Tatsuo Matsunaga

7PUBLICATIONS
27CO-AUTHORS
Predictive and prognostic markersGene expression (incl. microarray and other genome-wide approaches)NeonatologyCentral nervous systemSensory systems
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Publications (7)

|Mar 06, 2022
Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.

Hideki Mutai, Yukihide Momozawa, Yoichiro Kamatani

|Dec 18, 2021
A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder.

Kazuki Yamazawa, Kenji Shimizu, Hirofumi Ohashi

|Nov 13, 2021
A High Risk of Missing Congenital Cytomegalovirus-Associated Hearing Loss through Newborn Hearing Screening in Japan.

Shujiro Bando Minami, Yoshiharu Yamanobe, Atsuko Nakano

|Jun 05, 2019
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel.

Jun Shen, Andrea M Oza, Ignacio Del Castillo

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