Your account is not claimed yet. You can sign up with ORCID to claim your account.

Miao-Xin Li (Miaoxin Li)

Scopus Author ID ResearcherID HKU ResearcherPage ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 14

Top Venues

Nature communications

Nucleic acids research

Genome biology

PLoS genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Weiwei Qi, Dan Zhu, Ping Yin, Xiaoqiong Gu, Zhen Zhao, Miao-Xin Li, Chang Dong, Qilong Tang, Wanting Xie, Ti Zhou, Huimin Xia, Xiu Qiu, Xia Yang, Guoquan Gao
Pigment epithelium-derived factor (PEDF), a novel adipokine contributes to gestational diabetes mellitus (GDM). The Journal of clinical endocrinology and metabolism (2023)
Ruiyang Li, Wenben Chen, Mingyuan Li, Ruixin Wang, Lanqin Zhao, Yuanfan Lin, Xinwei Chen, Yuanjun Shang, Xueer Tu, Duoru Lin, Xiaohang Wu, Zhenzhe Lin, Andi Xu, Xun Wang, Dongni Wang, Xulin Zhang, Meimei Dongye, Yunjian Huang, Chuan Chen, Yi Zhu, Chunqiao Liu, Youjin Hu, Ling Zhao, Hong Ouyang, Miao-Xin Li, Xuri Li, Haotian Lin
LensAge index as a deep learning-based biological age for self-monitoring the risks of age-related diseases and mortality. Nature communications 14 (1) (2023)
Zipeng Liu, Yiming Qin, Tian Wu, Justin D Tubbs, Larry Baum, Timothy Shin Heng Mak, Miao-Xin Li, Yan Dora Zhang, Pak-Chung Sham
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data. Nature communications 14 (1) (2023)
Zipeng Liu, Yiming Qin, Tian Wu, Justin D Tubbs, Larry Baum, Timothy Shin Heng Mak, Miao-Xin Li, Yan Dora Zhang, Pak-Chung Sham
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data. Nature communications 14 (1) (2023)
Zipeng Liu, Yiming Qin, Tian Wu, Justin D Tubbs, Larry Baum, Timothy Shin Heng Mak, Miao-Xin Li, Yan Dora Zhang, Pak-Chung Sham
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data. Nature communications 14 (1) (2023)
Yunqi Huang, Dongru Chen, Albert M Levin, Brian K Ahmedani, Cathrine Frank, Miao-Xin Li, Qiang Wang, Hongsheng Gui, Pak-Chung Sham
Cross-phenotype relationship between opioid use disorder and suicide attempts: new evidence from polygenic association and Mendelian randomization analyses. Molecular psychiatry (2023)
Zipeng Liu, Yiming Qin, Tian Wu, Justin D Tubbs, Larry Baum, Timothy Shin Heng Mak, Miao-Xin Li, Yan Dora Zhang, Pak-Chung Sham
Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data. Nature communications 14 (1) (2023)
Liubin Zhang, Yangyang Yuan, Wenjie Peng, Bin Tang, Mulin Jun Li, Hongsheng Gui, Qiang Wang, Miao-Xin Li
GBC: a parallel toolkit based on highly addressable byte-encoding blocks for extremely large-scale genotypes of species. Genome biology 24 (1) (2023)
Chao Xue, Lin Jiang, Miao Zhou, Qihan Long, Ying Chen, Xiangyi Li, Wenjie Peng, Qi Yang, Miao-Xin Li
PCGA: a comprehensive web server for phenotype-cell-gene association analysis. Nucleic acids research (2022)
Xiangyi Li, Lin Jiang, Chao Xue, Mulin Jun Li, Miao-Xin Li
A conditional gene-based association framework integrating isoform-level eQTL data reveals new susceptibility genes for schizophrenia. eLife 11 (2022)
Lin Jiang, Hui Jiang, Sheng Dai, Ying Chen, You-Qiang Song, Clara Sze-Man Tang, Shirley Yin-Yu Pang, Shu-Leong Ho, Binbin Wang, Maria-Mercedes Garcia-Barcelo, Paul Kwong-Hang Tam, Stacey S Cherny, Mulin Jun Li, Pak Chung Sham, Miao-Xin Li
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases. Nucleic acids research 50 (6) (2022)
Nana Liu, Jiayuan Xu, Huaigui Liu, Shijie Zhang, Miao-Xin Li, Yao Zhou, Wen Qin, Mulin Jun Li, Chunshui Yu, null null
Hippocampal transcriptome-wide association study and neurobiological pathway analysis for Alzheimer's disease. PLoS genetics 17 (2) (2021)
Hui Jiang, Chunmiao Guo, Jie Xie, Jingxin Pan, Ying Huang, Miao-Xin Li, Yibin Guo
Case report: exome sequencing achieved a definite diagnosis in a Chinese family with muscle atrophy. BMC neurology 21 (1) (2021)
Jia-En Deng, Pak C Sham, Miao-Xin Li
SNPTracker: A Swift Tool for Comprehensive Tracking and Unifying dbSNP rs IDs and Genomic Coordinates of Massive Sequence Variants. G3 (Bethesda, Md.) 6 (1) (2015)

Miao-Xin Li.css-eqlu8i{font-size:small;padding-left:4px;} (Miaoxin Li)

Publication Activity (10 Years)

Top Topics

Top Venues

Miao-Xin Li (Miaoxin Li)