Yin-hung Lin
TPQ, Taiwan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 publications
Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment.
Journal: The Journal of molecular diagnostics : JMD
Published: January 18, 2023
pubmedKB: an interactive web server for exploring biomedical entity relations in the biomedical literature.
Journal: Nucleic acids research
Published: February 27, 2022
Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
Journal: The Journal of molecular diagnostics : JMD
Published: October 09, 2020
Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: January 14, 2020
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response.
Journal: Scientific reports
Published: November 07, 2019
Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations.
Journal: Ear and hearing
Published: June 28, 2019
Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations.
Journal: PloS one
Published: September 22, 2018
Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan.
Journal: The Journal of pediatrics
Published: December 21, 2017
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct.
Journal: The Journal of molecular diagnostics : JMD
Published: October 31, 2017
Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss.
Journal: JAMA otolaryngology-- head & neck surgery
Published: July 09, 2017
Last Updated: 09/26/2026