Kishin Koh

1.0k total citations
38 papers, 295 citations indexed

About

Kishin Koh is a scholar working on Cellular and Molecular Neuroscience, Neurology and Genetics. According to data from OpenAlex, Kishin Koh has authored 38 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cellular and Molecular Neuroscience, 19 papers in Neurology and 11 papers in Genetics. Recurrent topics in Kishin Koh's work include Neurological diseases and metabolism (18 papers), Hereditary Neurological Disorders (15 papers) and Genetic Neurodegenerative Diseases (14 papers). Kishin Koh is often cited by papers focused on Neurological diseases and metabolism (18 papers), Hereditary Neurological Disorders (15 papers) and Genetic Neurodegenerative Diseases (14 papers). Kishin Koh collaborates with scholars based in Japan, United Kingdom and Italy. Kishin Koh's co-authors include Yoshihisa Takiyama, Shoji Tsuji, Hiroyuki Ishiura, Yuta Ichinose, Haitian Nan, Kazumasa Shindo, Mai Tsuchiya, Toshihisa Ohtsuka, Haruo Shimazaki and Jun Mitsui and has published in prestigious journals such as Journal of the Neurological Sciences, Journal of Neural Transmission and Parkinsonism & Related Disorders.

In The Last Decade

Kishin Koh

35 papers receiving 293 citations

Peers

Kishin Koh

CMN

NEURO

GENET

Pedro José Tomaselli Brazil

Elisa Sarto Italy

Yo-Tsen Liu Taiwan

Sonia Nouioua Algeria

Alexander P. Drew Australia

Amir Boukhris Tunisia

Claudia Crimella Italy

Anne Kjersti Erichsen Norway

Marie‐France Rioux Canada

Ana Cuesta Spain

Pedro José Tomaselli Brazil

Kishin Koh

256 ×1.3

CMN

160 ×1.2

87 ×0.9

NEURO

102 ×1.4

NEURO

40 ×0.6

GENET

Citations per year, relative to Kishin Koh Kishin Koh (= 1×) peers Pedro José Tomaselli

Countries citing papers authored by Kishin Koh

Since Specialization

Citations

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

Fields of papers citing papers by Kishin Koh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kishin Koh

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

Koh, Kishin, et al.. (2024). Hereditary sensory and autonomic neuropathy 1E showing hyperreflexia: a case report. Rinsho Shinkeigaku. 64(4). 286–291.

Koh, Kishin, Haruo Shimazaki, Matsuo Ogawa, & Yoshihisa Takiyama. (2022). A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia. Human Genome Variation. 9(1). 27–27. 2 indexed citations

Nan, Haitian, et al.. (2022). A clinical and genetic study of SPG31 in Japan. Journal of Human Genetics. 67(7). 421–425.

Koh, Kishin, Mai Tsuchiya, Hiroyuki Ishiura, et al.. (2021). Chédiak–Higashi syndrome presenting as a hereditary spastic paraplegia. Journal of Human Genetics. 67(2). 119–121. 4 indexed citations

Nan, Haitian, et al.. (2021). A Nepalese family with an REEP2 mutation: clinical and genetic study. Journal of Human Genetics. 66(7). 749–752. 1 indexed citations

Shindo, Kazumasa, et al.. (2021). Sympathetic nerve outflow to skin in a case with dentatorubral-pallidoluysian atrophy. Journal of Clinical Neuroscience. 87. 80–83. 1 indexed citations

Koh, Kishin, et al.. (2021). SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report. BMC Neurology. 21(1). 64–64. 1 indexed citations

Ono, Kenjiro, Kishin Koh, Hiroyuki Ishiura, et al.. (2020). A novel mutation in the GBA2 gene in a Japanese patient with SPG46: A case report. eNeurologicalSci. 19. 100238–100238. 4 indexed citations

Nagasaka, Takamura, Kishin Koh, Mai Tsuchiya, et al.. (2019). Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene; a case report. BMC Neurology. 19(1). 125–125. 2 indexed citations

10.

Nan, Haitian, Yuta Ichinose, Masaki Tanaka, et al.. (2019). UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes. Journal of Human Genetics. 64(11). 1055–1065. 18 indexed citations

11.

Koh, Kishin, Yuta Ichinose, Hiroyuki Ishiura, et al.. (2018). PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia. Journal of Human Genetics. 64(1). 55–59. 17 indexed citations

12.

Suzuki, Naoki, Masashi Aoki, Takehiko Inui, et al.. (2018). A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy. Journal of Human Genetics. 64(2). 171–176. 5 indexed citations

13.

Ichinose, Yuta, Hiroyuki Ishiura, Masaki Tanaka, et al.. (2018). Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. Parkinsonism & Related Disorders. 61. 57–63. 6 indexed citations

14.

Koh, Kishin, Hiroyuki Ishiura, Shoji Tsuji, & Yoshihisa Takiyama. (2018). JASPAC: Japan Spastic Paraplegia Research Consortium. Brain Sciences. 8(8). 153–153. 34 indexed citations

15.

Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2017). Pre- and postganglionic vasomotor dysfunction causes distal limb coldness in multiple system atrophy. Journal of the Neurological Sciences. 380. 191–195. 4 indexed citations

16.

Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2016). Vasomotor regulation in patients with multiple system atrophy. Journal of Neural Transmission. 124(4). 477–481. 5 indexed citations

17.

Ichinose, Yuta, Kishin Koh, Takamura Nagasaka, et al.. (2016). Exome sequencing reveals a novel missense mutation in the KIAA0196 gene in a Japanese patient with SPG8. Clinical Neurology and Neurosurgery. 144. 36–38. 10 indexed citations

18.

Shindo, Kazumasa, Mai Tsuchiya, Yuta Ichinose, et al.. (2015). No relation between sympathetic outflow to muscles and respiratory function in amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 358(1-2). 66–71. 1 indexed citations

19.

Koh, Kishin, Kazumasa Shindo, Eiji Isozaki, et al.. (2015). Novel mutations in the PNPLA6 gene in Boucher-Neuhäuser syndrome. Journal of Human Genetics. 60(4). 217–220. 12 indexed citations

20.

Wang, Ying, et al.. (2014). A Japanese SCA5 family with a novel three-nucleotide in-frame deletion mutation in the SPTBN2 gene: a clinical and genetic study. Journal of Human Genetics. 59(10). 569–573. 18 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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