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
Inglês
| MEDLINE | ID: mdl-25487149
2.
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.
PLoS Genet
; 7(6): e1002158, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21738491
3.
Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).
Ann Noninvasive Electrocardiol
; 18(1): 29-40, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23347024
4.
Common genetic determinants of vitamin D insufficiency: a genome-wide association study.
Lancet
; 376(9736): 180-8, 2010 Jul 17.
Artigo
Inglês
| MEDLINE | ID: mdl-20541252
5.
Chest Pain Risk Stratification: A Comparison of the 2-Hour Accelerated Diagnostic Protocol (ADAPT) and the HEART Pathway.
Crit Pathw Cardiol
; 15(2): 46-9, 2016 06.
Artigo
Inglês
| MEDLINE | ID: mdl-27183253
6.
Null association between abdominal muscle and calcified atherosclerosis in community-living persons without clinical cardiovascular disease: the multi-ethnic study of atherosclerosis.
Metabolism
; 62(11): 1562-9, 2013 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-23916063