Tomohiro Kohmoto

672 total citations
30 papers, 359 citations indexed

About

Tomohiro Kohmoto is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Tomohiro Kohmoto has authored 30 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 4 papers in Oncology. Recurrent topics in Tomohiro Kohmoto's work include Genomic variations and chromosomal abnormalities (7 papers), Epigenetics and DNA Methylation (5 papers) and Genomics and Rare Diseases (3 papers). Tomohiro Kohmoto is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Epigenetics and DNA Methylation (5 papers) and Genomics and Rare Diseases (3 papers). Tomohiro Kohmoto collaborates with scholars based in Japan. Tomohiro Kohmoto's co-authors include Issei Imoto, Kiyoshi Masuda, Takuya Naruto, Miki Watanabe, Shoichiro Tange, Shoji Kagami, Daisuke Ichikawa, Eigo Otsuji, Katsutoshi Shoda and Nobuhiko Okamoto and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Oncotarget.

In The Last Decade

Tomohiro Kohmoto

30 papers receiving 351 citations

Peers

Tomohiro Kohmoto

GENET

ONCOL

PRM

Azadeh Reyahi Sweden

Donatella Conconi Italy

Zulekha A. Qadeer United States

Lucia Pedace Italy

G. Praveen Raju United States

Enrique Salero United States

Rosa Ferrentino Italy

Michele Kyle United States

Rachana R. Chandran United States

Rubing Xing United States

Azadeh Reyahi Sweden

Tomohiro Kohmoto

256 ×1.2

68 ×0.6

GENET

51 ×0.9

51 ×1.1

ONCOL

17 ×0.4

PRM

Citations per year, relative to Tomohiro Kohmoto Tomohiro Kohmoto (= 1×) peers Azadeh Reyahi

Countries citing papers authored by Tomohiro Kohmoto

Since Specialization

Citations

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

Fields of papers citing papers by Tomohiro Kohmoto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomohiro Kohmoto

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

All Works

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20 of 20 papers shown

Harazono, Yosuke, et al.. (2022). TP63 mutation mapping information in TP63 mutation-associated syndromes. SHILAP Revista de lepidopterología. 5. 100253–100253. 2 indexed citations

Okamoto, Nobuhiko, Tatsuyuki Ohto, Yoshinao Wada, et al.. (2021). Siblings with MAN1B1-CDG Showing Novel Biochemical Profiles. Cells. 10(11). 3117–3117. 8 indexed citations

Imoto, Issei, Masako Saitō, Kenichi Suga, et al.. (2021). Functionally confirmed compound heterozygous ADAM17 missense loss-of-function variants cause neonatal inflammatory skin and bowel disease 1. Scientific Reports. 11(1). 9552–9552. 13 indexed citations

Makita, Yoshio, Akihiro Katada, Yasuaki Harabuchi, et al.. (2019). Novel compound heterozygous CDH23 variants in a patient with Usher syndrome type I. Human Genome Variation. 6(1). 8–8. 5 indexed citations

Mori, Tatsuo, Yoshihiro Toda, Hiromichi Ito, et al.. (2019). A 16q22.2-q23.1 deletion identified in a male infant with West syndrome. Brain and Development. 41(10). 888–893. 5 indexed citations

Okamoto, Nobuhiko, Tomohiro Kohmoto, Takuya Naruto, Kiyoshi Masuda, & Issei Imoto. (2018). Primary microcephaly caused by novel compound heterozygous mutations in ASPM. Human Genome Variation. 5(1). 18015–18015. 8 indexed citations

Okamoto, Nobuhiko, Miki Watanabe, Takuya Naruto, et al.. (2017). Genome-first approach diagnosed Cabezas syndrome via novel CUL4B mutation detection. Human Genome Variation. 4(1). 16045–16045. 11 indexed citations

Kohmoto, Tomohiro, Takuya Naruto, Chie Murata, et al.. (2017). A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements. Molecular Cytogenetics. 10(1). 15–15. 5 indexed citations

Kohmoto, Tomohiro, Takuya Naruto, Miki Watanabe, et al.. (2017). A 590 kb deletion caused by non‐allelic homologous recombination between two LINE‐1 elements in a patient with mesomelia‐synostosis syndrome. American Journal of Medical Genetics Part A. 173(4). 1082–1086. 2 indexed citations

10.

Kohmoto, Tomohiro, et al.. (2017). Novel CLCN7 compound heterozygous mutations in intermediate autosomal recessive osteopetrosis. Human Genome Variation. 4(1). 17036–17036. 7 indexed citations

11.

Kohmoto, Tomohiro, Atsumi Tsuji‐Hosokawa, Keiichi Morita, et al.. (2016). A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndrome. Human Genome Variation. 3(1). 16003–16003. 3 indexed citations

12.

Watanabe, Miki, Yasunobu Hayabuchi, A. Ono, et al.. (2016). Detection of 1p36 deletion by clinical exome-first diagnostic approach. Human Genome Variation. 3(1). 16006–16006. 20 indexed citations

13.

Kohmoto, Tomohiro, Takuya Naruto, Miki Watanabe, et al.. (2016). A novel frameshift mutation of CHD7 in a Japanese patient with CHARGE syndrome. Human Genome Variation. 3(1). 16004–16004. 7 indexed citations

14.

Watanabe, Miki, Ryuji Nakagawa, Takuya Naruto, et al.. (2016). A novel missense mutation of COL5A2 in a patient with Ehlers–Danlos syndrome. Human Genome Variation. 3(1). 16030–16030. 23 indexed citations

15.

Naruto, Takuya, Nobuhiko Okamoto, Kiyoshi Masuda, et al.. (2015). Deep intronic GPR143 mutation in a Japanese family with ocular albinism. Scientific Reports. 5(1). 11334–11334. 21 indexed citations

16.

Kohmoto, Tomohiro, et al.. (2015). A FRMD7 variant in a Japanese family causes congenital nystagmus. Human Genome Variation. 2(1). 15002–15002. 3 indexed citations

17.

Kohmoto, Tomohiro, Takuya Naruto, Miki Watanabe, et al.. (2015). A novel COL11A1 mutation affecting splicing in a patient with Stickler syndrome. Human Genome Variation. 2(1). 15043–15043. 6 indexed citations

18.

Naruto, Takuya, et al.. (2014). A novel PTCH1 mutation in a patient with Gorlin syndrome. Human Genome Variation. 1(1). 14022–14022. 26 indexed citations

19.

Ikeda, Masahiko, et al.. (2002). Equilibrium solid solubility of Mg in aluminum below 523 K.. Journal of Japan Institute of Light Metals. 52(5). 210–215. 7 indexed citations

20.

Komatsu, Shin-ya, et al.. (1998). Corrected Nordheim's Rule in high concentration Al-Mg solid solution.. Journal of Japan Institute of Light Metals. 48(6). 294–298. 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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