Mutsuko Hayakawa

1.3k total citations
41 papers, 880 citations indexed

About

Mutsuko Hayakawa is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mutsuko Hayakawa has authored 41 papers receiving a total of 880 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 17 papers in Ophthalmology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mutsuko Hayakawa's work include Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (11 papers) and Photoreceptor and optogenetics research (7 papers). Mutsuko Hayakawa is often cited by papers focused on Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (11 papers) and Photoreceptor and optogenetics research (7 papers). Mutsuko Hayakawa collaborates with scholars based in Japan, United States and Taiwan. Mutsuko Hayakawa's co-authors include Atsushi Kanai, Keiko Fujiki, Yoshihiro Hotta, Noriyuki Azuma, Fumino Iwata, Xiaodong Jiao, J. Fielding Hejtmancik, Masao Yamada, Muriel I. Kaiser‐Kupfer and Hiroshi Handa and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Ophthalmology and British Journal of Ophthalmology.

In The Last Decade

Mutsuko Hayakawa

41 papers receiving 852 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mutsuko Hayakawa Japan 16 736 391 155 129 124 41 880
Suddhasil Mookherjee India 13 517 0.7× 366 0.9× 81 0.5× 132 1.0× 143 1.2× 18 719
K. Saidas Nair United States 17 754 1.0× 413 1.1× 300 1.9× 198 1.5× 154 1.2× 27 1.1k
Shirley He United States 11 995 1.4× 548 1.4× 173 1.1× 265 2.1× 376 3.0× 14 1.3k
Whitney M. Cleghorn United States 16 940 1.3× 131 0.3× 319 2.1× 60 0.5× 50 0.4× 24 1.1k
Melanie M. Sohocki United States 14 1.0k 1.4× 501 1.3× 267 1.7× 93 0.7× 177 1.4× 18 1.1k
H.J. Winkens Netherlands 18 697 0.9× 607 1.6× 178 1.1× 73 0.6× 83 0.7× 35 1.1k
Jeffrey Adijanto United States 8 738 1.0× 205 0.5× 145 0.9× 85 0.7× 56 0.5× 8 887
Jinshan Wang United States 15 781 1.1× 222 0.6× 251 1.6× 56 0.4× 48 0.4× 25 1.1k
S.S. Sidney United States 4 402 0.5× 181 0.5× 164 1.1× 54 0.4× 45 0.4× 6 496
James R. Mertz United States 14 543 0.7× 371 0.9× 63 0.4× 313 2.4× 107 0.9× 17 942

Countries citing papers authored by Mutsuko Hayakawa

Since Specialization
Citations

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

Fields of papers citing papers by Mutsuko Hayakawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mutsuko Hayakawa

This figure shows the co-authorship network connecting the top 25 collaborators of Mutsuko Hayakawa. A scholar is included among the top collaborators of Mutsuko Hayakawa 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 Mutsuko Hayakawa. Mutsuko Hayakawa 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.
Jin, Zi‐Bing, Mutsuko Hayakawa, Akira Murakami, & Nobuhisa Nao‐i. (2007). RCC1-Like Domain and ORF15: Essentials in RPGR Gene. Advances in experimental medicine and biology. 572. 29–33. 7 indexed citations
2.
Jin, Zi‐Bing, Xiaoqiang Liu, Mutsuko Hayakawa, Akira Murakami, & Nobuhisa Nao‐i. (2006). Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations.. PubMed. 12. 1167–74. 32 indexed citations
3.
Li, Anren, Xiaodong Jiao, Francis L. Munier, et al.. (2004). Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2. The American Journal of Human Genetics. 74(5). 817–826. 207 indexed citations
4.
Igarashi, Jun, et al.. (2002). Retinal neurodevelopmental assessment with electroretinogram in patients with biliary atresia. Pediatrics International. 44(2). 141–144. 5 indexed citations
5.
Yokoyama, Akiko, Mutsuko Hayakawa, Atsushi Kanai, et al.. (2001). Three novel mutations of theRPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa. American Journal of Medical Genetics. 104(3). 232–238. 32 indexed citations
6.
Yokoyama, Akiko, Mutsuko Hayakawa, Atsushi Kanai, et al.. (2001). Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X‐linked retinitis pigmentosa. American Journal of Medical Genetics. 104(3). 232–238. 5 indexed citations
7.
Jiao, Xiaodong, Francis L. Munier, Fumino Iwata, et al.. (2000). Genetic Linkage of Bietti Crystallin Corneoretinal Dystrophy to Chromosome 4q35. The American Journal of Human Genetics. 67(5). 1309–1313. 62 indexed citations
8.
Fujiki, Keiko, Yoshihiro Hotta, Mutsuko Hayakawa, et al.. (1999). REP-1 gene mutations in Japanese patients with choroideremia. Graefe s Archive for Clinical and Experimental Ophthalmology. 237(9). 735–740. 24 indexed citations
9.
Hotta, Yoshihiro, Keiko Fujiki, Mutsuko Hayakawa, et al.. (1998). Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene. Human Genetics. 103(2). 142–144. 24 indexed citations
10.
Sakuma, Hitoshi, George Inana, Akira Murakami, et al.. (1995). A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa. Genomics. 27(2). 384–386. 23 indexed citations
11.
Fujiki, Keiko, Yoshihiro Hotta, Akira Murakami, et al.. (1995). Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa. The Japanese Journal of Human Genetics. 40(3). 271–277. 17 indexed citations
12.
Hotta, Yoshihiro, et al.. (1994). ACUTE RETINAL NECROSIS SYNDROME ASSOCIATED WITH HERPES SIMPLEX KERATITIS. Retina. 14(3). 260–263. 10 indexed citations
13.
Hayakawa, Mutsuko, Yoshihiro Hotta, Keiko Fujiki, et al.. (1993). Clinical Features of Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Gene Codon 17 Mutation and Retinal Neovascularization in a Japanese Patient. American Journal of Ophthalmology. 115(2). 168–173. 45 indexed citations
14.
Hotta, Yoshihiro, Mutsuko Hayakawa, Keiko Fujiki, et al.. (1993). An atypical Leber's hereditary optic neuropathy with the 11778 mutation.. British Journal of Ophthalmology. 77(11). 748–750. 8 indexed citations
15.
Fujiki, Keiko, Mutsuko Hayakawa, A Kanai, et al.. (1992). [An epidemiogenetic study of typical retinitis pigmentosa in Japan--a preliminary report of nationwide, multicenter study].. PubMed. 96(2). 225–30. 3 indexed citations
16.
Hayakawa, Mutsuko, et al.. (1992). A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity. Ophthalmic Paediatrics and Genetics. 13(4). 211–217. 4 indexed citations
17.
Hotta, Yoshihiro, Takeshi Shiono, Mutsuko Hayakawa, et al.. (1992). [Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa].. PubMed. 96(2). 237–42. 18 indexed citations
18.
Fujiki, Keiko, Yoshihiro Hotta, Mutsuko Hayakawa, et al.. (1992). Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP). The Japanese Journal of Human Genetics. 37(2). 125–132. 39 indexed citations
19.
Hotta, Yoshihiro, et al.. (1989). Diagnosis of Leber's Optic Neuropathy by Means of Polymerase Chain Reaction Amplification. American Journal of Ophthalmology. 108(5). 601–602. 15 indexed citations
20.
Yoshiike, Takuya, Motomu Manabe, Mutsuko Hayakawa, & Hideyuki Ogawa. (1985). Macromelanosomes in X-linked ocular albinism (XLOA). Acta Dermato Venereologica. 65(1). 66–69. 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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