Giovanna D’Andrea

University of Foggia — Italy

Medicine · Health Sciences

24h-index2.9kcitations64works5.82yr avg
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Research Topics

Blood Coagulation and Thrombosis Mechanisms(25), Venous Thromboembolism Diagnosis and Management(12), Platelet Disorders and Treatments(10), Coagulation, Bradykinin, Polyphosphates, and Angioedema(10), Atrial Fibrillation Management and Outcomes(8)

Publications64 total

Clinical and Genetic Heterogeneity of Factor XI Deficiency: Insights from a Southern Italian Cohort
International Journal of Molecular Sciences·2025Open Access
Bleeding Predictability in Patients with Factor XI Deficiency: The Experience of Reference Centers in Southern Italy
Preprints.org·2025Open Access
Vasculopathy: a possible factor affecting hereditary angioedema
Bleeding Thrombosis and Vascular Biology·2025Open Access
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing Study
International Journal of Molecular Sciences·2025· 2 citedOpen Access
Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome
Genes·2024· 1 citedOpen Access
DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology
Journal of Allergy and Clinical Immunology·2024· 41 citedOpen Access
Homozygous MTHFR C677T carriers develop idiopathic portal vein thrombosis 20 years earlier than wild type
Blood Coagulation & Fibrinolysis·2024· 3 cited
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis
International Journal of Molecular Sciences·2024· 5 citedOpen Access
Homozygous MTHFR C667T carriers ≤45 years old develop central retinal vein occlusion five years earlier than wild type
Ophthalmic Genetics·2024
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Genetics & Genomic Sciences·2023Open Access
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis
Genes·2023· 14 citedOpen Access
Juvenile patients with the homozygous MTHFR C677T genotype develop ischemic stroke 5 years earlier than wild type
Journal of Thrombosis and Thrombolysis·2022· 3 cited
Homozygous Mthfr C677t Carriers Develop Idiopathic Portal Vein Thrombosis Twenty Years Earlier Than Wild Type
Research Square (Research Square)·2022Open Access
Associations Between Personality Traits, Perceived Stress and Depressive Symptoms in Gynecological Cancer Patients Characterized by the Short and Long Allele Variant of the 5-HTTLPR Genotype: Preliminary Results.
PubMed·2022· 3 citedOpen Access
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism
Thrombosis and Haemostasis·2022· 3 cited
Earlier onset of peripheral arterial thrombosis in homozygous MTHFR C677T carriers than in other MTHFR genotypes: a cohort study
Clinical and Experimental Medicine·2022· 5 cited
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients
PLoS ONE·2022· 14 citedOpen Access
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients
SHILAP Revista de lepidopterología·2022Open Access
Homozygous methylentetrahydrofolate reductase C667T genotype anticipates age at venous thromboembolism by one decade
Blood Coagulation & Fibrinolysis·2021· 5 cited
The Genetics of Hereditary Angioedema: A Review
Journal of Clinical Medicine·2021· 101 citedOpen Access
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Frequent Co-authors

Maurizio Margaglione(47), Elvira Grandone(21), Vincenzo Brancaccio(17), Rosa Santacroce(12), Giovanni Di Minno(11), Paul R. J. Ames(9), Donatella Colaizzo(8), Luigi Iannaccone(8), Gennaro Vecchione(7), Maria D’Apolito(7), Lucio Amitrano(5), Maria Anna Guardascione(5), Giuseppe Cappucci(5), Giovanni Luca Tiscia(5), Vincenzo Marottoli(5), Rosa D’Ambrosio(4), Nicola Giuliani(4), Filomena Cappucci(4), Mario Altamura(4), Antonello Bellomo(4)