Detalhe da pesquisa
1.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Nature
; 518(7537): 102-6, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25487149
2.
Biological, clinical and population relevance of 95 loci for blood lipids.
Nature
; 466(7307): 707-13, 2010 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20686565
3.
LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias.
J Lipid Res
; 55(4): 765-72, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24503134
4.
Allelic and phenotypic spectrum of plasma triglycerides.
Biochim Biophys Acta
; 1821(5): 833-42, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22033228
5.
Sortilin: an unusual suspect in cholesterol metabolism: from GWAS identification to in vivo biochemical analyses, sortilin has been identified as a novel mediator of human lipoprotein metabolism.
Bioessays
; 33(6): 430-7, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21462369
6.
Genetic variation in hyaluronan metabolism loci is associated with plasma plasminogen activator inhibitor-1 concentration.
Blood
; 116(12): 2160-3, 2010 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20558613
7.
The complex genetic basis of plasma triglycerides.
Curr Atheroscler Rep
; 14(3): 227-34, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22528520
8.
An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia.
Arterioscler Thromb Vasc Biol
; 31(8): 1916-26, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21597005
9.
Genetic bases of hypertriglyceridemic phenotypes.
Curr Opin Lipidol
; 22(4): 247-53, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21519249
10.
Genetic determinants of plasma triglycerides.
J Lipid Res
; 52(2): 189-206, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21041806
11.
Rare ATGL haplotypes are associated with increased plasma triglyceride concentrations in the Greenland Inuit.
Int J Circumpolar Health
; 69(1): 3-12, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20167152
12.
Predictive genetic testing for coronary artery disease.
Crit Rev Clin Lab Sci
; 46(5-6): 343-60, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19958218
13.
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution.
Atherosclerosis
; 250: 63-8, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27182959
14.
Common low-density lipoprotein receptor p.G116S variant has a large effect on plasma low-density lipoprotein cholesterol in circumpolar inuit populations.
Circ Cardiovasc Genet
; 8(1): 100-5, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25414273
15.
Genetic determinants of "cognitive impairment, no dementia".
J Alzheimers Dis
; 33(3): 831-40, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23042215
16.
Western Database of Lipid Variants (WDLV): a catalogue of genetic variants in monogenic dyslipidemias.
Can J Cardiol
; 29(8): 934-9, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23623477
17.
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia.
Circ Cardiovasc Genet
; 5(1): 66-72, 2012 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22135386
18.
The transcription factor cyclic AMP-responsive element-binding protein H regulates triglyceride metabolism.
Nat Med
; 17(7): 812-5, 2011 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21666694
19.
Translating genomic analyses into improved management of coronary artery disease.
Future Cardiol
; 6(4): 507-21, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20608823
20.
A translational view of the genetics of lipodystrophy and ectopic fat deposition.
Prog Mol Biol Transl Sci
; 94: 159-96, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21036325