–769.
4.
Kondo, H., et al.. (2022). Severe congenital myasthenic syndrome with novel variants in the CHRND gene. Pediatrics International. 64(1). e15342–e15342. 2 indexed citations
5.
Lee, Tomoko, Naoko Taniguchi, Hideki Shimomura, et al.. (2021). Underlying diseases in sporadic presentation of high creatine kinase levels in girls. Clinica Chimica Acta. 519. 198–203. 3 indexed citations
6.
Shimomura, Hideki, Tomoko Lee, Yasuhiko Tanaka, et al.. (2019). Two closely spaced mutations in cis result in Ullrich congenital muscular dystrophy. Human Genome Variation. 6(1). 21–21. 2 indexed citations
7.
Lee, Tomoko, Hideki Shimomura, Yasuhiko Tanaka, et al.. (2018). Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutation. Human Genome Variation. 5(1). 22–22. 10 indexed citations
8.
Matsumoto, Masaaki, Hiroyuki Awano, Tomoko Lee, et al.. (2017). Patients with Duchenne muscular dystrophy are significantly shorter than those with Becker muscular dystrophy, with the higher incidence of short stature in Dp71 mutated subgroup. Neuromuscular Disorders. 27(11). 1023–1028. 16 indexed citations
9.
Nishida, Atsushi, Atsuko Takeuchi, Tomoko Lee, et al.. (2016). Staurosporine allows dystrophin expression by skipping of nonsense-encoding exon. Brain and Development. 38(8). 738–745. 6 indexed citations
10.
Nishida, Atsushi, Atsuko Takeuchi, Hiroyuki Awano, et al.. (2016). HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71ab. Histochemistry and Cell Biology. 146(3). 301–309. 15 indexed citations
11.
Taniguchi‐Ikeda, Mariko, Yasuhiro Takeshima, Tomoko Lee, et al.. (2016). Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother. Journal of Human Genetics. 61(4). 351–355. 9 indexed citations
12.
Niba, Emma Tabe Eko, Văn Khanh Trần, Dũng Chí Vũ, et al.. (2014). Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene. Clinica Chimica Acta. 436. 155–159. 11 indexed citations
13.
Lee, Tomoko, Mariko Yagi, Tsubasa Koda, et al.. (2014). Standard values for the urine HVA/VMA ratio in neonates as a screen for Menkes disease. Brain and Development. 37(1). 114–119. 14 indexed citations
14.
Nishida, Atsushi, et al.. (2014). Resveratrol enhances splicing of insulin receptor exon 11 in myotonic dystrophy type 1 fibroblasts. Brain and Development. 37(7). 661–668. 13 indexed citations
15.
Dwianingsih, Ery Kus, Rusdy Ghazali Malueka, Atsushi Nishida, et al.. (2014). A novel splicing silencer generated by DMD exon 45 deletion junction could explain upstream exon 44 skipping that modifies dystrophinopathy. Journal of Human Genetics. 59(8). 423–429. 20 indexed citations
16.
Lee, Tomoko, Yasuhiro Takeshima, Hiroyuki Awano, et al.. (2013). Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients. Journal of Human Genetics. 59(1). 46–50. 35 indexed citations
17.
Malueka, Rusdy Ghazali, Yutaka Takaoka, Mariko Yagi, et al.. (2012). Categorization of 77 dystrophinexons into 5 groups by a decision tree using indexes of splicing regulatory factors as decision markers. BMC Genetics. 13(1). 23–23. 12 indexed citations
18.
Yamamoto, Tetsushi, Hidekazu Tanaka, Kensuke Matsumoto, et al.. (2012). Utility of Transmural Myocardial Strain Profile for Prediction of Early Left Ventricular Dysfunction in Patients With Duchenne Muscular Dystrophy. The American Journal of Cardiology. 111(6). 902–907. 20 indexed citations
19.
Takeshima, Yasuhiro, Atsushi Nishida, Hiroyuki Awano, et al.. (2011). A G-to-T Transversion at the Splice Acceptor Site of Dystrophin Exon 14 Shows Multiple Splicing Outcomes That Are Not Exemplified by Transition Mutations. Genetic Testing and Molecular Biomarkers. 16(1). 3–8. 1 indexed citations
20.
Yagi, Mariko, Tomoko Lee, Hiroyuki Awano, et al.. (2011). A patient with mitochondrial trifunctional protein deficiency due to the mutations in the HADHB gene showed recurrent myalgia since early childhood and was diagnosed in adolescence. Molecular Genetics and Metabolism. 104(4). 556–559. 11 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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