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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 2 |
2010 | 1 |
2011 | 1 |
2012 | 1 |
2013 | 1 |
2014 | 1 |
2024 | 0 |
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7 results
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Page 1
Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations.
BMC Genet. 2014 Jul 9;15:81. doi: 10.1186/1471-2156-15-81.
BMC Genet. 2014.
PMID: 25007794
Free PMC article.
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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Using family-based imputation in genome-wide association studies with large complex pedigrees: the Framingham Heart Study.
Chen MH, Huang J, Chen WM, Larson MG, Fox CS, Vasan RS, Seshadri S, O'Donnell CJ, Yang Q.
Chen MH, et al.
PLoS One. 2012;7(12):e51589. doi: 10.1371/journal.pone.0051589. Epub 2012 Dec 17.
PLoS One. 2012.
PMID: 23284720
Free PMC article.
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A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees.
Chen MH, Liu X, Wei F, Larson MG, Fox CS, Vasan RS, Yang Q.
Chen MH, et al.
Genet Epidemiol. 2011 Nov;35(7):650-7. doi: 10.1002/gepi.20614. Epub 2011 Aug 4.
Genet Epidemiol. 2011.
PMID: 21818773
Free PMC article.
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Development of a risk score for atrial fibrillation (Framingham Heart Study): a community-based cohort study.
Schnabel RB, Sullivan LM, Levy D, Pencina MJ, Massaro JM, D'Agostino RB Sr, Newton-Cheh C, Yamamoto JF, Magnani JW, Tadros TM, Kannel WB, Wang TJ, Ellinor PT, Wolf PA, Vasan RS, Benjamin EJ.
Schnabel RB, et al.
Lancet. 2009 Feb 28;373(9665):739-45. doi: 10.1016/S0140-6736(09)60443-8.
Lancet. 2009.
PMID: 19249635
Free PMC article.
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Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Smith NL, Felix JF, Morrison AC, Demissie S, Glazer NL, Loehr LR, Cupples LA, Dehghan A, Lumley T, Rosamond WD, Lieb W, Rivadeneira F, Bis JC, Folsom AR, Benjamin E, Aulchenko YS, Haritunians T, Couper D, Murabito J, Wang YA, Stricker BH, Gottdiener JS, Chang PP, Wang TJ, Rice KM, Hofman A, Heckbert SR, Fox ER, O'Donnell CJ, Uitterlinden AG, Rotter JI, Willerson JT, Levy D, van Duijn CM, Psaty BM, Witteman JC, Boerwinkle E, Vasan RS.
Smith NL, et al.
Circ Cardiovasc Genet. 2010 Jun;3(3):256-66. doi: 10.1161/CIRCGENETICS.109.895763. Epub 2010 May 5.
Circ Cardiovasc Genet. 2010.
PMID: 20445134
Free PMC article.
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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel RB, Bis JC, Boerwinkle E, Sinner MF, Dehghan A, Lubitz SA, D'Agostino RB Sr, Lumley T, Ehret GB, Heeringa J, Aspelund T, Newton-Cheh C, Larson MG, Marciante KD, Soliman EZ, Rivadeneira F, Wang TJ, Eiríksdottir G, Levy D, Psaty BM, Li M, Chamberlain AM, Hofman A, Vasan RS, Harris TB, Rotter JI, Kao WH, Agarwal SK, Stricker BH, Wang K, Launer LJ, Smith NL, Chakravarti A, Uitterlinden AG, Wolf PA, Sotoodehnia N, Köttgen A, van Duijn CM, Meitinger T, Mueller M, Perz S, Steinbeck G, Wichmann HE, Lunetta KL, Heckbert SR, Gudnason V, Alonso A, Kääb S, Ellinor PT, Witteman JC.
Benjamin EJ, et al.
Nat Genet. 2009 Aug;41(8):879-81. doi: 10.1038/ng.416. Epub 2009 Jul 13.
Nat Genet. 2009.
PMID: 19597492
Free PMC article.
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