Katsuhiro Hosono

1.0k total citations
45 papers, 507 citations indexed

About

Katsuhiro Hosono is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Katsuhiro Hosono has authored 45 papers receiving a total of 507 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 16 papers in Ophthalmology and 12 papers in Genetics. Recurrent topics in Katsuhiro Hosono's work include Retinal Development and Disorders (23 papers), Retinal Diseases and Treatments (12 papers) and Ocular Disorders and Treatments (7 papers). Katsuhiro Hosono is often cited by papers focused on Retinal Development and Disorders (23 papers), Retinal Diseases and Treatments (12 papers) and Ocular Disorders and Treatments (7 papers). Katsuhiro Hosono collaborates with scholars based in Japan and China. Katsuhiro Hosono's co-authors include Yoshihiro Hotta, Satoshi Minoshima, Kentaro Kurata, Nobuyoshi Shimizu, Sachiko Nishina, Noriyuki Azuma, Masafumi Ohtsubo, Takashi Sasaki, Miho Sato and Tadashi Yokoi and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Ophthalmology.

In The Last Decade

Katsuhiro Hosono

40 papers receiving 501 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Katsuhiro Hosono Japan 13 407 197 132 68 64 45 507
Béatrice Bocquet France 16 527 1.3× 264 1.3× 80 0.6× 90 1.3× 53 0.8× 37 607
Yanrong Shi United States 10 485 1.2× 104 0.5× 97 0.7× 90 1.3× 79 1.2× 14 594
Ji‐Neng Lv China 12 551 1.4× 121 0.6× 110 0.8× 52 0.8× 39 0.6× 21 679
Dhani Tracey‐White United Kingdom 14 395 1.0× 155 0.8× 78 0.6× 134 2.0× 64 1.0× 24 506
Daniel Navarro-Gomez United States 13 495 1.2× 178 0.9× 204 1.5× 30 0.4× 29 0.5× 19 621
F.P.M. Cremers Netherlands 8 377 0.9× 243 1.2× 83 0.6× 45 0.7× 55 0.9× 10 443
Tina M. Lamey Australia 13 474 1.2× 324 1.6× 80 0.6× 77 1.1× 102 1.6× 63 557
Penny Clouston United Kingdom 12 613 1.5× 201 1.0× 452 3.4× 56 0.8× 43 0.7× 34 850
Michael W. Stuck United States 15 491 1.2× 111 0.6× 149 1.1× 192 2.8× 37 0.6× 22 547
M. Ashwin Reddy United Kingdom 7 591 1.5× 268 1.4× 273 2.1× 76 1.1× 50 0.8× 10 673

Countries citing papers authored by Katsuhiro Hosono

Since Specialization
Citations

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

Fields of papers citing papers by Katsuhiro Hosono

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katsuhiro Hosono

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

All Works

20 of 20 papers shown
1.
2.
Takeda, Yu, Katsuhiro Hosono, Akiko Hikoya, et al.. (2022). Exophthalmos associated with chronic progressive external ophthalmoplegia. Japanese Journal of Ophthalmology. 66(3). 314–319.
3.
Nishina, Sachiko, Katsuhiro Hosono, Shizuka Ishitani, et al.. (2021). Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome. Journal of Human Genetics. 66(10). 1021–1027. 3 indexed citations
4.
Ohishi, Kentaro, Katsuhiro Hosono, Akira Obana, et al.. (2021). Identification of susceptibility loci for light-induced visual impairment in rats. Experimental Eye Research. 210. 108688–108688.
5.
Mizobuchi, Kei, Takaaki Hayashi, Shuhei Kameya, et al.. (2021). Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN. Journal of Clinical Medicine. 10(11). 2265–2265. 16 indexed citations
6.
Ohtsubo, Masafumi, Sachiko Nishina, Kazue Yoshida, et al.. (2020). Analysis of IKBKG/NEMO gene in five Japanese cases of incontinentia pigmenti with retinopathy: fine genomic assay of a rare male case with mosaicism. Journal of Human Genetics. 66(2). 205–214. 6 indexed citations
7.
Yamazaki, Hiroshi, et al.. (2020). Sensorineural hearing loss and hypoplastic cochlea in Axenfeld-Rieger syndrome with FOXC1 mutation. Auris Nasus Larynx. 48(6). 1204–1208. 5 indexed citations
8.
Hayashi, Takaaki, Katsuhiro Hosono, Akiko Kubo, et al.. (2020). Long‐term observation of a Japanese mucolipidosis IV patient with a novel homozygous p.F313del variant of MCOLN1. American Journal of Medical Genetics Part A. 182(6). 1500–1505. 7 indexed citations
9.
Nishiguchi, Koji M., Yasuhiro Ikeda, Kosuke Fujita, et al.. (2019). Phenotypic Features of Oguchi Disease and Retinitis Pigmentosa in Patients with S-Antigen Mutations. Ophthalmology. 126(11). 1557–1566. 25 indexed citations
10.
Hayashi, Takaaki, Katsuhiro Hosono, Kentaro Kurata, et al.. (2019). Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy. Documenta Ophthalmologica. 140(2). 147–157. 17 indexed citations
11.
Kurata, Kentaro, Katsuhiro Hosono, Masafumi Ohtsubo, et al.. (2019). A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variants. Human Genome Variation. 6(1). 18–18. 4 indexed citations
12.
Katagiri, Satoshi, Takaaki Hayashi, Katsuhiro Hosono, et al.. (2018). Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy. Scientific Reports. 8(1). 11507–11507. 8 indexed citations
13.
Hosono, Katsuhiro, Sachiko Nishina, Tadashi Yokoi, et al.. (2018). Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing. Investigative Ophthalmology & Visual Science. 59(9). 5414–5414.
14.
Katagiri, Satoshi, Katsuhiro Hosono, Takaaki Hayashi, et al.. (2018). Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants.. PubMed. 24. 286–296. 20 indexed citations
15.
Hosono, Katsuhiro, Sachiko Nishina, Tadashi Yokoi, et al.. (2018). Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing. Scientific Reports. 8(1). 8279–8279. 36 indexed citations
16.
Nishina, Sachiko, Katsuhiro Hosono, Tadashi Yokoi, et al.. (2017). Changes in macular structure and retinal function in patients with Leber congenital amaurosis with RPGRIP1 mutations. Investigative Ophthalmology & Visual Science. 58(8). 574–574. 1 indexed citations
17.
Hosono, Katsuhiro, et al.. (2015). Visual Outcomes of Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations. Investigative Ophthalmology & Visual Science. 56(7). 2901–2901. 1 indexed citations
18.
Hosono, Katsuhiro, Yuko Harada, Kentaro Kurata, et al.. (2015). NovelGUCY2DGene Mutations in Japanese Male Twins with Leber Congenital Amaurosis. Journal of Ophthalmology. 2015. 1–10. 11 indexed citations
19.
Hosono, Katsuhiro, Setsuko Noda, Atsushi Shimizu, et al.. (2010). YPEL5 protein of the YPEL gene family is involved in the cell cycle progression by interacting with two distinct proteins RanBPM and RanBP10. Genomics. 96(2). 102–111. 52 indexed citations
20.
Ohtsubo, Masafumi, Miho Sato, Akiko Hikoya, et al.. (2010). Case of a Japanese patient with X-linked ocular albinism associated with the GPR143 gene mutation. Japanese Journal of Ophthalmology. 54(6). 624–626.

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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