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1.
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
2.
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
3.
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
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