SNPTracker: A Swift Tool for Comprehensive Tracking and Unifying dbSNP rs IDs and Genomic Coordinates of Massive Sequence Variants

por Deng, Jia-En, Sham, Pak C., Li, Miao-Xin
Publicado 2015

A Knowledge-Based Weighting Framework to Boost the Power of Genome-Wide Association Studies

por Li, Miao-Xin, Sham, Pak C., Cherny, Stacey S., Song, You-Qiang
Publicado 2010

Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets

por Li, Miao-Xin, Yeung, Juilian M. Y., Cherny, Stacey S., Sham, Pak C.
Publicado 2011

A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases

por Li, Miao-Xin, Gui, Hong-Sheng, Kwan, Johnny S. H., Bao, Su-Ying, Sham, Pak C.
Publicado 2012

MGAS: a powerful tool for multivariate gene-based genome-wide association analysis

por Van der Sluis, Sophie, Dolan, Conor V., Li, Jiang, Song, Youqiang, Sham, Pak, Posthuma, Danielle, Li, Miao-Xin
Publicado 2015

Predicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing Studies

por Li, Miao-Xin, Kwan, Johnny S. H., Bao, Su-Ying, Yang, Wanling, Ho, Shu-Leong, Song, Yong-Qiang, Sham, Pak C.
Publicado 2013

Identification of Genes with Allelic Imbalance on 6p Associated with Nasopharyngeal Carcinoma in Southern Chinese

por Li, Yan, Fu, Li, Wong, Alissa Michelle Go, Fan, Yan-Hui, Li, Miao-Xin, Bei, Jin-Xin, Jia, Wei-Hua, Zeng, Yi-Xin, Chan, Danny, Cheung, Kenneth M. C., Sham, Pak, Chua, Daniel, Guan, Xin-Yuan, Song, You-Qiang
Publicado 2011

An NT-3-releasing bioscaffold supports the formation of TrkC-modified neural stem cell-derived neural network tissue with efficacy in repairing spinal cord injury

por Li, Ge, Zhang, Bao, Sun, Jia-hui, Shi, Li-yang, Huang, Meng-yao, Huang, Li-jun, Lin, Zi-jing, Lin, Qiong-yu, Lai, Bi-qin, Ma, Yuan-huan, Jiang, Bin, Ding, Ying, Zhang, Hong-bo, Li, Miao-xin, Zhu, Ping, Wang, Ya-qiong, Zeng, Xiang, Zeng, Yuan-shan
Publicado 2021