Mutsuko Hayakawa

1.3k citations

41 papers · 880 indexed · h-index 16

Ophthalmology top 1%
- Retinal Diseases and Treatments 11
- Glaucoma and retinal disorders 5
Molecular Biology top 10%
- Retinal Development and Disorders 25
- Mitochondrial Function and Pathology 4
- Advanced biosensing and bioanalysis techniques 4
Cellular and Molecular Neuroscience top 10%
- Photoreceptor and optogenetics research 7
Cell Biology
- melanin and skin pigmentation 5
Radiology, Nuclear Medicine and Imaging top 10%
Genetics
- Ocular Disorders and Treatments 5

Co-authors: Atsushi Kanai Keiko Fujiki Yoshihiro Hotta Noriyuki Azuma Fumino Iwata Muriel I. Kaiser‐Kupfer Francis L. Munier J. Fielding Hejtmancik
Cited by: Ophthalmology Molecular Biology Cellular and Molecular Neuroscience
Journals: The American Journal of Human Genetics (4 papers)American Journal of Ophthalmology (2 papers)British Journal of Ophthalmology (2 papers)
Partner nations: Japan United States United Kingdom

In The Last Decade

Mutsuko Hayakawa

41 papers receiving 852 citations

Peers

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

The 25 scholars most cited alongside Mutsuko Hayakawa, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mutsuko Hayakawa Line = papers co-authored together Mutsuko Hayakawa links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	RCC1-Like Domain and ORF15: Essentials in RPGR Gene Advances in experimental medicine and biology ·Zi‐Bing Jin,Mutsuko Hayakawa,Akira Murakami,Nobuhisa Nao‐i	2007	7
2	Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations. PubMed ·Zi‐Bing Jin,Xiaoqiang Liu,Mutsuko Hayakawa,Akira Murakami,Nobuhisa Nao‐i	2006	32
3	Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2 The American Journal of Human Genetics ·Anren Li,Xiaodong Jiao,Francis L. Munier,Daniel F. Schorderet,Wenliang Yao,Fumino Iwata,Mutsuko Hayakawa,Atsushi Kanai,Muh Shy Chen,Richard A. Lewis,John R. Heckenlively,Richard G. Weleber,Elias I. Traboulsi,Qingjiong Zhang,Xueshan Xiao,Muriel I. Kaiser‐Kupfer,Yuri V. Sergeev,J. Fielding Hejtmancik	2004	207
4	Retinal neurodevelopmental assessment with electroretinogram in patients with biliary atresia Pediatrics International ·Jun Igarashi,Toshiaki Shimizu,S. Oguchi,Yuichiro Yamashiro,Tekeshi Miyano,Mutsuko Hayakawa	2002	5
5	Genetic Linkage of Bietti Crystallin Corneoretinal Dystrophy to Chromosome 4q35 The American Journal of Human Genetics ·Xiaodong Jiao,Francis L. Munier,Fumino Iwata,Mutsuko Hayakawa,Atsushi Kanai,June Lee,Daniel F. Schorderet,Muh‐Shy Chen,Muriel I. Kaiser‐Kupfer,J. Fielding Hejtmancik	2000	62
6	REP-1 gene mutations in Japanese patients with choroideremia Graefe s Archive for Clinical and Experimental Ophthalmology ·Keiko Fujiki,Yoshihiro Hotta,Mutsuko Hayakawa,Akio Saito,Yukihiko Mashima,Mikiro Mori,Masaru Yoshii,Akira Murakami,Masayuki Matsumoto,Seiji Hayasaka,Nobuko Tagami,Yasushi Isashiki,Norio Ohba,Atsushi Kanai	1999	24
7	Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene Human Genetics ·Yoshihiro Hotta,Keiko Fujiki,Mutsuko Hayakawa,Takashi Ohta,Takuro Fujimaki,Kouichi Tamaki,Toshiyuki Yokoyama,Atsushi Kanai,Akito Hirakata,Tetsuo Hida,Sachiko Nishina,Noriyuki Azuma	1998	24
8	A hemizygous A to CC base change of theCHM gene causing choroideremia associated with pinealoma Graefe s Archive for Clinical and Experimental Ophthalmology ·Yoshihiro Hotta,Keiko Fujiki,Mutsuko Hayakawa,Nao Kohno,Hitoshi KITAGAWA,Rie Doi,Atsushi Kanai	1997	7
9	Analysis of Herpes Virus Group (DNA) from Cerebrospinal Fluid in Vogt-Koyanagi-Harada Disease Ocular Immunology and Inflammation ·Yoshihiro Hotta,Mutsuko Hayakawa,Hiroyuki Kawano,Hitoshi Sakuma,Takayuki Momose,Kishiko Ohkoshi,Sumio Usuba,Utako Ogasa,Ryuji Kawaguchi,Kazumasa Hikiji,Atsushi Kanai	1996	5
10	A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa Genomics ·Hitoshi Sakuma,George Inana,Akira Murakami,Toshihiro Yajima,Richard G. Weleber,William H. Murphey,J. Donald M. Gass,Yoshihiro Hotta,Mutsuko Hayakawa,Keiko Fujiki,Yong Gao,Michael Danciger,Debora B. Farber,Artur V. Cideciyan,Samuel G. Jacobson	1995	23
11	Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa The Japanese Journal of Human Genetics ·Keiko Fujiki,Yoshihiro Hotta,Akira Murakami,Masaru Yoshii,Mutsuko Hayakawa,Takafumi Ichikawa,Misako Takeda,Kiyoshi Akeo,Shigekuni Okisaka,Atsushi Kanai	1995	17
12	ACUTE RETINAL NECROSIS SYNDROME ASSOCIATED WITH HERPES SIMPLEX KERATITIS Retina ·Kazushige Sado,Tairo Kimura,Yoshihiro Hotta,Hitoshi Sakuma,Mutsuko Hayakawa,Kazuo Kato,Atsushi Kanai	1994	10
13	Clinical Features of Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Gene Codon 17 Mutation and Retinal Neovascularization in a Japanese Patient American Journal of Ophthalmology ·Mutsuko Hayakawa,Yoshihiro Hotta,Yoshie Imai,Keiko Fujiki,Atsuo Nakamura,Kenji Yanashima,Atsushi Kanai	1993	45
14	An atypical Leber's hereditary optic neuropathy with the 11778 mutation. British Journal of Ophthalmology ·Yoshihiro Hotta,Mutsuko Hayakawa,Keiko Fujiki,Kosei Shinohara,Keina Sado,A Kanai,Kenji Yanashima	1993	8
15	A Japanese pedigree of autosomal dominant congenital stationary night blindness with variable expressivity Ophthalmic Paediatrics and Genetics ·Mutsuko Hayakawa,Yoshie Imai,M Wakita,Kazuo Kato,Kenji Yanashima,Yozo Miyake,Atsushi Kanai	1992	4
16	Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP) The Japanese Journal of Human Genetics ·Keiko Fujiki,Yoshihiro Hotta,Mutsuko Hayakawa,Hitoshi Sakuma,Takeshi Shiono,Michiru Noro,Takehiko Sakuma,Makoto Tamai,Kazumasa Hikiji,Ryuji Kawaguchi,Akihiko Hoshi,Akira Nakajima,Atsushi Kanai	1992	39
17	[An epidemiogenetic study of typical retinitis pigmentosa in Japan--a preliminary report of nationwide, multicenter study]. PubMed ·Keiko Fujiki,Mutsuko Hayakawa,A Kanai,Miyo Matsumura,Hideki Koizumi,Makoto Tamai,Takeshi Shiono,T Tokoro,Yoshihiko Akazawa,N Kubota	1992	3
18	A mutation of mitochondrial DNA in Japanese families with Leber's hereditary optic neuropathy The Japanese Journal of Human Genetics ·Keiko Fujiki,Yoshihiro Hotta,Mutsuko Hayakawa,Kimiko Saito,Fumino Ara,Syunsuke Ueda,Toshiko Goto,Misako Ishida,Kenji Yanashima,Takeshi Shiono,Jo Sakai,Atsushi Kanai,Akira Nakajima	1991	3
19	Diagnosis of Leber's Optic Neuropathy by Means of Polymerase Chain Reaction Amplification American Journal of Ophthalmology ·Yoshihiro Hotta,Mutsuko Hayakawa,Kimiko Saito,Atsushi Kanai,Akira Nakajima,Keiko Fujiki	1989	15
20	Macromelanosomes in X-linked ocular albinism (XLOA) Acta Dermato Venereologica ·Takuya Yoshiike,Motomu Manabe,Mutsuko Hayakawa,Hideyuki Ogawa	1985	12

About Mutsuko Hayakawa

Mutsuko Hayakawa is a scholar working on Ophthalmology, Molecular Biology and Cell Biology, having authored 41 papers that have together received 880 indexed citations. Recurring topics across this work include Retinal Development and Disorders (25 papers), Retinal Diseases and Treatments (11 papers), Photoreceptor and optogenetics research (7 papers), melanin and skin pigmentation (5 papers), Ocular Disorders and Treatments (5 papers), Glaucoma and retinal disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Advanced biosensing and bioanalysis techniques (4 papers). The work is most often cited by research in Ophthalmology (391 citations), Molecular Biology (736 citations) and Cellular and Molecular Neuroscience (155 citations). Mutsuko Hayakawa has collaborated with scholars based in Japan, United States and United Kingdom. Frequent co-authors include Atsushi Kanai, Keiko Fujiki, Yoshihiro Hotta, Noriyuki Azuma, Fumino Iwata, Muriel I. Kaiser‐Kupfer, Francis L. Munier, J. Fielding Hejtmancik, Xiaodong Jiao and Masao Yamada. Their work appears in journals such as The American Journal of Human Genetics, American Journal of Ophthalmology and British Journal of Ophthalmology.

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