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Sandra Mastroianno

Observed names: Mastroianno Sandra, S Mastroianno, S. Mastroianno
Observed institutions: University of Foggia, Casa Sollievo della Sofferenza, Magna Graecia University, University of Catania, University of Chieti-Pescara, Ospedale Garibaldi, Mario Negri Sud Foundation, Sapienza University of Rome
ORCID: 0000-0001-6898-4657
Observed ORCID: 0000-0001-6898-4657
OpenAlex ID: A5045025946
A Variation in 3′ UTR of hPTP1B Increases Specific Gene Expression and Associates with Insulin Resistance
2002 · Rosa Di Paola, Lucia Frittitta, et al. · The American Journal of Human Genetics · 188
Increased Urinary Albumin Excretion, Insulin Resistance, and Related Cardiovascular Risk Factors in Patients With Type 2 Diabetes
2005 · Salvatore De Cosmo, Antonio Minenna, et al. · Diabetes Care · 103
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Heterogeneous Effect of Peroxisome Proliferator‐activated Receptor γ2 Ala12 Variant on Type 2 Diabetes Risk
2007 · Ornella Ludovico, Fabio Pellegrini, et al. · Obesity · 101
Screening for silent myocardial ischaemia in type 2 diabetic patients with additional atherogenic risk factors: applicability and accuracy of the exercise stress test
2002 · S Bacci, M Villella, et al. · European Journal of Endocrinology · 88
Cardiac valvular Ehlers‐Danlos syndrome is a well‐defined condition due to recessive null variants in COL1A2
2019 · Vito Guarnieri, Silvia Morlino, et al. · American Journal of Medical Genetics Part A · 31
ENPP1 Q121 Variant, Increased Pulse Pressure and Reduced Insulin Signaling, and Nitric Oxide Synthase Activity in Endothelial Cells
2009 · Simonetta Bacci, Rosa Di Paola, et al. · Arteriosclerosis Thrombosis and Vascular Biology · 22
Serum uric acid as a prognostic marker in the setting of advanced vascular disease: a prospective study in the elderly.
2015 · Giuseppe Di Stolfo, Sandra Mastroianno, et al. · Europe PMC (PubMed Central) · 21
Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family
2011 · Sandra Mastroianno, Massimo Torlontano, et al. · Endocrine · 19
Association of the Q121 Variant of ENPP1 Gene With Decreased Kidney Function Among Patients With Type 2 Diabetes
2008 · Salvatore De Cosmo, Antonio Minenna, et al. · American Journal of Kidney Diseases · 19
Emery‐Dreifuss muscular dystrophy type 4: A new SYNE1 mutation associated with hypertrophic cardiomyopathy masked by a perinatal distress‐related spastic diplegia
2019 · Mastroianno Sandra, Leone Maria Pia, et al. · Clinical Case Reports · 15
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Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athlete
2019 · Stefano Castellana, Sandra Mastroianno, et al. · Journal of Electrocardiology · 15
Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Nav 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic role
2018 · Giuseppe Di Stolfo, Pietro Palumbo, et al. · Journal of Electrocardiology · 15
Identification and Clinical Characterization of Adult Patients with Multigenerational Diabetes Mellitus
2015 · Ornella Ludovico, Massimo Carella, et al. · PLoS ONE · 14
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COMPASS criteria applied to a contemporary cohort of unselected patients with stable coronary artery diseases: insights from the START registry
2020 · Leonardo De Luca, Dario Formigli, et al. · European Heart Journal - Quality of Care and Clinical Outcomes · 8
Double missense mutations in cardiac myosin‐binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathy
2019 · Sandra Mastroianno, Pietro Palumbo, et al. · Annals of Noninvasive Electrocardiology · 8
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Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription
2019 · Giuseppe Di Stolfo, Maria Accadia, et al. · Molecular Genetics & Genomic Medicine · 8
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Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction
2021 · Maria Pia Leone, Pietro Palumbo, et al. · Frontiers in Cardiovascular Medicine · 7
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MODY type 2 P59S GCK mutant: founder effect in South of Italy
2012 · M Delvecchio, O Ludovico, et al. · Clinical Genetics · 7
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Role of the APOE polymorphism in carotid and lower limb revascularization: A prospective study from Southern Italy
2017 · Sandra Mastroianno, Giuseppe Di Stolfo, et al. · PLoS ONE · 6
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Sustainable and effective lipid-lowering management: prevention strategies from the BRING-UP prevention study
2026 · Furio Colivicchi, Pier Luigi Temporelli, et al. · European Heart Journal - Quality of Care and Clinical Outcomes · 5
Molecular diagnostic workflow, clinical interpretation of sequence variants, and data repository procedures in 140 individuals with familial cerebral cavernous malformations
2019 · Carmela Fusco, Massimiliano Copetti, et al. · Human Mutation · 5
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The Role of TOMM40 in Cardiovascular Mortality and Conduction Disorders: An Observational Study
2024 · Giuseppe Di Stolfo, Sandra Mastroianno, et al. · Journal of Clinical Medicine · 4
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Role of C-Reactive Protein as a Predictor of Early Revascularization and Mortality in Advanced Peripheral Arterial Disease
2025 · Giuseppe Di Stolfo, Mario Mastroianno, et al. · Journal of Clinical Medicine · 3
Biallelic LZTR1 variants in a 49‐year‐old woman with hypertrophic cardiomyopathy: A clue for considering LZTR1 in adults
2023 · Giuseppe Di Stolfo, Antonio Petracca, et al. · American Journal of Medical Genetics Part A · 3
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Involvement of APOE in Incidence of Revascularization in Patients Affected by Peripheral Arterial Disease: A Prospective Study from Southern Italy
2023 · Giuseppe Di Stolfo, Michele Antonio Pacilli, et al. · Journal of Clinical Medicine · 3
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Works count: 49
Citation count: 742
H-index: 13
I10-index: 13
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