Xiangzhong Sun
Shenzhen, China
Last Updated: 09/26/2026
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Found 12 publications
Concurrent physiologic and gene-based genetic newborn hearing screening in a general population.
Journal: Human genomics
Published: September 08, 2025
Genome Sequencing Unveils the Role of Copy Number Variants in Hearing Loss and Identifies Novel Deletions With Founder Effect in the DFNB1 Locus.
Journal: Human mutation
Published: May 18, 2024
The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data.
Journal: Clinical chemistry
Published: December 29, 2022
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss.
Journal: Human genetics
Published: March 16, 2022
Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.
Journal: BMC medical genomics
Published: February 28, 2022
Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in Newborns.
Journal: Frontiers in genetics
Published: February 25, 2022
Rational Design of a Polymer-Based Ratiometric K+ Indicator for High-Throughput Monitoring Intracellular K+ Fluctuations.
Journal: ACS applied bio materials
Published: January 11, 2022
Magnetically Reusable and Well-dispersed Nanoparticles for Oxygen Detection in Water.
Journal: Journal of fluorescence
Published: October 30, 2021
Tricolor dual sensor for ratiometrically analyzing potassium ions and dissolved oxygen.
Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
Published: January 15, 2020
Pyrazinamide and derivatives block ethylene biosynthesis by inhibiting ACC oxidase.
Journal: Nature communications
Published: November 14, 2016
Showing 1-12 of 12
Last Updated: 09/26/2026