Mitsuhiro Kato

13.9k total citations
214 papers, 5.0k citations indexed

About

Mitsuhiro Kato is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mitsuhiro Kato has authored 214 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 104 papers in Molecular Biology, 96 papers in Genetics and 40 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mitsuhiro Kato's work include Genetics and Neurodevelopmental Disorders (55 papers), Genomics and Rare Diseases (32 papers) and Epilepsy research and treatment (27 papers). Mitsuhiro Kato is often cited by papers focused on Genetics and Neurodevelopmental Disorders (55 papers), Genomics and Rare Diseases (32 papers) and Epilepsy research and treatment (27 papers). Mitsuhiro Kato collaborates with scholars based in Japan, United States and Malaysia. Mitsuhiro Kato's co-authors include Naomichi Matsumoto, Hirotomo Saitsu, Kiyoshi Hayasaka, Jun Tohyama, Mitsuko Nakashima, Noriko Miyake, William B. Dobyns, Yoshinori Tsurusaki, Hitoshi Osaka and Shinji Saitoh and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Mitsuhiro Kato

207 papers receiving 4.9k citations

Peers

Countries citing papers authored by Mitsuhiro Kato

Since Specialization

Citations

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

Fields of papers citing papers by Mitsuhiro Kato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitsuhiro Kato

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

#	Work	Indexed citations
1	Refractory myoclonic epilepsy and progressive movement disorder arising from recurrent DHDDS variants in Japanese patients: a case series 2025 ·Brain and Development ·Yu Kobayashi, Satoru Sakuma, Emiko Morimoto, Hitomi Fujii, Kei Yamada, (unknown), (unknown), Jun Tohyama, Fuyuki Miya, Mitsuhiro Kato, Hirotomo Saitsu, Naomichi Matsumoto	0
2	A new case of developmental and epileptic encephalopathy and macrocytic anemia with stretched-activated ion channel TMEM63B variant 2024 ·(unknown), Mitsuko Nakashima, Yuji Fujii, (unknown), Hirotomo Saitsu, Mitsuhiro Kato	1
3	Sibling cases of DEPDC5-related developmental and epileptic encephalopathy successfully treated with lacosamide 2024 ·(unknown), Ritsuo Nishiuchi, Fuyuki Miya, Katsuhiro Kobayashi, Mitsuhiro Kato	1
4	Detection of hidden intronic DDC variant in aromatic L-amino acid decarboxylase deficiency by adaptive sampling 2024 ·Journal of Human Genetics ·Eriko Koshimizu, Mitsuhiro Kato, Kazuharu Misawa, Yuri Uchiyama, Naomi Tsuchida, Kohei Hamanaka, Atsushi Fujita, Takeshi Mizuguchi, Satoko Miyatake, Naomichi Matsumoto	1
5	Limb-clasping, cognitive deficit and increased vulnerability to kainic acid-induced seizures in neuronal glycosylphosphatidylinositol deficiency mouse models 2021 ·Human Molecular Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), Mitsuhiro Kato, Naomichi Matsumoto, Junji Takeda, Shigeyoshi Itohara, Sonoko Ogawa, Larry J. Young, Qí Zhāng	7
6	A homozygous ABHD16A variant causes a complex hereditary spastic paraplegia with developmental delay, absent speech, and characteristic face 2021 ·Clinical Genetics ·Noriko Miyake, (unknown), M. Troncoso, Nobuhiko Okamoto, Yoshiki Andachi, Mitsuhiro Kato, (unknown), (unknown), Atsushi Fujita, Yuri Uchiyama, Naomichi Matsumoto	5
7	Four pedigrees with aminoacyl-tRNA synthetase abnormalities 2021 ·Neurological Sciences ·Nobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, Yonehiro Kanemura, Shinji Saitoh, Mitsuhiro Kato, Kumiko Yanagi, Tadashi Kaname, Kenjiro Kosaki	10
8	Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review 2021 ·Journal of Human Genetics ·Kazuki Watanabe, Mitsuko Nakashima, Satoko Kumada, (unknown), Mikako Enokizono, Keitaro Yamada, Mitsuhiro Kato, Hirotomo Saitsu	16
9	Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability 2021 ·Neurological Sciences ·Nobuhiko Okamoto, Fuyuki Miya, (unknown), Tatsuhiko Tsunoda, Mitsuhiro Kato, Shinji Saitoh, Yonehiro Kanemura, Kenjiro Kosaki	5
10	A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome 2018 ·Journal of Human Genetics ·Ikumi Hori, Fuyuki Miya, Yutaka Negishi, Ayako Hattori, N Ando, Keith A. Boroevich, Nobuhiko Okamoto, Mitsuhiro Kato, Tatsuhiko Tsunoda, Mami Yamasaki, Yonehiro Kanemura, Kenjiro Kosaki, Shinji Saitoh	10
11	A case of tubulinopathy presenting with porencephaly caused by a novel missense mutation in the TUBA1A gene 2018 ·Brain and Development ·Tatsuharu Sato, Mitsuhiro Kato, (unknown), (unknown), Hirotomo Saitsu, Naomichi Matsumoto, Hiroyuki Moriuchi	5
12	PRUNE1‐related disorder: Expanding the clinical spectrum 2018 ·Clinical Genetics ·Eri Imagawa, Yutaka Yamamoto, Satomi Mitsuhashi, Bertrand Isidor, Tetsuhiro Fukuyama, Mitsuhiro Kato, Masayuki Sasaki, Saori Tanabe, Satoko Miyatake, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Naomichi Matsumoto	8
13	GRIN2D variants in three cases of developmental and epileptic encephalopathy 2018 ·Clinical Genetics ·Naomi Tsuchida, Keisuke Hamada, Masaaki Shiina, Mitsuhiro Kato, Yu Kobayashi, Jun Tohyama, Kazue Kimura, Kyoko Hoshino, (unknown), Keng Wee Teik, Mitsuko Nakashima, Satomi Mitsuhashi, Takeshi Mizuguchi, Atsushi Takata, Noriko Miyake, Hirotomo Saitsu, Kazuhiro Ogata, Satoko Miyatake, Naomichi Matsumoto	16
14	Novel MCA/ID syndrome with ASH1L mutation 2017 ·American Journal of Medical Genetics Part A ·Nobuhiko Okamoto, Fuyuki Miya, Tatsuhiko Tsunoda, Mitsuhiro Kato, Shinji Saitoh, Mami Yamasaki, Yonehiro Kanemura, Kenjiro Kosaki	29
15	A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology 2017 ·American Journal of Medical Genetics Part A ·Nobuhiko Okamoto, (unknown), Fuyuki Miya, Tatsuhiko Tsunoda, (unknown), Keith A. Boroevich, Mitsuhiro Kato, Shinji Saitoh, Mami Yamasaki, Yonehiro Kanemura, Kenjiro Kosaki, Daiju Kitagawa	7
16	Progressive subglottic stenosis in a child with Pallister‐Killian syndrome 2017 ·Congenital Anomalies ·Tadashi Shiohama, Katsunori Fujii, Kenji Shimizu, Hirofumi Ohashi, Tomozumi Takatani, Nobuhiko Okamoto, Gen Nishimura, Mitsuhiro Kato, Naoki Shimojo	2
17	Identification of novel BCL11A variants in patients with epileptic encephalopathy: Expanding the phenotypic spectrum 2017 ·Clinical Genetics ·Michiko Yoshida, Mitsuko Nakashima, Tohru Okanishi, (unknown), Ayataka Fujimoto, Kazuya Itomi, Masafumi Morimoto, Hirotomo Saitsu, Mitsuhiro Kato, Naomichi Matsumoto, Tomohiro Chiyonobu	26
18	Novel biallelic SZT2 mutations in 3 cases of early‐onset epileptic encephalopathy 2017 ·Clinical Genetics ·Naomi Tsuchida, Mitsuko Nakashima, Akihiko Miyauchi, (unknown), (unknown), (unknown), Keng Wee Teik, (unknown), Mitsuhiro Kato, Takeshi Mizuguchi, Atsushi Takata, Satoko Miyatake, Noriko Miyake, Hitoshi Osaka, Takanori Yamagata, Hideaki Nakajima, Hirotomo Saitsu, Naomichi Matsumoto	23
19	Eleven‐year clinical outcome of schizophrenia in Bali 2005 ·Acta Psychiatrica Scandinavica ·Toshiyuki Kurihara, Mitsuhiro Kato, Robert Reverger, (unknown)	26
20	INFLUENCE OF GASTRIC SURGERY ON ENTERO-INSULAR AXIS : WITH SPECIAL REFERENCE TO PATHOGENESIS OF LATE DUMPING SYNDROME AFTER GASTRECTOMY 1986 ·The Japanese Journal of Gastroenterological Surgery ·Iwao Sasaki, Mitsuhiro Kato, (unknown), (unknown), (unknown)	1

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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