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All papers authored by M. Li

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2023 Lin Miao, Lin Jiang, Bin Tang, Pak Chung Sham, Miaoxin Li

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Dissecting the high-resolution genetic architecture of complex phenotypes by accurately estimating gene-based conditional heritability

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Liubin Zhang, Yangyang Yuan, Wenjie Peng, Bin Tang, Mulin Jun Li, Hongsheng Gui, Qiang Wang, Miaoxin Li

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GBC: a parallel toolkit based on highly addressable byte-encoding blocks for extremely large-scale genotypes of species

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Zipeng Liu, Yiming Qin

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, Tian Wu

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, Justin D. Tubbs

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, Timothy Shin Heng Mak, Miaoxin Li

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, Yan Dora Zhang

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, Pak Chung Sham

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Reciprocal causation mixture model for robust Mendelian randomization analysis using genome-scale summary data

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2022 Qihan Long, Yangyang Yuan, Miaoxin Li

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RNA-SSNV: A Reliable Somatic Single Nucleotide Variant Identification Framework for Bulk RNA-Seq Data

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Chao Xue

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, Lin Jiang, Miao Zhou, Qihan Long, Ying Chen, Xiangyi Li, Wenjie Peng, Qi Yang, Miaoxin Li

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PCGA: a comprehensive web server for phenotype-cell-gene association analysis

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Lin Jiang, Lin Miao, Guorong Yi, Xiangyi Li, Chao Xue, Mulin Jun Li, Hailiang Huang, Miaoxin Li

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Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization

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Miao Zhou, Chao Xue, Zhongdao Wu, Xiaoying Wu, Miaoxin Li

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Genome-Wide Association Study Identifies New Risk Loci for Progression of Schistosomiasis Among the Chinese Population

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Xiangyi Li

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, Lin Jiang, Chao Xue, Mulin Jun Li, Miaoxin Li

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A conditional gene-based association framework integrating isoform-level eQTL data reveals new susceptibility genes for schizophrenia

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Vassily Trubetskoy, Alp Üçok, Antonio F. Pardiñas, Ting Qi, Georgia Panagiotaropoulou, Swapnil Awasthi, Tim B. Bigdeli, Julien Bryois, Chia-Yen Chen, Lynsey S. Hall, Charlotte A. Dennison, Max Lam, Kyoko Watanabe, Oleksandr Frei, Tian Ge and 606 other authors

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

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Yangyang Yuan, Liubin Zhang, Qihan Long, Hui Jiang, Miaoxin Li

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An accurate prediction model of digenic interaction for estimating pathogenic gene pairs of human diseases

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2021 Lin Jiang, Hui Jiang, Sheng Dai, Ying Chen, Youqiang Song

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, 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, Miaoxin Li

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Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases

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Hui Jiang, Chunmiao Guo, Jie Xie, Jingxin Pan, Ying Huang, Miaoxin Li

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, Yibin Guo

Case report: exome sequencing achieved a definite diagnosis in a Chinese family with muscle atrophy

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2020 Deke Jiang

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, Jiaen Deng, Changzheng Dong, Xiaopin Ma, Qianyi Xiao, Bin Zhou, Chou Yang, Lin Wei, Carly Conran, S. Lilly Zheng, Irene Oi-Lin Ng, Long Yu, Jianfeng Xu, Pak C. Sham, Xiaolong Qi and 4 other authors

Knowledge-based analyses reveal new candidate genes associated with risk of hepatitis B virus related hepatocellular carcinoma

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2019 Lin Jiang, Chao Xue, Sheng Dai, Shangzhen Chen, Peikai Chen, Pak Chung Sham, Haijun Wang, Miaoxin Li

ORCID

DESE: estimating driver tissues by selective expression of genes associated with complex diseases or traits

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Lin Jiang, Jingjing Zheng, Johnny S. H. Kwan, Sheng Dai, Cong Li, Mulin Jun Li, Bolan Yu, Ka F. To, Pak C. Sham, Yonghong Zhu, Miaoxin Li

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WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation counts

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Jacob Shujui Hsu

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, Ruizhong Zhang, Fanny Yeung, Clara S. M. Tang, John K. L. Wong, Man-Ting So, Huimin Xia, Pak Sham, Paul K. Tam, Miaoxin Li

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, Kenneth K. Y. Wong

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, Maria-Mercè Garcia-Barcelo

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Cancer gene mutations in congenital pulmonary airway malformation patients

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2018 Wenliang Zhang, Haiyue Zhang, Huan Yang, Miaoxin Li

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, Zhi Xie, Weizhong Li

Computational resources associating diseases with genotypes, phenotypes and exposures

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Miaoxin Li

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, Lin Jiang, Timothy Shin Heng Mak, Johnny Sheung Him Kwan, Chao Xue, Peikai Chen, Henry Chi-Ming Leung, Liqian Cui, Tao Li, Pak Chung Sham

A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia

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Zhenxing Yang, Longkun Li

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, Miaoxin Li

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De novo mutations as causes of schizophrenia

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Dingge Ying, Mulin Jun Li, Pak Chung Sham, Miaoxin Li

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A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissues

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