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BMC Medical Genomics|May 16, 2022
Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing lossWeixun Zhang, Jing Song, Busheng Tong, et al.
Hearing Research|May 20, 2019
A humanized mouse model, demonstrating progressive hearing loss caused by MYO6 p.C442Y, is inherited in a semi-dominant patternJinghan Wang, Jun Shen, Luo Guo, et al.
Frontiers in Molecular Neuroscience|May 16, 2018
Characterization of Wnt and Notch-Responsive Lgr5+ Hair Cell Progenitors in the Striolar Region of the Neonatal Mouse UtricleDan You, Luo Guo, Wenyan Li, et al.
BMC Medical Genomics|June 17, 2022
Novel homozygous variant in the PDZD7 gene in a family with nonsyndromic sensorineural hearing lossQiang Du, Qin Sun, Xiaodong Gu, et al.
International Journal of Pediatric Otorhinolaryngology|January 27, 2016
A novel recessive truncating mutation in MYO15A causing prelingual sensorineural hearing lossWei Li, Luo Guo, Yu Li, et al.
International Journal of Pediatric Otorhinolaryngology|April 2, 2015
Novel biallelic OTOGL mutations in a Chinese family with moderate non-syndromic sensorineural hearing lossXiaodong Gu, Shan Sun, Luo Guo, et al.
Clinical and Translational Medicine|September 30, 2022
The heterogeneity of mammalian utricular cells over the course of developmentDan You, Jin Guo, Yunzhong Zhang, et al.
BMC Medical Genomics|March 19, 2024
A novel intronic TCOF1 pathogenic variant in a Chinese family with Treacher Collins syndromeHaojie Sun, Xinda Xu, Binjun Chen, et al.
Hearing Research|October 20, 2025
Unraveling the genetic basis of post-infancy diagnosed sensorineural hearing loss using whole exome sequencingWeitao Li, Sha Yu, Biyun Zhu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 19, 2016
Extensive Supporting Cell Proliferation and Mitotic Hair Cell Generation by In Vivo Genetic Reprogramming in the Neonatal Mouse CochleaWenli Ni, Chen Lin, Luo Guo, et al.
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