Tomoki Kosho

7.3k total citations
143 papers, 2.5k citations indexed

About

Tomoki Kosho is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Tomoki Kosho has authored 143 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Genetics, 80 papers in Molecular Biology and 31 papers in Cell Biology. Recurrent topics in Tomoki Kosho's work include Connective tissue disorders research (58 papers), Proteoglycans and glycosaminoglycans research (23 papers) and Dermatological and Skeletal Disorders (15 papers). Tomoki Kosho is often cited by papers focused on Connective tissue disorders research (58 papers), Proteoglycans and glycosaminoglycans research (23 papers) and Dermatological and Skeletal Disorders (15 papers). Tomoki Kosho collaborates with scholars based in Japan, United States and United Kingdom. Tomoki Kosho's co-authors include Yoshimitsu Fukushima, Noriko Miyake, Keiko Wakui, Nobuhiko Okamoto, Fransiska Malfait, Cecilia Giunta, John C. Carey, Tomomi Yamaguchi, Hiroshi Kawame and Clair A. Francomano and has published in prestigious journals such as Molecular Cell, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Tomoki Kosho

134 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tomoki Kosho Japan 26 1.4k 1.3k 396 357 301 143 2.5k
Rika Kosaki Japan 25 846 0.6× 1.3k 1.0× 379 1.0× 297 0.8× 255 0.8× 113 2.3k
David Geneviève France 24 1.1k 0.8× 1.3k 1.1× 233 0.6× 285 0.8× 202 0.7× 80 2.3k
John Tolmie United Kingdom 32 1.7k 1.2× 2.1k 1.7× 463 1.2× 312 0.9× 402 1.3× 108 3.5k
Yasemin Alanay Türkiye 26 1.0k 0.7× 994 0.8× 162 0.4× 370 1.0× 179 0.6× 108 2.1k
Geneviève Baujat France 31 1.8k 1.2× 1.4k 1.1× 210 0.5× 293 0.8× 233 0.8× 130 3.0k
Samia A. Temtamy Egypt 29 1.6k 1.1× 1.4k 1.1× 179 0.5× 407 1.1× 288 1.0× 127 2.9k
Jürgen Kohlhase Germany 33 1.0k 0.7× 1.7k 1.4× 463 1.2× 287 0.8× 195 0.6× 91 2.7k
Helga V. Toriello United States 32 1.4k 1.0× 1.3k 1.1× 242 0.6× 430 1.2× 707 2.3× 97 3.1k
Keiko Wakui Japan 28 1.4k 1.0× 1.3k 1.1× 190 0.5× 192 0.5× 283 0.9× 89 2.3k
F. Dagna Bricarelli Italy 19 1.8k 1.3× 2.1k 1.7× 557 1.4× 336 0.9× 271 0.9× 51 4.4k

Countries citing papers authored by Tomoki Kosho

Since Specialization
Citations

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

Fields of papers citing papers by Tomoki Kosho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomoki Kosho

This figure shows the co-authorship network connecting the top 25 collaborators of Tomoki Kosho. A scholar is included among the top collaborators of Tomoki Kosho 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 Tomoki Kosho. Tomoki Kosho 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.
Tachimori, Hisateru, et al.. (2025). Current Nationwide Landscape of Cardiac Surgery for Children With Trisomy 18 in Japan. American Journal of Medical Genetics Part A. 200(1). 77–83.
2.
Mizumoto, Shuji, Yuko Nitahara‐Kasahara, Takahiro Yoshizawa, et al.. (2023). Collagen Network Formation in In Vitro Models of Musculocontractural Ehlers–Danlos Syndrome. Genes. 14(2). 308–308. 3 indexed citations
3.
Koike, Yuta, et al.. (2023). The detailed obstetric course of the first Japanese patient with AEBP1‐related Ehlers–Danlos syndrome (classical‐like EDS, type 2). Journal of obstetrics and gynaecology research. 49(3). 1043–1047. 2 indexed citations
4.
Tsuji‐Hosokawa, Atsumi, Kei Takasawa, Tomomi Yamaguchi, et al.. (2023). A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 109(3). 750–760. 4 indexed citations
5.
6.
Kitazawa, Masato, Yusuke Miyagawa, Tomoaki Suga, et al.. (2023). Hereditary diffuse gastric cancer in a Japanese family with CDH1 mutation three case reports. Discover Oncology. 14(1). 14–14. 1 indexed citations
7.
Miyake, Noriko, et al.. (2021). Expanding the phenotypic spectrum of cardiospondylocarpofacial syndrome: From a detailed clinical and radiological observation of a boy with a novel missense variant in MAP3K7. American Journal of Medical Genetics Part A. 188(1). 350–356. 2 indexed citations
8.
Uekawa, Ken, Yasuyuki Kaku, Hiroaki Matsuzaki, et al.. (2020). Intracranial and extracranial multiple arterial dissecting aneurysms in rheumatoid arthritis: A case report. Interventional Neuroradiology. 27(2). 212–218. 4 indexed citations
9.
Lautrup, Charlotte Kvist, Keng Wee Teik, Shuji Mizumoto, et al.. (2020). Delineation of musculocontractural Ehlers–Danlos Syndrome caused by dermatan sulfate epimerase deficiency. Molecular Genetics & Genomic Medicine. 8(5). e1197–e1197. 18 indexed citations
10.
Ghali, Neeti, Duncan Baker, Angela F. Brady, et al.. (2020). Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome. American Journal of Medical Genetics Part A. 182(5). 994–1007. 14 indexed citations
11.
Koitabashi, Norimichi, Tomomi Yamaguchi, Daisuke Fukui, et al.. (2018). Peripartum Iliac Arterial Aneurysm and Rupture in a Patient with Vascular Ehlers-Danlos Syndrome Diagnosed by Next-Generation Sequencing. International Heart Journal. 59(5). 1180–1185. 7 indexed citations
12.
Uehara, Masashi, Yukio Nakamura, Jun Takahashi, et al.. (2018). Efficacy of denosumab therapy for neurofibromatosis type I with osteoporosis and history of fractures: a case report. Therapeutics and Clinical Risk Management. Volume 14. 1243–1246. 7 indexed citations
13.
Akazawa, Yohei, Yuji Inaba, Akira Hachiya, et al.. (2015). Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome in a boy with Loeys‐Dietz syndrome. American Journal of Medical Genetics Part A. 167(10). 2435–2439. 15 indexed citations
14.
Kosho, Tomoki, Noriko Miyake, & John C. Carey. (2014). Coffin–Siris syndrome and related disorders involving components of the BAF (mSWI/SNF) complex: Historical review and recent advances using next generation sequencing. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 241–251. 82 indexed citations
15.
Narumi, Yoko, Sachiko Nishina, Yoko Aoki, et al.. (2014). Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: A clinical report and review of literature. American Journal of Medical Genetics Part A. 164(5). 1272–1276. 28 indexed citations
16.
Kono, Michihiro, Kazumitsu Sugiura, M. Ono, et al.. (2014). A 45-year-old Woman with Ehlers-Danlos Syndrome Caused by Dermatan 4-O-sulfotransferase-1 Deficiency: Implications for Early Ageing. Acta Dermato Venereologica. 96(6). 0–0. 11 indexed citations
17.
Kosho, Tomoki, et al.. (2013). Natural history and parental experience of children with trisomy 18 based on a questionnaire given to a Japanese trisomy 18 parental support group. American Journal of Medical Genetics Part A. 161(7). 1531–1542. 55 indexed citations
18.
Nishi, Eriko, Satoshi Takamizawa, Yasumasa Yamada, et al.. (2013). Surgical intervention for esophageal atresia in patients with trisomy 18. American Journal of Medical Genetics Part A. 164(2). 324–330. 36 indexed citations
19.
20.
Torii, Chiharu, Rika Kosaki, Kenji Kurosawa, et al.. (2007). Screening for Alagille Syndrome Mutations in the JAG1 and NOTCH2 Genes Using Denaturing High-Performance Liquid Chromatography. Genetic Testing. 11(3). 216–227. 7 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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