Published in BMC Med Genet on March 27, 2013
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Factors related to the selection of surgical versus percutaneous revascularization in diabetic patients with multivessel coronary artery disease in the BARI 2D (Bypass Angioplasty Revascularization Investigation in Type 2 Diabetes) trial. JACC Cardiovasc Interv (2009) 1.38
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Hum Mol Genet (2012) 1.34
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Three endothelial nitric oxide (NOS3) gene polymorphisms in hypertensive and normotensive individuals: meta-analysis of 53 studies reveals evidence of publication bias. J Hypertens (2007) 1.14
APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population. Lipids Health Dis (2010) 1.14
Assessment of the relationship between self-declared ethnicity, mitochondrial haplogroups and genomic ancestry in Brazilian individuals. PLoS One (2013) 1.11
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Brazilian urban population genetic structure reveals a high degree of admixture. Eur J Hum Genet (2011) 1.10
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Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development. Proc Natl Acad Sci U S A (2012) 1.08
Heritability of cardiovascular risk factors in a Brazilian population: Baependi Heart Study. BMC Med Genet (2008) 1.08
CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population. BMC Med Genet (2011) 1.05
One-year outcomes of coronary artery bypass graft surgery versus percutaneous coronary intervention with multiple stenting for multisystem disease: a meta-analysis of individual patient data from randomized clinical trials. J Thorac Cardiovasc Surg (2005) 1.04
Circulating dipeptidyl peptidase IV activity correlates with cardiac dysfunction in human and experimental heart failure. Circ Heart Fail (2013) 1.04
Exercise training delays cardiac dysfunction and prevents calcium handling abnormalities in sympathetic hyperactivity-induced heart failure mice. J Appl Physiol (1985) (2007) 1.04
Structural shifts of aldehyde dehydrogenase enzymes were instrumental for the early evolution of retinoid-dependent axial patterning in metazoans. Proc Natl Acad Sci U S A (2010) 1.04
Further evidence of the importance of RIT1 in Noonan syndrome. Am J Med Genet A (2014) 1.03
Impact of diabetes on five-year outcomes of patients with multivessel coronary artery disease. Ann Thorac Surg (2007) 1.02
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Prevalence and risk factors associated with peripheral arterial disease in the Hearts of Brazil Project. Arq Bras Cardiol (2008) 1.02
Ethnicity and arterial stiffness in Brazil. Am J Hypertens (2010) 1.01
Gene variation in resistant hypertension: multilocus analysis of the angiotensin 1-converting enzyme, angiotensinogen, and endothelial nitric oxide synthase genes. DNA Cell Biol (2011) 1.01
Effect of the G-308A polymorphism of the tumor necrosis factor alpha gene on the risk of ischemic heart disease and ischemic stroke: a meta-analysis. Am Heart J (2007) 1.01
Mutations in the human phospholamban gene in patients with heart failure. Am Heart J (2011) 0.99
SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group. BMC Med Genet (2011) 0.98
Association between platelet P2Y12 haplotype and risk of cardiovascular events in chronic coronary disease. Thromb Res (2006) 0.97
Derivation and external validation of a simple prediction model for the diagnosis of type 2 diabetes mellitus in the Brazilian urban population. Eur J Epidemiol (2009) 0.95
Non-HFE hemochromatosis. Rev Bras Hematol Hemoter (2012) 0.95
Effectiveness of coadministration of varenicline, bupropion, and serotonin reuptake inhibitors in a smoking cessation program in the real-life setting. Nicotine Tob Res (2012) 0.94
Effects of depression, anxiety, comorbidity, and antidepressants on resting-state heart rate and its variability: an ELSA-Brasil cohort baseline study. Am J Psychiatry (2014) 0.93
ALDH1A2 (RALDH2) genetic variation in human congenital heart disease. BMC Med Genet (2009) 0.92
Angiotensinogen M235T polymorphism is associated with coronary artery disease severity. Clin Chim Acta (2005) 0.92
Lower heart rate variability is associated with higher serum high-sensitivity C-reactive protein concentration in healthy individuals aged 46 years or more. Int J Cardiol (2006) 0.92
Two new mutations in the HIF2A gene associated with erythrocytosis. Am J Hematol (2012) 0.92
Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in Brazilian populations. Obesity (Silver Spring) (2011) 0.91
Influence of pregnancy on clinical course and fetal outcome of women with hypertrophic cardiomyopathy. Arq Bras Cardiol (2007) 0.90
Metabolic syndrome determinants in an urban population from Brazil: social class and gender-specific interaction. Int J Cardiol (2007) 0.90
Thioredoxin interacting protein genetic variation is associated with diabetes and hypertension in the Brazilian general population. Atherosclerosis (2011) 0.90
High-sensitivity C-reactive protein concentration in a healthy Brazilian population. Int J Cardiol (2004) 0.89
Adipose tissue-derived stem cells from humans and mice differ in proliferative capacity and genome stability in long-term cultures. Stem Cells Dev (2010) 0.89
Association of mannose-binding lectin gene polymorphism but not of mannose-binding serine protease 2 with chronic severe aortic regurgitation of rheumatic etiology. Clin Vaccine Immunol (2008) 0.89
Identification of two novel shear stress responsive elements in rat angiotensin I converting enzyme promoter. Physiol Genomics (2004) 0.89
Additional value of dipyridamole stress myocardial perfusion by 64-row computed tomography in patients with coronary stents. J Cardiovasc Comput Tomogr (2011) 0.89
Association of genetic variants in the adiponectin encoding gene (ADIPOQ) with type 2 diabetes in Japanese Brazilians. J Diabetes Complications (2009) 0.89
The effect of Sao Paulo's smoke-free legislation on carbon monoxide concentration in hospitality venues and their workers. Tob Control (2010) 0.88
Cell biology, MRI and geometry: insight into a microscopic/macroscopic marriage. Eur J Cardiothorac Surg (2006) 0.88
Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design. Int J Cardiol (2005) 0.88
Nuclear Factor (NF) kappaB polymorphism is associated with heart function in patients with heart failure. BMC Med Genet (2010) 0.88
Determinants of left ventricular mass and presence of metabolic risk factors in normotensive individuals. Int J Cardiol (2008) 0.88
Heritability of physical activity traits in Brazilian families: the Baependi Heart Study. BMC Med Genet (2011) 0.87
Cell therapy plus transmyocardial laser revascularization for refractory angina. Ann Thorac Surg (2005) 0.87
Shear stress induces nitric oxide-mediated vascular endothelial growth factor production in human adipose tissue mesenchymal stem cells. Stem Cells Dev (2010) 0.87
Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy. Am Heart J (2013) 0.87
Association between genetics of diabetes, coronary artery disease, and macrovascular complications: exploring a common ground hypothesis. Rev Diabet Stud (2011) 0.87
Holt-Oram syndrome: novel TBX5 mutation and associated anomalous right coronary artery. Cardiol Young (2011) 0.86
Impact of metabolic syndrome on the outcome of patients with stable coronary artery disease: 2-year follow-up of the MASS II study. Coron Artery Dis (2008) 0.86
Cardiovascular adaptations in rats submitted to a resistance-training model. Clin Exp Pharmacol Physiol (2005) 0.86
Survival analysis of patients with heart failure: implications of time-varying regression effects in modeling mortality. PLoS One (2012) 0.86
Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene. J Hum Genet (2007) 0.86
Revision of the Sokolow-Lyon-Rappaport and cornell voltage criteria for left ventricular hypertrophy. Arq Bras Cardiol (2008) 0.85
Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation. Am J Med Genet A (2004) 0.85
A novel TBX5 missense mutation (V263M) in a family with atrial septal defects and postaxial hexodactyly. Int J Cardiol (2008) 0.85
NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis. J Nephrol (2006) 0.85
Reduced expression of systemic proinflammatory and myocardial biomarkers after off-pump versus on-pump coronary artery bypass surgery: a prospective randomized study. J Crit Care (2009) 0.85
Skeletal muscle cells expressing VEGF induce capillary formation and reduce cardiac injury in rats. Int J Cardiol (2006) 0.85
Echocardiographic reference values in a sample of asymptomatic adult Brazilian population. Arq Bras Cardiol (2007) 0.85
Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients. Blood Cells Mol Dis (2011) 0.85
In vitro simultaneous transfer of lipids to HDL in coronary artery disease and in statin treatment. Lipids (2009) 0.85
Genetic polymorphism, medical therapy and sequential cardiac function in patients with heart failure. Arq Bras Cardiol (2008) 0.85
Glu298Asp eNOS gene polymorphism causes attenuation in nonexercising muscle vasodilatation. Physiol Genomics (2009) 0.85
The influence of tumor necrosis factor -308 and C-reactive protein G1059C gene variants on serum concentration of C-reactive protein: evidence for an age-dependent association. Clin Chim Acta (2004) 0.84
Association between ADAMTS13 polymorphisms and risk of cardiovascular events in chronic coronary disease. Thromb Res (2009) 0.84
Association of alpha1a-adrenergic receptor polymorphism and blood pressure phenotypes in the Brazilian population. BMC Cardiovasc Disord (2008) 0.84
Design and baseline characteristics of a coronary heart disease prospective cohort: two-year experience from the strategy of registry of acute coronary syndrome study (ERICO study). Clinics (Sao Paulo) (2013) 0.84
Lactase persistence/non-persistence variants, C/T_13910 and G/A_22018, as a diagnostic tool for lactose intolerance in IBS patients. Clin Chim Acta (2007) 0.84