Results
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1.
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Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study. MedStar authors:
Year: 2019
Citation: - Scientific Reports. 9(1):17899, 2019 11 29.
Institution: - MedStar Health Research Institute
Medline publication type:
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
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Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development. MedStar authors:
Year: 2019
Citation: - Circulation. 140(16):1318-1330, 2019 10 15.
Institution: - MedStar Health Research Institute
Medline publication type:
All authors: - Aung N, Barnes MR, Bluemke DA, Cabrera CP, Fung K, Lima JAC, Manichaikul AW, Munroe PB, Neubauer S, Petersen SE, Piechnik SK, Rotter JI, Taylor KD, Tzanis E, Vargas JD, Warren HR, Yang C
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3.
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Genetic and Nongenetic Implications of Racial Variation in Response to Antiplatelet Therapy. [Review] MedStar authors:
- Attaran, Saina
- Buchanan, Kyle
- Gajanana, Deepakraj
- Garcia-Garcia, Hector M
- Iantorno, Micaela
- Rogers, Toby
- Torguson, Rebecca
- Waksman, Ron
- Weintraub, William S
Year: 2019
Citation: - American Journal of Cardiology. 123(11):1878-1883, 2019 Jun 01.
Institution: - MedStar Heart & Vascular Institute
Medline publication type:
All authors: - Attaran S, Buchanan KD, Gajanana D, Garcia-Garcia HM, Iantorno M, Rogers T, Torguson R, Waksman R, Weintraub WS
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Association of APOL1 With Heart Failure With Preserved Ejection Fraction in Postmenopausal African American Women. MedStar authors:
Year: 2018
Citation: - JAMA Cardiology. 3(8):712-720, 2018 Aug 01.
Institution: - MedStar Heart & Vascular Institute
Medline publication type:
All authors: - Barac A, Franceschini N, Kopp JB, Li Y, Martin LW, Pollak M, Qian H, Reiner AP, Rosamond WD, Wallace RB, Winkler CA
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6.
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Association of caspase-1 polymorphisms with Chagas cardiomyopathy among individuals in Santa Cruz, Bolivia. MedStar authors:
Year: 2017
Citation: - Revista Da Sociedade Brasileira de Medicina Tropical. 50(4):516-523, 2017 Jul-Aug
Institution: - MedStar Heart & Vascular Institute
Medline publication type:
All authors: - Almuedo A, Alyesh D, Bern C, Clipman SJ, Colanzi R, Crawford T, Duran G, Flores J, Fu KY, Gilman RH, Henderson-Frost J, Marcus R, Steinberg H, Zamudio R
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7.
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Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study. MedStar authors:
Year: 2014
Citation: - Circulation. Cardiovascular Genetics. 7(4):505-13, 2014 Aug.
Institution: - MedStar Health Research Institute
Medline publication type:
- Journal Article
- Meta-Analysis
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't
All authors: - Aroda V, Bhattacharjee S, Carlson CS, Carty CL, Chatterjee N, Cheng I, Haessler J, Hindorff LA, Hsu CN, Jackson R, Kooperberg C, Liu S, North KE, Pankow JS, Peters U, Selvin E, Wilkens L
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8.
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Both rare and common variants in PCSK9 influence plasma low-density lipoprotein cholesterol level in American Indians. MedStar authors:
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
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
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9.
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Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians. MedStar authors:
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
All authors: - Cole SA, Comuzzie AG, Franceschini N, Haack K, Laston S, MacCluer JW, North KE, Umans JG, Voruganti VS
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10.
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Leukotriene haplotype x diet interaction on carotid artery hypertrophy and atherosclerosis in American Indians: the Strong Heart Family Study. MedStar authors:
Citation: - Atherosclerosis. 233(1):165-71, 2014 Mar.
Institution: - MedStar Health Research Institute
Medline publication type:
- Journal Article
- Research Support, N.I.H., Extramural
All authors: - Best LG, Cole SA, Devereux RB, Haack K, Howard BV, Lee ET, Roman MJ, Yeh F, Zhang Y, Zhao J
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11.
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Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage.[Erratum appears in Stroke. 2012 Nov;43(11):e171] MedStar authors:
Citation: - Stroke. 43(11):2877-83, 2012 Nov.
Institution: - MedStar Heart & Vascular Institute
Medline publication type:
- Journal Article
- Multicenter Study
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't
All authors: - Ayres AM, Biffi A, Broderick JP, Brown DL, Cuadrado-Godia E, Delgado P, Devan WJ, Elosua R, Enzinger C, Falcone GJ, Fernandez-Cadenas I, Flaherty ML, Giralt-Steinhauer E, Goldstein JN, Greenberg SM, Hansen BM, International Stroke Genetics Consortium, Jagiella JM, Jimenez-Conde J, Kidwell CS, Kissela B, Kleindorfer DO, Langefeld CD, Lindgren A, Meschia JF, Montaner J, Norrving B, Pera J, Pichler A, Roquer J, Rosand J, Rost NS, Schmidt H, Schmidt R, Schwab K, Selim M, Silliman SL, Slowik A, Soriano C, Tirschwell DL, Urbanik A, Viswanathan A, Woo D, Worrall BB
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12.
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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:
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
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
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13.
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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
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
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
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14.
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Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage. MedStar authors:
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
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
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