Detalhe da pesquisa
1.
Validation of a genetic risk score for atrial fibrillation: A prospective multicenter cohort study.
PLoS Med
; 15(3): e1002525, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29534064
2.
A Multigene Test Could Cost-Effectively Help Extend Life Expectancy for Women at Risk of Hereditary Breast Cancer.
Value Health
; 20(4): 547-555, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28407996
3.
Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history.
Eur Heart J
; 37(6): 561-7, 2016 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26392438
4.
Use of low density lipoprotein particle number levels as an aid in statin treatment decisions for intermediate risk patients: a cost-effectiveness analysis.
BMC Cardiovasc Disord
; 16(1): 251, 2016 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27927162
5.
Genetic risk for atrial fibrillation could motivate patient adherence to warfarin therapy: a cost effectiveness analysis.
BMC Cardiovasc Disord
; 15: 104, 2015 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26419225
6.
Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke.
Stroke
; 45(10): 2856-2862, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25123217
7.
Multiple SNP testing improves risk prediction of first venous thrombosis.
Blood
; 120(3): 656-63, 2012 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22586183
8.
A multigene test could cost-effectively help extend life expectancy for women at risk of hereditary breast cancer-Reply to letter to the editor by Petelin et al.
Value Health
; 21(7): 893-894, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30005763
9.
Polymorphisms and noncardioembolic stroke in three case-control studies.
Cerebrovasc Dis
; 33(1): 80-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22134093
10.
Genetic variants in the KIF6 region and coronary event reduction from statin therapy.
Hum Genet
; 129(1): 17-23, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20886236
11.
Replication of LDL GWAs hits in PROSPER/PHASE as validation for future (pharmaco)genetic analyses.
BMC Med Genet
; 12: 131, 2011 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-21977987
12.
The contribution of a 9p21.3 variant, a KIF6 variant, and C-reactive protein to predicting risk of myocardial infarction in a prospective study.
BMC Cardiovasc Disord
; 11: 10, 2011 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21406102
13.
Assessment of the Association of Vitamin D Level With SARS-CoV-2 Seropositivity Among Working-Age Adults.
JAMA Netw Open
; 4(5): e2111634, 2021 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34009346
14.
Association of changes in lipid levels with changes in vitamin D levels in a real-world setting.
Sci Rep
; 11(1): 21536, 2021 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34728785
15.
KIF6 Trp719Arg polymorphism and the effect of statin therapy in elderly patients: results from the PROSPER study.
Eur J Cardiovasc Prev Rehabil
; 17(4): 455-61, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20215968
16.
Outreach and Connection to Care for Chronic Kidney Disease in a Workplace Wellness Setting: A Cost-Effectiveness Analysis.
Popul Health Manag
; 23(6): 487-494, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31895617
17.
Cost-effectiveness of nucleic acid amplification testing to guide treatment for vaginitis: a decision-modeling analysis.
Diagn Microbiol Infect Dis
; 98(2): 115119, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32683205
18.
Concordance of Cardiovascular Risk Factors and Behaviors in a Multiethnic US Nationwide Cohort of Married Couples and Domestic Partners.
JAMA Netw Open
; 3(10): e2022119, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33104207
19.
Gaps in Dyslipidemia Care Among Working-Aged Individuals With Employer-Sponsored Health Care.
J Am Heart Assoc
; 9(9): e015807, 2020 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32319337
20.
Gene variants associated with ischemic stroke: the cardiovascular health study.
Stroke
; 40(2): 363-8, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19023099