Zhiyu Peng

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 16

Top Venues

BMC medical genomics

Scientific reports

Human mutation

European journal of human genetics : EJHG

Peking University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Peking University Aug 01 2004 - Jul 01 2009

China

PHD

Publications

Yeqing Qian, Yan Sun, Xueqin Guo, Lijie Song, Yixi Sun, Xiaoyang Gao, Bei Liu, Yuqing Xu, Na Chen, Min Chen, Yuqin Luo, Zhihong Qiao, Linlin Fan, Jianfen Man, Kang Zhang, Xiaoli Wang, Tingting Rong, Zhonghua Wang, Fengxia Liu, Jing Zhao, Xiaoming Wei, Minfeng Chen, Zhiyu Peng, Huanhuan Peng, Jun Sun, Min-Yue Dong
Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples. Journal of medical genetics (2023)
Jiale Xiang, Xiangzhong Sun, Nana Song, Sathishkumar Ramaswamy, Ahmad N Abou Tayoun, Zhiyu Peng
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss. Human genetics (2022)
Yaya Guo, Dandan Yu, Kaisu Zhou, Jie Wang, Dongzhu Lei, Zhenpeng Xu, Weijiang Tang, Miaofeng Wu, Xingxing Fang, Jiankun Shen, Zhiyu Peng, Jiale Xiang
The effect of hemolysis on quality control metrics for noninvasive prenatal testing. BMC medical genomics 15 (1) (2022)
Jiale Xiang, Yuan Jin, Nana Song, Sen Chen, Jiankun Shen, Wen Xie, Xiangzhong Sun, Zhiyu Peng, Yu Sun
Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss. BMC medical genomics 15 (1) (2022)
Chao Chen, Ru Li, Jun Sun, Yaping Zhu, Lu Jiang, Jian Li, Fang Fu, Junhui Wan, Fengyu Guo, Xiaoying An, Yaoshen Wang, Linlin Fan, Yan Sun, Xiaosen Guo, Sumin Zhao, Wanyang Wang, Fanwei Zeng, Yun Yang, Peixiang Ni, Yi Ding, Bixia Xiang, Zhiyu Peng, Can Liao
Noninvasive prenatal testing of α-thalassemia and β-thalassemia through population-based parental haplotyping. Genome medicine 13 (1) (2021)
Yan Sun, Fengxia Liu, Chunna Fan, Yaoshen Wang, Lijie Song, Zhonghai Fang, Rui Han, Zhonghua Wang, Xiaodan Wang, Ziying Yang, Zhenpeng Xu, Jiguang Peng, Chaonan Shi, Hongyun Zhang, Wei Dong, Hui Huang, Yun Li, Yanqun Le, Jun Sun, Zhiyu Peng
Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders. BMC medical genomics 14 (1) (2021)
Jiguang Peng, Jiale Xiang, Xiangqian Jin, Junhua Meng, Nana Song, Lisha Chen, Ahmad N Abou Tayoun, Zhiyu Peng
VIP-HL: Semi-automated ACMG/AMP variant interpretation platform for genetic hearing loss. Human mutation 42 (12) (2021)
Jiale Xiang, Jiguang Peng, Samantha Baxter, Zhiyu Peng
AutoPVS1: An automatic classification tool for PVS1 interpretation of null variants. Human mutation 41 (9) (2020)
Ling Guo, Jiale Xiang, Lei Sun, Xinyi Yan, Jingjing Yang, Haiyan Wu, Kejian Guo, Jiguang Peng, Xiaomei Xie, Ye Yin, Jian Wang, Huanming Yang, Jun Shen, Lijian Zhao, Zhiyu Peng
Concurrent hearing and genetic screening in a general newborn population. Human genetics 139 (4) (2020)
Jiale Xiang, Jiyun Yang, Lisha Chen, Qiang Chen, Haiyan Yang, Chengcheng Sun, Qing Zhou, Zhiyu Peng
Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades. Scientific reports 10 (1) (2020)
Xiaoming Wei, Fanwei Zeng, Baitong Fan, Nan Yu, Jing Wu, Yun Yang, Hui Huang, Sheng-Li Li, Zhiyu Peng
Impact of ultrasonography on identifying noninvasive prenatal screening false-negative aneuploidy. Molecular genetics & genomic medicine 8 (6) (2020)
Sumin Zhao, Wanyang Wang, Yaoshen Wang, Rui Han, Chunna Fan, Peixiang Ni, Fengyu Guo, Fanwei Zeng, Qiaona Yang, Yun Yang, Yan Sun, Xinhua Zhang, Yan Chen, Baosheng Zhu, Wangwei Cai, Shaoke Chen, Ren Cai, Xiaoling Guo, Chonglin Zhang, Yuqiu Zhou, Shuodan Huang, Yanhui Liu, Biyan Chen, Shanhuo Yan, Yajun Chen, Hongmei Ding, Xuan Shang, Xiangmin Xu, Jun Sun, Zhiyu Peng
NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study. European journal of human genetics : EJHG 29 (1) (2020)
Jiale Xiang, Jiyun Yang, Lisha Chen, Qiang Chen, Haiyan Yang, Chengcheng Sun, Qing Zhou, Zhiyu Peng
Author Correction: Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades. Scientific reports 10 (1) (2020)
Yu Sun, Jiale Xiang, Yidong Liu, Sen Chen, Jintao Yu, Jiguang Peng, Zijing Liu, Lisha Chen, Jun Sun, Yun Yang, Yaping Yang, Yulin Zhou, Zhiyu Peng
Increased diagnostic yield by reanalysis of data from a hearing loss gene panel. BMC medical genomics 12 (1) (2019)
Qiuju Wang, Jiale Xiang, Jun Sun, Yun Yang, Jing Guan, Dayong Wang, Cui Song, Ling Guo, Hongyang Wang, Yaqiu Chen, Junhong Leng, Xiaman Wang, Junqing Zhang, Bing Han, Jing Zou, Chengbin Yan, Lidong Zhao, Hongyu Luo, Yuan Han, Wen Yuan, Hongyun Zhang, Wei Wang, Jian Wang, Huanming Yang, Xun Xu, Ye Yin, Cynthia C Morton, Lijian Zhao, Shi-da Zhu, Jun Shen, Zhiyu Peng
Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China. Genetics in medicine : official journal of the American College of Medical Genetics 21 (10) (2019)
Sumin Zhao, Jiale Xiang, Chunna Fan, null Asan, Xuan Shang, Xinhua Zhang, Yan Chen, Baosheng Zhu, Wangwei Cai, Shaoke Chen, Ren Cai, Xiaoling Guo, Chonglin Zhang, Yuqiu Zhou, Shuodan Huang, Yanhui Liu, Biyan Chen, Shanhuo Yan, Yajun Chen, Hongmei Ding, Fengyu Guo, Yaoshen Wang, Wenwei Zhong, Yaping Zhu, Yaling Wang, Chao Chen, Yun Li, Hui Huang, Mao Mao, Ye Yin, Jian Wang, Huanming Yang, Xiangmin Xu, Jun Sun, Zhiyu Peng
Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples. European journal of human genetics : EJHG 27 (2) (2018)

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Publication Activity (10 Years)

Top Topics

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Zhiyu Peng