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Miaoxin Li

Showing results (31-40 of 71) with videos related to

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Plos Genetics|February 25, 2021
Hippocampal transcriptome-wide association study and neurobiological pathway analysis for Alzheimer's diseaseNana Liu, Jiayuan Xu, Huaigui Liu, et al.
Human Mutation|February 14, 2015
wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited DisordersMulin Jun Li, Jiaen Deng, Panwen Wang, et al.
Cellular and Molecular Life Sciences : CMLS|December 20, 2016
Dynamic landscape of alternative polyadenylation during retinal developmentWenyan Hu, Shengguo Li, Ji Yeon Park, et al.
Molecular Psychiatry|December 12, 2023
Correction: Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analysesYunqi Huang, Dongru Chen, Albert M Levin, et al.
Molecular Psychiatry|June 20, 2023
Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analysesYunqi Huang, Dongru Chen, Albert M Levin, et al.
Translational Neurodegeneration|October 20, 2017
The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a reviewShirley Yin-Yu Pang, Kay-Cheong Teo, Jacob Shujui Hsu, et al.
BMC Genomics|May 1, 2025
Ge-SAND: an explainable deep learning-driven framework for disease risk prediction by uncovering complex genetic interactions in parallelLihang Ye, Liubin Zhang, Bin Tang, et al.
Nature Communications|February 28, 2023
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary dataZipeng Liu, Yiming Qin, Tian Wu, et al.
Plos One|August 15, 2014
PMCA4 (ATP2B4) mutation in familial spastic paraplegiaMiaoxin Li, Philip Wing-Lok Ho, Shirley Yin-Yu Pang, et al.
Brain and Behavior|March 24, 2015
PMCA4 (ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusionPhilip Wing-Lok Ho, Shirley Yin-Yu Pang, Miaoxin Li, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Plos Genetics|February 25, 2021
Hippocampal transcriptome-wide association study and neurobiological pathway analysis for Alzheimer's diseaseNana Liu, Jiayuan Xu, Huaigui Liu, et al.
Human Mutation|February 14, 2015
wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited DisordersMulin Jun Li, Jiaen Deng, Panwen Wang, et al.
Cellular and Molecular Life Sciences : CMLS|December 20, 2016
Dynamic landscape of alternative polyadenylation during retinal developmentWenyan Hu, Shengguo Li, Ji Yeon Park, et al.
Molecular Psychiatry|December 12, 2023
Correction: Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analysesYunqi Huang, Dongru Chen, Albert M Levin, et al.
Molecular Psychiatry|June 20, 2023
Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analysesYunqi Huang, Dongru Chen, Albert M Levin, et al.
Translational Neurodegeneration|October 20, 2017
The role of gene variants in the pathogenesis of neurodegenerative disorders as revealed by next generation sequencing studies: a reviewShirley Yin-Yu Pang, Kay-Cheong Teo, Jacob Shujui Hsu, et al.
BMC Genomics|May 1, 2025
Ge-SAND: an explainable deep learning-driven framework for disease risk prediction by uncovering complex genetic interactions in parallelLihang Ye, Liubin Zhang, Bin Tang, et al.
Nature Communications|February 28, 2023
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary dataZipeng Liu, Yiming Qin, Tian Wu, et al.
Plos One|August 15, 2014
PMCA4 (ATP2B4) mutation in familial spastic paraplegiaMiaoxin Li, Philip Wing-Lok Ho, Shirley Yin-Yu Pang, et al.
Brain and Behavior|March 24, 2015
PMCA4 (ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusionPhilip Wing-Lok Ho, Shirley Yin-Yu Pang, Miaoxin Li, et al.
Pageof 8