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Miaoxin Li

Showing results (61-70 of 71) with videos related to

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Nucleic Acids Research|December 21, 2021
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseasesLin Jiang, Hui Jiang, Sheng Dai, et al.
Cell Genomics|August 29, 2025
Endogenous fine-mapping and prioritization of functional regulatory elements in complex genetic lociKe Zhao, Yao Zhou, Xueqi Wang, et al.
Hepatology (Baltimore, Md.)|November 25, 2014
The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis BLiang Peng, Qiang Zhao, Qibin Li, et al.
Genome Biology|October 31, 2023
Landscape of enhancer disruption and functional screen in melanoma cellsZhao Wang, Menghan Luo, Qian Liang, et al.
Nature Communications|November 6, 2023
LensAge index as a deep learning-based biological age for self-monitoring the risks of age-related diseases and mortalityRuiyang Li, Wenben Chen, Mingyuan Li, et al.
Human Molecular Genetics|November 28, 2017
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloacaJacob S J Hsu, Manting So, Clara S M Tang, et al.
Schizophrenia Bulletin|September 18, 2013
Common variants on Xq28 conferring risk of schizophrenia in Han ChineseEmily H M Wong, Hon-Cheong So, Miaoxin Li, et al.
Neurobiology of Aging|April 17, 2018
A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese populationBinbin Wang, Suying Bao, Zhigang Zhang, et al.
Hepatology (Baltimore, Md.)|May 22, 2012
Rare inborn errors associated with chronic hepatitis B virus infectionQiang Zhao, Liang Peng, Weijun Huang, et al.
Schizophrenia Bulletin|May 27, 2014
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations, Jim van Os, Bart P Rutten, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|December 21, 2021
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseasesLin Jiang, Hui Jiang, Sheng Dai, et al.
Cell Genomics|August 29, 2025
Endogenous fine-mapping and prioritization of functional regulatory elements in complex genetic lociKe Zhao, Yao Zhou, Xueqi Wang, et al.
Hepatology (Baltimore, Md.)|November 25, 2014
The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis BLiang Peng, Qiang Zhao, Qibin Li, et al.
Genome Biology|October 31, 2023
Landscape of enhancer disruption and functional screen in melanoma cellsZhao Wang, Menghan Luo, Qian Liang, et al.
Nature Communications|November 6, 2023
LensAge index as a deep learning-based biological age for self-monitoring the risks of age-related diseases and mortalityRuiyang Li, Wenben Chen, Mingyuan Li, et al.
Human Molecular Genetics|November 28, 2017
De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloacaJacob S J Hsu, Manting So, Clara S M Tang, et al.
Schizophrenia Bulletin|September 18, 2013
Common variants on Xq28 conferring risk of schizophrenia in Han ChineseEmily H M Wong, Hon-Cheong So, Miaoxin Li, et al.
Neurobiology of Aging|April 17, 2018
A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese populationBinbin Wang, Suying Bao, Zhigang Zhang, et al.
Hepatology (Baltimore, Md.)|May 22, 2012
Rare inborn errors associated with chronic hepatitis B virus infectionQiang Zhao, Liang Peng, Weijun Huang, et al.
Schizophrenia Bulletin|May 27, 2014
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations, Jim van Os, Bart P Rutten, et al.
Pageof 8