Jiale Xiang

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 11

Top Venues

University of Helsinki (MSC)

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

Education History

University of Helsinki Aug 01 2012 - Dec 31 2014

Finland

MSC

Publications

Jiale Xiang, Jiguang Peng, Xiangzhong Sun, Zibin Lin, Dongdong Li, Haodong Ye, Sibao Wang, Yushi Bai, Xiaohong Wang, Peina Du, Ya Gao, Jun Sun, Silin Pan, Zhiyu Peng
The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing Data. Clinical chemistry (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)
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)
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)
Jing Zhang, Gugan Eswaran, Juan Alonso-Serra, Melis Kucukoglu Topcu, Jiale Xiang, Weibing Yang, Annakaisa Elo, Kaisa Nieminen, Teddy Damén, Je-Gun Joung, Jae-Young Yun, Jung-Hun Lee, Laura Ragni, Pierre Barbier de Reuille, Sebastian E Ahnert, Ji-Young Lee, Anne-Maarit Bågman, Yrjö Helariutta
Transcriptional regulatory framework for vascular cambium development in Arabidopsis roots. Nature plants 5 (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)

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Jiale Xiang