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Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study.
Kocarnik JM, Pendergrass SA, Carty CL, Pankow JS, Schumacher FR, Cheng I, Durda P, Ambite JL, Deelman E, Cook NR, Liu S, Wactawski-Wende J, Hutter C, Brown-Gentry K, Wilson S, Best LG, Pankratz N, Hong CP, Cole SA, Voruganti VS, Bůžkova P, Jorgensen NW, Jenny NS, Wilkens LR, Haiman CA, Kolonel LN, Lacroix A, North K, Jackson R, Le Marchand L, Hindorff LA, Crawford DC, Gross M, Peters U. Kocarnik JM, et al. Among authors: jenny ns. Circ Cardiovasc Genet. 2014 Apr;7(2):178-88. doi: 10.1161/CIRCGENETICS.113.000173. Epub 2014 Mar 12. Circ Cardiovasc Genet. 2014. PMID: 24622110 Free PMC article.
Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation.
Reiner AP, Wurfel MM, Lange LA, Carlson CS, Nord AS, Carty CL, Rieder MJ, Desmarais C, Jenny NS, Iribarren C, Walston JD, Williams OD, Nickerson DA, Jarvik GP. Reiner AP, et al. Among authors: jenny ns. Arterioscler Thromb Vasc Biol. 2008 Jul;28(7):1407-12. doi: 10.1161/ATVBAHA.108.167437. Epub 2008 May 1. Arterioscler Thromb Vasc Biol. 2008. PMID: 18451331 Free PMC article.
Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study.
Reiner AP, Gross MD, Carlson CS, Bielinski SJ, Lange LA, Fornage M, Jenny NS, Walston J, Tracy RP, Williams OD, Jacobs DR Jr, Nickerson DA. Reiner AP, et al. Among authors: jenny ns. Circ Cardiovasc Genet. 2009 Jun;2(3):244-54. doi: 10.1161/CIRCGENETICS.108.839506. Epub 2009 Apr 6. Circ Cardiovasc Genet. 2009. PMID: 20031592 Free PMC article.
Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.
Franceschini N, Carty C, Bůzková P, Reiner AP, Garrett T, Lin Y, Vöckler JS, Hindorff LA, Cole SA, Boerwinkle E, Lin DY, Bookman E, Best LG, Bella JN, Eaton C, Greenland P, Jenny N, North KE, Taverna D, Young AM, Deelman E, Kooperberg C, Psaty B, Heiss G. Franceschini N, et al. Circ Cardiovasc Genet. 2011 Dec;4(6):661-72. doi: 10.1161/CIRCGENETICS.111.960096. Epub 2011 Oct 31. Circ Cardiovasc Genet. 2011. PMID: 22042884 Free PMC article.
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study.
Buyske S, Wu Y, Carty CL, Cheng I, Assimes TL, Dumitrescu L, Hindorff LA, Mitchell S, Ambite JL, Boerwinkle E, Buzkova P, Carlson CS, Cochran B, Duggan D, Eaton CB, Fesinmeyer MD, Franceschini N, Haessler J, Jenny N, Kang HM, Kooperberg C, Lin Y, Le Marchand L, Matise TC, Robinson JG, Rodriguez C, Schumacher FR, Voight BF, Young A, Manolio TA, Mohlke KL, Haiman CA, Peters U, Crawford DC, North KE. Buyske S, et al. PLoS One. 2012;7(4):e35651. doi: 10.1371/journal.pone.0035651. Epub 2012 Apr 23. PLoS One. 2012. PMID: 22539988 Free PMC article.
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
Emond MJ, Louie T, Emerson J, Zhao W, Mathias RA, Knowles MR, Wright FA, Rieder MJ, Tabor HK, Nickerson DA, Barnes KC; National Heart, Lung, and Blood Institute (NHLBI) GO Exome Sequencing Project; Lung GO; Gibson RL, Bamshad MJ. Emond MJ, et al. Nat Genet. 2012 Jul 8;44(8):886-9. doi: 10.1038/ng.2344. Nat Genet. 2012. PMID: 22772370 Free PMC article.
205 results