Da-yong Wang

D. Bing, L. Lan, Z. Yin, 2019, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

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.

Family trio-based sequencing in 404 sporadic bilateral hearing loss patients discovers recessive and De novo genetic variants in multiple ways.

L. Lan, J. Guan, Qiuju Wang, 2021, European journal of medical genetics.

High Frequency of AIFM1 Variants and Phenotype Progression of Auditory Neuropathy in a Chinese Population

D. Bing, L. Lan, J. Guan, 2020, Neural plasticity.

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family

L. Lan, J. Guan, B. Han, 2017, Chinese medical journal.

[Cinical and genetic characteristics of familial Meniere's disease: three families report].

L. Lan, J. Guan, Lan Yu, 2015, Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery.

Comparison between Bilateral and Unilateral Sudden Sensorineural Hearing Loss

D. Bing, L. Lan, Z. Yin, 2018, Chinese medical journal.

Phenotype prediction of Mohr-Tranebjaerg syndrome (MTS) by genetic analysis and initial auditory neuropathy

L. Lan, J. Guan, Qiuju Wang, 2019, BMC Medical Genetics.

Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss

L. Lan, J. Guan, Qiuju Wang, 2020, Molecular genetics & genomic medicine.

A novel variant in diaphanous homolog 1 (DIAPH1) as the cause of auditory neuropathy in a Chinese family.

L. Lan, J. Guan, Mengqian Zhang, 2020, International journal of pediatric otorhinolaryngology.

A novel de novo mutation of ACTG1 in two sporadic non-syndromic hearing loss cases

L. Lan, J. Guan, Lan Yu, 2018, Science China Life Sciences.

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.

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China

L. Lan, Qiuju Wang, Q. Zheng, 2011, Acta oto-laryngologica.

[Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].

L. Lan, Qiuju Wang, Yu-bin Ji, 2009, Zhonghua yi xue za zhi.

Identification of four TMC1 variations in different Chinese families with hereditary hearing loss

L. Lan, J. Guan, Qiuju Wang, 2018, Molecular genetics & genomic medicine.

A Novel DFNA36 Mutation in TMC1 Orthologous to the Beethoven (Bth) Mouse Associated with Autosomal Dominant Hearing Loss in a Chinese Family

Ling Yang, Xin Jin, L. Lan, 2014, PloS one.

Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of China.

Qiuju Wang, Yan-Li Wang, Yu-bin Ji, 2010, Genetic testing and molecular biomarkers.

[The curative effect analysis of combined medical therapy for auditory neuropathy spectrum disorder].

L. Lan, Lan Yu, Qiuju Wang, 2014, Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery.

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.

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China

Huanming Yang, Jian Wang, Zhiyu Peng, 2018, Genetics in Medicine.

Clinical characteristics of patients with unilateral auditory neuropathy.

L. Lan, J. Guan, Lan Yu, 2021, American journal of otolaryngology.

Predicting the hearing outcome in sudden sensorineural hearing loss via machine learning models

D. Bing, J. Ying, J. Miao, 2018, Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery.