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Yaping Yang

Showing results (271-280 of 410) with videos related to

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Human Mutation|August 30, 2008
Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridizationDaniela del Gaudio, Yaping Yang, Barbara A Boggs, et al.
The Oncologist|June 2, 2020
Prognostic Value of Modified IHC4 Score in Patients with Estrogen Receptor-Positive Metastatic Breast CancerLiang Jin, Kai Chen, Cui Tan, et al.
BMJ (Clinical Research Ed.)|September 11, 2025
Effect of methylcobalamin on capecitabine induced hand-foot syndrome in patients with HER2 negative early breast cancer: multicentre, double blind, randomised, placebo controlled, phase 3 trialYuan Xia, Yingying Zhu, Li Ling, et al.
Nano Letters|October 31, 2019
Stacking Order in Graphite Films Controlled by van der Waals TechnologyYaping Yang, Yi-Chao Zou, Colin R Woods, et al.
Neurology. Genetics|November 11, 2016
FHF1 (FGF12) epileptic encephalopathySameer Al-Mehmadi, Miranda Splitt, , et al.
Investigative Ophthalmology & Visual Science|November 26, 2009
Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese populationYaping Yang, Xin Zhang, Li Jia Chen, et al.
Nature Genetics|October 1, 2013
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autismChristian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophyLinyan Meng, Taraka Donti, Fan Xia, et al.
Circulation. Arrhythmia and Electrophysiology|April 14, 2017
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test ReferralsAndrew P Landstrom, Andrew L Dailey-Schwartz, Jill A Rosenfeld, et al.
Genome Medicine|February 4, 2016
A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnosticsRegis A James, Ian M Campbell, Edward S Chen, et al.
Pageof 41

Showing results (271-280 of 410) with videos related to

Sort By:
Pageof 41
Human Mutation|August 30, 2008
Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridizationDaniela del Gaudio, Yaping Yang, Barbara A Boggs, et al.
The Oncologist|June 2, 2020
Prognostic Value of Modified IHC4 Score in Patients with Estrogen Receptor-Positive Metastatic Breast CancerLiang Jin, Kai Chen, Cui Tan, et al.
BMJ (Clinical Research Ed.)|September 11, 2025
Effect of methylcobalamin on capecitabine induced hand-foot syndrome in patients with HER2 negative early breast cancer: multicentre, double blind, randomised, placebo controlled, phase 3 trialYuan Xia, Yingying Zhu, Li Ling, et al.
Nano Letters|October 31, 2019
Stacking Order in Graphite Films Controlled by van der Waals TechnologyYaping Yang, Yi-Chao Zou, Colin R Woods, et al.
Neurology. Genetics|November 11, 2016
FHF1 (FGF12) epileptic encephalopathySameer Al-Mehmadi, Miranda Splitt, , et al.
Investigative Ophthalmology & Visual Science|November 26, 2009
Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese populationYaping Yang, Xin Zhang, Li Jia Chen, et al.
Nature Genetics|October 1, 2013
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autismChristian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, et al.
American Journal of Medical Genetics. Part A|November 19, 2016
Homozygous variants in pyrroline-5-carboxylate reductase 2 (PYCR2) in patients with progressive microcephaly and hypomyelinating leukodystrophyLinyan Meng, Taraka Donti, Fan Xia, et al.
Circulation. Arrhythmia and Electrophysiology|April 14, 2017
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test ReferralsAndrew P Landstrom, Andrew L Dailey-Schwartz, Jill A Rosenfeld, et al.
Genome Medicine|February 4, 2016
A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnosticsRegis A James, Ian M Campbell, Edward S Chen, et al.
Pageof 41