Mingyao Li
Mingyao Li
Professor of Biostatistics, University of Pennsylvania School of Medicine
Geverifieerd e-mailadres voor mail.med.upenn.edu - Homepage
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ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
K Wang, M Li, H Hakonarson
Nucleic acids research 38 (16), e164-e164, 2010
77172010
Biological, clinical and population relevance of 95 loci for blood lipids
TM Teslovich, K Musunuru, AV Smith, AC Edmondson, IM Stylianou, ...
Nature 466 (7307), 707-713, 2010
32982010
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ...
The Lancet 380 (9841), 572-580, 2012
19422012
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
GB Ehret, PB Munroe, KM Rice, M Bochud, AD Johnson, DI Chasman, ...
Nature 478 (7367), 103, 2011
18672011
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ...
Nature genetics 43 (4), 333-338, 2011
17502011
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
K Wang, M Li, D Hadley, R Liu, J Glessner, SFA Grant, H Hakonarson, ...
Genome research 17 (11), 1665-1674, 2007
16472007
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
S Kathiresan, BF Voight, S Purcell, K Musunuru, D Ardissino, ...
Nature genetics 41 (3), 334-341, 2009
11212009
Pathway-based approaches for analysis of genomewide association studies
K Wang, M Li, M Bucan
The American Journal of Human Genetics 81 (6), 1278-1283, 2007
9272007
Analysing biological pathways in genome-wide association studies
K Wang, M Li, H Hakonarson
Nature Reviews Genetics 11 (12), 843-854, 2010
8192010
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
7142016
Meta-analysis and imputation refines the association of 15q25 with smoking quantity
JZ Liu, F Tozzi, DM Waterworth, SG Pillai, P Muglia, L Middleton, ...
Nature genetics 42 (5), 436-440, 2010
6052010
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ...
Nature 518 (7537), 102-106, 2015
5452015
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
N Soranzo, TD Spector, M Mangino, B Kühnel, A Rendon, A Teumer, ...
Nature genetics 41 (11), 1182-1190, 2009
5352009
Widespread RNA and DNA sequence differences in the human transcriptome
M Li, IX Wang, Y Li, A Bruzel, AL Richards, JM Toung, VG Cheung
science 333 (6038), 53-58, 2011
520*2011
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two …
MP Reilly, M Li, J He, JF Ferguson, IM Stylianou, NN Mehta, MS Burnett, ...
The Lancet 377 (9763), 383-392, 2011
4782011
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration
S Zareparsi, KEH Branham, M Li, S Shah, RJ Klein, J Ott, J Hoh, ...
The American Journal of Human Genetics 77 (1), 149-153, 2005
4332005
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies
BJ Keating, S Tischfield, SS Murray, T Bhangale, TS Price, JT Glessner, ...
PloS one 3 (10), e3583, 2008
4272008
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
M Bucan, BS Abrahams, K Wang, JT Glessner, EI Herman, LI Sonnenblick, ...
PLoS Genet 5 (6), e1000536, 2009
4172009
A genome-wide association meta-analysis identifies new childhood obesity loci
JP Bradfield, HR Taal, NJ Timpson, A Scherag, C Lecoeur, ...
Nature genetics 44 (5), 526, 2012
4102012
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration
M Li, P Atmaca-Sonmez, M Othman, KEH Branham, R Khanna, MS Wade, ...
Nature genetics 38 (9), 1049-1054, 2006
3782006
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