Kazuhiro Ogata

9.4k total citations
137 papers, 5.3k citations indexed

About

Kazuhiro Ogata is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Kazuhiro Ogata has authored 137 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 96 papers in Molecular Biology, 30 papers in Genetics and 15 papers in Oncology. Recurrent topics in Kazuhiro Ogata's work include RNA and protein synthesis mechanisms (26 papers), RNA modifications and cancer (23 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Kazuhiro Ogata is often cited by papers focused on RNA and protein synthesis mechanisms (26 papers), RNA modifications and cancer (23 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Kazuhiro Ogata collaborates with scholars based in Japan, United States and Malaysia. Kazuhiro Ogata's co-authors include Akinori Sarai, Shunsuke Ishii, Yoshifumi Nishimura, Masaaki Shiina, Haruki Nakamura, Naomichi Matsumoto, Hirotomo Saitsu, M. Takagi, Noriko Miyake and T.H. Tahirov and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Kazuhiro Ogata

130 papers receiving 5.2k citations

Peers

Kazuhiro Ogata

GENET

ONCOL

Sepideh Khorasanizadeh United States

Sharleen Zhou United States

Hisaaki Taniguchi Japan

Oleg Georgiev Switzerland

Tom Moss Canada

Anne Marie Quinn United States

C. David Allis United States

Wolfgang Fischer United States

Anthony P. H. Wright Sweden

Daniel Bogenhagen United States

Sepideh Khorasanizadeh United States

Kazuhiro Ogata

5.2k ×1.3

898 ×0.9

GENET

1.1k ×1.7

373 ×0.7

452 ×1.2

ONCOL

Citations per year, relative to Kazuhiro Ogata Kazuhiro Ogata (= 1×) peers Sepideh Khorasanizadeh

Countries citing papers authored by Kazuhiro Ogata

Since Specialization

Citations

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

Fields of papers citing papers by Kazuhiro Ogata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kazuhiro Ogata

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

Hayashi, Y., Keisuke Hamada, Naomi Tsuchida, et al.. (2025). Biallelic TSEN2 variants causing pontocerebellar hypoplasia type 2. Journal of Human Genetics. 70(12). 649–654.

Hamada, Keisuke, Hidenori Ito, Marcello Scala, et al.. (2025). A p.N92K variant of the GTPase RAC3 disrupts cortical neuron migration and axon elongation. Journal of Biological Chemistry. 301(4). 108346–108346.

Mizuguchi, Takeshi, Keisuke Hamada, Kotaro Yuge, et al.. (2025). Hemizygous SMARCA1 variants cause X-linked intellectual disability. Journal of Human Genetics. 70(7). 359–363.

Fu, Lina, Yuka Yamamoto, Takashi Yao, et al.. (2024). Biallelic missense CEP55 variants cause prenatal MARCH syndrome. Journal of Human Genetics. 70(1). 63–66.

Hamada, Keisuke, Kohei Hamanaka, Keita Miyoshi, et al.. (2023). Novel missense variants cause intermediate phenotypes in the phenotypic spectrum of SLC5A6-related disorders. Journal of Human Genetics. 69(2). 69–77. 5 indexed citations

Hamada, Keisuke, Dinh Thanh Nguyen, Masayuki Satake, et al.. (2022). LimF is a versatile prenyltransferase for histidine-C-geranylation on diverse non-natural substrates. Nature Catalysis. 5(8). 682–693. 31 indexed citations

Tsuchida, Naomi, Shuichi Shimakawa, Kei Ohashi, et al.. (2022). Three KINSSHIP syndrome patients with mosaic and germline AFF3 variants. Clinical Genetics. 103(5). 590–595. 1 indexed citations

Saida, Ken, Masayuki Sasaki, Eriko Koshimizu, et al.. (2021). Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Clinical Genetics. 100(6). 722–730. 18 indexed citations

Tsuchida, Naomi, Y. Okada, Sonoko Sakata, et al.. (2021). Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms. Journal of Human Genetics. 67(3). 157–164. 13 indexed citations

10.

Miyado, Mami, Maki Fukami, Shuji Takada, et al.. (2019). Germline-Derived Gain-of-Function Variants of Gsα-Coding GNAS Gene Identified in Nephrogenic Syndrome of Inappropriate Antidiuresis. Journal of the American Society of Nephrology. 30(5). 877–889. 20 indexed citations

11.

Uchiyama, Yuri, Shinji Kunishima, Masaaki Shiina, et al.. (2018). A novel CYCS mutation in the α‐helix of the CYCS C‐terminal domain causes non‐syndromic thrombocytopenia. Clinical Genetics. 94(6). 548–553. 20 indexed citations

12.

Tsuchida, Naomi, Keisuke Hamada, Masaaki Shiina, et al.. (2018). GRIN2D variants in three cases of developmental and epileptic encephalopathy. Clinical Genetics. 94(6). 538–547. 16 indexed citations

13.

Saitsu, Hirotomo, Hitoshi Osaka, Masayuki Sasaki, et al.. (2011). Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy. The American Journal of Human Genetics. 89(5). 644–651. 111 indexed citations

14.

Takahashi, Nobukazu, Masaaki Shiina, Keisuke Hamada, et al.. (2010). Rational Approach to the Synthesis, Evaluation, and ⁶⁸ Ga Labeling of a Novel 4-Anilinoquinoline Epidermal Growth Factor Receptor Inhibitor as a New Imaging Agent That Selectively Targets the Epidermal Growth Factor Receptor Tyrosine Kinase. Cancer Biotherapy and Radiopharmaceuticals. 25(4). 479–485. 8 indexed citations

15.

Furuta, Akiko, et al.. (2008). . Kyushu Plant Protection Research. 54. 105–108. 2 indexed citations

16.

Yamada, Hiroaki, et al.. (2001). Filling a cavity dramatically increases pressure stability of the c‐Myb R2 subdomain. Proteins Structure Function and Bioinformatics. 45(1). 96–101. 37 indexed citations

17.

Matsui, Hidenori, Kazuhiro Ogata, Kiyoshi Tajima, et al.. (2001). Prevotella ruminicola由来セルラーゼ遺伝子のクローニング,発現及び特徴. Animal Science Journal. 72(5). 421–426. 1 indexed citations

18.

Tamura, Minoru, Kazuhiro Ogata, & M Takeshita. (1993). Phosphatidic Acid-Induced Superoxide Generation in Electropermeabilized Human Neutrophils. Archives of Biochemistry and Biophysics. 305(2). 477–482. 13 indexed citations

19.

Ogata, Kazuhiro, et al.. (1960). Release studies on the dispersion of the lesser house fly, Fannia canicularis, in the residential area of Bibai, Hokkaido.. 25. 1 indexed citations

20.

Ogata, Kazuhiro & M. Sasa. (1954). Taxonomic notes on Simullidae or black flies of Japan, with special references on the subgenera Eusimulium roubaud and Nevermannia enderlein (Diptera).. PubMed. 24(5). 325–33. 12 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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