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	1.	Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study. MedStar authors: Umans, Jason G PMID: 31784582 Year: 2019 Citation: Scientific Reports. 9(1):17899, 2019 11 29. Institution: MedStar Health Research Institute Medline publication type: Journal Article Form of publication: Journal Article All authors: Balakrishnan P, Best LG, Bharadwaj D, Bizon C, Canizales-Quinteros S, Chittoor G, Cole SA, Franceschini N, Haack K, Laston S, MacCluer JW, Macias-Kauffer L, Navas-Acien A, North KE, Prasad G, Umans JG, Villarreal-Molina T, Voruganti VS DOI: https://dx.doi.org/10.1038/s41598-019-52924-w Add to cart (remove)
	2.	Both rare and common variants in PCSK9 influence plasma low-density lipoprotein cholesterol level in American Indians. MedStar authors: Howard, Barbara V PMID: 25412415 Citation: Journal of Clinical Endocrinology & Metabolism. 100(2):E345-9, 2015 Feb. Institution: MedStar Health Research Institute Medline publication type: Journal Article Research Support, N.I.H., Extramural Form of publication: Journal Article All authors: Beaty TH, Best LG, Franceschini N, Haack K, Howard BV, Kao WH, Laston S, MacCluer JW, Navas-Acien A, North KE, Saroja Voruganti V, Tin A, Tsai CW, Zhang Y DOI: http://dx.doi.org/10.1210/jc.2014-3340 Add to cart (remove)
	3.	Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians. MedStar authors: Umans, Jason G PMID: 24301058 Year: 2014 Citation: European Journal of Human Genetics. 22(7):938-43, 2014 Jul. Institution: MedStar Health Research Institute Medline publication type: Clinical Trial Journal Article Multicenter Study Research Support, American Recovery and Reinvestment Act Research Support, N.I.H., Extramural Form of publication: Journal Article All authors: Cole SA, Comuzzie AG, Franceschini N, Haack K, Laston S, MacCluer JW, North KE, Umans JG, Voruganti VS DOI: http://dx.doi.org/10.1038/ejhg.2013.264 Add to cart (remove)
	4.	Leukotriene haplotype x diet interaction on carotid artery hypertrophy and atherosclerosis in American Indians: the Strong Heart Family Study. MedStar authors: Howard, Barbara V PMID: 24529139 Citation: Atherosclerosis. 233(1):165-71, 2014 Mar. Institution: MedStar Health Research Institute Medline publication type: Journal Article Research Support, N.I.H., Extramural Form of publication: Journal Article All authors: Best LG, Cole SA, Devereux RB, Haack K, Howard BV, Lee ET, Roman MJ, Yeh F, Zhang Y, Zhao J DOI: http://dx.doi.org/10.1016/j.atherosclerosis.2013.12.007 Add to cart (remove)
	5.	Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium. MedStar authors: Najjar, Samer S PMID: 22068335 Citation: Circulation. Cardiovascular Genetics. 5(1):81-90, 2012 Feb 1. Institution: MedStar Heart & Vascular Institute Medline publication type: Journal Article Meta-Analysis Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, Non-U.S. Gov't Form of publication: Journal Article All authors: Abecasis GR, Andrews JS, Arfan Ikram M, Aspelund T, Bekaert S, Benjamin EJ, Cockcroft JR, De Backer GG, De Bacquer D, De Buyzere ML, De Meyer T, Dehghan A, Ding J, Eiriksdottir G, Elliott P, Erdmann J, Felix JF, Ferrucci L, Fuchsberger C, Gibson Q, Gillebert TC, Gudnason V, Hamburg NM, Harris TB, Herrington DM, Hofman A, Howard TD, Isaacs A, Jewell ES, Johnson AD, Lakatta EG, Larson MG, Launer LJ, Levy D, Liu Y, Mattace-Raso FU, McArdle PF, McEniery CM, Mitchell GF, Najjar SS, Newhouse SJ, Newman AB, O'Shaughnessy KM, Olden M, Oostra BA, Parsa A, Post WS, Psaty BM, Rietzschel ER, Rivadeneira F, Sanna S, Schut AF, Scuteri A, Segers P, Shuldiner AR, Sie MP, Sigurdsson S, Sijbrands EJ, Smith AV, Smith NL, Sutton-Tyrrell K, Tanaka T, Tarasov KV, Uda M, Uitterlinden AG, Van Bortel L, van Duijn CM, van Rijn MJ, Vasan RS, Verwoert GC, Vita JA, Wain LV, Wilkinson IB, Witteman JC, Yasmin DOI: http://dx.doi.org/10.1161/CIRCGENETICS.111.959817 Add to cart (remove)
	6.	Haptoglobin genotype is a consistent marker of coronary heart disease risk among individuals with elevated glycosylated hemoglobin. MedStar authors: Howard, Barbara V Shara, Nawar M Wang, Hong PMID: 23312704 Year: 2013 Citation: Journal of the American College of Cardiology. 61(7):728-37, 2013 Feb 19. Institution: MedStar Health Research Institute Medline publication type: Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Form of publication: Journal Article All authors: Blum S, Cahill LE, Chiuve SE, Howard BV, Jensen MK, Levy AP, Mukamal KJ, Pai JK, Rexrode KM, Rimm EB, Shara NM, Wang H DOI: Click here to access online Add to cart (remove)
	7.	Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage. MedStar authors: Kidwell, Chelsea S PMID: 23559261 Citation: Stroke. 44(6):1578-83, 2013 Jun. Institution: MedStar Heart & Vascular Institute Medline publication type: Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Form of publication: Journal Article All authors: Anderson CD, Ayres AM, Biffi A, Brown DL, Cuadrado-Godia E, Delgado P, Devan WJ, Falcone GJ, Fernandez-Cadenas I, Freudenberger P, Giralt-Steinhauer E, Goldstein JN, Greenberg SM, Hansen BM, International Stroke Genetics Consortium, Jagiella JM, Jimenez-Conde J, Kassis SB, Kidwell CS, Lindgren A, Meschia JF, Montaner J, Norrving B, Pera J, Roquer J, Rosand J, Rost NS, Schmidt H, Schmidt R, Schwab K, Selim M, Silliman SL, Slowik A, Soriano C, Stogerer EM, Tirschwell DL, Urbanik A, Valant V, Viswanathan A, Woo D, Worrall BB DOI: http://dx.doi.org/10.1161/STROKEAHA.111.000089 Add to cart (remove)

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