Dongyang Y. Kang - Publications

Hearing phenotype and genotypic characteristics in GSDME-related deafness pedigrees

Journal: Zhonghua yi xue za zhi

Published: January 11, 2026

Reevaluation of Enlarged Vestibular Aqueduct.

Journal: JAMA otolaryngology-- head & neck surgery

Published: October 09, 2025

An in situ non-contact 3D microscopic measurement system for temporal bone anatomy based on stereo imaging.

Journal: Scientific reports

Published: September 23, 2025

Origin of mitochondrial A1555G heterogeneous mutation and its correlation with hearing loss severity

Journal: Zhonghua yi xue za zhi

Published: February 12, 2025

Clinical Application of the 4K-3D Exoscope System in Cochlear Implantation.

Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology

Published: May 10, 2024

Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population.

Journal: Orphanet journal of rare diseases

Published: April 02, 2024

Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells.

Journal: Clinical chemistry

Published: July 26, 2023

Phenotype-genotype analysis of the autosomal recessive hereditary hearing loss caused by OTOA variations

Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery

Published: April 28, 2023

Correction to: Preimplantation genetic testing for hereditary hearing loss in Chinese population.

Journal: Journal of assisted reproduction and genetics

Published: April 24, 2023

Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy.

Journal: Genes & diseases

Published: January 17, 2023

Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome.

Journal: Human genetics

Published: July 25, 2022

Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10.

Journal: Stem cell research

Published: May 28, 2022