Miaoxin LI
Miaoxin LI
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Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets
MX Li, JMY Yeung, SS Cherny, PC Sham
Human genetics 131 (5), 747-756, 2012
GATES: a rapid and powerful gene-based association test using extended Simes procedure
MX Li, HS Gui, JSH Kwan, PC Sham
The American Journal of Human Genetics 88 (3), 283-293, 2011
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases
MX Li, HS Gui, JSH Kwan, SY Bao, PC Sham
Nucleic acids research 40 (7), e53-e53, 2012
Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies
MX Li, JSH Kwan, SY Bao, W Yang, SL Ho, YQ Song, PC Sham
PLoS genetics 9 (1), e1003143, 2013
HYST: a hybrid set-based test for genome-wide association studies, with application to protein-protein interaction-based association analysis
MX Li, JSH Kwan, PC Sham
The American Journal of Human Genetics 91 (3), 478-488, 2012
Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis
K Zhou, L Donnelly, J Yang, M Li, H Deshmukh, N Van Zuydam, ...
The lancet Diabetes & endocrinology 2 (6), 481-487, 2014
TSC1/2 mutations define a molecular subset of HCC with aggressive behaviour and treatment implication
DWH Ho, LK Chan, YT Chiu, IMJ Xu, RTP Poon, TT Cheung, CN Tang, ...
Gut 66 (8), 1496-1506, 2017
White-matter microstructure in previously drug-naive patients with schizophrenia after 6 weeks of treatment
Q Wang, C Cheung, W Deng, M Li, C Huang, X Ma, Y Wang, L Jiang, ...
Psychological medicine 43 (11), 2301-2309, 2013
The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis B
L Peng, Q Zhao, Q Li, M Li, C Li, T Xu, X Jing, X Zhu, Y Wang, F Li, R Liu, ...
Hepatology 61 (4), 1251-1260, 2015
Uncovering the total heritability explained by all true susceptibility variants in a genome‐wide association study
HC So, M Li, PC Sham
Genetic epidemiology 35 (6), 447-456, 2011
Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset
H Gui, M Li, PC Sham, SS Cherny
BMC research notes 4 (1), 1-9, 2011
Estrogen receptor α gene polymorphisms and peak bone density in Chinese nuclear families
YJ Qin, H Shen, QR Huang, LJ Zhao, Q Zhou, MX Li, JW He, XY Mo, ...
Journal of Bone and Mineral Research 18 (6), 1028-1035, 2003
Genetic determination and correlation of body mass index and bone mineral density at the spine and hip in Chinese Han ethnicity
FY Deng, SF Lei, MX Li, C Jiang, V Dvornyk, HW Deng
Osteoporosis international 17 (1), 119-124, 2006
Association between myostatin gene polymorphisms and peak BMD variation in Chinese nuclear families
ZL Zhang, JW He, YJ Qin, YQ Hu, M Li, H Zhang, WW Hu, YJ Liu, JM Gu
Osteoporosis International 19 (1), 39-47, 2008
Common variants on Xq28 conferring risk of schizophrenia in Han Chinese
EHM Wong, HC So, M Li, Q Wang, AW Butler, B Paul, HM Wu, TCK Hui, ...
Schizophrenia bulletin 40 (4), 777-786, 2014
A knowledge-based weighting framework to boost the power of genome-wide association studies
MX Li, PC Sham, SS Cherny, YQ Song
PloS one 5 (12), e14480, 2010
The schizophrenia risk gene ZNF804A: clinical associations, biological mechanisms and neuronal functions
H Chang, X Xiao, M Li
Molecular psychiatry 22 (7), 944-953, 2017
Bone mineral density in elderly Chinese: effects of age, sex, weight, height, and body mass index
SF Lei, FY Deng, MX Li, V Dvornyk, HW Deng
Journal of bone and mineral metabolism 22 (1), 71-78, 2004
Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies
X Xiao, H Chang, M Li
Molecular psychiatry 22 (4), 497-511, 2017
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