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Issue Date	Title	Journal Title
2022	OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin	AUTOPHAGY
2015	Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure	PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
2019	Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency	Scientific Reports
2019	The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report	BMC MEDICAL GENETICS