Takeshi Iwata

Tokyo, Japan

Last Updated: 09/26/2026

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Found 145 publications

Initial Site of Macular Involvement in Central Retinal Dystrophies Revealed by Fundus Autofluorescence and Optical Coherence Tomography.

Initial Site of Macular Involvement in Central Retinal Dystrophies Revealed by Fundus Autofluorescence and Optical Coherence Tomography.

Journal: Investigative ophthalmology & visual science

Published: May 19, 2026

Age-dependent association of the METTL23 c.84+60delAT variant with normal-tension glaucoma.

Age-dependent association of the METTL23 c.84+60delAT variant with normal-tension glaucoma.

Journal: Journal of human genetics

Published: March 12, 2026

DELETION INVOLVING EXON 18 OF RPGRIP1 IS a MAJOR CAUSE OF ACHROMATOPSIA.

DELETION INVOLVING EXON 18 OF RPGRIP1 IS a MAJOR CAUSE OF ACHROMATOPSIA.

Journal: Retina (Philadelphia, Pa.)

Published: February 10, 2026

Genotype-Phenotype Correlations in RPGRIP1-Associated Retinal Dystrophy in a Nationwide Japanese Cohort.

Genotype-Phenotype Correlations in RPGRIP1-Associated Retinal Dystrophy in a Nationwide Japanese Cohort.

Journal: American journal of ophthalmology

Published: January 29, 2026

A de novo splice-site variant in the retinitis pigmentosa 2 (RP2) gene identified in a symptomatic carrier woman.

A de novo splice-site variant in the retinitis pigmentosa 2 (RP2) gene identified in a symptomatic carrier woman.

Journal: Ophthalmic genetics

Published: December 17, 2025

Longitudinal evaluation of peripheral photoreceptor atrophy in fundus albipunctatus.

Longitudinal evaluation of peripheral photoreceptor atrophy in fundus albipunctatus.

Journal: Japanese journal of ophthalmology

Published: October 06, 2025

Clinical and genetic characterization of REEP6-associated retinopathy in a Japanese cohort.

Clinical and genetic characterization of REEP6-associated retinopathy in a Japanese cohort.

Journal: Japanese journal of ophthalmology

Published: September 08, 2025

Protocol for differentiating patient-derived iPSCs into photoreceptor-like cells.

Protocol for differentiating patient-derived iPSCs into photoreceptor-like cells.

Journal: STAR protocols

Published: September 02, 2025

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs).

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs).

Journal: bioRxiv : the preprint server for biology

Published: July 15, 2025

A novel NR2F1-associated microdeletion underlying Bosch-Boonstra-Schaaf optic atrophy syndrome.

A novel NR2F1-associated microdeletion underlying Bosch-Boonstra-Schaaf optic atrophy syndrome.

Journal: Ophthalmic genetics

Published: June 26, 2025

Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.

Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: June 23, 2025

RetiGene, a comprehensive gene atlas for inherited retinal diseases.

RetiGene, a comprehensive gene atlas for inherited retinal diseases.

Journal: American journal of human genetics

Published: June 10, 2025

Showing 1-12 of 145

Last Updated: 09/26/2026