Guohui Chen
Beijing, China
Last Updated: 09/26/2026
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Found 13 publications
Auditory Function and Natural History of 645 Auditory Neuropathy Patients Over a 27-Year Span in China.
Journal: Ear and hearing
Published: December 26, 2025
Comparative Prognostic Analysis of Sudden Sensorineural Hearing Loss With Vertigo in Pediatric and Adult Patients.
Journal: Laryngoscope investigative otolaryngology
Published: November 05, 2025
Comparable Outcomes in Pediatric and Adult Patients With Sudden Sensorineural Hearing Loss.
Journal: The Laryngoscope
Published: October 21, 2025
Characteristic cortical alterations in auditory neuropathy: An EEG study.
Journal: Hearing research
Published: June 25, 2025
Identification of a Novel Likely Pathogenic Variant of DIAPH3 Associated With New Phenotype of Sensorineural Hearing Loss.
Journal: Molecular genetics & genomic medicine
Published: May 03, 2025
Interpretation of de novo mutations (DNM) and genetic counseling for sporadic hearing loss based on family trio-based sequencing.
Journal: Yi chuan = Hereditas
Published: March 11, 2025
Clinical application of preimplantation genetic testing based on low-coverage next-generation sequencing with linkage analyses in hereditary hearing loss families.
Journal: Journal of assisted reproduction and genetics
Published: November 24, 2024
Effect of sudden sensorineural hearing loss patients with or without dizziness/vertigo on auditory prognosis in patients with moderately severe hearing loss and above
Journal: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery
Published: May 17, 2024
Sudden sensorineural hearing loss as the initial symptom in patients with acoustic neuroma.
Journal: Frontiers in neurology
Published: May 26, 2022
Family trio-based sequencing in 404 sporadic bilateral hearing loss patients discovers recessive and De novo genetic variants in multiple ways.
Journal: European journal of medical genetics
Published: January 30, 2021
Discovery of sensorineural hearing loss and ossicle deformity in a Chinese Li nationality family with spondyloepiphyseal dysplasia congenita caused by p.G504S mutation of COL2A1.
Journal: BMC medical genomics
Published: December 16, 2020
Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.
Journal: Molecular genetics & genomic medicine
Published: April 05, 2020
Last Updated: 09/26/2026