| 36696749 | Efficacy, safety, adherence and persistence of PCSK9 inhibitors in clinical practice: A single country, multicenter, observational study (AT-TARGET-IT). | | 2023 |
| 35176406 | Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA). | International Journal of Cardiology | 2022 |
| 35367005 | Acute coronary syndromes. | Lancet, The | 2022 |
| 35859592 | Sex-Related Differences in Long-Term Outcomes After Early-Onset Myocardial Infarction. | Frontiers in Cardiovascular Medicine | 2022 |
| 36613613 | Lipoprotein(a): Cardiovascular Disease, Aortic Stenosis and New Therapeutic Option. | | 2022 |
| 33611623 | The efficacy and safety of dapagliflozin in women and men with type 2 diabetes mellitus. | Diabetologia | 2021 |
| 33587659 | Comparison of the Efficacy and Safety Outcomes of Edoxaban in 8040 Women Versus 13 065 Men With Atrial Fibrillation in the ENGAGE AF-TIMI 48 Trial. | Circulation | 2021 |
| 31699787 | Rare variants lowering the levels of coagulation factor X are protective against ischemic heart disease. | Haematologica | 2020 |
| 31479721 | Long-Term Outcomes After Early-Onset Myocardial Infarction. | Journal of the American College of Cardiology | 2019 |
| 31311244 | Compound sarcomeric mutations causing hypertrophic cardiomyopathy in a young Sardinian soccer player: a family affair. | Journal of Sports Medicine and Physical Fitness | 2019 |
| 29540324 | Pharmacogenomic Approach to Selecting Antiplatelet Therapy in Patients With Acute Coronary Syndromes: The PHARMCLO Trial. | Journal of the American College of Cardiology | 2018 |
| 29321131 | Efficacy of Ranolazine in Patients With Symptomatic Hypertrophic Cardiomyopathy: The RESTYLE-HCM Randomized, Double-Blind, Placebo-Controlled Study. | Circulation: Heart Failure | 2018 |
| 28209224 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. | J Am Coll Cardiol | 2017 |
| 28506971 | Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease. | Circ Res | 2017 |
| 28267856 | Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease. | JAMA | 2017 |
| 28007139 | Phenotypic Characterization of Genetically Lowered Human Lipoprotein(a) Levels. | J Am Coll Cardiol | 2016 |
| 27440003 | Atherothrombotic Risk Stratification and the Efficacy and Safety of Vorapaxar in Patients With Stable Ischemic Heart Disease and Previous Myocardial Infarction. | Circulation | 2016 |
| 26934567 | Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. | N Engl J Med | 2016 |
| 27431644 | Universal Classification System Type of Incident Myocardial Infarction in Patients With Stable Atherosclerosis: Observations From Thrombin Receptor Antagonist in Secondary Prevention of Atherothrombotic Ischemic Events (TRA 2°P)-TIMI 50. | J Am Heart Assoc | 2016 |
| 27050191 | Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. | J Am Coll Cardiol | 2016 |
| 25252039 | Association of bleeding, mortality and sex in acute coronary syndromes: the missing triangle. | Journal of Cardiovascular Medicine | 2015 |
| 25487149 | Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. | Nature | 2015 |
| 25647241 | Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction. | PLoS Genet | 2015 |
| 26453416 | Rapid and portable, lab-on-chip, point-of-care genotyping for evaluating clopidogrel metabolism. | Clinica Chimica Acta | 2015 |
| 24507774 | Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. | Am J Hum Genet | 2014 |
| 25390462 | Inactivating mutations in NPC1L1 and protection from coronary heart disease. | N Engl J Med | 2014 |
| 25173926 | Novel α-actinin 2 variant associated with familial hypertrophic cardiomyopathy and juvenile atrial arrhythmias: a massively parallel sequencing study. | Circulation: Cardiovascular Genetics | 2014 |
| 24941081 | Loss-of-function mutations in APOC3, triglycerides, and coronary disease. | N Engl J Med | 2014 |
| 24925728 | Eleven-year trends in gender differences of treatments and mortality in ST-elevation acute myocardial infarction in northern Italy, 2000 to 2010. | American Journal of Cardiology | 2014 |
| 24378836 | Genetic and nongenetic factors influencing the response to clopidogrel. | Journal of Cardiovascular Medicine | 2013 |
| 22914306 | Relevance of gender in patients with acute myocardial infarction undergoing coronary interventions. | Journal of Cardiovascular Medicine | 2013 |
| 23071564 | Protein kinase C ε expression in platelets from patients with acute myocardial infarction. | PLoS ONE | 2012 |
| 22932716 | Vorapaxar for secondary prevention of thrombotic events for patients with previous myocardial infarction: a prespecified subgroup analysis of the TRA 2°P-TIMI 50 trial. | Lancet | 2012 |
| 22582980 | Genetic predisposition to atorvastatin-induced myopathy: a case report. | Journal of Clinical Pharmacy and Therapeutics | 2012 |
| 22341397 | A quantitative-PCR protocol rapidly detects αGAL deletions/duplications in patients with Anderson-Fabry disease. | Molecular Genetics and Metabolism | 2012 |
| 22622116 | [Genetic basis of ischemic heart disease. Do women have distinctive characteristics?]. | Giornale Italiano di Cardiologia | 2012 |
| 22907696 | A case of compound mutations in the MYBPC3 gene associated with biventricular hypertrophy and neonatal death. | | 2012 |
| 22449240 | The first Caucasian patient with p.Val122Ile mutated-transthyretin cardiac amyloidosis treated with isolated heart transplantation. | Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis | 2012 |
| 21901231 | Common variants in the haemostatic gene pathway contribute to risk of early-onset myocardial infarction in the Italian population. | Thrombosis and Haemostasis | 2011 |
| 21130994 | Strong association of the APOA5-1131T>C gene variant and early-onset acute myocardial infarction. | Atherosclerosis | 2011 |
| 21378990 | Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. | Nat Genet | 2011 |
| 21757122 | Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction. | J Am Coll Cardiol | 2011 |
| 20626623 | The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease. | Journal of Thrombosis and Haemostasis | 2010 |
| 20699424 | Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population. | Journal of Lipid Research | 2010 |
| 21111936 | Familial aggregation of early-onset myocardial infarction. | Eur J Intern Med | 2010 |
| 21246778 | [Genomics in cardiological clinical practice: from the individual response to drug therapy and monogenic cardiovascular disorders]. | Giornale Italiano di Cardiologia | 2010 |
| 20385930 | Clinical features and outcomes of women with unstable ischemic heart disease: observations from metabolic efficiency with ranolazine for less ischemia in non-ST-elevation acute coronary syndromes-thrombolysis in myocardial infarction 36 (MERLIN-TIMI 36). | Circulation | 2010 |
| 20456747 | Active platelet-binding conformation of plasma von Willebrand factor in young women with acute myocardial infarction. | Journal of Thrombosis and Haemostasis | 2010 |
| 18049795 | Comparison of the effects of pretreatment with tirofiban, clopidogrel or both on the inhibition of platelet aggregation and activation in patients with acute coronary syndromes. | Journal of Thrombosis and Thrombolysis | 2009 |
| 19198612 | New susceptibility locus for coronary artery disease on chromosome 3q22.3. | Nat Genet | 2009 |