Jiale Xiang

12PUBLICATIONS
16CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsFoetal development and medicinePsycholinguistics (incl. speech production and comprehension)
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Publications (12)

|Apr 14, 2025
Genome Sequencing Unveils the Role of Copy Number Variants in Hearing Loss and Identifies Novel Deletions With Founder Effect in the DFNB1 Locus.

Zibin Lin, Jiale Xiang, Xiangzhong Sun

|May 19, 2023
The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data.

Jiale Xiang, Jiguang Peng, Xiangzhong Sun

|Sep 01, 2022
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss.

Jiale Xiang, Xiangzhong Sun, Nana Song

|Jun 27, 2022
Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.

Jiale Xiang, Yuan Jin, Nana Song

|Jun 06, 2022
The effect of hemolysis on quality control metrics for noninvasive prenatal testing.

Yaya Guo, Dandan Yu, Kaisu Zhou

|Aug 24, 2021
VIP-HL: Semi-automated ACMG/AMP variant interpretation platform for genetic hearing loss.

Jiguang Peng, Jiale Xiang, Xiangqian Jin

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Frequent Collaborators

10 joint publications

Zhiyu Peng

3 joint publications

Jiguang Peng

2 joint publications

Yu Sun

2 joint publications

Ahmad N Abou Tayoun