Zhiyu Peng
19PUBLICATIONS
13CO-AUTHORS
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Publications (19)
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|Feb 17, 2026
Application of Non-Invasive Prenatal Testing for Dominant Single-Gene Disorders in an Intermediate-Risk Population: A Prospective Cohort Study.Qun Lu, Chao Chen, Ying Lin
|Feb 13, 2026
Novel Haplotype-Based Noninvasive Prenatal Diagnosis for Recessive Single-Gene Disorders: A Proof-of-Concept Study.Chao Chen, Yaping Zhu, Lu Jiang
|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
|Apr 03, 2023
Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples.Yeqing Qian, Yan Sun, Xueqin Guo
|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
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Frequent Collaborators
10 joint publications
Jiale Xiang
2 joint publications
Yaoshen Wang
2 joint publications
Jiguang Peng
2 joint publications
Ahmad N Abou Tayoun
2 joint publications
Yu Sun
1 joint publications
Shida Zhu
1 joint publications
Wei Li
1 joint publications
Baosheng Zhu
1 joint publications
Minyue Dong
1 joint publications
Zibin Lin
