Takeshi Iwata

16PUBLICATIONS
196CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Sensory systemsNeurology and neuromuscular diseasesMolecular targets
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Publications (16)

|Jul 03, 2026
Age-dependent association of the METTL23 c.84+60delAT variant with normal-tension glaucoma.

|Jan 19, 2026
Clinical and genetic characterization of REEP6-associated retinopathy in a Japanese cohort.

Takeru Tsuboi, Kei Mizobuchi, Kazutoshi Yoshitake

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Dec 17, 2025
A de novo splice-site variant in the retinitis pigmentosa 2 (RP2) gene identified in a symptomatic carrier woman.

Aya Domoto, Kazuki Kuniyoshi, Akiko Suga

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Jun 03, 2024
Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance.

Akiko Suga, Yuriko Minegishi, Megumi Yamamoto

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Frequent Collaborators

6 joint publications

Takaaki Hayashi

5 joint publications

Kei Mizobuchi

4 joint publications

Satoshi Katagiri

3 joint publications

Akiko Suga