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Fengxiao Bu

Showing results (11-20 of 34) with videos related to

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Frontiers in Genetics|January 28, 2025
Genetic variation in patent foramen ovale: a case-control genome-wide association studyBosi Dong, Yajiao Li, Fandi Ai, et al.
BMC Medical Genomics|August 9, 2024
Genotype-phenotype spectrum and correlation of PHARC Syndrome due to pathogenic ABHD12 variantsXicui Long, Wenyu Xiong, Xuegang Wang, et al.
Neuroendocrinology|October 12, 2023
Identifying Genetic Factors of Polycystic Ovary Syndrome in Women with Epilepsy: A Whole-Genome Sequencing StudyWanlin Lai, Yiming Wu, Leihao Sha, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 16, 2025
GDC: Integration of Multi-Omic and Phenotypic Resources to Unravel the Genetic Pathogenesis of Hearing LossHui Cheng, Xuegang Wang, Mingjun Zhong, et al.
Science Advances|April 3, 2026
Complex peopling history and expansion events inferred from large-scale modern and ancient Y chromosome sequencesGuanglin He, Zhiyong Wang, Yutong Jiang, et al.
Psychiatric Genetics|April 24, 2010
Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han populationXiaoping Li, Zhengmao Hu, Yiqun He, et al.
Molecular Genetics and Genomics : MGG|June 23, 2025
Enhanced identification of novel pathogenic variants in hereditary hearing loss through physical phasing with integrated short and long-read sequencing dataLu Kang, Qian Zhang, Chao Wang, et al.
Molecular Biology and Evolution|November 17, 2025
Human Population Genetic History and Evolutionary Dynamics on the Eastern Tibetan PlateauGuanglin He, Shuhan Duan, Gang Chen, et al.
Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.
Genome Medicine|December 19, 2023
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing lossSihan Liu, Mingjun Zhong, Yu Huang, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Frontiers in Genetics|January 28, 2025
Genetic variation in patent foramen ovale: a case-control genome-wide association studyBosi Dong, Yajiao Li, Fandi Ai, et al.
BMC Medical Genomics|August 9, 2024
Genotype-phenotype spectrum and correlation of PHARC Syndrome due to pathogenic ABHD12 variantsXicui Long, Wenyu Xiong, Xuegang Wang, et al.
Neuroendocrinology|October 12, 2023
Identifying Genetic Factors of Polycystic Ovary Syndrome in Women with Epilepsy: A Whole-Genome Sequencing StudyWanlin Lai, Yiming Wu, Leihao Sha, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 16, 2025
GDC: Integration of Multi-Omic and Phenotypic Resources to Unravel the Genetic Pathogenesis of Hearing LossHui Cheng, Xuegang Wang, Mingjun Zhong, et al.
Science Advances|April 3, 2026
Complex peopling history and expansion events inferred from large-scale modern and ancient Y chromosome sequencesGuanglin He, Zhiyong Wang, Yutong Jiang, et al.
Psychiatric Genetics|April 24, 2010
Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han populationXiaoping Li, Zhengmao Hu, Yiqun He, et al.
Molecular Genetics and Genomics : MGG|June 23, 2025
Enhanced identification of novel pathogenic variants in hereditary hearing loss through physical phasing with integrated short and long-read sequencing dataLu Kang, Qian Zhang, Chao Wang, et al.
Molecular Biology and Evolution|November 17, 2025
Human Population Genetic History and Evolutionary Dynamics on the Eastern Tibetan PlateauGuanglin He, Shuhan Duan, Gang Chen, et al.
Human Mutation|April 15, 2014
TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing lossHela Azaiez, Kevin T Booth, Fengxiao Bu, et al.
Genome Medicine|December 19, 2023
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing lossSihan Liu, Mingjun Zhong, Yu Huang, et al.
Pageof 4