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Mutsuko Hayakawa
Observed names:
M Hayakawa,
M. Hayakawa,
MUTSUKO HAYAKAWA,
MUtsUko Hayakawa
Institution:
Juntendo University
Observed institutions:
Kagoshima University,
University of Miami,
Chiba University,
University of California, Los Angeles,
Oregon Health & Science University,
Tohoku University,
Juntendo University,
National Rehabilitation Center for Persons with Disabilities
show all 8
OpenAlex ID:
A5109081586
Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
2004
·
Anren Li
, Xiaodong Jiao
, et al.
·
The American Journal of Human Genetics
·
287
PDF
Missense Mutation in the Alternative Splice Region of the PAX6 Gene in Eye Anomalies
1999
·
Noriyuki Azuma
, Yuki Yamaguchi
, et al.
·
The American Journal of Human Genetics
·
141
Genetic Linkage of Bietti Crystallin Corneoretinal Dystrophy to Chromosome 4q35
2000
·
Xiaodong Jiao
, Francis L. Munier
, et al.
·
The American Journal of Human Genetics
·
78
PDF
Clinical Features of Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Gene Codon 17 Mutation and Retinal Neovascularization in a Japanese Patient
1993
·
Mutsuko Hayakawa
, Yoshihiro Hotta
, et al.
·
American Journal of Ophthalmology
·
76
Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)
1992
·
Keiko Fujiki
, Yoshihiro Hotta
, et al.
·
The Japanese Journal of Human Genetics
·
67
Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.
1992
·
T Shiono
, Y Hotta
, et al.
·
PubMed
·
57
[Molecular biological study of the rhodopsin gene in Japanese patients with autosomal dominant retinitis pigmentosa].
1992
·
Y Hotta
, T Shiono
, et al.
·
PubMed
·
47
Mutational analysis of RPGR and RP2 genes in Japanese patients with retinitis pigmentosa: identification of four mutations.
2006
·
Zi-Bing Jin
, Xiao-Qiang Liu
, et al.
·
PubMed
·
44
Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X‐linked retinitis pigmentosa
2001
·
Akiko Yokoyama
, Futoshi Maruiwa
, et al.
·
American Journal of Medical Genetics
·
42
A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa
1995
·
Hitoshi Sakuma
, George Inana
, et al.
·
Genomics
·
34
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene
1998
·
Y. Hotta
, Keiko Fujiki
, et al.
·
Human Genetics
·
32
Studies on the Mechanism of Early Onset Macular Degeneration in Cynomolgus (Macaca fascicularis) Monkeys. I. Abnormal Concentrations of Two Proteins in the Retina
1996
·
MARILOU G. NICOLAS
, KEIKO FUJIKI
, et al.
·
Experimental Eye Research
·
32
Mutations in the Norrie disease gene: a new mutation in a Japanese family.
1995
·
Y Isashiki
, N Ohba
, et al.
·
British Journal of Ophthalmology
·
32
PDF
REP-1 gene mutations in Japanese patients with choroideremia
1999
·
K. Fujiki
, Yoshihiro Hotta
, et al.
·
Graefe s Archive for Clinical and Experimental Ophthalmology
·
31
Visual impairment and REP-1 gene mutations in Japanese choroideremia patients
1999
·
M. Hayakawa
, K. Fujiki
, et al.
·
Ophthalmic Genetics
·
27
Multicenter genetic study of retinitis pigmentosa in Japan: I. Genetic heterogeneity in typical retinitis pigmentosa
1997
·
M Hayakawa
·
Japanese Journal of Ophthalmology
·
23
Multicenter genetic study of retinitis pigmentosa in Japan: II. Prevalence of autosomal recessive retinitis pigmentosa
1997
·
M Hayakawa
·
Japanese Journal of Ophthalmology
·
21
Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa
1995
·
Keiko Fujiki
, Yoshihiro Hotta
, et al.
·
The Japanese Journal of Human Genetics
·
19
Diagnosis of Leber's Optic Neuropathy by Means of Polymerase Chain Reaction Amplification
1989
·
Yoshihiro Hotta
, Mutsuko Hayakawa
, et al.
·
American Journal of Ophthalmology
·
18
Acute Retinal Necrosis Syndrome Associated With Herpes Simplex Keratitis
1994
·
KAZUSHIGE SADO
, TAIRO KIMURA
, et al.
·
Retina
·
15
Macromelanosomes in X-linked ocular albinism (XLOA)
1985
·
T Yoshiike
, M Manabe
, et al.
·
Acta Dermato Venereologica
·
14
PDF
Analysis of phosducin as a candidate gene for retinopathies
1996
·
Fumino Ara-iwata
, Samuel G. Jacobson
, et al.
·
Ophthalmic Genetics
·
12
Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)
1989
·
Mutsuko Hayakawa
, Kenji Yanashima
, et al.
·
Ophthalmic Paediatrics and Genetics
·
12
Gyrate atrophy of the choroid and retina: 15 Japanese patients.
1986
·
S Hayasaka
, T Shiono
, et al.
·
British Journal of Ophthalmology
·
12
PDF
A multicenter study of typical retinitis pigmentosa in Japan.
1993
·
M Hayakawa
, M Matsumura
, et al.
·
PubMed
·
10
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Works count:
65
Citation count:
1,287
H-index:
18
I10-index:
26
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