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Items: 1 to 20 of 110

1.

Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.

Ronald J, Rajagopalan R, Cerrato F, Nord AS, Hatsukami T, Kohler T, Marcovina S, Heagerty P, Jarvik GP.

Stroke. 2011 Jan;42(1):2-9. doi: 10.1161/STROKEAHA.110.591230. Epub 2010 Dec 2.

2.

Functional Variant in the SLC22A3-LPAL2-LPA Gene Cluster Contributes to the Severity of Coronary Artery Disease.

Wang L, Chen J, Zeng Y, Wei J, Jing J, Li G, Su L, Tang X, Wu T, Zhou L.

Arterioscler Thromb Vasc Biol. 2016 Sep;36(9):1989-96. doi: 10.1161/ATVBAHA.116.307311. Epub 2016 Jul 14.

3.

Genetic variants associated with Lp(a) lipoprotein level and coronary disease.

Clarke R, Peden JF, Hopewell JC, Kyriakou T, Goel A, Heath SC, Parish S, Barlera S, Franzosi MG, Rust S, Bennett D, Silveira A, Malarstig A, Green FR, Lathrop M, Gigante B, Leander K, de Faire U, Seedorf U, Hamsten A, Collins R, Watkins H, Farrall M; PROCARDIS Consortium.

N Engl J Med. 2009 Dec 24;361(26):2518-28. doi: 10.1056/NEJMoa0902604.

4.

LPA and PLG sequence variation and kringle IV-2 copy number in two populations.

Crawford DC, Peng Z, Cheng JF, Boffelli D, Ahearn M, Nguyen D, Shaffer T, Yi Q, Livingston RJ, Rieder MJ, Nickerson DA.

Hum Hered. 2008;66(4):199-209. doi: 10.1159/000143403. Epub 2008 Jul 9.

5.

Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study.

Lv X, Zhang Y, Rao S, Liu F, Zuo X, Su D, Wang M, Xia M, Guo H, Feng D, Hong C, Li D, Ma W, Ouyang P, Li X, Feng X, Yang Y, Ling W, Qiu J.

Lipids Health Dis. 2012 Oct 4;11:128. doi: 10.1186/1476-511X-11-128.

6.

Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous Thromboembolism.

Sticchi E, Magi A, Kamstrup PR, Marcucci R, Prisco D, Martinelli I, Mannucci PM, Abbate R, Giusti B.

PLoS One. 2016 Feb 22;11(2):e0149427. doi: 10.1371/journal.pone.0149427. eCollection 2016.

7.

Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.

Qi Q, Workalemahu T, Zhang C, Hu FB, Qi L.

Eur Heart J. 2012 Feb;33(3):325-34. doi: 10.1093/eurheartj/ehr350. Epub 2011 Sep 6.

8.

Determination of lipoprotein(a) kringle repeat number from genomic DNA: copy number variation genotyping using qPCR.

Lanktree MB, Rajakumar C, Brunt JH, Koschinsky ML, Connelly PW, Hegele RA.

J Lipid Res. 2009 Apr;50(4):768-72. doi: 10.1194/jlr.D800050-JLR200. Epub 2008 Dec 5.

9.

Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysis.

Saleheen D, Haycock PC, Zhao W, Rasheed A, Taleb A, Imran A, Abbas S, Majeed F, Akhtar S, Qamar N, Zaman KS, Yaqoob Z, Saghir T, Rizvi SNH, Memon A, Mallick NH, Ishaq M, Rasheed SZ, Memon FU, Mahmood K, Ahmed N, Frossard P, Tsimikas S, Witztum JL, Marcovina S, Sandhu M, Rader DJ, Danesh J.

Lancet Diabetes Endocrinol. 2017 Jul;5(7):524-533. doi: 10.1016/S2213-8587(17)30088-8. Epub 2017 Apr 10. Erratum in: Lancet Diabetes Endocrinol. 2017 Sep;5(9):e6.

10.

Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.

Ronald J, Rajagopalan R, Ranchalis JE, Marshall JK, Hatsukami TS, Heagerty PJ, Jarvik GP.

Lipids Health Dis. 2009 Dec 1;8:52. doi: 10.1186/1476-511X-8-52.

11.

Validation and quantification of genetic determinants of lipoprotein-a levels and predictive value for angiographic coronary artery disease.

Anderson JL, Knight S, May HT, Horne BD, Bair TL, Huntinghouse JA, Rollo JS, Muhlestein JB, Carlquist JF.

Am J Cardiol. 2013 Sep 15;112(6):799-804. doi: 10.1016/j.amjcard.2013.05.009. Epub 2013 Jun 1. Erratum in: Am J Cardiol. 2013 Dec 15;112(12):1986.

PMID:
23735648
13.

Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.

Deo RC, Wilson JG, Xing C, Lawson K, Kao WH, Reich D, Tandon A, Akylbekova E, Patterson N, Mosley TH Jr, Boerwinkle E, Taylor HA Jr.

PLoS One. 2011 Jan 24;6(1):e14581. doi: 10.1371/journal.pone.0014581.

14.

Three single-nucleotide polymorphisms in LPA account for most of the increase in lipoprotein(a) level elevation in African Americans compared with European Americans.

Chretien JP, Coresh J, Berthier-Schaad Y, Kao WH, Fink NE, Klag MJ, Marcovina SM, Giaculli F, Smith MW.

J Med Genet. 2006 Dec;43(12):917-23. Epub 2006 Jul 13.

15.

Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels.

Lu W, Cheng YC, Chen K, Wang H, Gerhard GS, Still CD, Chu X, Yang R, Parihar A, O'Connell JR, Pollin TI, Angles-Cano E, Quon MJ, Mitchell BD, Shuldiner AR, Fu M.

Hum Mol Genet. 2015 Apr 15;24(8):2390-400. doi: 10.1093/hmg/ddu731. Epub 2015 Jan 9.

16.

Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.

Ober C, Nord AS, Thompson EE, Pan L, Tan Z, Cusanovich D, Sun Y, Nicolae R, Edelstein C, Schneider DH, Billstrand C, Pfaffinger D, Phillips N, Anderson RL, Philips B, Rajagopalan R, Hatsukami TS, Rieder MJ, Heagerty PJ, Nickerson DA, Abney M, Marcovina S, Jarvik GP, Scanu AM, Nicolae DL.

J Lipid Res. 2009 May;50(5):798-806. doi: 10.1194/jlr.M800515-JLR200. Epub 2009 Jan 5.

17.

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.

Trégouët DA, König IR, Erdmann J, Munteanu A, Braund PS, Hall AS, Grosshennig A, Linsel-Nitschke P, Perret C, DeSuremain M, Meitinger T, Wright BJ, Preuss M, Balmforth AJ, Ball SG, Meisinger C, Germain C, Evans A, Arveiler D, Luc G, Ruidavets JB, Morrison C, van der Harst P, Schreiber S, Neureuther K, Schäfer A, Bugert P, El Mokhtari NE, Schrezenmeir J, Stark K, Rubin D, Wichmann HE, Hengstenberg C, Ouwehand W; Wellcome Trust Case Control Consortium; Cardiogenics Consortium, Ziegler A, Tiret L, Thompson JR, Cambien F, Schunkert H, Samani NJ.

Nat Genet. 2009 Mar;41(3):283-5. doi: 10.1038/ng.314. Epub 2009 Feb 8.

PMID:
19198611
18.

Lack of association between lipoprotein(a) genetic variants and subsequent cardiovascular events in Chinese Han patients with coronary artery disease after percutaneous coronary intervention.

Li ZG, Li G, Zhou YL, Chen ZJ, Yang JQ, Zhang Y, Sun S, Zhong SL.

Lipids Health Dis. 2013 Aug 27;12:127. doi: 10.1186/1476-511X-12-127.

19.

LPA Gene, Ethnicity, and Cardiovascular Events.

Lee SR, Prasad A, Choi YS, Xing C, Clopton P, Witztum JL, Tsimikas S.

Circulation. 2017 Jan 17;135(3):251-263. doi: 10.1161/CIRCULATIONAHA.116.024611. Epub 2016 Nov 9.

20.

LPA rs10455872 polymorphism is associated with coronary lesions in Brazilian patients submitted to coronary angiography.

Santos PC, Bueno CT, Lemos PA, Krieger JE, Pereira AC.

Lipids Health Dis. 2014 Apr 29;13:74. doi: 10.1186/1476-511X-13-74.

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