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Page 1
Epigenomes of Human Hearts Reveal New Genetic Variants Relevant for Cardiac Disease and Phenotype.
Circ Res. 2020 Aug 28;127(6):761-777. doi: 10.1161/CIRCRESAHA.120.317254. Epub 2020 Jun 12.
Circ Res. 2020.
PMID: 32529949
Free PMC article.
Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype.
Tragante V, Gho JMIH, Felix JF, Vasan RS, Smith NL, Voight BF; CHARGE Heart Failure Working Group; Palmer C, van der Harst P, Moore JH, Asselbergs FW.
Tragante V, et al.
BioData Min. 2017 May 26;10:18. doi: 10.1186/s13040-017-0137-5. eCollection 2017.
BioData Min. 2017.
PMID: 28559929
Free PMC article.
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Aptamer-Based Proteomic Platform Identifies Novel Protein Predictors of Incident Heart Failure and Echocardiographic Traits.
Nayor M, Short MI, Rasheed H, Lin H, Jonasson C, Yang Q, Hveem K, Felix JF, Morrison AC, Wild PS, Morley MP, Cappola TP, Benson MD; CHARGE-Heart Failure Working Group; CHARGE-EchoGen Consortium; Ngo D, Sinha S, Keyes MJ, Shen D, Wang TJ, Larson MG, Brumpton BM, Gerszten RE, Omland T, Vasan RS.
Nayor M, et al.
Circ Heart Fail. 2020 May;13(5):e006749. doi: 10.1161/CIRCHEARTFAILURE.119.006749. Epub 2020 May 15.
Circ Heart Fail. 2020.
PMID: 32408813
Free PMC article.
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Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.
Ho JE, Chen WY, Chen MH, Larson MG, McCabe EL, Cheng S, Ghorbani A, Coglianese E, Emilsson V, Johnson AD, Walter S, Franceschini N, O'Donnell CJ; CARDIoGRAM Consortium; CHARGE Inflammation Working Group; Dehghan A, Lu C, Levy D, Newton-Cheh C; CHARGE Heart Failure Working Group; Lin H, Felix JF, Schreiter ER, Vasan RS, Januzzi JL, Lee RT, Wang TJ.
Ho JE, et al.
J Clin Invest. 2013 Oct;123(10):4208-18. doi: 10.1172/JCI67119. Epub 2013 Sep 3.
J Clin Invest. 2013.
PMID: 23999434
Free PMC article.
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