Xue Gao

ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 9

Top Venues

BioMed research international

Neural plasticity

Molecular genetics & genomic medicine

Journal of medical genetics

Fourth Military Medical University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Fourth Military Medical University Aug 01 2005 - Jul 01 2008

China

PHD

The Fourth Military Medical University Aug 01 1997 - Jul 01 2002

China

BSC

Publications

Kun Yang, Xi Wang, Wei-Qian Wang, Ming-Yu Han, Li-Min Hu, Dong-Yang Kang, Jin-Yuan Yang, Min Liu, Xue Gao, Yong-Yi Yuan, Jin-Cao Xu
A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3-4. Molecular genetics & genomic medicine (2022)
Jie Wu, Zongfu Cao, Yu Su, Yang Wang, Ruikun Cai, Jiyue Chen, Bo Gao, Mingyu Han, Xiaohong Li, DeJun Zhang, Xue Gao, Shasha Huang, Quanfei Huang, Yongyi Yuan, Xu Ma, Pu Dai
Molecular diagnose of a large hearing loss population from China by targeted genome sequencing. Journal of human genetics 67 (11) (2022)
Xue Gao, Pu Dai, Yong-Yi Yuan
Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes. Human genetics (2021)
Xue Gao, Sha-Sha Huang, Shi-Wei Qiu, Yu Su, Wei-Qian Wang, Hui-Yan Xu, Jin-Cao Xu, Dong-Yang Kang, Pu Dai, Yong-Yi Yuan
Congenital sensorineural hearing loss as the initial presentation of PTPN11-associated Noonan syndrome with multiple lentigines or Noonan syndrome: clinical features and underlying mechanisms. Journal of medical genetics 58 (7) (2020)
Chang Guo, Sha-Sha Huang, Yong-Yi Yuan, Ying Zhou, Ning Wang, Dong-Yang Kang, Su-Yan Yang, Xin Zhang, Xue Gao, Pu Dai
Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation. Neural plasticity 2020 (2020)
Shasha Huang, Xue Gao, Yufeng Wang, Dongyang Kang, Xin Zhang, Suyan Yang, Pu Dai
Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family. BioMed research international 2020 (2020)
Xue Gao, Jin-Cao Xu, Wei-Qian Wang, Yong-Yi Yuan, Dan Bai, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jia Li, Dong-Yang Kang, Mei-Guang Zhang, Xi Lin, Pu Dai
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family. BioMed research international 2018 (2018)
Xue Gao, Yong-Yi Yuan, Guo-Jian Wang, Jin-Cao Xu, Yu Su, Xi Lin, Pu Dai
Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment. BioMed research international 2017 (2017)
Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, Jin-Cao Xu, Ping Gu, Dan Bai, Dong-Yang Kang, Ming-Yu Han, Guo-Jian Wang, Mei-Guang Zhang, Jia Li, Pu Dai
Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population. Neural plasticity 2017 (2017)

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Publication Activity (10 Years)

Top Topics

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Xue Gao