Morrison AC - Search Results

1

Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.

He KY, Li X, Kelly TN, Liang J, Cade BE, Assimes TL, Becker LC, Beitelshees AL, Bress AP, Chang YC, Chen YI, de Vries PS, Fox ER, Franceschini N, Furniss A, Gao Y, Guo X, Haessler J, Hwang SJ, Irvin MR, Kalyani RR, Liu CT, Liu C, Martin LW, Montasser ME, Muntner PM, Mwasongwe S, Palmas W, Reiner AP, Shimbo D, Smith JA, Snively BM, Yanek LR, Boerwinkle E, Correa A, Cupples LA, He J, Kardia SLR, Kooperberg C, Mathias RA, Mitchell BD, Psaty BM, Vasan RS, Rao DC, Rich SS, Rotter JI, Wilson JG; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Blood Pressure Working Group; Chakravarti A, Morrison AC, Levy D, Arnett DK, Redline S, Zhu X. He KY, et al. Among authors: morrison ac. Hum Genet. 2019 Feb;138(2):199-210. doi: 10.1007/s00439-019-01975-0. Epub 2019 Jan 22. Hum Genet. 2019. PMID: 30671673 Free PMC article.

2

Beta3-adrenergic receptor Trp64Arg polymorphism does not predict incident CHD or carotid intima-media thickness in a community-based sample of whites: the ARIC study. Atherosclerosis Risk in Communities.

Morrison AC, Brancati FL, Folsom AR, Smith L, Boerwinkle E. Morrison AC, et al. Hum Genet. 1999 Oct;105(4):314-9. doi: 10.1007/s004399900096. Hum Genet. 1999. PMID: 10543398

3

Parental history of stroke predicts subclinical but not clinical stroke: the Atherosclerosis Risk in Communities Study.

Morrison AC, Fornage M, Liao D, Boerwinkle E. Morrison AC, et al. Stroke. 2000 Sep;31(9):2098-102. doi: 10.1161/01.str.31.9.2098. Stroke. 2000. PMID: 10978036

4

G-protein beta3 subunit and alpha-adducin polymorphisms and risk of subclinical and clinical stroke.

Morrison AC, Doris PA, Folsom AR, Nieto FJ, Boerwinkle E; Atherosclerosis Risk in Communities Study. Morrison AC, et al. Stroke. 2001 Apr;32(4):822-9. doi: 10.1161/01.str.32.4.822. Stroke. 2001. PMID: 11283377

5

Linkage disequilibrium structure and its impact on the localization of a candidate functional mutation.

Huang Q, Morrison AC, Boerwinkle E. Huang Q, et al. Among authors: morrison ac. Genet Epidemiol. 2001;21 Suppl 1:S620-5. doi: 10.1002/gepi.2001.21.s1.s620. Genet Epidemiol. 2001. PMID: 11793750

6

LPL polymorphism predicts stroke risk in men.

Morrison AC, Ballantyne CM, Bray M, Chambless LE, Sharrett AR, Boerwinkle E. Morrison AC, et al. Genet Epidemiol. 2002 Mar;22(3):233-42. doi: 10.1002/gepi.0191. Genet Epidemiol. 2002. PMID: 11921083

7

ADD1 460W allele associated with cardiovascular disease in hypertensive individuals.

Morrison AC, Bray MS, Folsom AR, Boerwinkle E. Morrison AC, et al. Hypertension. 2002 Jun;39(6):1053-7. doi: 10.1161/01.hyp.0000019128.94483.3a. Hypertension. 2002. PMID: 12052841

8

Evaluating the context-dependent effect of family history of stroke in a genome scan for hypertension.

Morrison AC, Brown A, Kardia SL, Turner ST, Boerwinkle E; Genetic Epidemiology Network of Arteriopathy (GENOA) Study. Morrison AC, et al. Stroke. 2003 May;34(5):1170-5. doi: 10.1161/01.STR.0000068780.47411.16. Epub 2003 Apr 24. Stroke. 2003. PMID: 12714704

9

Genome scan for hypertension in nonobese African Americans: the National Heart, Lung, and Blood Institute Family Blood Pressure Program.

Morrison AC, Cooper R, Hunt S, Lewis CE, Luke A, Mosley TH, Boerwinkle E. Morrison AC, et al. Am J Hypertens. 2004 Sep;17(9):834-8. doi: 10.1016/j.amjhyper.2004.04.009. Am J Hypertens. 2004. PMID: 15363828

10

Genome-wide linkage study of erythrocyte sodium-lithium countertransport.

Morrison AC, Boerwinkle E, Turner ST, Ferrell RE. Morrison AC, et al. Am J Hypertens. 2005 May;18(5 Pt 1):653-6. doi: 10.1016/j.amjhyper.2004.11.030. Am J Hypertens. 2005. PMID: 15882547

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