Linwei Yin

The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide

L. Lan, J. Guan, Hong-yang Wang, 2022, Ear and hearing.

Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss

J. Guan, Qiuju Wang, Huifang Zhou, 2019, BMC Medical Genetics.

Novel de novo interstitial deletion in 2q36.1q36.3 causes syndromic hearing loss and further delineation of the 2q36 deletion syndrome

J. Guan, Qiuju Wang, Da-yong Wang, 2019, Acta oto-laryngologica.

Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy

L. Lan, J. Guan, Qiuju Wang, 2019, BMC Medical Genetics.

Effect of the Pulsed Electromagnetic Field Treatment in a Rat Model of Senile Osteoporosis In Vivo

Jun Zhou, P. Zhong, M. Qu, 2022, Bioelectromagnetics.

Treadmill training mitigates bone deterioration via inhibiting NLRP3/Caspase1/IL-1β signaling in aged rats

Jun Zhou, P. Zhong, Qi Wu, 2022, BMC musculoskeletal disorders.