W. Xiong

发表

Further evidence for “gain-of-function” mechanism of DFNA5 related hearing loss

L. Lan, J. Guan, Lan Yu, 2018, Scientific Reports.

A novel dominant GJB2 (DFNA3) mutation in a Chinese family

J. Guan, Lan Yu, Hong-yang Wang, 2017, Scientific Reports.

Understanding auditory neuropathy spectrum disorder: a systematic review in transgenic mouse models

L. Lan, J. Guan, Hong-yang Wang, 2016, Science China Life Sciences.

Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome

L. Lan, J. Guan, Lan Yu, 2017, Chinese medical journal.

Idiopathic Sudden Sensorineural Hearing Loss in Different Ages: Prognosis of Patients With Initial Total Hearing Loss

Dao-gong Zhang, Kunpeng Lu, Ying-jun Wang, 2022, Frontiers in Psychology.

Understanding auditory neuropathy spectrum disorder: a systematic review in transgenic mouse models

L. Lan, J. Guan, Qiuju Wang, 2016, Science China Life Sciences.

Novel recessive PDZD7 biallelic mutations in two Chinese families with non‐syndromic hearing loss

L. Lan, Z. Yin, J. Guan, 2017, American journal of medical genetics. Part A.

Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder

Suhua Chang, Jing Wang, L. Lan, 2015, Journal of Medical Genetics.

Phenotypic Heterogeneity of Post-lingual and/or Milder Hearing Loss for the Patients With the GJB2 c.235delC Homozygous Mutation

L. Lan, J. Guan, Lan Yu, 2021, Frontiers in Cell and Developmental Biology.

Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment

L. Lan, Z. Yin, B. Han, 2015, Science China Life Sciences.

[Prognostic factors of sudden sensorineural hearing loss in children].

L. Lan, Z. Yin, J. Guan, 2015, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

Targeted High-Throughput Sequencing Identifies Pathogenic Mutations in KCNQ4 in Two Large Chinese Families with Autosomal Dominant Hearing Loss

X. Yi, Ling Yang, L. Lan, 2014, PloS one.

Characteristics and prognostic analysis of simultaneous bilateral sudden sensorineural hearing loss

Kunpeng Lu, Mingming Wang, W. Xiong, 2023, Frontiers in Neurology.

Reproductive management through integration of PGD and MPS-based noninvasive prenatal screening/diagnosis for a family with GJB2-associated hearing impairment

L. Lan, Z. Yin, B. Han, 2015, Science China Life Sciences.