Anhai Chen - Publications

A Novel EYA1 Splicing Mutation in a Chinese Family With Branchio-Oto Syndrome: A Functional Analysis and Reproductive Intervention.

Journal: Clinical and experimental otorhinolaryngology

Published: October 14, 2024

The Distribution and Therapeutic Effectiveness of Clinical Unilateral Ménière's Disease Phenotypes.

Journal: Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery

Published: August 23, 2024

ABCC1 deficiency potentiated noise-induced hearing loss in mice by impairing cochlear antioxidant capacity.

Journal: Redox biology

Published: March 07, 2024

Construction and validation of a folate metabolism-related gene signature for predicting prognosis in HNSCC.

Journal: Journal of cancer research and clinical oncology

Published: January 30, 2024

A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application.

Journal: Clinical and experimental otorhinolaryngology

Published: May 12, 2023

Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss.

Journal: PloS one

Published: November 14, 2022

Genetic research progress in branchio-oto syndrome/ branchio-oto-renal syndrome.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Published: May 11, 2022

Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysis.

Journal: Clinical genetics

Published: December 13, 2020

Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.

Journal: Human molecular genetics

Published: May 30, 2019