Yohei Nitta
Niigata, Japan
Last Updated: 09/26/2026
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Found 21 publications
Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.
Journal: European journal of human genetics : EJHG
Published: August 04, 2025
Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype.
Journal: Frontiers in genetics
Published: February 07, 2024
Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.
Journal: Nature communications
Published: November 03, 2023
Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences.
Journal: European journal of medical genetics
Published: May 23, 2023
Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes.
Journal: Scientific reports
Published: March 09, 2023
Identification of genes regulating stimulus-dependent synaptic assembly in Drosophila using an automated synapse quantification system.
Journal: Genes & genetic systems
Published: March 06, 2023
A novel NONO variant that causes developmental delay and cardiac phenotypes.
Journal: Scientific reports
Published: November 18, 2022
Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA.
Journal: Human molecular genetics
Published: August 08, 2022
A Quantitative Model of Sporadic Axonal Degeneration in the Drosophila Visual System.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: October 13, 2021
De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.
Journal: Human molecular genetics
Published: June 01, 2021
Last Updated: 09/26/2026