Li L - Search Results

1

ADCY9 Genetic Variants and Cardiovascular Outcomes With Evacetrapib in Patients With High-Risk Vascular Disease: A Nested Case-Control Study.

Nissen SE, Pillai SG, Nicholls SJ, Wolski K, Riesmeyer JS, Weerakkody GJ, Foster WM, McErlean E, Li L, Bhatnagar P, Ruotolo G, Lincoff AM. Nissen SE, et al. Among authors: li l. JAMA Cardiol. 2018 May 1;3(5):401-408. doi: 10.1001/jamacardio.2018.0569. JAMA Cardiol. 2018. PMID: 29525816 Free PMC article.

2

Trimethyllysine, a trimethylamine N-oxide precursor, provides near- and long-term prognostic value in patients presenting with acute coronary syndromes.

Li XS, Obeid S, Wang Z, Hazen BJ, Li L, Wu Y, Hurd AG, Gu X, Pratt A, Levison BS, Chung YM, Nissen SE, Tang WHW, Mach F, Räber L, Nanchen D, Matter CM, Lüscher TF, Hazen SL. Li XS, et al. Among authors: li l. Eur Heart J. 2019 Aug 21;40(32):2700-2709. doi: 10.1093/eurheartj/ehz259. Eur Heart J. 2019. PMID: 31049589 Free PMC article.

3

Genome-Wide Polygenic Score and Cardiovascular Outcomes With Evacetrapib in Patients With High-Risk Vascular Disease: A Nested Case-Control Study.

Emdin CA, Bhatnagar P, Wang M, Pillai SG, Li L, Qian HR, Riesmeyer JS, Lincoff AM, Nicholls SJ, Nissen SE, Ruotolo G, Kathiresan S, Khera AV. Emdin CA, et al. Among authors: li l. Circ Genom Precis Med. 2020 Feb;13(1):e002767. doi: 10.1161/CIRCGEN.119.002767. Epub 2020 Jan 3. Circ Genom Precis Med. 2020. PMID: 31898914 Free PMC article. Clinical Trial.

4

rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis.

Teo K, Abeysekera KWM, Adams L, Aigner E, Anstee QM, Banales JM, Banerjee R, Basu P, Berg T, Bhatnagar P, Buch S, Canbay A, Caprio S, Chatterjee A, Ida Chen YD, Chowdhury A, Daly AK, Datz C, de Gracia Hahn D, DiStefano JK, Dong J, Duret A; EU-PNAFLD Investigators; Emdin C, Fairey M, Gerhard GS; GOLD Consortium; Guo X, Hampe J, Hickman M, Heintz L, Hudert C, Hunter H, Kelly M, Kozlitina J, Krawczyk M, Lammert F, Langenberg C, Lavine J, Li L, Lim HK, Loomba R, Luukkonen PK, Melton PE, Mori TA, Palmer ND, Parisinos CA, Pillai SG, Qayyum F, Reichert MC, Romeo S, Rotter JI, Im YR, Santoro N, Schafmayer C, Speliotes EK, Stender S, Stickel F, Still CD, Strnad P, Taylor KD, Tybjærg-Hansen A, Umano GR, Utukuri M, Valenti L, Wagenknecht LE, Wareham NJ, Watanabe RM, Wattacheril J, Yaghootkar H, Yki-Järvinen H, Young KA, Mann JP. Teo K, et al. Among authors: li l. J Hepatol. 2021 Jan;74(1):20-30. doi: 10.1016/j.jhep.2020.08.027. Epub 2020 Aug 31. J Hepatol. 2021. PMID: 32882372 Free PMC article.

5

Relation of Statin Use to Gut Microbial Trimethylamine N-Oxide and Cardiovascular Risk.

Li DY, Li XS, Chaikijurajai T, Li L, Wang Z, Hazen SL, Tang WHW. Li DY, et al. Among authors: li l, li xs. Am J Cardiol. 2022 Sep 1;178:26-34. doi: 10.1016/j.amjcard.2022.05.010. Epub 2022 Jul 2. Am J Cardiol. 2022. PMID: 35787338

6

Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

Abdullah KG, Li L, Shen GQ, Hu Y, Yang Y, MacKinlay KG, Topol EJ, Wang QK. Abdullah KG, et al. Among authors: li l. Ann Hum Genet. 2008 Sep;72(Pt 5):654-7. doi: 10.1111/j.1469-1809.2008.00454.x. Epub 2008 May 26. Ann Hum Genet. 2008. PMID: 18505420 Free PMC article.

7

A Novel Cell-Free Fluorescent Assay for HDL Function: Low Apolipoprotein A1 Exchange Rate Associated with Increased Incident Cardiovascular Events.

Lorkowski SW, Brubaker G, Li L, Li XS, Hazen SL, Smith JD. Lorkowski SW, et al. Among authors: li l, li xs. J Appl Lab Med. 2020 May 1;5(3):544-557. doi: 10.1093/jalm/jfaa002. J Appl Lab Med. 2020. PMID: 32445357 Free PMC article.

8

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

Shen GQ, Li L, Rao S, Abdullah KG, Ban JM, Lee BS, Park JE, Wang QK. Shen GQ, et al. Among authors: li l. Arterioscler Thromb Vasc Biol. 2008 Feb;28(2):360-5. doi: 10.1161/ATVBAHA.107.157248. Epub 2007 Nov 29. Arterioscler Thromb Vasc Biol. 2008. PMID: 18048766

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. Wang AZ, et al. Among authors: li l. Ann Hum Genet. 2011 Jul;75(4):475-82. doi: 10.1111/j.1469-1809.2011.00646.x. Epub 2011 Apr 4. Ann Hum Genet. 2011. PMID: 21463265 Free PMC article.

10

Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.

Shen GQ, Girelli D, Li L, Olivieri O, Martinelli N, Chen Q, Topol EJ, Wang QK. Shen GQ, et al. Among authors: li l. Gene. 2013 May 25;521(1):78-81. doi: 10.1016/j.gene.2013.03.022. Epub 2013 Mar 21. Gene. 2013. PMID: 23524007 Free PMC article.

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