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Yaping Yang

Showing results (291-300 of 410) with videos related to

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International Journal of Surgery (London, England)|February 13, 2024
Deep learning combining mammography and ultrasound images to predict the malignancy of BI-RADS US 4A lesions in women with dense breasts: a diagnostic studyYaping Yang, Ying Zhong, Junwei Li, et al.
Genome Medicine|June 29, 2013
Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathyJames R Lupski, Claudia Gonzaga-Jauregui, Yaping Yang, et al.
Med (New York, N.Y.)|December 28, 2024
Targeting autophagy plus high-dose CDK4/6 inhibitors in advanced HR+HER2- breast cancer: A phase 1b/2 trialChang Gong, Qun Lin, Tao Qin, et al.
Pediatric Blood & Cancer|October 18, 2016
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemiaSamara L Potter, Rajkumar Venkatramani, Scott Wenderfer, et al.
Annals of Translational Medicine|December 14, 2020
Development and validation of a nomogram in survival prediction among advanced breast cancer patientsJianli Zhao, Yaping Yang, Danmei Pang, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
American Journal of Medical Genetics. Part A|December 29, 2019
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONOMaham Sewani, Kimberly Nugent, Patrick R Blackburn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 28, 2013
A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health recordPeter Tarczy-Hornoch, Laura Amendola, Samuel J Aronson, et al.
Genome Medicine|September 30, 2022
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traitsBo Yuan, Katharina V Schulze, Nurit Assia Batzir, et al.
Molecular Genetics & Genomic Medicine|October 1, 2019
Characterization of the renal phenotype in RMND1-related mitochondrial diseaseBrian J Shayota, Nhon T Le, Nasim Bekheirnia, et al.
Pageof 41

Showing results (291-300 of 410) with videos related to

Sort By:
Pageof 41
International Journal of Surgery (London, England)|February 13, 2024
Deep learning combining mammography and ultrasound images to predict the malignancy of BI-RADS US 4A lesions in women with dense breasts: a diagnostic studyYaping Yang, Ying Zhong, Junwei Li, et al.
Genome Medicine|June 29, 2013
Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathyJames R Lupski, Claudia Gonzaga-Jauregui, Yaping Yang, et al.
Med (New York, N.Y.)|December 28, 2024
Targeting autophagy plus high-dose CDK4/6 inhibitors in advanced HR+HER2- breast cancer: A phase 1b/2 trialChang Gong, Qun Lin, Tao Qin, et al.
Pediatric Blood & Cancer|October 18, 2016
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemiaSamara L Potter, Rajkumar Venkatramani, Scott Wenderfer, et al.
Annals of Translational Medicine|December 14, 2020
Development and validation of a nomogram in survival prediction among advanced breast cancer patientsJianli Zhao, Yaping Yang, Danmei Pang, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
American Journal of Medical Genetics. Part A|December 29, 2019
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONOMaham Sewani, Kimberly Nugent, Patrick R Blackburn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 28, 2013
A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health recordPeter Tarczy-Hornoch, Laura Amendola, Samuel J Aronson, et al.
Genome Medicine|September 30, 2022
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traitsBo Yuan, Katharina V Schulze, Nurit Assia Batzir, et al.
Molecular Genetics & Genomic Medicine|October 1, 2019
Characterization of the renal phenotype in RMND1-related mitochondrial diseaseBrian J Shayota, Nhon T Le, Nasim Bekheirnia, et al.
Pageof 41