| Year |
Citation |
Score |
| 2020 |
Liu E, Radmanesh B, Chung BH, Donnan MD, Yi D, Dadi A, Smith KD, Himmelfarb J, Li M, Freedman BS, Lin J. Profiling Nephropathy Risk Variants in Genome-Edited Kidney Organoids with Single-Cell Transcriptomics. Kidney360. 1: 203-215. PMID 32656538 DOI: 10.34067/Kid.0000422019 |
0.39 |
|
| 2020 |
Hu Y, Wang K, Li M. Detecting differential alternative splicing events in scRNA-seq with or without Unique Molecular Identifiers. Plos Computational Biology. 16: e1007925. PMID 32502143 DOI: 10.1371/Journal.Pcbi.1007925 |
0.334 |
|
| 2020 |
Fan J, Hu J, Xue C, Zhang H, Susztak K, Reilly MP, Xiao R, Li M. ASEP: Gene-based detection of allele-specific expression cross individuals in a population by RNA sequencing. Plos Genetics. 16: e1008786. PMID 32392242 DOI: 10.1371/Journal.Pgen.1008786 |
0.383 |
|
| 2020 |
Li YR, Glessner JT, Coe BP, Li J, Mohebnasab M, Chang X, Connolly J, Kao C, Wei Z, Bradfield J, Kim C, Hou C, Khan M, Mentch F, Qiu H, ... ... Li M, et al. Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations. Nature Communications. 11: 255. PMID 31937769 DOI: 10.1038/S41467-019-13624-1 |
0.509 |
|
| 2019 |
Fang L, Kao C, Gonzalez MV, Mafra FA, Pellegrino da Silva R, Li M, Wenzel SS, Wimmer K, Hakonarson H, Wang K. LinkedSV for detection of mosaic structural variants from linked-read exome and genome sequencing data. Nature Communications. 10: 5585. PMID 31811119 DOI: 10.1038/S41467-019-13397-7 |
0.305 |
|
| 2019 |
Wang X, Park J, Susztak K, Zhang NR, Li M. Bulk tissue cell type deconvolution with multi-subject single-cell expression reference. Nature Communications. 10: 380. PMID 30670690 DOI: 10.1038/S41467-018-08023-X |
0.309 |
|
| 2018 |
Wang J, Huang M, Torre E, Dueck H, Shaffer S, Murray J, Raj A, Li M, Zhang NR. Gene expression distribution deconvolution in single-cell RNA sequencing. Proceedings of the National Academy of Sciences of the United States of America. PMID 29946020 DOI: 10.1073/Pnas.1721085115 |
0.321 |
|
| 2018 |
Huang M, Wang J, Torre E, Dueck H, Shaffer S, Bonasio R, Murray JI, Raj A, Li M, Zhang NR. SAVER: gene expression recovery for single-cell RNA sequencing. Nature Methods. PMID 29941873 DOI: 10.1038/S41592-018-0033-Z |
0.318 |
|
| 2018 |
Li G, Feng D, Wang Y, Fu J, Han L, Li L, Grant SFA, Li M, Li M, Gao S. Loss of Cardio-Protective Effects at the CDH13 Locus Due to Gene-Sleep Interaction: The BCAMS Study. Ebiomedicine. PMID 29903569 DOI: 10.1016/J.Ebiom.2018.05.033 |
0.334 |
|
| 2018 |
Zhang H, Zhang NR, Li M, Reilly MP. First Giant Steps Toward a Cell Atlas of Atherosclerosis. Circulation Research. 122: 1632-1634. PMID 29880495 DOI: 10.1161/Circresaha.118.313076 |
0.316 |
|
| 2018 |
Park J, Shrestha R, Qiu C, Kondo A, Huang S, Werth M, Li M, Barasch J, Suszták K. Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease. Science (New York, N.Y.). PMID 29622724 DOI: 10.1126/Science.Aar2131 |
0.306 |
|
| 2017 |
Fu J, Li G, Li L, Yin J, Cheng H, Han L, Zhang Q, Li N, Xiao X, Grant SFA, Li M, Gao S, Mi J, Li M. The role of established East Asian obesity-related loci on pediatric leptin levels highlights a neuronal influence on body weight regulation in Chinese children and adolescents: the BCAMS study. Oncotarget. 8: 93593-93607. PMID 29212175 DOI: 10.18632/Oncotarget.20547 |
0.395 |
|
| 2017 |
Jia C, Hu Y, Kelly D, Kim J, Li M, Zhang NR. Accounting for technical noise in differential expression analysis of single-cell RNA sequencing data. Nucleic Acids Research. PMID 29036714 DOI: 10.1093/Nar/Gkx754 |
0.311 |
|
| 2017 |
Li M, Zauhar RJ, Grazal C, Curcio CA, DeAngelis MM, Stambolian D. RNA expression in human retina. Human Molecular Genetics. 26: R68-R74. PMID 28854577 DOI: 10.1093/Hmg/Ddx219 |
0.414 |
|
| 2017 |
DeAngelis MM, Owen LA, Morrison MA, Morgan DJ, Li M, Shakoor A, Vitale A, Iyengar S, Stambolian D, Kim IK, Farrer LA. Genetics of age-related macular degeneration (AMD). Human Molecular Genetics. 26: R45-R50. PMID 28854576 DOI: 10.1093/Hmg/Ddx228 |
0.364 |
|
| 2017 |
Jiang Y, Zhang NR, Li M. SCALE: modeling allele-specific gene expression by single-cell RNA sequencing. Genome Biology. 18: 74. PMID 28446220 DOI: 10.1186/S13059-017-1200-8 |
0.368 |
|
| 2017 |
Xue C, Zhang X, Zhang H, Ferguson JF, Wang Y, Hinkle C, Li M, Reilly MP. De novo RNA sequence assembly during in vivo inflammatory stress reveals hundreds of unannotated lincRNAs in human blood CD14+ monocytes and in adipose tissue. Physiological Genomics. physiolgenomics.0000. PMID 28389524 DOI: 10.1152/Physiolgenomics.00001.2017 |
0.302 |
|
| 2017 |
Wang X, Xiao R, Zhu X, Li M. Gene Mapping in Admixed Families: A Cautionary Note on the Interpretation of the Transmission Disequilibrium Test and a Possible Solution. Human Heredity. 81: 106-116. PMID 28076865 DOI: 10.1159/000446956 |
0.372 |
|
| 2016 |
Shi J, Hua X, Goedert JJ, Landi MT, Äijö T, Bonneau R, Zhou W, Sherwood B, Ji H, Zappala Z, Montgomery SB, Wang X, Xiao R, Zhu X, Li M, et al. SAGES 2015. Symposium of Advances in Genomics, Epidemiology and Statistics 2015: Abstracts Human Heredity. 81: 51-61. PMID 28076868 DOI: 10.1159/000447110 |
0.304 |
|
| 2016 |
Ballantyne RL, Zhang X, Nuñez S, Xue C, Zhao W, Reed E, Salaheen D, Foulkes AS, Li M, Reilly MP. Genome-wide interrogation reveals hundreds of long intergenic noncoding RNAs that associate with cardiometabolic traits. Human Molecular Genetics. PMID 27288454 DOI: 10.1093/Hmg/Ddw154 |
0.471 |
|
| 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 |
0.334 |
|
| 2016 |
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications. 7: 10023. PMID 26831199 DOI: 10.1038/Ncomms10023 |
0.367 |
|
| 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 |
0.58 |
|
| 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 |
0.621 |
|
| 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 |
0.305 |
|
| 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 |
0.501 |
|
| 2015 |
Xu Z, Duan Q, Yan S, Chen W, Li M, Lange E, Li Y. DISSCO: direct imputation of summary statistics allowing covariates. Bioinformatics (Oxford, England). PMID 25810429 DOI: 10.1093/Bioinformatics/Btv168 |
0.499 |
|
| 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 |
0.471 |
|
| 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 |
0.307 |
|
| 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 |
0.495 |
|
| 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 |
0.419 |
|
| 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 |
0.331 |
|
| 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 |
0.341 |
|
| 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 |
0.588 |
|
| 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 |
0.361 |
|
| 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 |
0.337 |
|
| 2014 |
Hu Y, Liu Y, Mao X, Jia C, Ferguson JF, Xue C, Reilly MP, Li H, Li M. PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distribution. Nucleic Acids Research. 42: e20. PMID 24362841 DOI: 10.1093/Nar/Gkt1304 |
0.331 |
|
| 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 |
0.435 |
|
| 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 |
0.444 |
|
| 2013 |
Liu Y, Ferguson JF, Xue C, Silverman IM, Gregory B, Reilly MP, Li M. Evaluating the impact of sequencing depth on transcriptome profiling in human adipose. Plos One. 8: e66883. PMID 23826166 DOI: 10.1371/Journal.Pone.0066883 |
0.319 |
|
| 2013 |
Chen HY, Reilly MP, Li M. Semiparametric odds ratio model for case-control and matched case-control designs. Statistics in Medicine. 32: 3126-42. PMID 23307592 DOI: 10.1002/Sim.5742 |
0.333 |
|
| 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 |
0.464 |
|
| 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 |
0.444 |
|
| 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 |
0.459 |
|
| 2013 |
Zemel B, Kalkwarf H, Li M, Deliard S, Kim C, Qu L, Chiavacci R, Paulhamus D, Lappe J, Gilsanz V, Hakonarson H, Oberfield S, Shepherd J, Voight B, Kelly A, et al. Role of bone-associated loci identified in GWAS meta-analyses in the context of longitudinal pediatric BMD in European Americans Bone Abstracts. DOI: 10.1530/Boneabs.2.Oc6 |
0.311 |
|
| 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 |
0.489 |
|
| 2012 |
Morris AP, Voight BF, Teslovich TM, Ferreira T, Segrè AV, Steinthorsdottir V, Strawbridge RJ, Khan H, Grallert H, Mahajan A, Prokopenko I, Kang HM, Dina C, Esko T, Fraser RM, ... ... Li M, et al. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nature Genetics. 44: 981-90. PMID 22885922 DOI: 10.1038/Ng.2383 |
0.498 |
|
| 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 |
0.458 |
|
| 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 |
0.376 |
|
| 2012 |
Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... ... Li M, ... ... Li M, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
0.533 |
|
| 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 |
0.451 |
|
| 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 |
0.522 |
|
| 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 |
0.414 |
|
| 2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, ... ... Li M, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.589 |
|
| 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 |
0.442 |
|
| 2012 |
Lanktree M, Guo Y, Murtaza M, Glessner J, Bailey S, Onland-Moret N, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson C, 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 The American Journal of Human Genetics. 90: 1116-1117. DOI: 10.1016/J.Ajhg.2012.05.017 |
0.387 |
|
| 2012 |
Saxena R, Elbers C, Guo Y, Peter I, Gaunt T, Mega J, Lanktree M, Tare A, Castillo B, Li Y, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight B, ... ... Li M, et al. Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci The American Journal of Human Genetics. 90: 753. DOI: 10.1016/J.Ajhg.2012.03.001 |
0.312 |
|
| 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 |
0.404 |
|
| 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 |
0.447 |
|
| 2011 |
Chen HY, Li M. Improving power and robustness for detecting genetic association with extreme-value sampling design. Genetic Epidemiology. 35: 823-30. PMID 22006659 DOI: 10.1002/Gepi.20631 |
0.363 |
|
| 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 |
0.361 |
|
| 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 |
0.343 |
|
| 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 |
0.311 |
|
| 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 |
0.466 |
|
| 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 |
0.356 |
|
| 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 |
0.412 |
|
| 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 |
0.406 |
|
| 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 |
0.329 |
|
| 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 |
0.376 |
|
| 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 |
0.425 |
|
| 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 |
0.436 |
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| 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 |
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| 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 |
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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 |
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Zhao J, Bradfield JP, Li M, Zhang H, Mentch FD, Wang K, Sleiman PM, Kim CE, Glessner JT, Frackelton EC, Chiavacci RM, Berkowitz RI, Zemel BS, Hakonarson H, Grant SF. BMD-associated variation at the Osterix locus is correlated with childhood obesity in females. Obesity (Silver Spring, Md.). 19: 1311-4. PMID 21212767 DOI: 10.1038/Oby.2010.324 |
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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 |
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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 |
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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 |
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Butterworth AS, Braund PS, Farrall M, Hardwick RJ, Saleheen D, Peden JF, Soranzo N, Chambers JC, Sivapalaratnam S, Kleber ME, Keating B, Qasim A, Klopp N, Erdmann J, Assimes TL, ... ... Li M, et al. Large-scale gene-centric analysis identifies novel variants for coronary artery disease Plos Genetics. 7. DOI: 10.1371/Journal.Pgen.1002260 |
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Wang K, Li M, Hakonarson H. Analysing biological pathways in genome-wide association studies. Nature Reviews. Genetics. 11: 843-54. PMID 21085203 DOI: 10.1038/Nrg2884 |
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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 |
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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 |
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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 |
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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 |
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Qin H, Morris N, Kang SJ, Li M, Tayo B, Lyon H, Hirschhorn J, Cooper RS, Zhu X. Interrogating local population structure for fine mapping in genome-wide association studies. Bioinformatics (Oxford, England). 26: 2961-8. PMID 20889494 DOI: 10.1093/Bioinformatics/Btq560 |
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Soranzo N, Sanna S, Wheeler E, Gieger C, Radke D, Dupuis J, Bouatia-Naji N, Langenberg C, Prokopenko I, Stolerman E, Sandhu MS, Heeney MM, Devaney JM, Reilly MP, Ricketts SL, ... ... Li M, ... ... Li M, et al. Common variants at 10 genomic loci influence hemoglobin Aâ‚(C) levels via glycemic and nonglycemic pathways. Diabetes. 59: 3229-39. PMID 20858683 DOI: 10.2337/Db10-0502 |
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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 |
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Zhao J, Schug J, Li M, Kaestner KH, Grant SFA. Disease-associated loci are significantly over-represented among genes bound by transcription factor 7-like 2 (TCF7L2) in vivo Diabetologia. 53: 2340-2346. PMID 20640398 DOI: 10.1007/S00125-010-1852-3 |
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Wang K, Li M, Hakonarson H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Research. 38: e164. PMID 20601685 DOI: 10.1093/Nar/Gkq603 |
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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 |
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Voight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, Zeggini E, Huth C, Aulchenko YS, Thorleifsson G, McCulloch LJ, Ferreira T, Grallert H, Amin N, Wu G, ... ... Li M, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics. 42: 579-89. PMID 20581827 DOI: 10.1038/Ng.609 |
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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 |
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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 |
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Cappola TP, Li M, He J, Ky B, Gilmore J, Qu L, Keating B, Reilly M, Kim CE, Glessner J, Frackelton E, Hakonarson H, Syed F, Hindes A, Matkovich SJ, et al. Common variants in HSPB7 and FRMD4B associated with advanced heart failure. Circulation. Cardiovascular Genetics. 3: 147-54. PMID 20124441 DOI: 10.1161/Circgenetics.109.898395 |
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Li M, Reilly MP, Rader DJ, Wang LS. Correcting population stratification in genetic association studies using a phylogenetic approach. Bioinformatics (Oxford, England). 26: 798-806. PMID 20097913 DOI: 10.1093/Bioinformatics/Btq025 |
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Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, ... ... Li M, et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics. 42: 105-16. PMID 20081858 DOI: 10.1038/Ng.520 |
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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 |
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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 |
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Qasim A, Matthews L, Qu L, Movva R, Parcham-Azad K, DerOhannessian S, Ferguson J, Li M, Rader DJ, Reilly MP. ASSOCIATION OF GENOME WIDE LOCI FOR CAD WITH DISTRIBUTION OF CORONARY DISEASE Journal of the American College of Cardiology. 55: A124.E1161. DOI: 10.1016/S0735-1097(10)61162-X |
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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 |
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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 |
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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 |
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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 |
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Zhao J, Bradfield JP, Li M, Wang K, Zhang H, Kim CE, Annaiah K, Glessner JT, Thomas K, Garris M, Frackelton EC, Otieno FG, Shaner JL, Smith RM, Chiavacci RM, et al. The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI. Obesity (Silver Spring, Md.). 17: 2254-7. PMID 19478790 DOI: 10.1038/Oby.2009.159 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, Erdmann J, Reilly MP, Rader DJ, Morgan T, ... ... Li M, et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nature Genetics. 41: 334-41. PMID 19198609 DOI: 10.1038/Ng.327 |
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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 |
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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 |
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Wang K, Chen Z, Tadesse MG, Glessner J, Grant SF, Hakonarson H, Bucan M, Li M. Modeling genetic inheritance of copy number variations. Nucleic Acids Research. 36: e138. PMID 18832372 DOI: 10.1093/Nar/Gkn641 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Li C, Li M, Lange EM, Watanabe RM. Prioritized subset analysis: improving power in genome-wide association studies. Human Heredity. 65: 129-41. PMID 17934316 DOI: 10.1159/000109730 |
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Wei Z, Li M. Genome-wide linkage and association analysis of rheumatoid arthritis in a Canadian population. Bmc Proceedings. 1: S19. PMID 18466515 |
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Li C, Li M. GWAsimulator: a rapid whole-genome simulation program. Bioinformatics (Oxford, England). 24: 140-2. PMID 18006546 DOI: 10.1093/Bioinformatics/Btm549 |
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Wang K, Li M, Bucan M. Pathway-based approaches for analysis of genomewide association studies. American Journal of Human Genetics. 81: 1278-83. PMID 17966091 DOI: 10.1086/522374 |
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Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA, Hakonarson H, Bucan M. PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome Research. 17: 1665-1674. PMID 17921354 DOI: 10.1101/Gr.6861907 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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