Get started
Award

2023YFC2508400

Funded outputs count: 7
Funder award ID: 2023YFC2508400
OpenAlex ID: G1106810578
POU4F3 variants are prevalent in Chinese patients with autosomal dominant non-syndromic hearing loss and concurrent tinnitus
2026 · Qiujing Zhang, Lingling Zeng, et al. · Journal of Translational Medicine
The hidden gut–brain connection in tinnitus: Insight from a cross-sectional and genetic causal mediation study in over 900,000 individuals
2025 · Chanmei Fang, Liling Lin, et al. · NeuroImage · 4
Effect of hearing ability on inflammation and glymphatic function affecting cognition in older adults
2025 · Weijie Ye, Chunhua Xing, et al. · GeroScience · 3
PDF
Variant frequency of GJB2 c.109G>A (p.Val37Ile) in the general Chinese population: A systematic review and meta-analysis
2025 · Jiao Zhang, Dayong Wang, et al. · International Journal of Pediatric Otorhinolaryngology · 1
Seasonal and monthly variation in benign paroxysmal positional vertigo: a systematic review and meta‑analysis
2025 · Linlin Wang, Haixia Wang, et al. · European Archives of Oto-Rhino-Laryngology · 1
Predominant white matter microstructural changes over gray matter in tinnitus brain
2025 · Qianhui Xu, Tingting Chai, et al. · NeuroImage · 4
Comparison of vHIT deficits with Ramsay Hunt syndrome with dizziness, vestibular neuritis, and idiopathic sudden sensorineural hearing loss with vertigo
2025 · Yingzhao Liu, Xiaoye Chen, et al. · Journal of Vestibular Research · 1
Year
Topic