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Hongyang Wang

Chinese PLA General Hospital

47

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301

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Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo.

2021
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Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype-Phenotype Study and CI Management.

2021 Frontiers in Cell and Developmental Biology
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A porous ceramic separator prepared from natural minerals: Research on the mechanism of high liquid absorption and electrochemical properties of mineral material separator

2021 Materials Chemistry and Physics
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A Novel Variant in Diaphanous Homolog 1 (DIAPH1) as the Cause of Auditory Neuropathy in a Chinese Family

2020 International Journal of Pediatric Otorhinolaryngology
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Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China

2019 Genetics in Medicine
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Molecular genetic studies of familial Meniere’s disease

2019 Science China-life Sciences
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Novel de novo interstitial deletion in 2q36.1q36.3 causes syndromic hearing loss and further delineation of the 2q36 deletion syndrome

2019 Acta Oto-laryngologica
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Identification of four TMC1 variations in different Chinese families with hereditary hearing loss

2018 Molecular Genetics & Genomic Medicine
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Further evidence for “gain-of-function” mechanism of DFNA5 related hearing loss

2018 Scientific Reports
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Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype–phenotype review for DFNA11

2018 Acta Oto-laryngologica
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