Kohji Kato

758 total citations
21 papers, 384 citations indexed

About

Kohji Kato is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Kohji Kato has authored 21 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Kohji Kato's work include Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Kohji Kato is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Kohji Kato collaborates with scholars based in Japan, United Kingdom and France. Kohji Kato's co-authors include H. Shinohara, Taku Asano, Hirohisa Watanabe, Mizuki Ito, Kimiteru Ito, Gen Sobue, Takeshi Kato, Fumiaki Tanaka, Yohei Kawai and Shinji Naganawa and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Neurology.

In The Last Decade

Kohji Kato

21 papers receiving 378 citations

Peers

Countries citing papers authored by Kohji Kato

Since Specialization

Citations

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

Fields of papers citing papers by Kohji Kato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kohji Kato

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	MYCN in human development and diseases 2024 ·Frontiers in Oncology ·(unknown), Kohji Kato, Hisashi Oishi, Yoshiyuki Takahashi, Shinji Saitoh	2
2	Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome 2023 ·Human Genetics and Genomics Advances ·(unknown), Kohji Kato, Frédéric Tran Mau‐Them, (unknown), Chloé Quēlin, (unknown), Antonio Vitobello, (unknown), Hossam H. Shawki, Hisashi Oishi, Christel Thauvin‐Robinet, Toshiki Takenouchi, Kenjiro Kosaki, Yoshiyuki Takahashi, Shinji Saitoh	2
3	Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome 2022 ·Journal of Medical Genetics ·(unknown), (unknown), Maki Tsujita, Marlène Rio, Céline Huber, Carlos Antón-Plágaro, Seiji Mizuno, Yoshihiko Kawano, Satoko Miyatake, Marleen Simon, Ellen van Binsbergen, Richard H. van Jaarsveld, Naomichi Matsumoto, Valérie Cormier‐Daire, Peter J. Cullen, Shinji Saitoh, Kohji Kato	9
4	Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes 2020 ·PLoS ONE ·Daisuke Ieda, Yutaka Negishi, Tomomi Miyamoto, Yoshikazu Johmura, Natsuko Kumamoto, Kohji Kato, Ichiro Miyoshi, Makoto Nakanishi, Shinya Ugawa, Hisashi Oishi, Shinji Saitoh	7
5	Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect 2020 ·International Journal of Cardiology ·(unknown), S. Hayano, Yusuke Okuno, Atsuto Onoda, Kohji Kato, Noriko Nagai, (unknown), Shinji Saitoh, Yoshiyuki Takahashi, Taichi Kato	3
6	NUS1 mutation in a family with epilepsy, cerebellar ataxia, and tremor 2020 ·Epilepsy Research ·Kunihiko Araki, Ryoichi Nakamura, Daisuke Ito, Kohji Kato, Yohei Iguchi, Kentaro Sahashi, (unknown), K Hamada, Nobuhiko Okamoto, Yoshinao Wada, Tomohiko Nakamura, Tomoo Ogi, Masahisa Katsuno	18
7	A novel missense variant in CUL3 shows altered binding ability to BTB-adaptor proteins leading to diverse phenotypes of CUL3-related disorders 2020 ·Journal of Human Genetics ·Kohji Kato, Fuyuki Miya, Yasuyoshi Oka, Seiji Mizuno, Shinji Saitoh	7
8	Expanding the phenotype of biallelic loss‐of‐function variants in the NSUN2 gene: Description of four individuals with juvenile cataract, chronic nephritis, or brain anomaly as novel complications 2020 ·American Journal of Medical Genetics Part A ·Kohji Kato, Seiji Mizuno, Jenny Morton, (unknown), Yuichiro Hara, (unknown), Alan R. Lehmann, Tomoo Ogi	5
9	Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case report 2020 ·Molecular Genetics & Genomic Medicine ·(unknown), Masaki Matsushita, Kenichi Mishima, (unknown), Kohji Kato, (unknown), Tomoo Ogi, Naoki Ishiguro, Hiroshi Kitoh	1
10	MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndrome 2019 ·Kohji Kato	1
11	Novel compound heterozygous MCOLN1 mutations identified in a Japanese girl with severe developmental delay and thin corpus callosum 2019 ·Brain and Development ·Naoya Yamaguchi, Kyoko Ban, Atsushi Suzuki, Y. Nakamura, Kohji Kato, Hideki Muramatsu, Yusuke Okuno, Ayako Hattori, Tadashi Kaname, Yoshiyuki Takahashi, Shinji Saitoh	3
12	Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegeneration 2019 ·Brain and Development ·(unknown), Takayuki Sassa, Hiroyuki Kidokoro, Tomohiko Nakata, Kohji Kato, Hideki Muramatsu, Yusuke Okuno, Hiroyuki Yamamoto, Tadashi Kaname, Akio Kihara, Jun Natsume	7
13	Elucidation of the pathogenic mechanism and potential treatment strategy for a female patient with spastic paraplegia derived from a single-nucleotide deletion in PLP1 2019 ·Journal of Human Genetics ·(unknown), (unknown), Yusuke Aoki, Ken Inoue, Tadashi Kaname, Yusuke Okuno, Hideki Muramatsu, Kohji Kato, Toshiyuki Yamamoto	12
14	Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease 2019 ·PLoS ONE ·Y. Nakamura, Kohji Kato, Naomi Tsuchida, Naomichi Matsumoto, Yoshiyuki Takahashi, Shinji Saitoh	8
15	Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex 2019 ·Journal of Medical Genetics ·Kohji Kato, Yasuyoshi Oka, Hideki Muramatsu, (unknown), Takanobu Otomo, Hisashi Oishi, Yoshihiko Kawano, Hiroyuki Kidokoro, Yuka Nakazawa, Tomoo Ogi, Yoshiyuki Takahashi, Shinji Saitoh	22
16	Distinctive facies, macrocephaly, and developmental delay are signs of a PTEN mutation in childhood 2018 ·Brain and Development ·Kohji Kato, Seiji Mizuno, (unknown), Shinobu Fukumura, N. Kurahashi, Koichi Maruyama, Daisuke Ieda, Kei Ohashi, Ikumi Hori, Yutaka Negishi, Ayako Hattori, Shinji Saitoh	16
17	MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndrome 2018 ·Journal of Medical Genetics ·Kohji Kato, Fuyuki Miya, Nanako Hamada, Yutaka Negishi, (unknown), Hiroshi Ozawa, Hidenori Ito, Ikumi Hori, Ayako Hattori, Nobuhiko Okamoto, Mitsuhiro Kato, Tatsuhiko Tsunoda, Yonehiro Kanemura, Kenjiro Kosaki, Yoshiyuki Takahashi, Koh-ichi Nagata, Shinji Saitoh	9
18	Disruption of Atherosclerotic Neointima Seven Years After Bare Metal Stent Deployment 2012 ·International Heart Journal ·Shigenobu Inami, Masamichi Takano, Kohji Kato, (unknown), Shunsuke Nakamura, Koji Murai, Yukichi Tokita, Gen Takagi, Hitoshi Takano, Kuniya Asai, Masahiro Yasutake, Kyoichi Mizuno	3
19	Prefrontal hypoperfusion and cognitive dysfunction correlates in spinocerebellar ataxia type 6 2008 ·Journal of the Neurological Sciences ·Y. Kawai, (unknown), Hirohisa Watanabe, Mizuki Ito, Kohji Kato, Takeshi Kato, Kimiteru Ito, Fumiaki Tanaka, Gen Sobue	31
20	Differential localization of G-proteins Gi and Go in the accessory olfactory bulb of the rat 1992 ·Journal of Neuroscience ·H. Shinohara, Taku Asano, Kohji Kato	92

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.

Explore authors with similar magnitude of impact