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Maurizio Margaglione

Maurizio Margaglione

D-Index & Metrics

Medicine

D-Index
71
Citations
17755
World Ranking
19998
National Ranking
805

Overview

Maurizio Margaglione is affiliated with the University of Foggia in Italy and has an extensive research portfolio primarily concentrated in the field of Medicine. Their scholarly work covers multiple subfields including Infectious Diseases, Hematology, Cardiology and Cardiovascular Medicine, Genetics, and Internal Medicine.

Their research topics emphasize mechanisms and diagnosis related to blood coagulation and thrombosis, as well as conditions involving coagulation factors such as bradykinin and polyphosphates linked to angioedema. Studies on venous thromboembolism management, clinical research on COVID-19, and investigations into cardiac electrophysiology and arrhythmias also form significant pillars of their scientific contributions. Specific subject areas they address include:

  • Blood Coagulation and Thrombosis Mechanisms
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Venous Thromboembolism Diagnosis and Management
  • COVID-19 Clinical Research Studies
  • SARS-CoV-2 and COVID-19 Research
  • Cardiac electrophysiology and arrhythmias
  • Hemophilia Treatment and Research

Maurizio Margaglione has contributed to numerous recent publications including:

  • "A myoferlin gain-of-function variant associates with a new type of hereditary angioedema," 2020, Allergy
  • "The Genetics of Hereditary Angioedema: A Review," 2021, Journal of Clinical Medicine
  • "Summary of the Available Molecular Methods for Detection of SARS-CoV-2 during the Ongoing Pandemic," 2021, International Journal of Molecular Sciences
  • "Results from a survey in healthy blood donors in South Eastern Italy indicate that we are far away from herd immunity to SARS-CoV-2," 2020, Journal of Medical Virology
  • "Findings from a multicentre, observational study on reproductive outcomes in women with unexplained recurrent pregnancy loss: the OTTILIA registry," 2021, Human Reproduction

Their work frequently appears in journals such as the International Journal of Molecular Sciences, Genes, Journal of Thrombosis and Thrombolysis, PubMed, and Preprints.org.

Collaborations have been established with a number of coauthors, reflecting an interdisciplinary approach. Frequent coauthors include Rosa Santacroce, Elvira Grandone, Maria D'Apolito, Giovanna D'Andrea, and Giovanni Luca Tiscia.

Best Publications

  • A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.

    Giovanna D'Andrea;Rosa Lucia D'Ambrosio;Rosa Lucia D'Ambrosio;Pasquale Di Perna;Pasquale Di Perna;Massimiliano Chetta;Massimiliano Chetta

  • Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis

    Lucio Amitrano;Maria Anna Guardascione;Vincenzo Brancaccio;Maurizio Margaglione

  • Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism - Pooled analysis of 8 case-control studies including 2310 cases and 3204 controls

    Joseph Emmerich;Frits R. Rosendaal;Marco Cattaneo;Maurizio Margaglione

  • F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis

    Samantha C. Gouw;Samantha C. Gouw;H. Marijke van den Berg;Johannes Oldenburg;Jan Astermark

  • Factor V Leiden is associated with repeated and recurrent unexplained fetal losses

    Elvira Grandone;Elvira Grandone;Maurizio Margaglione;Maurizio Margaglione;Donatella Colaizzo;Donatella Colaizzo;Marina d'Addedda;Marina d'Addedda

  • Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis

    Lucio Amitrano;Vincenzo Brancaccio;Maria Anna Guardascione;Maurizio Margaglione

  • Prognostic factors in noncirrhotic patients with splanchnic vein thromboses.

    Lucio Amitrano;Maria Anna Guardascione;Mariano Scaglione;Luca Pezzullo

  • Factor V Leiden, C>T MTHFR Polymorphism and Genetic Susceptibility to Preeclampsia

    Elvira Grandone;Maurizio Margaglione;Donatella Colaizzo;Giuseppe Cappucci

  • Prothrombotic Genetic Risk Factors in Young Survivors of Myocardial Infarction

    D. Ardissino;P.M. Mannucci;P.A. Merlini;F. Duca

  • Genetic modulation of oral anticoagulation with warfarin.

    Maurizio Margaglione;Donatella Colaizzo;Giovanna D’Andrea;Vincenzo Brancaccio

  • Increased Risk for Venous Thrombosis in Carriers of the Prothrombin G→A20210 Gene Variant

    Maurizio Margaglione;Vincenzo Brancaccio;Nicola Giuliani;Giovanna D'Andrea

  • Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema

    Valeria Bafunno;Davide Firinu;Maria D'Apolito;Giorgia Cordisco

  • No evidence of association between prothrombotic gene Polymorphisms and the development of acute myocardial infarction at a young age

    P. M. Mannucci;P. A. Merlini;D. Ardissino;C. Barzuini

  • Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations.

    Elvira Grandone;Maurizio Margaglione;Donatella Colaizzo;Giovanna D’Andrea

  • Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism.

    G Di Minno;G Davì;M Margaglione;F Cirillo

  • Plasma Thrombin-Activatable Fibrinolysis Inhibitor Antigen Concentration and Genotype in Relation to Myocardial Infarction in the North and South of Europe

    I. Juhan-Vague;P.E. Morange;H. Aubert;M. Henry

  • The PAI-1 gene locus 4g/5G polymorphism is associated with a family history of coronary artery disease

    Maurizio Margaglione;Giuseppe Cappucci;Donatella Colaizzo;Nicola Giuliani

  • Low-grade inflammation may play a role in the etiology of the metabolic syndrome in patients with coronary heart disease: the HIFMECH study.

    J.S Yudkin;I Juhan-Vague;E Hawe;S.E Humphries

  • Insight into the nature of the CRP–coronary event association using Mendelian randomization

    Juan P Casas;Tina Shah;Jackie Cooper;Emma Hawe

  • The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis

    D. Colaizzo;L. Amitrano;G. L. Tiscia;G. Scenna

Frequent Co-Authors

Irène Juhan-Vague
Irène Juhan-Vague Hôpital de la Timone
Walter Ageno
Walter Ageno University of Insubria
John S Yudkin
John S Yudkin University College London
Anders Hamsten
Anders Hamsten Karolinska Institute
Angelo Andriulli
Angelo Andriulli Casa Sollievo della Sofferenza
Salvatore Panico
Salvatore Panico University of Naples Federico II
Elena Tremoli
Elena Tremoli University of Milan
Vito Michele Fazio
Vito Michele Fazio Università Campus Bio-Medico
V. De Stefano
V. De Stefano Catholic University of the Sacred Heart
Paolo Fortina
Paolo Fortina Thomas Jefferson University

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