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	1.	Burden of risk alleles for hypertension increases risk of intracerebral hemorrhage.[Erratum appears in Stroke. 2012 Nov;43(11):e171] MedStar authors: Kidwell, Chelsea S PMID: 22933587 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 Form of publication: Journal Article 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 DOI: http://dx.doi.org/10.1161/STROKEAHA.112.659755 Add to cart (remove)
	2.	The association of mannose binding lectin genotype and immune response to Chlamydia pneumoniae: The Strong Heart Study. MedStar authors: DeCroo, Susan Zhu, Jianhui PMID: 30629683 Year: 2019 Citation: PLoS ONE [Electronic Resource]. 14(1):e0210640, 2019. Institution: MedStar Health Research Institute Medline publication type: Journal Article Form of publication: Journal Article All authors: Anderson MZ, Best LG, DeCroo S, Monsey L, Zhu J DOI: https://dx.doi.org/10.1371/journal.pone.0210640 Add to cart (remove)
	3.	Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. MedStar authors: Epstein, Stephen E PMID: 25487149 Citation: Nature. 518(7537):102-6, 2015 Feb 5. Institution: MedStar Health Research 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: Abecasis GR, Allayee H, Altshuler D, Angelica Merlini P, Ardissino D, Asselta R, Assimes TL, Auer PL, Bamshad MJ, Boerwinkle E, Burke GL, Carlson CS, Clarke R, Cresci S, Cupples LA, Danesh J, Davies R, DePristo MA, Do R, Donnelly P, Duga S, Epstein SE, Erdmann J, Farlow DN, Farrall M, Folsom AR, Gabriel S, Girelli D, Goel A, Gross M, Guella I, Hamsten A, Hartiala J, Hazen SL, Hechter E, Hegele RA, Heiss G, Herrington DM, Hovingh GK, Huang J, Jackson RD, Johansen CT, Johnson AD, Jorgensen AB, Kastelein JJ, Kathiresan S, Kiezun A, Kleber ME, Kooperberg C, Kraus WE, Lander ES, Lange EM, Lange LA, Li M, Liu Y, Martinelli N, Marz W, McPherson R, NHLBI Exome Sequencing Project, Nickerson DA, Nikpay M, O'Donnell CJ, Olivieri O, Peloso GM, Psaty BM, Rader DJ, Reilly DF, Reilly MP, Reiner AP, Rich SS, Rivas MA, Roberts R, Rossouw JE, Saleheen D, Samani NJ, Schunkert H, Schwartz SM, Shah SH, Siscovick DS, Sivapalaratnam S, Spertus JA, Stewart AF, Stitziel NO, Sunyaev SR, Tang WH, Taylor HA, Tracy RP, Tybjaerg-Hansen A, Wang J, Watkins H, Wilson JG, Won HH, Yin W, Zuk O DOI: http://dx.doi.org/10.1038/nature13917 Add to cart (remove)

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