Kentaro Kurata

641 total citations
30 papers, 326 citations indexed

About

Kentaro Kurata is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Kentaro Kurata has authored 30 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 13 papers in Ophthalmology and 11 papers in Genetics. Recurrent topics in Kentaro Kurata's work include Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (12 papers) and Ocular Disorders and Treatments (7 papers). Kentaro Kurata is often cited by papers focused on Retinal Development and Disorders (17 papers), Retinal Diseases and Treatments (12 papers) and Ocular Disorders and Treatments (7 papers). Kentaro Kurata collaborates with scholars based in Japan, United States and Germany. Kentaro Kurata's co-authors include Katsuhiro Hosono, Yoshihiro Hotta, Tadashi Nakano, Kei Mizobuchi, Takaaki Hayashi, Satoshi Katagiri, Miho Sato, Satoshi Minoshima, Noriyuki Azuma and Akiko Hikoya and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Ophthalmology.

In The Last Decade

Kentaro Kurata

29 papers receiving 321 citations

Peers

Countries citing papers authored by Kentaro Kurata

Since Specialization

Citations

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

Fields of papers citing papers by Kentaro Kurata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kentaro Kurata

This figure shows the co-authorship network connecting the top 25 collaborators of Kentaro Kurata. A scholar is included among the top collaborators of Kentaro Kurata 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 Kentaro Kurata. Kentaro Kurata 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	The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1-Related Retinal Dystrophy in Japanese Patients 2023 ·International Journal of Molecular Sciences ·(unknown), Sachiko Nishina, (unknown), Kei Mizobuchi, (unknown), (unknown), Kentaro Kurata, Akiko Hikoya, Miho Sato, Tadashi Nakano, Maki Fukami, Noriyuki Azuma, Takaaki Hayashi, Hirotomo Saitsu, Yoshihiro Hotta	3
2	Maternal Uniparental Isodisomy of Chromosome 4 and 8 in Patients with Retinal Dystrophy: SRD5A3-Congenital Disorders of Glycosylation and RP1-Related Retinitis Pigmentosa 2022 ·Genes ·(unknown), Katsuhiro Hosono, Shuhei Nomura, Shinji ARAI, (unknown), Kentaro Kurata, Miho Sato, Shuichi Shimakawa, Noriyuki Azuma, Tsutomu Ogata, Yoshinao Wada, Nobuhiko Okamoto, Hirotomo Saitsu, Sachiko Nishina, Yoshihiro Hotta	7
3	Retinitis pigmentosa with optic neuropathy and COQ2 mutations: A case report 2022 ·American Journal of Ophthalmology Case Reports ·Kentaro Kurata, Katsuhiro Hosono, (unknown), Masahisa Katsuno, Hirotomo Saitsu, Tsutomu Ogata, Yoshihiro Hotta	2
4	Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN 2021 ·Journal of Clinical Medicine ·Kei Mizobuchi, Takaaki Hayashi, (unknown), (unknown), Shuhei Kameya, Koichiro Higasa, (unknown), Hiroyuki Kondo, Katsuhiro Hosono, Kentaro Kurata, Yoshihiro Hotta, Kazutoshi Yoshitake, Takeshi Iwata, Tomokazu Matsuura, Tadashi Nakano	16
5	Usefulness of handheld electroretinogram system for diagnosing blue-cone monochromatism in children 2020 ·Japanese Journal of Ophthalmology ·(unknown), (unknown), Kentaro Kurata, Shinji ARAI, (unknown), (unknown), Akiko Hikoya, (unknown), Yoshihiro Hotta, Miho Sato	3
6	Novel biallelic splice-site BBS1 variants in Bardet–Biedle syndrome: a case report of the first Japanese patient 2020 ·Documenta Ophthalmologica ·Satoshi Katagiri, Katsuhiro Hosono, Takaaki Hayashi, Noriyuki Murai, (unknown), Ichiro Miyata, Kei Mizobuchi, Kentaro Kurata, Tomokazu Matsuura, Tadashi Nakano, Yoshihiro Hotta	5
7	Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations 2019 ·Ophthalmology ·Koji M. Nishiguchi, Yasuhiro Ikeda, Kosuke Fujita, Hiroshi Kunikata, (unknown), Kazuki Hashimoto, Katsuhiro Hosono, Kentaro Kurata, Yoshito Koyanagi, Masato Akiyama, Takefumi Suzuki, Ryo Kawasaki, Yuko Wada, Yoshihiro Hotta, Koh‐Hei Sonoda, Akira Murakami, Mitsuru Nakazawa, Toru Nakazawa, Toshiaki Abe	25
8	Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy 2019 ·Documenta Ophthalmologica ·Takaaki Hayashi, Katsuhiro Hosono, Kentaro Kurata, Satoshi Katagiri, Kei Mizobuchi, Shinji Ueno, Mineo Kondo, Tadashi Nakano, Yoshihiro Hotta	17
9	A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variants 2019 ·Human Genome Variation ·(unknown), Kentaro Kurata, Katsuhiro Hosono, Masafumi Ohtsubo, Kentaro Ohishi, Miho Sato, Satoshi Minoshima, Yoshihiro Hotta	4
10	Retinal structure in Leber’s congenital amaurosis caused by RPGRIP1 mutations 2019 ·Human Genome Variation ·(unknown), Sachiko Nishina, Katsuhiro Hosono, Tadashi Yokoi, Kentaro Kurata, Miho Sato, Yoshihiro Hotta, Noriyuki Azuma	8
11	Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing 2018 ·Scientific Reports ·Katsuhiro Hosono, Sachiko Nishina, Tadashi Yokoi, Satoshi Katagiri, Hirotomo Saitsu, Kentaro Kurata, (unknown), Akiko Hikoya, Kei Mizobuchi, Tadashi Nakano, Satoshi Minoshima, Maki Fukami, Hiroyuki Kondo, Miho Sato, Takaaki Hayashi, Noriyuki Azuma, Yoshihiro Hotta	36
12	Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants. 2018 ·PubMed ·Satoshi Katagiri, Katsuhiro Hosono, Takaaki Hayashi, Kentaro Kurata, Kei Mizobuchi, Tomokazu Matsuura, Kazutoshi Yoshitake, Takeshi Iwata, Tadashi Nakano, Yoshihiro Hotta	20
13	Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing 2018 ·Investigative Ophthalmology & Visual Science ·Katsuhiro Hosono, Sachiko Nishina, Tadashi Yokoi, Satoshi Katagiri, Kentaro Kurata, (unknown), Kei Mizobuchi, Tadashi Nakano, Satoshi Minoshima, Maki Fukami, Hiroyuki Kondo, Miho Sato, Takaaki Hayashi, Noriyuki Azuma, Yoshihiro Hotta	0
14	Long-term clinical course of 2 Japanese patients with PRPF31-related retinitis pigmentosa 2018 ·Japanese Journal of Ophthalmology ·Kentaro Kurata, Katsuhiro Hosono, Yoshihiro Hotta	5
15	Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations 2018 ·Japanese Journal of Ophthalmology ·Kentaro Kurata, Katsuhiro Hosono, Akiko Hikoya, Akihiko Kato, Hirotomo Saitsu, Satoshi Minoshima, Tsutomu Ogata, Yoshihiro Hotta	10
16	Changes in macular structure and retinal function in patients with Leber congenital amaurosis with RPGRIP1 mutations 2017 ·Investigative Ophthalmology & Visual Science ·(unknown), Sachiko Nishina, Katsuhiro Hosono, Tadashi Yokoi, Kentaro Kurata, Miho Sato, Satoshi Minoshima, Maki Fukami, Yoshihiro Hotta, Noriyuki Azuma	1
17	Nisin-induced expression of recombinant T cell epitopes of major Japanese cedar pollen allergens in Lactococcus lactis 2017 ·Applied Microbiology and Biotechnology ·(unknown), (unknown), Kentaro Kurata, (unknown), (unknown), Keiichi Enomoto	15
18	NovelGUCY2DGene Mutations in Japanese Male Twins with Leber Congenital Amaurosis 2015 ·Journal of Ophthalmology ·Katsuhiro Hosono, Yuko Harada, Kentaro Kurata, Akiko Hikoya, Miho Sato, Satoshi Minoshima, Yoshihiro Hotta	11
19	Expression of recombinant T-cell epitopes of major Japanese cedar pollen allergens fused with cholera toxin B subunit in Escherichia coli 2015 ·Protein Expression and Purification ·(unknown), (unknown), Kentaro Kurata, Keiichi Enomoto	5
20	Isolation and characterization of native Cry j 3 from Japanese cedar (Cryptomeria japonica) pollen 2007 ·Allergy ·Takashi Fujimura, Norihiro Futamura, Terumi Midoro‐Horiuti, (unknown), Randall M. Goldblum, Hiroshi Yasueda, Atsushi Saito, Kenji Shinohara, Kenichi Masuda, Kentaro Kurata, Masahiro Sakaguchi	39

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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