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Frontiers in Genetics|September 8, 2022
Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in ChinaKeya Tong, Wenbin He, Yao He, et al.
Gene|February 23, 2020
Profiling of mitochondrial genomes in SCA3/MJD patients from mainland ChinaHongyu Yuan, Huihua Yang, Linliu Peng, et al.
The Journal of Molecular Diagnostics : JMD|March 6, 2016
Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation SequencingLan Qin, Jing Wang, Xia Tian, et al.
Eye and Vision (London, England)|April 1, 2025
Randomized controlled trial on corneal denervation, neuroinflammation and ocular surface in corneal lenticule extraction for advanced refractive correction (CLEAR) and small incision lenticule extraction (SMILE)Mingyi Yu, Chang Liu, Isabelle Xin Yu Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 6, 2020
Correction: Interpretation of mitochondrial tRNA variantsLee-Jun C Wong, Ting Chen, Jing Wang, et al.
Frontiers in Genetics|August 8, 2022
Discovery of Novel Variants on the CHD7 Gene: A Case Series of CHARGE SyndromeXiangtao Wu, Liang Chen, Weihong Lu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 10, 2020
Correction: Interpretation of mitochondrial tRNA variantsLee-Jun C Wong, Ting Chen, Jing Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2020
Interpretation of mitochondrial tRNA variantsLee-Jun C Wong, Ting Chen, Jing Wang, et al.
The Journal of Molecular Diagnostics : JMD|June 7, 2025
A Comparative Study of Medium-Coverage Genome Sequencing and SNP Array Technology in Identifying Chromosomal Abnormalities to Advance Prenatal and Postnatal DiagnosisJialun Pang, Lin Zhou, Jiancheng Hu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2015
Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation typesJing Wang, Hui Yu, Victor Wei Zhang, et al.
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