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Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk.
Turner AW, Hu SS, Mosquera JV, Ma WF, Hodonsky CJ, Wong D, Auguste G, Song Y, Sol-Church K, Farber E, Kundu S, Kundaje A, Lopez NG, Ma L, Ghosh SKB, Onengut-Gumuscu S, Ashley EA, Quertermous T, Finn AV, Leeper NJ, Kovacic JC, Björkegren JLM, Zang C, Miller CL. Turner AW, et al. Among authors: quertermous t. Nat Genet. 2022 Jun;54(6):804-816. doi: 10.1038/s41588-022-01069-0. Epub 2022 May 19. Nat Genet. 2022. PMID: 35590109 Free PMC article.
Pathway analysis of coronary atherosclerosis.
King JY, Ferrara R, Tabibiazar R, Spin JM, Chen MM, Kuchinsky A, Vailaya A, Kincaid R, Tsalenko A, Deng DX, Connolly A, Zhang P, Yang E, Watt C, Yakhini Z, Ben-Dor A, Adler A, Bruhn L, Tsao P, Quertermous T, Ashley EA. King JY, et al. Among authors: quertermous t. Physiol Genomics. 2005 Sep 21;23(1):103-18. doi: 10.1152/physiolgenomics.00101.2005. Epub 2005 Jun 7. Physiol Genomics. 2005. PMID: 15942018 Free article.
Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease.
Hlatky MA, Ashley E, Quertermous T, Boothroyd DB, Ridker P, Southwick A, Myers RM, Iribarren C, Fortmann SP, Go AS; Atherosclerotic Disease, Vascular Function and Genetic Epidemiology (ADVANCE) Study. Hlatky MA, et al. Among authors: quertermous t. Am Heart J. 2007 Dec;154(6):1043-51. doi: 10.1016/j.ahj.2007.06.042. Am Heart J. 2007. PMID: 18035073
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.
Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, Iribarren C, Boerwinkle E, Myers R, Risch N, Quertermous T. Assimes TL, et al. Among authors: quertermous t. Hum Genet. 2008 May;123(4):399-408. doi: 10.1007/s00439-008-0489-5. Epub 2008 Mar 28. Hum Genet. 2008. PMID: 18369664 Free PMC article.
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.
Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, Risch N, Quertermous T. Assimes TL, et al. Among authors: quertermous t. Hum Mol Genet. 2008 Aug 1;17(15):2320-8. doi: 10.1093/hmg/ddn132. Epub 2008 Apr 28. Hum Mol Genet. 2008. PMID: 18443000 Free PMC article.
388 results