Mingyao Li, Ph.D. - Publications

Affiliations: 
2005 University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Biostatistics Biology, Genetics

100 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Wang F, Zhao S, Zhou X, Li C, Li M, Zeng Z. An Recognition-Verification Mechanism for Real-Time Chinese Sign Language Recognition Based on Multi-Information Fusion. Sensors (Basel, Switzerland). 19. PMID 31159240 DOI: 10.3390/s19112495  0.6
2017 Li L, Fu J, Yu XT, Li G, Xu L, Yin J, Cheng H, Hou D, Zhao X, Gao S, Li W, Li C, Grant SF, Li M, Xiao Y, ... ... Li M, et al. Sleep Duration and Cardiometabolic Risk Among Chinese School-aged Children: Do Adipokines Play a Mediating Role? Sleep. PMID 28329079 DOI: 10.1093/sleep/zsx042  0.6
2016 Fu J, Hou C, Li L, Feng D, Li G, Li M, Li C, Gao S, Li M. Vitamin D modifies the associations between circulating betatrophin and cardiometabolic risk factors among youths at risk for metabolic syndrome. Cardiovascular Diabetology. 15: 142. PMID 27716289 DOI: 10.1186/s12933-016-0461-y  0.4
2016 Hughes AE, Bridgett S, Meng W, Li M, Curcio CA, Stambolian D, Bradley DT. Sequence and Expression of Complement Factor H Gene Cluster Variants and Their Roles in Age-Related Macular Degeneration Risk. Investigative Ophthalmology & Visual Science. 57: 2763-2769. PMID 27196323 DOI: 10.1167/iovs.15-18744  0.4
2016 Ferguson JF, Xue C, Hu Y, Li M, Reilly MP. Adipose tissue RNASeq reveals novel gene-nutrient interactions following n-3 PUFA supplementation and evoked inflammation in humans. The Journal of Nutritional Biochemistry. 30: 126-32. PMID 27012629 DOI: 10.1016/j.jnutbio.2015.12.010  0.4
2016 Li L, Yin J, Cheng H, Wang Y, Gao S, Li M, Grant SF, Li C, Mi J, Li M. Identification of genetic and environmental factors predicting metabolically healthy obesity in children: Data from the BCAMS study. The Journal of Clinical Endocrinology and Metabolism. jc20153760. PMID 26913634 DOI: 10.1210/jc.2015-3760  0.6
2016 Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, ... ... Li M, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/ng.3448  0.4
2015 Gaulton KJ, Ferreira T, Lee Y, Raimondo A, Mägi R, Reschen ME, Mahajan A, Locke A, William Rayner N, Robertson N, Scott RA, Prokopenko I, Scott LJ, Green T, Sparso T, ... ... Li M, et al. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature Genetics. PMID 26551672 DOI: 10.1038/ng.3437  0.4
2015 Lin JJ, Zhang X, Xue C, Zhang H, Shashaty MG, Gosai S, Meyer NJ, Grazioli A, Hinkle C, Caughey J, Li W, Susztak K, Gregory BD, Li M, Reilly MP. The Long Noncoding RNA Landscape in Hypoxic and Inflammatory Renal Epithelial Injury. American Journal of Physiology. Renal Physiology. ajprenal.00290.2015. PMID 26400545 DOI: 10.1152/ajprenal.00290.2015  0.4
2015 Christofidou P, Nelson CP, Nikpay M, Qu L, Li M, Loley C, Debiec R, Braund PS, Denniff M, Charchar FJ, Arjo AR, Trégouët DA, Goodall AH, Cambien F, Ouwehand WH, et al. Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages. American Journal of Human Genetics. PMID 26166477 DOI: 10.1016/j.ajhg.2015.06.001  0.4
2015 Jia C, Guan W, Yang A, Xiao R, Tang WH, Moravec CS, Margulies KB, Cappola TP, Li M, Li C. MetaDiff: differential isoform expression analysis using random-effects meta-regression. Bmc Bioinformatics. 16: 208. PMID 26134005 DOI: 10.1186/s12859-015-0623-z  0.4
2015 Hu M, Clark KL, Gong X, Noudoost B, Li M, Moore T, Liang H. Copula Regression Analysis of Simultaneously Recorded Frontal Eye Field and Inferotemporal Spiking Activity during Object-Based Working Memory. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 8745-57. PMID 26063909 DOI: 10.1523/JNEUROSCI.5041-14.2015  0.4
2015 Zhang H, Xue C, Shah R, Bermingham K, Hinkle CC, Li W, Rodrigues A, Tabita-Martinez J, Millar JS, Cuchel M, Pashos EE, Liu Y, Yan R, Yang W, Gosai SJ, ... ... Li M, et al. Functional Analysis and Transcriptomic Profiling of iPSC-Derived Macrophages and Their Application in Modeling Mendelian Disease. Circulation Research. 117: 17-28. PMID 25904599 DOI: 10.1161/CIRCRESAHA.117.305860  0.4
2015 Wang X, Zhang S, Li Y, Li M, Sha Q. A powerful approach to test an optimally weighted combination of rare variants in admixed populations. Genetic Epidemiology. 39: 294-305. PMID 25758547 DOI: 10.1002/gepi.21894  0.4
2015 Tian L, Kazmierkiewicz KL, Bowman AS, Li M, Curcio CA, Stambolian DE. Transcriptome of the human retina, retinal pigmented epithelium and choroid. Genomics. 105: 253-64. PMID 25645700 DOI: 10.1016/j.ygeno.2015.01.008  0.4
2015 Liu Y, Morley M, Brandimarto J, Hannenhalli S, Hu Y, Ashley EA, Tang WH, Moravec CS, Margulies KB, Cappola TP, Li M. RNA-Seq identifies novel myocardial gene expression signatures of heart failure. Genomics. 105: 83-9. PMID 25528681 DOI: 10.1016/j.ygeno.2014.12.002  0.4
2015 Do R, Stitziel NO, Won HH, Jørgensen AB, Duga S, Angelica Merlini P, Kiezun A, Farrall M, Goel A, Zuk O, Guella I, Asselta R, Lange LA, Peloso GM, Auer PL, ... ... Li M, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 518: 102-6. PMID 25487149 DOI: 10.1038/nature13917  0.4
2015 Ferguson JF, Meyer NJ, Qu L, Xue C, Liu Y, DerOhannessian SL, Rushefski M, Paschos GK, Tang S, Schadt EE, Li M, Christie JD, Reilly MP. Integrative genomics identifies 7p11.2 as a novel locus for fever and clinical stress response in humans. Human Molecular Genetics. 24: 1801-12. PMID 25416278 DOI: 10.1093/hmg/ddu589  0.4
2014 Meyer NJ, Ferguson JF, Feng R, Wang F, Patel PN, Li M, Xue C, Qu L, Liu Y, Boyd JH, Russell JA, Christie JD, Walley KR, Reilly MP. A functional synonymous coding variant in the IL1RN gene is associated with survival in septic shock. American Journal of Respiratory and Critical Care Medicine. 190: 656-64. PMID 25089931 DOI: 10.1164/rccm.201403-0586OC  0.4
2014 Li M, Jia C, Kazmierkiewicz KL, Bowman AS, Tian L, Liu Y, Gupta NA, Gudiseva HV, Yee SS, Kim M, Dentchev T, Kimble JA, Parker JS, Messinger JD, Hakonarson H, et al. Comprehensive analysis of gene expression in human retina and supporting tissues. Human Molecular Genetics. 23: 4001-14. PMID 24634144 DOI: 10.1093/hmg/ddu114  0.4
2014 Mahajan A, Go MJ, Zhang W, Below JE, Gaulton KJ, Ferreira T, Horikoshi M, Johnson AD, Ng MC, Prokopenko I, ... ... Li M, et al. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics. 46: 234-44. PMID 24509480 DOI: 10.1038/ng.2897  0.4
2014 Peloso GM, Auer PL, Bis JC, Voorman A, Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M, Isaacs A, Jakobsdottir J, Feitosa MF, Davies G, Huffman JE, ... ... Li M, et al. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. American Journal of Human Genetics. 94: 223-32. PMID 24507774 DOI: 10.1016/j.ajhg.2014.01.009  0.4
2014 Liu Y, Ferguson JF, Xue C, Ballantyne RL, Silverman IM, Gosai SJ, Serfecz J, Morley MP, Gregory BD, Li M, Reilly MP. Tissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 902-12. PMID 24504737 DOI: 10.1161/ATVBAHA.113.303123  0.4
2013 Baldwin DA, Sarnowski CP, Reddy SA, Blair IA, Clapper M, Lazarus P, Li M, Muscat JE, Penning TM, Vachani A, Whitehead AS. Development of a genotyping microarray for studying the role of gene-environment interactions in risk for lung cancer. Journal of Biomolecular Techniques : Jbt. 24: 198-217. PMID 24294113 DOI: 10.7171/jbt.13-2404-004  0.4
2013 Holmes MV, Simon T, Exeter HJ, Folkersen L, Asselbergs FW, Guardiola M, Cooper JA, Palmen J, Hubacek JA, Carruthers KF, Horne BD, Brunisholz KD, Mega JL, van Iperen EP, Li M, et al. Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study. Journal of the American College of Cardiology. 62: 1966-76. PMID 23916927 DOI: 10.1016/j.jacc.2013.06.044  0.4
2013 Wojczynski MK, Li M, Bielak LF, Kerr KF, Reiner AP, Wong ND, Yanek LR, Qu L, White CC, Lange LA, Ferguson JF, He J, Young T, Mosley TH, Smith JA, et al. Genetics of coronary artery calcification among African Americans, a meta-analysis. Bmc Medical Genetics. 14: 75. PMID 23870195 DOI: 10.1186/1471-2350-14-75  0.4
2013 Byrnes AE, Wu MC, Wright FA, Li M, Li Y. The value of statistical or bioinformatics annotation for rare variant association with quantitative trait. Genetic Epidemiology. 37: 666-74. PMID 23836599 DOI: 10.1002/gepi.21747  0.4
2013 Ferguson JF, Matthews GJ, Townsend RR, Raj DS, Kanetsky PA, Budoff M, Fischer MJ, Rosas SE, Kanthety R, Rahman M, Master SR, Qasim A, Li M, Mehta NN, Shen H, et al. Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort). Journal of the American College of Cardiology. 62: 789-98. PMID 23727086 DOI: 10.1016/j.jacc.2013.01.103  0.4
2013 Meyer NJ, Feng R, Li M, Zhao Y, Sheu CC, Tejera P, Gallop R, Bellamy S, Rushefski M, Lanken PN, Aplenc R, O'Keefe GE, Wurfel MM, Christiani DC, Christie JD. IL1RN coding variant is associated with lower risk of acute respiratory distress syndrome and increased plasma IL-1 receptor antagonist. American Journal of Respiratory and Critical Care Medicine. 187: 950-9. PMID 23449693 DOI: 10.1164/rccm.201208-1501OC  0.4
2013 Ng MC, Saxena R, Li J, Palmer ND, Dimitrov L, Xu J, Rasmussen-Torvik LJ, Zmuda JM, Siscovick DS, Patel SR, Crook ED, Sims M, Chen YD, Bertoni AG, Li M, et al. Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. Diabetes. 62: 965-76. PMID 23193183 DOI: 10.2337/db12-0266  0.4
2013 Liu EY, Li M, Wang W, Li Y. MaCH-admix: genotype imputation for admixed populations. Genetic Epidemiology. 37: 25-37. PMID 23074066 DOI: 10.1002/gepi.21690  0.4
2013 Mao X, Li Y, Liu Y, Lange L, Li M. Testing genetic association with rare variants in admixed populations. Genetic Epidemiology. 37: 38-47. PMID 23032398 DOI: 10.1002/gepi.21687  0.4
2012 Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, ... ... Li M, et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics. 91: 823-38. PMID 23063622 DOI: 10.1016/j.ajhg.2012.08.032  0.4
2012 Moberg PJ, Li M, Kanes SJ, Gur RE, Kamath V, Turetsky BI. Association of schizophrenia with the phenylthiocarbamide taste receptor haplotype on chromosome 7q. Psychiatric Genetics. 22: 286-9. PMID 22955840 DOI: 10.1097/YPG.0b013e32835863f0  0.4
2012 Voight BF, Peloso GM, Orho-Melander M, Frikke-Schmidt R, Barbalic M, Jensen MK, Hindy G, Hólm H, Ding EL, Johnson T, Schunkert H, Samani NJ, Clarke R, Hopewell JC, Thompson JF, ... Li M, et al. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet. 380: 572-80. PMID 22607825 DOI: 10.1016/S0140-6736(12)60312-2  0.4
2012 Bradfield JP, Taal HR, Timpson NJ, Scherag A, Lecoeur C, Warrington NM, Hypponen E, Holst C, Valcarcel B, Thiering E, Salem RM, Schumacher FR, Cousminer DL, Sleiman PM, Zhao J, ... ... Li M, et al. A genome-wide association meta-analysis identifies new childhood obesity loci. Nature Genetics. 44: 526-31. PMID 22484627 DOI: 10.1038/ng.2247  0.4
2012 Wassel CL, Lamina C, Nambi V, Coassin S, Mukamal KJ, Ganesh SK, Jacobs DR, Franceschini N, Papanicolaou GJ, Gibson Q, Yanek LR, van der Harst P, Ferguson JF, Crawford DC, Waite LL, ... ... Li M, et al. Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium. Atherosclerosis. 222: 138-47. PMID 22361517 DOI: 10.1016/j.atherosclerosis.2012.01.039  0.4
2012 Ferguson JF, Hinkle CC, Mehta NN, Bagheri R, Derohannessian SL, Shah R, Mucksavage MI, Bradfield JP, Hakonarson H, Wang X, Master SR, Rader DJ, Li M, Reilly MP. Translational studies of lipoprotein-associated phospholipase A₂ in inflammation and atherosclerosis. Journal of the American College of Cardiology. 59: 764-72. PMID 22340269 DOI: 10.1016/j.jacc.2011.11.019  0.4
2012 Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, ... ... Li M, et al. Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American Journal of Human Genetics. 90: 410-25. PMID 22325160 DOI: 10.1016/j.ajhg.2011.12.022  0.4
2012 Christie JD, Wurfel MM, Feng R, O'Keefe GE, Bradfield J, Ware LB, Christiani DC, Calfee CS, Cohen MJ, Matthay M, Meyer NJ, Kim C, Li M, Akey J, Barnes KC, et al. Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma. Plos One. 7: e28268. PMID 22295056 DOI: 10.1371/journal.pone.0028268  0.4
2012 He J, Li H, Edmondson AC, Rader DJ, Li M. A Gaussian copula approach for the analysis of secondary phenotypes in case-control genetic association studies. Biostatistics (Oxford, England). 13: 497-508. PMID 21933777 DOI: 10.1093/biostatistics/kxr025  0.4
2011 Wang K, Edmondson AC, Li M, Gao F, Qasim AN, Devaney JM, Burnett MS, Waterworth DM, Mooser V, Grant SF, Epstein SE, Reilly MP, Hakonarson H, Rader DJ. Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation. Frontiers in Genetics. 2: 41. PMID 22303337 DOI: 10.3389/fgene.2011.00041  0.4
2011 Khetarpal SA, Edmondson AC, Raghavan A, Neeli H, Jin W, Badellino KO, Demissie S, Manning AK, DerOhannessian SL, Wolfe ML, Cupples LA, Li M, Kathiresan S, Rader DJ. Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol. Plos Genetics. 7: e1002393. PMID 22174694 DOI: 10.1371/journal.pgen.1002393  0.4
2011 Bhatia G, Patterson N, Pasaniuc B, Zaitlen N, Genovese G, Pollack S, Mallick S, Myers S, Tandon A, Spencer C, Palmer CD, Adeyemo AA, Akylbekova EL, Cupples LA, Divers J, ... ... Li M, et al. Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. American Journal of Human Genetics. 89: 368-81. PMID 21907010 DOI: 10.1016/j.ajhg.2011.07.025  0.4
2011 Zhao J, Bradfield JP, Zhang H, Sleiman PM, Kim CE, Glessner JT, Deliard S, Thomas KA, Frackelton EC, Li M, Chiavacci RM, Berkowitz RI, Hakonarson H, Grant SF. Role of BMI-associated loci identified in GWAS meta-analyses in the context of common childhood obesity in European Americans. Obesity (Silver Spring, Md.). 19: 2436-9. PMID 21779088 DOI: 10.1038/oby.2011.237  0.4
2011 Rushefski M, Aplenc R, Meyer N, Li M, Feng R, Lanken PN, Gallop R, Bellamy S, Localio AR, Feinstein SI, Fisher AB, Albelda SM, Christie JD. Novel variants in the PRDX6 Gene and the risk of Acute Lung Injury following major trauma. Bmc Medical Genetics. 12: 77. PMID 21627785 DOI: 10.1186/1471-2350-12-77  0.4
2011 Wild PS, Zeller T, Schillert A, Szymczak S, Sinning CR, Deiseroth A, Schnabel RB, Lubos E, Keller T, Eleftheriadis MS, Bickel C, Rupprecht HJ, Wilde S, Rossmann H, Diemert P, ... ... Li M, et al. A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circulation. Cardiovascular Genetics. 4: 403-12. PMID 21606135 DOI: 10.1161/CIRCGENETICS.110.958728  0.4
2011 Li M, Wang IX, Li Y, Bruzel A, Richards AL, Toung JM, Cheung VG. Widespread RNA and DNA sequence differences in the human transcriptome. Science (New York, N.Y.). 333: 53-8. PMID 21596952 DOI: 10.1126/science.1207018  0.4
2011 Kanetsky PA, Mitra N, Vardhanabhuti S, Vaughn DJ, Li M, Ciosek SL, Letrero R, D'Andrea K, Vaddi M, Doody DR, Weaver J, Chen C, Starr JR, HÃ¥konarson H, Rader DJ, et al. A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility. Human Molecular Genetics. 20: 3109-17. PMID 21551455 DOI: 10.1093/hmg/ddr207  0.4
2011 Pasaniuc B, Zaitlen N, Lettre G, Chen GK, Tandon A, Kao WH, Ruczinski I, Fornage M, Siscovick DS, Zhu X, Larkin E, Lange LA, Cupples LA, Yang Q, Akylbekova EL, ... ... Li M, et al. Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. Plos Genetics. 7: e1001371. PMID 21541012 DOI: 10.1371/journal.pgen.1001371  0.4
2011 Toung JM, Morley M, Li M, Cheung VG. RNA-sequence analysis of human B-cells. Genome Research. 21: 991-8. PMID 21536721 DOI: 10.1101/gr.116335.110  0.4
2011 Shah R, Hinkle CC, Ferguson JF, Mehta NN, Li M, Qu L, Lu Y, Putt ME, Ahima RS, Reilly MP. Fractalkine is a novel human adipochemokine associated with type 2 diabetes. Diabetes. 60: 1512-8. PMID 21525510 DOI: 10.2337/db10-0956  0.4
2011 Mehta NN, Li M, William D, Khera AV, DerOhannessian S, Qu L, Ferguson JF, McLaughlin C, Shaikh LH, Shah R, Patel PN, Bradfield JP, He J, Stylianou IM, Hakonarson H, et al. The novel atherosclerosis locus at 10q11 regulates plasma CXCL12 levels. European Heart Journal. 32: 963-71. PMID 21415067 DOI: 10.1093/eurheartj/ehr091  0.4
2011 Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AF, Barbalic M, Gieger C, Absher D, Aherrahrou Z, Allayee H, Altshuler D, Anand SS, ... ... Li M, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nature Genetics. 43: 333-8. PMID 21378990 DOI: 10.1038/ng.784  0.4
2011 Lettre G, Palmer CD, Young T, Ejebe KG, Allayee H, Benjamin EJ, Bennett F, Bowden DW, Chakravarti A, Dreisbach A, Farlow DN, Folsom AR, Fornage M, Forrester T, Fox E, ... ... Li M, et al. Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Plos Genetics. 7: e1001300. PMID 21347282 DOI: 10.1371/journal.pgen.1001300  0.4
2011 Edmondson AC, Braund PS, Stylianou IM, Khera AV, Nelson CP, Wolfe ML, Derohannessian SL, Keating BJ, Qu L, He J, Tobin MD, Tomaszewski M, Baumert J, Klopp N, Döring A, ... ... Li M, et al. Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol. Circulation. Cardiovascular Genetics. 4: 145-55. PMID 21303902 DOI: 10.1161/CIRCGENETICS.110.957563  0.4
2011 Meyer NJ, Li M, Feng R, Bradfield J, Gallop R, Bellamy S, Fuchs BD, Lanken PN, Albelda SM, Rushefski M, Aplenc R, Abramova H, Atochina-Vasserman EN, Beers MF, Calfee CS, et al. ANGPT2 genetic variant is associated with trauma-associated acute lung injury and altered plasma angiopoietin-2 isoform ratio. American Journal of Respiratory and Critical Care Medicine. 183: 1344-53. PMID 21257790 DOI: 10.1164/rccm.201005-0701OC  0.4
2011 Cappola TP, Matkovich SJ, Wang W, van Booven D, Li M, Wang X, Qu L, Sweitzer NK, Fang JC, Reilly MP, Hakonarson H, Nerbonne JM, Dorn GW. Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation. Proceedings of the National Academy of Sciences of the United States of America. 108: 2456-61. PMID 21248228 DOI: 10.1073/pnas.1017494108  0.4
2011 Reilly MP, Li M, He J, Ferguson JF, Stylianou IM, Mehta NN, Burnett MS, Devaney JM, Knouff CW, Thompson JR, Horne BD, Stewart AF, Assimes TL, Wild PS, Allayee H, et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Lancet. 377: 383-92. PMID 21239051 DOI: 10.1016/S0140-6736(10)61996-4  0.4
2011 Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... ... Li M, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/j.ajhg.2010.11.007  0.4
2011 Wang X, Zhu X, Qin H, Cooper RS, Ewens WJ, Li C, Li M. Adjustment for local ancestry in genetic association analysis of admixed populations. Bioinformatics (Oxford, England). 27: 670-7. PMID 21169375 DOI: 10.1093/bioinformatics/btq709  0.4
2011 He J, Wang K, Edmondson AC, Rader DJ, Li C, Li M. Gene-based interaction analysis by incorporating external linkage disequilibrium information. European Journal of Human Genetics : Ejhg. 19: 164-72. PMID 20924406 DOI: 10.1038/ejhg.2010.164  0.4
2010 Li Y, Byrnes AE, Li M. To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests. American Journal of Human Genetics. 87: 728-35. PMID 21055717 DOI: 10.1016/j.ajhg.2010.10.014  0.4
2010 Glessner JT, Bradfield JP, Wang K, Takahashi N, Zhang H, Sleiman PM, Mentch FD, Kim CE, Hou C, Thomas KA, Garris ML, Deliard S, Frackelton EC, Otieno FG, Zhao J, ... ... Li M, et al. A genome-wide study reveals copy number variants exclusive to childhood obesity cases. American Journal of Human Genetics. 87: 661-6. PMID 20950786 DOI: 10.1016/j.ajhg.2010.09.014  0.4
2010 Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C, Patterson CC, Morgan TM, Burnett MS, Li M, Hlatky MA, et al. Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. Journal of the American College of Cardiology. 56: 1552-63. PMID 20933357 DOI: 10.1016/j.jacc.2010.06.022  0.4
2010 Preuss M, König IR, Thompson JR, Erdmann J, Absher D, Assimes TL, Blankenberg S, Boerwinkle E, Chen L, Cupples LA, Hall AS, Halperin E, Hengstenberg C, Holm H, Laaksonen R, ... Li M, et al. Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls. Circulation. Cardiovascular Genetics. 3: 475-83. PMID 20923989 DOI: 10.1161/CIRCGENETICS.109.899443  0.4
2010 Shen H, Bielak LF, Ferguson JF, Streeten EA, Yerges-Armstrong LM, Liu J, Post W, O'Connell JR, Hixson JE, Kardia SL, Sun YV, Jhun MA, Wang X, Mehta NN, Li M, et al. Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification. Arteriosclerosis, Thrombosis, and Vascular Biology. 30: 2648-54. PMID 20847308 DOI: 10.1161/ATVBAHA.110.211805  0.4
2010 Haas EJ, Zaoutis TE, Prasad P, Li M, Coffin SE. Risk Factors and Outcomes for Vancomycin-Resistant Enterococcus Bloodstream Infection in Children. Infection Control and Hospital Epidemiology : the Official Journal of the Society of Hospital Epidemiologists of America. PMID 20807035 DOI: 10.1086/655464  0.4
2010 Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, ... ... Li M, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 466: 707-13. PMID 20686565 DOI: 10.1038/nature09270  0.4
2010 Raychaudhuri S, Ripke S, Li M, Neale BM, Fagerness J, Reynolds R, Sobrin L, Swaroop A, Abecasis G, Seddon JM, Daly MJ. Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent. Nature Genetics. 42: 553-5; author reply . PMID 20581873 DOI: 10.1038/ng0710-553  0.4
2010 Zhao J, Li M, Bradfield JP, Zhang H, Mentch FD, Wang K, Sleiman PM, Kim CE, Glessner JT, Hou C, Keating BJ, Thomas KA, Garris ML, Deliard S, Frackelton EC, et al. The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature. Bmc Medical Genetics. 11: 96. PMID 20546612 DOI: 10.1186/1471-2350-11-96  0.4
2010 Liu JZ, Tozzi F, Waterworth DM, Pillai SG, Muglia P, Middleton L, Berrettini W, Knouff CW, Yuan X, Waeber G, Vollenweider P, Preisig M, Wareham NJ, Zhao JH, Loos RJ, ... ... Li M, et al. Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nature Genetics. 42: 436-40. PMID 20418889 DOI: 10.1038/ng.572  0.4
2010 Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, Tarasov KV, Müller M, Sotoodehnia N, Sinner MF, Verwoert GC, Li M, Kao WH, Köttgen A, Coresh J, et al. Genome-wide association study of PR interval. Nature Genetics. 42: 153-9. PMID 20062060 DOI: 10.1038/ng.517  0.4
2010 Zhao J, Bradfield JP, Zhang H, Annaiah K, Wang K, Kim CE, Glessner JT, Frackelton EC, Otieno FG, Doran J, Thomas KA, Garris M, Hou C, Chiavacci RM, Li M, et al. Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI. Diabetes. 59: 751-5. PMID 19933996 DOI: 10.2337/db09-0972  0.4
2009 Soranzo N, Spector TD, Mangino M, Kühnel B, Rendon A, Teumer A, Willenborg C, Wright B, Chen L, Li M, Salo P, Voight BF, Burns P, Laskowski RA, Xue Y, et al. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nature Genetics. 41: 1182-90. PMID 19820697 DOI: 10.1038/ng.467  0.4
2009 Zhao J, Li M, Bradfield JP, Wang K, Zhang H, Sleiman P, Kim CE, Annaiah K, Glaberson W, Glessner JT, Otieno FG, Thomas KA, Garris M, Hou C, Frackelton EC, et al. Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene. Diabetes. 58: 2414-8. PMID 19592620 DOI: 10.2337/db09-0506  0.4
2009 Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, ... ... Li M, et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. Plos Genetics. 5: e1000536. PMID 19557195 DOI: 10.1371/journal.pgen.1000536  0.4
2009 Kanetsky PA, Mitra N, Vardhanabhuti S, Li M, Vaughn DJ, Letrero R, Ciosek SL, Doody DR, Smith LM, Weaver J, Albano A, Chen C, Starr JR, Rader DJ, Godwin AK, et al. Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. Nature Genetics. 41: 811-5. PMID 19483682 DOI: 10.1038/ng.393  0.4
2009 Brown RJ, Edmondson AC, Griffon N, Hill TB, Fuki IV, Badellino KO, Li M, Wolfe ML, Reilly MP, Rader DJ. A naturally occurring variant of endothelial lipase associated with elevated HDL exhibits impaired synthesis. Journal of Lipid Research. 50: 1910-6. PMID 19411705 DOI: 10.1194/jlr.P900020-JLR200  0.4
2009 Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, et al. Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nature Genetics. 41: 407-14. PMID 19305409 DOI: 10.1038/ng.362  0.4
2009 Edmondson AC, Brown RJ, Kathiresan S, Cupples LA, Demissie S, Manning AK, Jensen MK, Rimm EB, Wang J, Rodrigues A, Bamba V, Khetarpal SA, Wolfe ML, Derohannessian S, Li M, et al. Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans. The Journal of Clinical Investigation. 119: 1042-50. PMID 19287092 DOI: 10.1172/JCI37176  0.4
2009 Grant SF, Bradfield JP, Zhang H, Wang K, Kim CE, Annaiah K, Santa E, Glessner JT, Thomas K, Garris M, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Imielinski M, ... ... Li M, et al. Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry. Obesity (Silver Spring, Md.). 17: 1461-5. PMID 19265794 DOI: 10.1038/oby.2009.53  0.4
2009 Wang K, Zhang H, Kugathasan S, Annese V, Bradfield JP, Russell RK, Sleiman PM, Imielinski M, Glessner J, Hou C, Wilson DC, Walters T, Kim C, Frackelton EC, Lionetti P, ... ... Li M, et al. Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease. American Journal of Human Genetics. 84: 399-405. PMID 19249008 DOI: 10.1016/j.ajhg.2009.01.026  0.4
2009 Li M, Wang K, Grant SF, Hakonarson H, Li C. ATOM: a powerful gene-based association test by combining optimally weighted markers. Bioinformatics (Oxford, England). 25: 497-503. PMID 19074959 DOI: 10.1093/bioinformatics/btn641  0.6
2008 Keating BJ, Tischfield S, Murray SS, Bhangale T, Price TS, Glessner JT, Galver L, Barrett JC, Grant SF, Farlow DN, Chandrupatla HR, Hansen M, Ajmal S, Papanicolaou GJ, Guo Y, ... Li M, et al. Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. Plos One. 3: e3583. PMID 18974833 DOI: 10.1371/journal.pone.0003583  0.4
2008 Christie JD, Ma SF, Aplenc R, Li M, Lanken PN, Shah CV, Fuchs B, Albelda SM, Flores C, Garcia JG. Variation in the myosin light chain kinase gene is associated with development of acute lung injury after major trauma. Critical Care Medicine. 36: 2794-800. PMID 18828194 DOI: 10.1097/CCM.0b013e318186b843  0.4
2008 Diskin SJ, Li M, Hou C, Yang S, Glessner J, Hakonarson H, Bucan M, Maris JM, Wang K. Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. Nucleic Acids Research. 36: e126. PMID 18784189 DOI: 10.1093/nar/gkn556  0.4
2008 Wei Z, Li M, Rebbeck T, Li H. U-statistics-based tests for multiple genes in genetic association studies. Annals of Human Genetics. 72: 821-33. PMID 18691161 DOI: 10.1111/j.1469-1809.2008.00473.x  0.4
2008 Becker DJ, Gordon RY, Morris PB, Yorko J, Gordon YJ, Li M, Iqbal N. Simvastatin vs therapeutic lifestyle changes and supplements: randomized primary prevention trial. Mayo Clinic Proceedings. 83: 758-64. PMID 18613992 DOI: 10.4065/83.7.758  0.4
2008 Vorovich EE, Chuai S, Li M, Averna J, Marwin V, Wolfe D, Reilly MP, Cappola TP. Comparison of matrix metalloproteinase 9 and brain natriuretic peptide as clinical biomarkers in chronic heart failure. American Heart Journal. 155: 992-7. PMID 18513509 DOI: 10.1016/j.ahj.2008.01.007  0.4
2008 Li M, Li C. Assessing departure from Hardy-Weinberg equilibrium in the presence of disease association. Genetic Epidemiology. 32: 589-99. PMID 18449919 DOI: 10.1002/gepi.20335  0.6
2008 Grant SF, Li M, Bradfield JP, Kim CE, Annaiah K, Santa E, Glessner JT, Casalunovo T, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Imielinski M, Eckert AW, Chiavacci RM, et al. Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP. Plos One. 3: e1746. PMID 18335027 DOI: 10.1371/journal.pone.0001746  0.4
2008 Li C, Li M, Long JR, Cai Q, Zheng W. Evaluating cost efficiency of SNP chips in genome-wide association studies. Genetic Epidemiology. 32: 387-95. PMID 18271056 DOI: 10.1002/gepi.20312  0.6
2008 Li M, Li C, Guan W. Evaluation of coverage variation of SNP chips for genome-wide association studies. European Journal of Human Genetics : Ejhg. 16: 635-43. PMID 18253166 DOI: 10.1038/sj.ejhg.5202007  0.6
2006 Li M, Atmaca-Sonmez P, Othman M, Branham KE, Khanna R, Wade MS, Li Y, Liang L, Zareparsi S, Swaroop A, Abecasis GR. CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration. Nature Genetics. 38: 1049-54. PMID 16936733 DOI: 10.1038/ng1871  0.4
2006 Li M, Boehnke M, Abecasis GR, Song PX. Quantitative trait linkage analysis using Gaussian copulas. Genetics. 173: 2317-27. PMID 16751671 DOI: 10.1534/genetics.105.054650  0.4
2006 Li M, Boehnke M, Abecasis GR. Efficient study designs for test of genetic association using sibship data and unrelated cases and controls. American Journal of Human Genetics. 78: 778-92. PMID 16642434 DOI: 10.1086/503711  0.4
2005 Zareparsi S, Branham KE, Li M, Shah S, Klein RJ, Ott J, Hoh J, Abecasis GR, Swaroop A. Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration. American Journal of Human Genetics. 77: 149-53. PMID 15895326 DOI: 10.1086/431426  0.4
2005 Li M, Boehnke M, Abecasis GR. Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal. American Journal of Human Genetics. 76: 934-49. PMID 15877278 DOI: 10.1086/430277  0.4
2005 Zareparsi S, Buraczynska M, Branham KE, Shah S, Eng D, Li M, Pawar H, Yashar BM, Moroi SE, Lichter PR, Petty HR, Richards JE, Abecasis GR, Elner VM, Swaroop A. Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration. Human Molecular Genetics. 14: 1449-55. PMID 15829498 DOI: 10.1093/hmg/ddi154  0.4
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