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Iwata Laboratory

Other IDs

Researcher Name Resolver ID: 1000090374157
Loop profile: 680119
SciProfiles: 1805818

Keywords

Retina, Genetics, iPS Cells, Knock-in mouse, Age-related macular degeneration, Glaucoma, Hereditary retinal diseases, Retinitis pigmentosa

Countries

Japan

Activities

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Employment (1)

National Institute of Sensory Organs, NHO Tokyo Medical Center: 2-5-1 Higashigaoka, Meguro-ku, Tokyo, JP

2000-04-01 to present | Division Director (Division of Molecular and Cellular Biology)
Employment
Source: Self-asserted source
Takeshi Iwata

Works (11)

Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance

Communications Biology
2024-06-03 | Journal article
DOI: 10.1038/s42003-024-06384-2
Contributors: Akiko Suga; Yuriko Minegishi; Megumi Yamamoto; Koji Ueda; Takeshi Iwata
Source: check_circle
Crossref

Exploring the Genetic Landscape of Childhood Glaucoma

Children
2024-04-09 | Journal article
DOI: 10.3390/children11040454
Contributors: Yang Pan; Takeshi Iwata
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degeneration

Progress in Retinal and Eye Research
2023-11 | Journal article
DOI: 10.1016/j.preteyeres.2022.101159
Contributors: Yang Pan; Yingbin Fu; Paul N. Baird; Robyn H. Guymer; Taraprasad Das; Takeshi Iwata
Source: check_circle
Crossref

Clinical course of a Japanese girl with Leber congenital amaurosis associated with a novel nonsense pathogenic variant in NMNAT1: a case report and mini review

Ophthalmic Genetics
2022-01-13 | Journal article
DOI: 10.1080/13816810.2021.2023195
Contributors: Tomoyasu Kayazawa; Kazuki Kuniyoshi; Yoshikazu Hatsukawa; Kaoru Fujinami; Kazutoshi Yoshitake; Kazushige Tsunoda; Hiroshi Shimojo; Takeshi Iwata; Shunji Kusaka
Source: check_circle
Crossref

ePat: extended PROVEAN annotation tool

2021-12-23 | Preprint
DOI: 10.1101/2021.12.21.468911
Contributors: Takumi Ito; Kazutoshi Yoshitake; Takeshi Iwata
Source: check_circle
Crossref

Genotype-Phenotype Correlations in <i>RP1</i>-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN

Journal of Clinical Medicine
2021-05 | Journal article | Author
DOI: 10.3390/jcm10112265
Contributors: kei mizobuchi; Takaaki Hayashi; Noriko Oishi; Daiki Kubota; Shuhei Kameya; Koichiro Higasa; Takuma Futami; Hiroyuki Kondo; Katsuhiro Hosono; Kentaro Kurata et al.
Source: check_circle
Multidisciplinary Digital Publishing Institute

Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques

Journal of Ophthalmology
2019-04-09 | Journal article
DOI: 10.1155/2019/1691064
Contributors: Yu Fujinami-Yokokawa; Nikolas Pontikos; Lizhu Yang; Kazushige Tsunoda; Kazutoshi Yoshitake; Takeshi Iwata; Hiroaki Miyata; Kaoru Fujinami; on behalf of Japan Eye Genetics Consortium
Source: check_circle
Crossref

Clinical findings of end-stage retinitis pigmentosa with a homozygous PDE6A variant (p.R653X)

American Journal of Ophthalmology Case Reports
2019-03 | Journal article
DOI: 10.1016/j.ajoc.2018.12.019
Contributors: Kei Mizobuchi; Satoshi Katagiri; Takaaki Hayashi; Kazutoshi Yoshitake; Kaoru Fujinami; Kazuki Kuniyoshi; Reimi Mishima; Kazushige Tsunoda; Takeshi Iwata; Tadashi Nakano
Source: check_circle
Crossref

LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells

Journal of Human Genetics
2018-08-14 | Journal article
DOI: 10.1038/s10038-018-0465-4
Contributors: Yuichi Kawamura; Akiko Suga; Takuro Fujimaki; Kazutoshi Yoshitake; Kazushige Tsunoda; Akira Murakami; Takeshi Iwata
Source: check_circle
Crossref

KUS121, an ATP regulator, mitigates chorioretinal pathologies in animal models of age-related macular degeneration

Heliyon
2018-05 | Journal article
DOI: 10.1016/j.heliyon.2018.e00624
Contributors: Yuki Muraoka; Yuto Iida; Hanako O. Ikeda; Sachiko Iwai; Masayuki Hata; Takeshi Iwata; Mao Nakayama; Nobuhiro Shimozawa; Yuko Katakai; Akira Kakizuka et al.
Source: check_circle
Crossref

Significance of optineurin mutations in glaucoma and other diseases

Progress in Retinal and Eye Research
2016-11 | Journal article
DOI: 10.1016/j.preteyeres.2016.08.002
Contributors: Yuriko Minegishi; Mao Nakayama; Daisuke Iejima; Kazuhide Kawase; Takeshi Iwata
Source: check_circle
Crossref

Peer review (14 reviews for 10 publications/grants)

Review activity for American journal of ophthalmology. (1)
Review activity for American journal of ophthalmology. (2)
Review activity for Biomedicines. (1)
Review activity for Cells. (1)
Review activity for Disease models & mechanisms (1)
Review activity for EMBO molecular medicine. (2)
Review activity for Gene therapy. (2)
Review activity for Journal of human genetics. (2)
Review activity for Ophthalmology and therapy. (1)
Review activity for Review Commons (1)
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