Zoekresultaten - Yiping Shen
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Evaluation of copy number variant detection from panel‐based next‐generation sequencing data door Ruen Yao, Tingting Yu, Yanrong Qing, Jian Wang, Yiping Shen
Gepubliceerd in 2018Artigo -
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Genome-wide detection of natural selection in African Americans pre- and post-admixture door Wenfei Jin, Shuhua Xu, Haifeng Wang, Yongguo Yu, Yiping Shen, Bai-Lin Wu, Jin Li
Gepubliceerd in 2011Artigo -
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Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data door Ruen Yao, Cheng Zhang, Tingting Yu, Niu Li, Xuyun Hu, Xiumin Wang, Jian Wang, Yiping Shen
Gepubliceerd in 2017Artigo -
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Whole Exome Sequencing to Identify Genetic Causes of Short Stature door Michael H. Guo, Yiping Shen, Emily C. Walvoord, Timothy C. Miller, Jennifer Moon, Joel N. Hirschhorn, Andrew Dauber
Gepubliceerd in 2014Artigo -
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Angiogenin loss‐of‐function mutations in amyotrophic lateral sclerosis door David M. Wu, Wenhao Yu, Hiroko Kishikawa, Rebecca D. Folkerth, A. John Iafrate, Yiping Shen, Winnie Xin, Katherine B. Sims, Guo‐fu Hu
Gepubliceerd in 2007Artigo -
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Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders door Lam Son Nguyen, Hyung‐Goo Kim, Jill A. Rosenfeld, Yiping Shen, James F. Gusella, Yves Lacassie, Lawrence C. Layman, Lisa G. Shaffer, Jozef Gécz
Gepubliceerd in 2013Artigo -
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Flap endonuclease 1 Facilitated Hepatocellular Carcinoma Progression by Enhancing USP7/MDM2-mediated P53 Inactivation door Saiyan Bian, Wenkai Ni, Mengqi Zhu, Xue Zhang, Yuwei Qiang, Jianping Zhang, Zhiyu Ni, Yiping Shen, Shi Qiu, Qianqian Song, Mingbing Xiao, Wenjie Zheng
Gepubliceerd in 2022Artigo -
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Applications of cerebrospinal fluid circulating tumor DNA in the diagnosis of gliomas door Zhenyu Zhao, Cheng Zhang, Mi Li, Yiping Shen, Shiyu Feng, Jialin Liu, Fangye Li, Lei Hou, Zhong Chen, Jingjing Jiang, Xiaodong Ma, Ling Chen, Xinguang Yu
Gepubliceerd in 2019Artigo -
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Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families door Lacey Williams, Durkadın Demir Ekşi, Yiping Shen, Amy C. Lossie, Lynn P. Chorich, Megan Sullivan, John A. Phillips, Münire Erman, Hyung‐Goo Kim, Özgül M. Alper, Lawrence C. Layman
Gepubliceerd in 2017Artigo -
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Proband-only medical exome sequencing as a cost-effective first-tier genetic diagnostic test for patients without prior molecular tests and clinical diagnosis in a developing count... door Xuyun Hu, Niu Li, Yufei Xu, Guoqiang Li, Tingting Yu, Ruen Yao, Lijun Fu, Jiwen Wang, Lei Yin, Yong Yin, Ying Wang, Xingming Jin, Xiumin Wang, Jian Wang, Yiping Shen
Gepubliceerd in 2017Artigo -
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Genome analysis and knowledge-driven variant interpretation with TGex door Dvir Dahary, Yaron Golan, Yaron Mazor, Ofer Zelig, Ruth Barshir, Michal Twik, Tsippi Iny Stein, Guy Rosner, Revital Kariv, Fei Chen, Qiang Zhang, Yiping Shen, Marilyn Safran, Doron Lancet, Simon Fishilevich
Gepubliceerd in 2019Artigo
Zoekinstrumenten:
Gerelateerde Onderwerpen
Biology
Genetics
Gene
Medicine
Genome
Internal medicine
Copy-number variation
Phenotype
Computational biology
Gene expression
Psychiatry
Mutation
Autism
Psychology
Cancer research
Endocrinology
Pathology
Autism spectrum disorder
Bioinformatics
Chromosome
Gene duplication
Cancer
Exome sequencing
Genotype
Intellectual disability
Neuroscience
Proband
Biochemistry
Breakpoint
Cell biology