B. Zuo

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.

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

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

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.

Perrault syndrome: Clinical report and retrospective analysis

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

Long non-coding RNA Rian promotes the expression of tight junction proteins in endothelial cells by regulating perivascular-resident macrophage-like melanocytes and PEDF secretion

Jinhui Zhang, Lingling Neng, Bei Chen, 2021, Human Cell.