S. Qiu

Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms

Xue Gao, Yongyi Yuan, Shasha Huang, 2020, Journal of Medical Genetics.

Syndromic Deafness Gene ATP6V1B2 Controls Degeneration of Spiral Ganglion Neurons Through Modulating Proton Flux

Dapeng Li, Xue Gao, Yongyi Yuan, 2021, Frontiers in Cell and Developmental Biology.

Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

L. Guan, Xue Gao, Guo-jian Wang, 2018, Journal of Medical Genetics.

Transcriptome analysis of the early stage ifnlr1-mutant zebrafish indicates the immune response to auditory dysfunction.

Xue Gao, Guo-jian Wang, Yongyi Yuan, 2021, Gene expression patterns : GEP.

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

Xue Gao, Yongyi Yuan, D. Kang, 2019, EBioMedicine.

Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2.

Xue Gao, Yongyi Yuan, Shasha Huang, 2020, Stem cell research.