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Items: 14

1.

Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.

Weissglas-Volkov D, Aguilar-Salinas CA, Sinsheimer JS, Riba L, Huertas-Vazquez A, Ordoñez-Sánchez ML, Rodriguez-Guillen R, Cantor RM, Tusie-Luna T, Pajukanta P.

Circ Cardiovasc Genet. 2010 Feb;3(1):31-8. doi: 10.1161/CIRCGENETICS.109.908004. Epub 2009 Dec 11.

2.

Genetic determinants of plasma triglycerides.

Johansen CT, Kathiresan S, Hegele RA.

J Lipid Res. 2011 Feb;52(2):189-206. doi: 10.1194/jlr.R009720. Epub 2010 Nov 1. Review.

3.

Update on the molecular biology of dyslipidemias.

Ramasamy I.

Clin Chim Acta. 2016 Feb 15;454:143-85. doi: 10.1016/j.cca.2015.10.033. Epub 2015 Nov 4. Review.

PMID:
26546829
4.

Allelic and phenotypic spectrum of plasma triglycerides.

Johansen CT, Hegele RA.

Biochim Biophys Acta. 2012 May;1821(5):833-42. doi: 10.1016/j.bbalip.2011.10.007. Epub 2011 Oct 12. Review.

PMID:
22033228
5.

Apolipoprotein A5 and triglyceridemia. Focus on the effects of the common variants.

Hubacek JA.

Clin Chem Lab Med. 2005;43(9):897-902. Review.

PMID:
16176166
6.

Genetic and environmental determinants of the susceptibility of Amerindian derived populations for having hypertriglyceridemia.

Aguilar-Salinas CA, Tusie-Luna T, Pajukanta P.

Metabolism. 2014 Jul;63(7):887-94. doi: 10.1016/j.metabol.2014.03.012. Epub 2014 Mar 30. Review.

7.

TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans.

Ollila HM, Utge S, Kronholm E, Aho V, Van Leeuwen W, Silander K, Partonen T, Perola M, Kaprio J, Salomaa V, Sallinen M, Härmä M, Porkka-Heiskanen T, Paunio T.

Transl Psychiatry. 2012 Mar 20;2:e97. doi: 10.1038/tp.2012.20. Review.

8.

Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

Panagiotou OA, Evangelou E, Ioannidis JP.

Am J Epidemiol. 2010 Oct 15;172(8):869-89. doi: 10.1093/aje/kwq234. Epub 2010 Sep 28. Review.

9.

Genetic causes of high and low serum HDL-cholesterol.

Weissglas-Volkov D, Pajukanta P.

J Lipid Res. 2010 Aug;51(8):2032-57. doi: 10.1194/jlr.R004739. Epub 2010 Apr 26. Review.

10.

Plasma lipoproteins: genetic influences and clinical implications.

Hegele RA.

Nat Rev Genet. 2009 Feb;10(2):109-21. doi: 10.1038/nrg2481. Epub 2009 Jan 13. Review.

PMID:
19139765
11.

Genetic Component of Type 2 Diabetes in a Mexican Population.

Sánchez-Pozos K, Menjívar M.

Arch Med Res. 2016 Oct;47(7):496-505. doi: 10.1016/j.arcmed.2016.12.007. Review.

PMID:
28262190
12.

Adaptive genetic variation and heart disease risk.

Parnell LD, Lee YC, Lai CQ.

Curr Opin Lipidol. 2010 Apr;21(2):116-22. doi: 10.1097/MOL.0b013e3283378e42. Review.

13.

Mining the genome for lipid genes.

Kuivenhoven JA, Hegele RA.

Biochim Biophys Acta. 2014 Oct;1842(10):1993-2009. doi: 10.1016/j.bbadis.2014.04.028. Epub 2014 May 2. Review.

14.

Comprehensive genotyping in dyslipidemia: mendelian dyslipidemias caused by rare variants and Mendelian randomization studies using common variants.

Tada H, Kawashiri MA, Yamagishi M.

J Hum Genet. 2017 Apr;62(4):453-458. doi: 10.1038/jhg.2016.159. Epub 2017 Jan 5. Review.

PMID:
28055004

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