Shushan Sang

Guangzhou University of Chinese Medicine — China

Neuroscience · Life Sciences

10h-index358citations21works3.02yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(9), Connexins and lens biology(5), Parkinson's Disease Mechanisms and Treatments(3), RNA regulation and disease(3), Glioma Diagnosis and Treatment(2)

Publications21 total

Potential Key Genes for Giant Cell Arteritis Revealed Based on Single-Cell Sequencing and Mendelian Randomization Analysis
International Archives of Allergy and Immunology·2025· 1 cited
Longitudinal faster anxiety progression of GBA variant carriers in the early Parkinson’s disease cohort
Frontiers in Neuroscience·2024· 5 citedOpen Access
P-83 Preoperative endoscopic biliary drainage procedures may affect intrahepatic recurrence of cholangiocarcinoma after surgical resection
Annals of Oncology·2023Open Access
Impact of GBA variants on longitudinal freezing of gait progression in early Parkinson’s disease
Journal of Neurology·2023· 6 cited
SNCA rs3910105 Is Associated With Development of Rapid Eye Movement Sleep Behavior Disorder in Parkinson’s Disease
Frontiers in Neuroscience·2022· 3 citedOpen Access
A nonsense <i>TMEM43</i> variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder
Proceedings of the National Academy of Sciences·2021· 29 citedOpen Access
Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with connexin-mediated passive conductance channels
2020Open Access
Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families
European Archives of Oto-Rhino-Laryngology·2020· 6 cited
[Application of PCR reverse dot blot in non-syndromic deafness gene detection].
PubMed·2020Open Access
Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families
Frontiers in Genetics·2019· 37 citedOpen Access
A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review
Gene·2019· 19 cited
Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families
International Journal of Pediatric Otorhinolaryngology·2018· 4 cited
Clinical Long-Term Follow-Up Evaluation of Functional Neuronavigation in Adult Cerebral Gliomas
World Neurosurgery·2018· 15 cited
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss
Human Genetics·2018· 22 cited
A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family
Journal of Human Genetics·2018· 19 cited
Corrigendum to “Neuroprotective and anti-apoptotic effects of valproic acid on adult rat cerebral cortex through ERK and Akt signaling pathway at acute phase of traumatic brain injury” [Brain Res.1555 (2014, Mar. 25) 1–9]
Brain Research·2016· 1 cited
Nitroproteins in Human Astrocytomas Discovered by Gel Electrophoresis and Tandem Mass Spectrometry
Journal of the American Society for Mass Spectrometry·2015· 42 cited
Anti-Cancer Effect of Metabotropic Glutamate Receptor 1 Inhibition in Human Glioma U87 Cells: Involvement of PI3K/Akt/mTOR Pathway
Cellular Physiology and Biochemistry·2015· 76 citedOpen Access
Neuroprotective and anti-apoptotic effects of valproic acid on adult rat cerebral cortex through ERK and Akt signaling pathway at acute phase of traumatic brain injury
Brain Research·2014· 48 cited
Downregualtion of dynamin-related protein 1 attenuates glutamate-induced excitotoxicity via regulating mitochondrial function in a calcium dependent manner in HT22 cells
Biochemical and Biophysical Research Communications·2013· 20 cited
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Frequent Co-authors

Chufeng He(9), Yong Feng(9), Jie Ling(8), Lingyun Mei(8), Yalan Liu(7), Hongsheng Chen(7), Jie Wen(6), Xinzhang Cai(5), Taoxi Li(5), Wu Li(5), Xianrui Yuan(4), Haoyu Li(4), Zijin Zhao(4), Yiwei Liao(4), Yuyuan Deng(4), Xianlin Liu(3), Zhijie Niu(3), Meng Li(3), Nannan Yang(3), Xiangyu Wang(2)