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Akiko Suga

Observed name: Suga, Akiko
Observed institutions: Keio University, Japan Science and Technology Agency, Tokyo Medical Center, RIKEN, RIKEN Advanced Science Institute, National Hospital Organization, The University of Tokyo, The University of Osaka
ORCID: 0000-0001-6609-2647
Observed ORCID: 0000-0001-6609-2647
OpenAlex ID: A5034725144
Characterization of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium Cell Sheets Aiming for Clinical Application
2014 · Hiroyuki Kamao, Michiko Mandai, et al. · Stem Cell Reports · 592
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Identification of Amino Acid Sequence in the Hinge Region of Human Vitamin D Receptor That Transfers a Cytosolic Protein to the Nucleus
1999 · Toshimi Michigami, Akiko Suga, et al. · Journal of Biological Chemistry · 70
Cellular FLIP Inhibits β-Catenin Ubiquitylation and Enhances Wnt Signaling
2004 · Mikihiko Naito, Ryohei Katayama, et al. · Molecular and Cellular Biology · 51
Proliferation Potential of Müller Glia after Retinal Damage Varies between Mouse Strains
2014 · Akiko Suga, Kazuyo Sadamoto, et al. · PLoS ONE · 45
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Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency
2020 · Lizhu Yang, Kaoru Fujinami, et al. · Scientific Reports · 40
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Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing
2022 · Akiko Suga, Kazutoshi Yoshitake, et al. · Human Mutation · 39
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METTL23 mutation alters histone H3R17 methylation in normal-tension glaucoma
2022 · Yang Pan, Akiko Suga, et al. · Journal of Clinical Investigation · 38
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Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association
2020 · Yu Fujinami-Yokokawa, Kaoru Fujinami, et al. · Scientific Reports · 33
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Identification of Novel Mutations in the LRR-Cap Domain of C21orf2 in Japanese Patients With Retinitis Pigmentosa and Cone–Rod Dystrophy
2016 · Akiko Suga, Atsushi Mizota, et al. · Investigative Ophthalmology & Visual Science · 32
LIM family transcription factors regulate the subtype-specific morphogenesis of retinal horizontal cells at post-migratory stages
2009 · Akiko Suga, Masanori Taira, et al. · Developmental Biology · 31
Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity
2006 · Akiko Suga, Hiroki Hikasa, et al. · Developmental Biology · 27
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Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy
2019 · Huiping Li, Shiqin Yuan, et al. · Human Molecular Genetics · 24
Retinal pigment epithelium-specific ablation of GPx4 in adult mice recapitulates key features of geographic atrophy in age-related macular degeneration
2024 · Kunihiro Azuma, Takafumi Suzuki, et al. · Cell Death and Disease · 20
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De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
2026 · Mathieu Quinodoz, Kim Rodenburg, et al. · Nature Genetics · 16
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De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
2025 · Mathieu Quinodoz, Kim Rodenburg, et al. · medRxiv · 15
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Binding of Gtf2i-β/δ transcription factors to the ARMS2 gene leads to increased circulating HTRA1 in AMD patients and in vitro
2021 · Yang Pan, Daisuke Iejima, et al. · Journal of Biological Chemistry · 15
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LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells
2018 · Yuichi Kawamura, Akiko Suga, et al. · Journal of Human Genetics · 9
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance
2024 · Akiko Suga, Yuriko Minegishi, et al. · Communications Biology · 6
Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis
2023 · Ayaka Nakajima, Kazuki Kuniyoshi, et al. · Frontiers in Medicine · 5
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Genetic Etiology and Clinical Features of Achromatopsia in Japan
2024 · Taiga Inooka, Takaaki Hayashi, et al. · Retina · 4
A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
2024 · Akiko Suga, Kei Mizobuchi, et al. · Genetics in Medicine Open · 3
DELETION INVOLVING EXON 18 OF RPGRIP1 IS a MAJOR CAUSE OF ACHROMATOPSIA
2026 · Taiga Inooka, Kei Mizobuchi, et al. · Retina · 1
A novel NR2F1 -associated microdeletion underlying Bosch-Boonstra-Schaaf optic atrophy syndrome
2025 · Takaaki Hayashi, Kei Mizobuchi, et al. · Ophthalmic Genetics · 1
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Genotype–Phenotype Correlations in RPGRIP1-Associated Retinal Dystrophy in a Nationwide Japanese Cohort
2026 · Kei Mizobuchi, Taiga Inooka, et al. · American Journal of Ophthalmology
Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene
2026 · Kazuma Oku, Kei Mizobuchi, et al. · Graefe s Archive for Clinical and Experimental Ophthalmology
Works count: 32
Citation count: 1,116
H-index: 15
I10-index: 16
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