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Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
De novo mutation in X-linked hearing loss-associated POU3F4 in a sporadic case of congenital hearing lossHideaki Moteki, A Eliot Shearer, Shuji Izumi, et al.The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptomsHideaki Moteki, Hidekane Yoshimura, Hela Azaiez, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 29, 2025
Intrathecal Gadolinium-Enhanced MR Cisternography Improves the Detection of Skull Base CSF LeaksDouglas J Totten, Nicholas A Koontz, Hunter L Elms, et al.Human Genetics|February 19, 2022
DVPred: a disease-specific prediction tool for variant pathogenicity classification for hearing lossFengxiao Bu, Mingjun Zhong, Qinyi Chen, et al.Biorxiv : the Preprint Server for Biology|November 28, 2023
PCDH15 Dual-AAV Gene Therapy for Deafness and Blindness in Usher Syndrome Type 1FMaryna V Ivanchenko, Daniel M Hathaway, Eric M Mulhall, et al.Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutationHideaki Moteki, Hela Azaiez, Kevin T Booth, et al.Biorxiv : the Preprint Server for Biology|March 18, 2024
The auditory midbrain mediates tactile vibration sensingErica L Huey, Josef Turecek, Michelle M Delisle, et al.Cell|December 19, 2024
The auditory midbrain mediates tactile vibration sensingErica L Huey, Josef Turecek, Michelle M Delisle, et al.Pageof 5