Hongen Xu

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Venues

Molecular genetics & genomic medicine

Biology

BioMed research international

NPJ genomic medicine

Technische Universität München (PHD)

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

Education History

Technische Universität München Sep 11 2012

Germany

PHD :: Genome-oriented bioinformatics

Southwest University Sep 01 2009 - Jul 01 2012

China

MSC

Publications

Qiang Li, Shuping Sun, Bin Zuo, Chengyu Lian, Wenxue Tang, Hongen Xu, Wei Lu
Novel Clinical Manifestation and Favorable Treatment Outcome of Cochlear Implant in a Chinese Family With Likely Pathogenic Variant of the P2RX2 Gene. American journal of medical genetics. Part A (2024)
Lu Mao, Yueqiang Wang, Lei An, Beiping Zeng, Yanyan Wang, Dmitrij Frishman, Mengli Liu, Yanyu Chen, Wenxue Tang, Hongen Xu
Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants. Biology 12 (4) (2023)
Lu Mao, Yueqiang Wang, Lei An, Beiping Zeng, Yanyan Wang, Dmitrij Frishman, Mengli Liu, Yanyu Chen, Wenxue Tang, Hongen Xu
Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants. Biology 12 (4) (2023)
Zhigang Wang, Hongen Xu, Tianchao Xiang, Danhua Liu, Fei Xu, Lixiang Zhao, Yonghua Feng, Linan Xu, Jialu Liu, Ye Fang, Huanfei Liu, Ruijun Li, Xinxin Hu, Jingyuan Guan, Longshan Liu, Guiwen Feng, Qian Shen, Hong Xu, Dmitrij Frishman, Wenxue Tang, Jiancheng Guo, Jia Rao, Wenjun Shang
An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease. NPJ genomic medicine 6 (1) (2021)
Jinying Li, Hongen Xu, Jianfeng Sun, Yongan Tian, Danhua Liu, Yaping Qin, Huanfei Liu, Ruijun Li, Lingling Neng, Xiaohua Deng, Binbin Xue, Changyun Yu, Wenxue Tang
Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype. BioMed research international 2021 (2021)
Yongan Tian, Hongen Xu, Danhua Liu, Juanli Zhang, Zengguang Yang, Sen Zhang, Huanfei Liu, Ruijun Li, Yingtao Tian, Beiping Zeng, Tong Li, Qianyu Lin, Haili Wang, Xiaohua Li, Wei Lu, Ying Shi, Yan Zhang, Hui Zhang, Chang Jiang, Ying Xu, Bei Chen, Jun Liu, Wenxue Tang
Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene. Molecular genetics & genomic medicine 9 (8) (2021)
Yanfang Mi, Danhua Liu, Beiping Zeng, Yongan Tian, Hui Zhang, Bei Chen, Juanli Zhang, Hong Xue, Wenxue Tang, Yulin Zhao, Hongen Xu
Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype. Molecular genetics & genomic medicine 9 (1) (2020)
Zhaoyu Pan, Hongen Xu, Bei Chen, Yongan Tian, Linlin Zhang, Sen Zhang, Danhua Liu, Huanfei Liu, Ruijun Li, Xinxin Hu, Jingyuan Guan, Wenxue Tang, Wei Lu
Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients. Molecular genetics & genomic medicine 9 (2) (2020)
Rong Qun Zhai, Haifeng Feng, Qingli Li, Wei Lu, Danhua Liu, Yongan Tian, Huanfei Liu, Ruijun Li, Bin Zuo, Wenxue Tang, Hongen Xu, Bei Chen
Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families. BioMed research international 2020 (2020)
Zhaoyu Pan, Hongen Xu, Yongan Tian, Danhua Liu, Huanfei Liu, Ruijun Li, Qian Dou, Bin Zuo, Rongqun Zhai, Wenxue Tang, Wei Lu
Perrault syndrome: Clinical report and retrospective analysis. Molecular genetics & genomic medicine 8 (10) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Hongen Xu