Educational applications of artificial intelligence in simulation-based learning: A systematic mapping review by Chih-Pu Dai, Fengfeng Ke

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Fast Depth Map Coding Based on Bayesian Decision Theorem for 3D-HEVC by Dongyao Zou, Pu Dai, Qiuwen Zhang

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Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene by Yi-Ming Zhu, Yi-Ming Zhu, Qi Li, Xue Gao, Yan-Fei Li, You-Li Liu, Pu Dai, Pu Dai, Xiang-Ping Li

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The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals. by Shasha Huang, Bangqing Huang, Guojian Wang, Yongyi Yuan, Pu Dai

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Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation by Ping Gu, Guojian Wang, Xue Gao, Dongyang Kang, Pu Dai, Shasha Huang

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Variant analysis of 92 Chinese Han families with hearing loss by Xiaohua Jin, Shasha Huang, Lisha An, Chuan Zhang, Pu Dai, Huafang Gao, Xu Ma

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Outcomes of cochlear implantation in 75 patients with auditory neuropathy by Jie Wu, Jiyue Chen, Zhiwei Ding, Jialin Fan, Qiuquan Wang, Pu Dai, Dongyi Han

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Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients by Ying Fu, Shasha Huang, Xue Gao, Mingyu Han, Guojian Wang, Dongyang Kang, Yongyi Yuan, Pu Dai

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Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene by Xue Gao, Shi–Wei Qiu, Wei-Qian Wang, Dong-Yang Kang, Ning Su, Pu Dai, Yong–Yi Yuan

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Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II. by Shuzhi Yang, Pu Dai, Xin Liu, Dongyang Kang, Xin Zhang, Weiyan Yang, Chengyong Zhou, Shiming Yang, Huijun Yuan

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Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families by Dejun Zhang, Jie Wu, Yongyi Yuan, Xiaohong Li, Xue Gao, Dongyang Kang, Xin Zhang, Sha-sha Huang, Pu Dai

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Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China. by Yi Jiang, Shasha Huang, Tao Deng, Lihua Wu, Juan Chen, Dongyang Kang, Xiufeng Xu, Ruiyu Li, Dongyi Han, Pu Dai

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A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityResearch in context by Weihao Zhao, Xue Gao, Shiwei Qiu, Bo Gao, Song Gao, Xin Zhang, Dongyang Kang, Weiju Han, Pu Dai, Yongyi Yuan

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Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China. by Yongyi Yuan, Weiwei Guo, Jie Tang, Guozheng Zhang, Guojian Wang, Mingyu Han, Xun Zhang, Shiming Yang, David Z Z He, Pu Dai

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Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment. by Zhengyue Li, Yilian Guo, Yu Lu, Jianzhong Li, Zhanguo Jin, Hongbo Li, Yanping Lu, Pu Dai, Dongyi Han, Jing Cheng, Huijun Yuan

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Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10 by Xiaohong Li, Xue Gao, Shasha Huang, Mingyu Han, Dongyang Kang, Jinyuan Yang, Xiedong Wu, Qiuchen Zheng, Yongyi Yuan, Pu Dai, Guojian Wang

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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 ATP6V1... by Xue Gao, Shi–Wei Qiu, Meng-Long Feng, Sha-Sha Huang, Dong-Yang Kang, Ming-Yu Han, Pu Dai, Yong–Yi Yuan

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Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population by Haifeng Feng, Shasha Huang, Ying Ma, Jinyuan Yang, Yijin Chen, Guojian Wang, Mingyu Han, Dongyang Kang, Xin Zhang, Pu Dai, Yongyi Yuan

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Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment. by Yongyi Yuan, Xun Zhang, Shasha Huang, Lujie Zuo, Guozheng Zhang, Yueshuai Song, Guojian Wang, Hongtian Wang, Deliang Huang, Dongyi Han, Pu Dai

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Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families by Yu Su, Xue Gao, Sha-Sha Huang, Jing-Ning Mao, Bang-Qing Huang, Jian-Dong Zhao, Dong-Yang Kang, Xin Zhang, Pu Dai

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