Atsushi Sugie

7PUBLICATIONS
35CO-AUTHORS
NeurogeneticsVision scienceMolecular targetsNeurosciences not elsewhere classifiedNeurology and neuromuscular diseases
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Publications (7)

|Jun 23, 2026
Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.

|Aug 23, 2024
Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy.

Yohei Nitta, Jiro Osaka, Ryuto Maki

|Jun 01, 2024
Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.

Samuel D Chauvin, Shoichiro Ando, Joe A Holley

|Mar 09, 2023
Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes.

Toshiyuki Itai, Atsushi Sugie, Yohei Nitta

|Jan 18, 2023
A novel NONO variant that causes developmental delay and cardiac phenotypes.

Toshiyuki Itai, Atsushi Sugie, Yohei Nitta

|Jan 07, 2023
Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA.

Yohei Nitta, Hiroki Kawai, Ryuto Maki

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Frequent Collaborators

3 joint publications

Yohei Nitta

2 joint publications

Toshiyuki Itai

2 joint publications

Yoichi Shinkai

2 joint publications

Yoshihiro Watanabe