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Jiale Xiang

Showing results (1-10 of 32) with videos related to

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Clinics in Laboratory Medicine|November 11, 2022
Applications of Noninvasive Prenatal Testing for Subchromosomal Copy Number Variations Using Cell-Free DNAJiale Xiang, Zhiyu Peng
Human Mutation|May 23, 2020
AutoPVS1: An automatic classification tool for PVS1 interpretation of null variantsJiale Xiang, Jiguang Peng, Samantha Baxter, et al.
Advanced Materials (Deerfield Beach, Fla.)|July 15, 2023
Robust and Sustainable Indium Anode Leading to Efficient and Stable Organic Solar CellsJiale Xiang, Zhi-Xi Liu, Hongzheng Chen, et al.
Foods (Basel, Switzerland)|December 30, 2025
Beluga Optimization Algorithm for Near-Infrared Spectral Variable Selection of Complex SamplesJavaria Kousar, Liping Yang, Jiale Xiang, et al.
Journal of Clinical Medicine|September 23, 2022
Analysis of the Results of Cytomegalovirus Testing Combined with Genetic Testing in Children with Congenital Hearing LossYuan Jin, Xiaozhou Liu, Sen Chen, et al.
BMC Medical Genomics|February 28, 2021
A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newbornsHaiyan Yang, Hongyu Luo, Guiwei Zhang, et al.
Human Genetics|September 1, 2022
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing lossJiale Xiang, Xiangzhong Sun, Nana Song, et al.
Frontiers in Genetics|May 16, 2022
Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in NewbornsJiale Xiang, Hongfu Zhang, Xiangzhong Sun, et al.
Scientific Reports|July 10, 2020
Author Correction: Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgradesJiale Xiang, Jiyun Yang, Lisha Chen, et al.
Scientific Reports|January 17, 2020
Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgradesJiale Xiang, Jiyun Yang, Lisha Chen, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Clinics in Laboratory Medicine|November 11, 2022
Applications of Noninvasive Prenatal Testing for Subchromosomal Copy Number Variations Using Cell-Free DNAJiale Xiang, Zhiyu Peng
Human Mutation|May 23, 2020
AutoPVS1: An automatic classification tool for PVS1 interpretation of null variantsJiale Xiang, Jiguang Peng, Samantha Baxter, et al.
Advanced Materials (Deerfield Beach, Fla.)|July 15, 2023
Robust and Sustainable Indium Anode Leading to Efficient and Stable Organic Solar CellsJiale Xiang, Zhi-Xi Liu, Hongzheng Chen, et al.
Foods (Basel, Switzerland)|December 30, 2025
Beluga Optimization Algorithm for Near-Infrared Spectral Variable Selection of Complex SamplesJavaria Kousar, Liping Yang, Jiale Xiang, et al.
Journal of Clinical Medicine|September 23, 2022
Analysis of the Results of Cytomegalovirus Testing Combined with Genetic Testing in Children with Congenital Hearing LossYuan Jin, Xiaozhou Liu, Sen Chen, et al.
BMC Medical Genomics|February 28, 2021
A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newbornsHaiyan Yang, Hongyu Luo, Guiwei Zhang, et al.
Human Genetics|September 1, 2022
Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing lossJiale Xiang, Xiangzhong Sun, Nana Song, et al.
Frontiers in Genetics|May 16, 2022
Utility of Whole Genome Sequencing for Population Screening of Deafness-Related Genetic Variants and Cytomegalovirus Infection in NewbornsJiale Xiang, Hongfu Zhang, Xiangzhong Sun, et al.
Scientific Reports|July 10, 2020
Author Correction: Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgradesJiale Xiang, Jiyun Yang, Lisha Chen, et al.
Scientific Reports|January 17, 2020
Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgradesJiale Xiang, Jiyun Yang, Lisha Chen, et al.
Pageof 4