Hongen Xu

发表

Somatic mutations in tumors: their detection, generation mechanisms and implications

Hongen Xu, Hongen Xu, 2017 .

Genome‐wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma

D. Frishman, S. Bielack, Yanping Zhang, 2017, International journal of cancer.

Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma

E. Collisson, W. Cao, Jia Liu, 2020, Nature Communications.

Early truncation of the N‐terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype

Hongen Xu, Wenxue Tang, Yulin Zhao, 2020, Molecular genetics & genomic medicine.

Genomic determinants of somatic copy number alterations across human cancers.

D. Frishman, Yanping Zhang, Hongen Xu, 2016, Human molecular genetics.

A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient

Hongen Xu, Wenxue Tang, Beiping Zeng, 2022, BMC Medical Genomics.

The N6-methyladenosine writer WTAP contributes to the induction of immune tolerance post kidney transplantation by targeting regulatory T cells

J Zhang, Hongen Xu, W. Shang, 2022, Laboratory Investigation.

Mechanisms of hearing loss and cell death in the cochlea of connexin mutant mice.

Hongen Xu, Wenxue Tang, Yulin Zhao, 2020, American journal of physiology. Cell physiology.

COVID-19 Resulting in Potential Hearing Damage of Rodents

Yongjun Guo, Jianbo Liu, Yaohe Wang, 2022, Chinese medicine and natural products.

Case report: Clinical and genetic analysis of a family with nonsyndromic auditory neuropathy

Lan Jiang, Hongen Xu, Danhua Liu, 2022, Frontiers in Pediatrics.

Defining the Sensitivity Landscape of EGFR Variants to Tyrosine Kinase Inhibitors.

Kongming Wu, Chenguang Niu, Xiaodong Li, 2022, Translational research : the journal of laboratory and clinical medicine.

A novel missense mutation in SMPX causes a rare form of X-linked postlingual sensorineural hearing loss in a Chinese family

Hongen Xu, Jie Bai, G. Guan, 2021, Translational pediatrics.

Increased diagnostic yield in a cohort of hearing loss families using a comprehensive stepwise strategy of molecular testing

Hongen Xu, Wenxue Tang, Yanan Yu, 2022, Frontiers in Genetics.

Identification and Validation of Ikaros (IKZF1) as a Cancer Driver Gene for Marek’s Disease Virus-Induced Lymphomas

Hans H. Cheng, D. Frishman, W. Muir, 2022, Microorganisms.

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

Hongen Xu, Wenxue Tang, Xiaohu Li, 2021, Frontiers in Genetics.

FishTEDB: a collective database of transposable elements identified in the complete genomes of fish

Feng Shao, Jianrong Wang, Hongen Xu, 2018, Database J. Biol. Databases Curation.

De ﬁ ning the sensitivity landscape of EGFR variants to tyrosine kinase inhibitors

Shuqing Chen, Chenguang Niu, Hongen Xu, 2022 .

Defining the Sensitivity Landscape of 74,389 EGFR Variants to Tyrosine Kinase Inhibitors

Shuqing Chen, Xiaodong Li, Chenguang Niu, 2021, bioRxiv.

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease

D. Frishman, Hongen Xu, Jiancheng Guo, 2021, npj Genomic Medicine.

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease

D. Frishman, Hongen Xu, Jiancheng Guo, 2021, NPJ genomic medicine.

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients

W. Lu, Hongen Xu, Wenxue Tang, 2020, Molecular genetics & genomic medicine.

Auditory Neuropathy Spectrum Disorder (ANSD)—Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families

W. Lu, Hongen Xu, Wenxue Tang, 2020, BioMed research international.

Maternal placenta modulates a deleterious fetal mutation†

D. Frishman, A. Schnieke, A. Kind, 2017, Biology of Reproduction.

Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome

Shuping Sun, Hongen Xu, Wenxue Tang, 2021, Frontiers in Genetics.

Identification of key genes in osteosarcoma by meta-analysis of gene expression microarray

Chi Zhang, Hongen Xu, Jianxiang Shi, 2019, Molecular medicine reports.

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

Hongen Xu, Wenxue Tang, Chang Yu, 2021, BioMed research international.

Case Report: A Case Report of a Histological Transformation of ALK-Rearranged Adenocarcinoma With High Expression of PD-L1 to Squamous Cell Carcinoma After Treatment With Alectinib

Jingli Ren, Hongen Xu, Yan Zhang, 2021, Pathology & Oncology Research.

Porcine familial adenomatous polyposis model enables systematic analysis of early events in adenoma progression

D. Frishman, D. Saur, A. Schnieke, 2017, Scientific Reports.

Perrault syndrome: Clinical report and retrospective analysis

W. Lu, Hongen Xu, Wenxue Tang, 2020, Molecular genetics & genomic medicine.

Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants

D. Frishman, Hongen Xu, Wenxue Tang, 2023, Biology.

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene

Hongen Xu, Wenxue Tang, Xiaohu Li, 2021, Molecular genetics & genomic medicine.

Genetic Epidemiology of Medication Safety and Efficacy Related Variants in the Central Han Chinese Population With Whole Genome Sequencing

Hongen Xu, Jiancheng Guo, Jianxiang Shi, 2022, Frontiers in Pharmacology.

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans

Jianbo Liu, Yaohe Wang, Hongen Xu, 2021, Scientific reports.

Dynamics of binding ability prediction between spike protein and human ACE2 reveals the adaptive strategy of SARS-CoV-2 in humans

Jianbo Liu, Yaohe Wang, Hongen Xu, 2020, Scientific Reports.

SARS-CoV-2 infecting the inner ear results in potential hearing damage at the early stage or prognosis of COVID-19 in rodents

Jianbo Liu, Yaohe Wang, Hongen Xu, 2020, bioRxiv.

Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria

Hongen Xu, Danhua Liu, Yongan Tian, 2023, BMC medical genomics.

Multiple Distinctive Demyelinating Lesions Caused by Eosinophilic Granulomatosis With Polyangiitis: Case Report and Literature Review

Hongen Xu, F. Wang, Fuyou Guo, 2019, Front. Neurol..

Differentially methylated region in bovine MIMT1 detected by small-scale whole-genome methylation sequencing

K. Flisikowski, Hongen Xu, K. Rutkowska, 2019, Journal of Applied Genetics.