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Items: 1 to 20 of 73

1.

[Evaluation of association between 9 genetic polymorphism and myocardial infarction in the Siberian population].

Maksimov VN, Kulikov IV, Orlov PS, Gafarov VV, Maliutina SK, Romashchenko AG, Voevoda MI.

Vestn Ross Akad Med Nauk. 2012;(5):24-9. Russian.

PMID:
22856164
2.

[Genetic predictors of myocardial infarction in subjects of young age].

Shesternia PA, Nikulina SIu, Shul'man VA, Martynova EA, Demkina AI, Orlov PS, Maksimov VN, Voevoda MI.

Kardiologiia. 2013;53(7):4-8. Russian.

PMID:
24087953
3.

Association of the genetic markers for myocardial infarction with sudden cardiac death.

Ivanova AA, Maksimov VN, Orlov PS, Ivanoshchuk DE, Savchenko SV, Voevoda MI.

Indian Heart J. 2017 Apr;69 Suppl 1:S8-S11. doi: 10.1016/j.ihj.2016.07.016. Epub 2016 Jul 30.

4.

Association of ANRIL polymorphism (rs1333049:C>G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia.

Ahmed W, Ali IS, Riaz M, Younas A, Sadeque A, Niazi AK, Niazi SH, Ali SH, Azam M, Qamar R.

Gene. 2013 Feb 25;515(2):416-20. doi: 10.1016/j.gene.2012.12.044. Epub 2012 Dec 21.

PMID:
23266621
5.

Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

Dehghan A, Bis JC, White CC, Smith AV, Morrison AC, Cupples LA, Trompet S, Chasman DI, Lumley T, Völker U, Buckley BM, Ding J, Jensen MK, Folsom AR, Kritchevsky SB, Girman CJ, Ford I, Dörr M, Salomaa V, Uitterlinden AG, Eiriksdottir G, Vasan RS, Franceschini N, Carty CL, Virtamo J, Demissie S, Amouyel P, Arveiler D, Heckbert SR, Ferrières J, Ducimetière P, Smith NL, Wang YA, Siscovick DS, Rice KM, Wiklund PG, Taylor KD, Evans A, Kee F, Rotter JI, Karvanen J, Kuulasmaa K, Heiss G, Kraft P, Launer LJ, Hofman A, Markus MR, Rose LM, Silander K, Wagner P, Benjamin EJ, Lohman K, Stott DJ, Rivadeneira F, Harris TB, Levy D, Liu Y, Rimm EB, Jukema JW, Völzke H, Ridker PM, Blankenberg S, Franco OH, Gudnason V, Psaty BM, Boerwinkle E, O'Donnell CJ.

PLoS One. 2016 Mar 7;11(3):e0144997. doi: 10.1371/journal.pone.0144997. eCollection 2016.

6.

Genetic Variant rs10757278 on Chromosome 9p21 Contributes to Myocardial Infarction Susceptibility.

Chen G, Fu X, Wang G, Liu G, Bai X.

Int J Mol Sci. 2015 May 21;16(5):11678-88. doi: 10.3390/ijms160511678.

7.

Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population.

Hiura Y, Fukushima Y, Yuno M, Sawamura H, Kokubo Y, Okamura T, Tomoike H, Goto Y, Nonogi H, Takahashi R, Iwai N.

Circ J. 2008 Aug;72(8):1213-7.

8.

Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease.

Virani SS, Brautbar A, Lee VV, MacArthur E, Morrison AC, Grove ML, Nambi V, Frazier L, Wilson JM, Willerson JT, Boerwinkle E, Ballantyne CM.

Circ J. 2012;76(4):950-6. Epub 2012 Feb 9.

9.

Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.

Wang AZ, Li L, Zhang B, Shen GQ, Wang QK.

Ann Hum Genet. 2011 Jul;75(4):475-82. doi: 10.1111/j.1469-1809.2011.00646.x. Epub 2011 Apr 4.

10.

Polymorphisms in dipeptidyl peptidase IV gene are associated with the risk of myocardial infarction in patients with atherosclerosis.

Aghili N, Devaney JM, Alderman LO, Zukowska Z, Epstein SE, Burnett MS.

Neuropeptides. 2012 Dec;46(6):367-71. doi: 10.1016/j.npep.2012.10.001. Epub 2012 Oct 31.

PMID:
23122333
11.

Variations of specific non-candidate genes and risk of myocardial infarction: a replication study.

Koch W, Hoppmann P, Schömig A, Kastrati A.

Int J Cardiol. 2011 Feb 17;147(1):38-41. doi: 10.1016/j.ijcard.2009.07.028. Epub 2009 Aug 25.

PMID:
19709766
12.

Polymorphisms in the long non-coding RNA CDKN2B-AS1 may contribute to higher systolic blood pressure levels in hypertensive patients.

Bayoglu B, Yuksel H, Cakmak HA, Dirican A, Cengiz M.

Clin Biochem. 2016 Jul;49(10-11):821-7. doi: 10.1016/j.clinbiochem.2016.02.012. Epub 2016 Mar 2.

PMID:
26944720
13.

Genetic variants associated with myocardial infarction and the risk factors in Chinese population.

Wang Y, Wang L, Liu X, Zhang Y, Yu L, Zhang F, Liu L, Cai J, Yang X, Wang X.

PLoS One. 2014 Jan 27;9(1):e86332. doi: 10.1371/journal.pone.0086332. eCollection 2014.

14.

Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study.

Dehghan A, van Hoek M, Sijbrands EJ, Oostra BA, Hofman A, van Duijn CM, Witteman JC.

BMC Med. 2008 Oct 16;6:30. doi: 10.1186/1741-7015-6-30.

15.

The chromosome 9p21 region and myocardial infarction in a European population.

Koch W, Türk S, Erl A, Hoppmann P, Pfeufer A, King L, Schömig A, Kastrati A.

Atherosclerosis. 2011 Jul;217(1):220-6. doi: 10.1016/j.atherosclerosis.2011.03.014. Epub 2011 Mar 24.

PMID:
21511257
16.

Associations with myocardial infarction of six polymorphisms selected from a three-stage genome-wide association study.

Horne BD, Carlquist JF, Muhlestein JB, Nicholas ZP, Anderson JL; Intermountain Heart Collaborative Study Group.

Am Heart J. 2007 Nov;154(5):969-75.

PMID:
17967605
17.

Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.

Szpakowicz A, Kiliszek M, Pepinski W, Waszkiewicz E, Franaszczyk M, Skawronska M, Ploski R, Niemcunowicz-Janica A, Dobrzycki S, Opolski G, Musial WJ, Kaminski KA.

PLoS One. 2014 Aug 8;9(8):e104635. doi: 10.1371/journal.pone.0104635. eCollection 2014.

18.

Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.

Szpakowicz A, Pepinski W, Waszkiewicz E, Maciorkowska D, Skawronska M, Niemcunowicz-Janica A, Milewski R, Dobrzycki S, Musial WJ, Kaminski KA.

PLoS One. 2013 Sep 12;8(9):e72333. doi: 10.1371/journal.pone.0072333. eCollection 2013. Retraction in: PLoS One. 2014;9(4):e95513.

19.

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

Shen GQ, Rao S, Martinelli N, Li L, Olivieri O, Corrocher R, Abdullah KG, Hazen SL, Smith J, Barnard J, Plow EF, Girelli D, Wang QK.

J Hum Genet. 2008;53(2):144-50. Epub 2007 Dec 8.

PMID:
18066490
20.

Chromosome 9p21 rs10757278 polymorphism is associated with the risk of metabolic syndrome.

Bayoglu B, Cakmak HA, Yuksel H, Can G, Karadag B, Ulutin T, Vural VA, Cengiz M.

Mol Cell Biochem. 2013 Jul;379(1-2):77-85. doi: 10.1007/s11010-013-1629-3. Epub 2013 Mar 28.

PMID:
23535969

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