|Mapping genomic loci implicates genes and synaptic biology in schizophrenia|
V Trubetskoy, AF Pardiņas, T Qi, G Panagiotaropoulou, S Awasthi, ...
Nature 604 (7906), 502-508, 2022
|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, 747-756, 2012
|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
|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
|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
|Schizophrenia Working Group of the Psychiatric Genomics Consortium Biological insights from 108 schizophrenia-associated genetic loci|
S Ripke, BM Neale, A Corvin, JT Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421-427, 2014
|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
|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
|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
|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
|A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts|
G Ni, J Zeng, JA Revez, Y Wang, Z Zheng, T Ge, R Restuadi, J Kiewa, ...
Biological psychiatry 90 (9), 611-620, 2021
|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, 1-9, 2011
|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
|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
|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
|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, 39-47, 2008
|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, 119-124, 2006