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Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis

Frontiers in physiology, 2017-08, Vol.8, p.612-612

2017

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Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome

Journal of vascular surgery, 2018-07, Vol.68 (1), p.225-233.e5

2018

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Sanger Validation of High-Throughput Sequencing in Genetic Diagnosis: Still the Best Practice?

Frontiers in genetics, 2020-12, Vol.11, p.592588-592588

2020

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CLOCK gene polymorphisms and quality of aging in a cohort of nonagenarians - The MUGELLO Study

Scientific reports, 2019-02, Vol.9 (1), p.1472-1472, Article 1472

2019

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Polymorphisms of genes involved in extracellular matrix remodeling and abdominal aortic aneurysm

Journal of vascular surgery, 2012, Vol.55 (1), p.171-179.e2

2012

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Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous Thromboembolism

PloS one, 2016-02, Vol.11 (2), p.e0149427-e0149427

2016

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Detection of Platelet-Activating Antibodies Associated with Vaccine-Induced Thrombotic Thrombocytopenia by Flow Cytometry: An Italian Experience

Viruses, 2022-05, Vol.14 (6), p.1133

2022

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Plasma PCSK9 levels and sepsis severity: an early assessment in the emergency department

Clinical and experimental medicine, 2021-02, Vol.21 (1), p.101-107

2021

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Association of rs1466535 LRP1 but not rs3019885 SLC30A8 and rs6674171 TDRD10 gene polymorphisms with abdominal aortic aneurysm in Italian patients

Journal of vascular surgery, 2015-03, Vol.61 (3), p.787-792

2015

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When should a rare inherited connective tissue disorder be suspected in bicuspid aortic valve by primary-care internists and cardiologists? Proposal of a score

Internal and emergency medicine, 2021-04, Vol.16 (3), p.609-615

2021

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Searching for a common mechanism for placenta-mediated pregnancy complications and cardiovascular disease: role of lipoprotein(a)

Fertility and sterility, 2016-05, Vol.105 (5), p.1287-1293.e3

2016

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Tracking an Elusive Killer: State of the Art of Molecular-Genetic Knowledge and Laboratory Role in Diagnosis and Risk Stratification of Thoracic Aortic Aneurysm and Dissection

Diagnostics (Basel), 2022-07, Vol.12 (8), p.1785

2022

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Differential Diagnosis between Marfan Syndrome and Loeys-Dietz Syndrome Type 4: A Novel Chromosomal Deletion Covering TGFB2

Genes, 2021-09, Vol.12 (10), p.1462

2021

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Fibrinolysis alterations in infertile women during controlled ovarian stimulation: Influence of BMI and genetic components

Thrombosis research, 2012-12, Vol.130 (6), p.919-924

2012

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Non-traumatic splenic rupture on dual antiplatelet therapy with aspirin and ticagrelor after stenting for acute coronary syndrome

Journal of cardiology cases, 2015-09, Vol.12 (3), p.65-67

2015

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Association between polymorphisms of the renin angiotensin system and carotid stenosis

Journal of vascular surgery, 2011-08, Vol.54 (2), p.467-473

2011

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Multilocus analysis in candidate genes ACE, AGT , and AGTR1 and predisposition to peripheral arterial disease: Role of ACE D/-240T haplotype

Journal of vascular surgery, 2009-12, Vol.50 (6), p.1399-1404

2009

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eNOS and ACE genes influence peripheral arterial disease predisposition in smokers

Journal of vascular surgery, 2010-07, Vol.52 (1), p.97-102.e1

2010

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Endothelial nitric oxide synthase gene influences the risk of pre-eclampsia, the recurrence of negative pregnancy events, and the maternal–fetal flow

Journal of hypertension, 2006-09, Vol.24 (9), p.1823-1829

2006

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Lipoprotein (a) [Lp(a)]: a possible link between migraine and stroke

Translational research : the journal of laboratory and clinical medicine, 2009, Vol.153 (1), p.44-47

2009

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Hemorheologic profile in healthy women undergoing controlled ovarian stimulation

Fertility and sterility, 2011, Vol.95 (1), p.327-329

2011

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S38G single-nucleotide polymorphism at the KCNE1 locus is associated with heart failure

Heart rhythm, 2010-03, Vol.7 (3), p.363-367

2010

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Role of C677T and A1298C MTHFR, A2756G MTR and -786 C/T eNOS gene polymorphisms in atrial fibrillation susceptibility

PloS one, 2007-06, Vol.2 (6), p.e495-e495

2007

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Whole Exome Sequencing in Vaccine‐Induced Thrombotic Thrombocytopenia (VITT)

BioMed research international, 2024-01, Vol.2024 (1), p.2860547

2024

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The serum metabolomic profiles of atrial fibrillation patients treated with direct oral anticoagulants or vitamin K antagonists

Life sciences (1973), 2024-08, Vol.351, p.122796, Article 122796

2024

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Genetic Bases of Bicuspid Aortic Valve: The Contribution of Traditional and High-Throughput Sequencing Approaches on Research and Diagnosis

Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome

Sanger Validation of High-Throughput Sequencing in Genetic Diagnosis: Still the Best Practice?

CLOCK gene polymorphisms and quality of aging in a cohort of nonagenarians - The MUGELLO Study

Polymorphisms of genes involved in extracellular matrix remodeling and abdominal aortic aneurysm

Apolipoprotein(a) Kringle-IV Type 2 Copy Number Variation Is Associated with Venous Thromboembolism

Detection of Platelet-Activating Antibodies Associated with Vaccine-Induced Thrombotic Thrombocytopenia by Flow Cytometry: An Italian Experience

Plasma PCSK9 levels and sepsis severity: an early assessment in the emergency department

Association of rs1466535 LRP1 but not rs3019885 SLC30A8 and rs6674171 TDRD10 gene polymorphisms with abdominal aortic aneurysm in Italian patients

When should a rare inherited connective tissue disorder be suspected in bicuspid aortic valve by primary-care internists and cardiologists? Proposal of a score

Searching for a common mechanism for placenta-mediated pregnancy complications and cardiovascular disease: role of lipoprotein(a)

Tracking an Elusive Killer: State of the Art of Molecular-Genetic Knowledge and Laboratory Role in Diagnosis and Risk Stratification of Thoracic Aortic Aneurysm and Dissection

Differential Diagnosis between Marfan Syndrome and Loeys-Dietz Syndrome Type 4: A Novel Chromosomal Deletion Covering TGFB2

Fibrinolysis alterations in infertile women during controlled ovarian stimulation: Influence of BMI and genetic components

Non-traumatic splenic rupture on dual antiplatelet therapy with aspirin and ticagrelor after stenting for acute coronary syndrome

Association between polymorphisms of the renin angiotensin system and carotid stenosis

Multilocus analysis in candidate genes ACE, AGT , and AGTR1 and predisposition to peripheral arterial disease: Role of ACE D/-240T haplotype

eNOS and ACE genes influence peripheral arterial disease predisposition in smokers

Endothelial nitric oxide synthase gene influences the risk of pre-eclampsia, the recurrence of negative pregnancy events, and the maternal–fetal flow

Lipoprotein (a) [Lp(a)]: a possible link between migraine and stroke

Hemorheologic profile in healthy women undergoing controlled ovarian stimulation

S38G single-nucleotide polymorphism at the KCNE1 locus is associated with heart failure

Role of C677T and A1298C MTHFR, A2756G MTR and -786 C/T eNOS gene polymorphisms in atrial fibrillation susceptibility

Whole Exome Sequencing in Vaccine‐Induced Thrombotic Thrombocytopenia (VITT)

The serum metabolomic profiles of atrial fibrillation patients treated with direct oral anticoagulants or vitamin K antagonists

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