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Items: 1 to 20 of 90

1.

GATA2 is associated with familial early-onset coronary artery disease.

Connelly JJ, Wang T, Cox JE, Haynes C, Wang L, Shah SH, Crosslin DR, Hale AB, Nelson S, Crossman DC, Granger CB, Haines JL, Jones CJ, Vance JM, Goldschmidt-Clermont PJ, Kraus WE, Hauser ER, Gregory SG.

PLoS Genet. 2006 Aug 25;2(8):e139. Epub 2006 Jul 20.

2.

Genetic and functional association of FAM5C with myocardial infarction.

Connelly JJ, Shah SH, Doss JF, Gadson S, Nelson S, Crosslin DR, Hale AB, Lou X, Wang T, Haynes C, Seo D, Crossman DC, Mooser V, Granger CB, Jones CJ, Kraus WE, Hauser ER, Gregory SG.

BMC Med Genet. 2008 Apr 22;9:33. doi: 10.1186/1471-2350-9-33.

3.

A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits.

Muiya NP, Wakil S, Al-Najai M, Tahir AI, Baz B, Andres E, Al-Boudari O, Al-Tassan N, Al-Shahid M, Meyer BF, Dzimiri N.

Gene. 2014 Jul 10;544(2):152-8. doi: 10.1016/j.gene.2014.04.064. Epub 2014 Apr 28.

PMID:
24786211
4.

Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.

Wang L, Hauser ER, Shah SH, Pericak-Vance MA, Haynes C, Crosslin D, Harris M, Nelson S, Hale AB, Granger CB, Haines JL, Jones CJ, Crossman D, Seo D, Gregory SG, Kraus WE, Goldschmidt-Clermont PJ, Vance JM.

Am J Hum Genet. 2007 Apr;80(4):650-63. Epub 2007 Feb 8.

5.

Association study of GATA-2 transcription factor gene (GATA2) polymorphism and Parkinson's disease.

Kurzawski M, Białecka M, Sławek J, Kłodowska-Duda G, Droździk M.

Parkinsonism Relat Disord. 2010 May;16(4):284-7. doi: 10.1016/j.parkreldis.2009.10.006. Epub 2009 Oct 27.

PMID:
19864173
6.

Polymorphisms in the IL6 gene in Asian Indian families with premature coronary artery disease--the Indian Atherosclerosis Research Study.

Maitra A, Shanker J, Dash D, John S, Sannappa PR, Rao VS, Ramanna JK, Kakkar VV.

Thromb Haemost. 2008 May;99(5):944-50. doi: 10.1160/TH07-11-0686.

PMID:
18449426
7.

The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies.

Dandona S, Chen L, Fan M, Alam MA, Assogba O, Belanger M, Williams K, Wells GA, Tang WH, Ellis SG, Hazen SL, McPherson R, Roberts R, Stewart AF.

Hum Genet. 2010 Jan;127(1):101-5. doi: 10.1007/s00439-009-0761-3. Epub 2009 Nov 3.

8.

A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease.

Chen Z, Qian Q, Ma G, Wang J, Zhang X, Feng Y, Shen C, Yao Y.

Mol Biol Rep. 2009 May;36(5):889-93. doi: 10.1007/s11033-008-9259-7. Epub 2008 May 6.

PMID:
18459066
9.

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.

Topol EJ, McCarthy J, Gabriel S, Moliterno DJ, Rogers WJ, Newby LK, Freedman M, Metivier J, Cannata R, O'Donnell CJ, Kottke-Marchant K, Murugesan G, Plow EF, Stenina O, Daley GQ.

Circulation. 2001 Nov 27;104(22):2641-4.

10.

Association of RAGE gene polymorphisms with coronary artery disease in the Korean population.

Yoon SJ, Park S, Shim CY, Park CM, Ko YG, Choi D, Park HY, Oh B, Kim H, Jang Y, Chung N.

Coron Artery Dis. 2007 Feb;18(1):1-8.

PMID:
17172923
11.

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.

Hauser ER, Crossman DC, Granger CB, Haines JL, Jones CJ, Mooser V, McAdam B, Winkelmann BR, Wiseman AH, Muhlestein JB, Bartel AG, Dennis CA, Dowdy E, Estabrooks S, Eggleston K, Francis S, Roche K, Clevenger PW, Huang L, Pedersen B, Shah S, Schmidt S, Haynes C, West S, Asper D, Booze M, Sharma S, Sundseth S, Middleton L, Roses AD, Hauser MA, Vance JM, Pericak-Vance MA, Kraus WE.

Am J Hum Genet. 2004 Sep;75(3):436-47. Epub 2004 Jul 22.

12.

Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.

Shah SH, Kraus WE, Crossman DC, Granger CB, Haines JL, Jones CJ, Mooser V, Huang L, Haynes C, Dowdy E, Vega GL, Grundy SM, Vance JM, Hauser ER.

Ann Hum Genet. 2006 Nov;70(Pt 6):738-48.

13.

The adiponectin gene SNP+276G>T associates with early-onset coronary artery disease and with lower levels of adiponectin in younger coronary artery disease patients (age <or=50 years).

Filippi E, Sentinelli F, Romeo S, Arca M, Berni A, Tiberti C, Verrienti A, Fanelli M, Fallarino M, Sorropago G, Baroni MG.

J Mol Med (Berl). 2005 Sep;83(9):711-9. Epub 2005 May 5.

PMID:
15877215
14.

Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.

Wang L, Hauser ER, Shah SH, Seo D, Sivashanmugam P, Exum ST, Gregory SG, Granger CB, Haines JL, Jones CJ, Crossman D, Haynes C, Kraus WE, Freedman NJ, Pericak-Vance MA, Goldschmidt-Clermont PJ, Vance JM.

Ann Hum Genet. 2008 Jul;72(Pt 4):443-53. doi: 10.1111/j.1469-1809.2008.00433.x. Epub 2008 Jul 3.

15.

Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.

Sutton BS, Crosslin DR, Shah SH, Nelson SC, Bassil A, Hale AB, Haynes C, Goldschmidt-Clermont PJ, Vance JM, Seo D, Kraus WE, Gregory SG, Hauser ER.

Hum Mol Genet. 2008 May 1;17(9):1318-28. doi: 10.1093/hmg/ddn020. Epub 2008 Jan 18.

16.

Family-based association studies of lipid gene polymorphisms in coronary artery disease.

Allen A, Belton C, Patterson C, Horan P, McGlinchey P, Spence M, Evans A, Fogarty D, McKeown P.

Am J Cardiol. 2005 Jul 1;96(1):52-5.

PMID:
15979432
17.

Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.

Ward-Caviness C, Haynes C, Blach C, Dowdy E, Gregory SG, Shah SH, Horne BD, Kraus WE, Hauser ER.

Hum Genet. 2013 Dec;132(12):1371-82. doi: 10.1007/s00439-013-1339-7. Epub 2013 Aug 2.

18.

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.

Ding H, Xu Y, Wang X, Wang Q, Zhang L, Tu Y, Yan J, Wang W, Hui R, Wang CY, Wang DW.

Circ Cardiovasc Genet. 2009 Aug;2(4):338-46. doi: 10.1161/CIRCGENETICS.108.810226. Epub 2009 May 28.

19.

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients.

Kyriakou T, Pontefract DE, Viturro E, Hodgkinson CP, Laxton RC, Bogari N, Cooper G, Davies M, Giblett J, Day IN, Simpson IA, Albrecht C, Ye S.

Hum Mol Genet. 2007 Jun 15;16(12):1412-22. Epub 2007 Apr 5.

20.

Multifactor dimensionality reduction analysis of MTHFR, PAI-1, ACE, PON1, and eNOS gene polymorphisms in patients with early onset coronary artery disease.

Agirbasli M, Guney AI, Ozturhan HS, Agirbasli D, Ulucan K, Sevinc D, Kirac D, Ryckman KK, Williams SM.

Eur J Cardiovasc Prev Rehabil. 2011 Dec;18(6):803-9. doi: 10.1177/1741826711398806. Epub 2011 Feb 22.

PMID:
21450592
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