Naoya Morisada

14PUBLICATIONS
21CO-AUTHORS
NeurogeneticsMechanobiologyDevelopmental genetics (incl. sex determination)NeonatologyCancer genetics
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Publications (14)

|Jul 14, 2025
Clinical characteristics of patients with SALL1-related disorder.

Yoshitaka Asagai, Yu Tanaka, Hiroaki Hanafusa

|Feb 20, 2025
Phenotype and genotype of autosomal dominant tubulointerstitial kidney disease in a Japanese cohort.

Yu Tanaka, China Nagano, Nana Sakakibara

|Mar 29, 2024
End-stage ADPKD with a low-frequency PKD1 mosaic variant accelerated by chemoradiotherapy.

Hiroaki Hanafusa, Hiroshi Yamaguchi, Naoya Morisada

|Mar 12, 2023
Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome.

Kana Hiromoto, Naoya Morisada, Shinya Tairaku

|Sep 01, 2020
A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy.

Ayumi Shishido, Naoya Morisada, Kenta Tominaga

|Mar 24, 2020
Clinical and genetic variability of PAX2-related disorder in the Japanese population.

Rini Rossanti, Naoya Morisada, Kandai Nozu

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