Prothrombin Gene Mutation

Prothrombin Gene Mutation is a genetic variant in the prothrombin (F2) gene characterized by a specific single nucleotide substitution (G20210A) that increases prothrombin plasma levels and confers a heightened risk for venous thrombosis.

1.3K

Publications

69.9K

Citations

5.9K

Authors

1.4K

Institutions

Publications per year

2017–2026

74

Variants

F2 Gene Mutation

Parents

Authors

5.9K

  1. FR
    Frits R. Rosendaal

    Leiden University Medical Center, Netherlands

    33 publications · 4.5K citations

    27

    h-index

  2. PM
    Pier Mannuccio Mannucci

    University of Milan, Italy

    31 publications · 3.7K citations

    26

    h-index

  3. VD
    Valerio De Stefano

    Università Cattolica del Sacro Cuore, Italy

    25 publications · 2.8K citations

    20

    h-index

  4. IM
    Ida Martinelli

    Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Italy

    20 publications · 3.1K citations

    19

    h-index

  5. DA
    David A. Lane

    Charing Cross Hospital, United Kingdom

    20 publications · 1.6K citations

    17

    h-index

1–5 of 5.9K

Venues

  1. Thrombosis and Haemostasis

    137 publications · 8.7K citations

    49

    h-index

  2. Blood

    96 publications · 9.6K citations

    46

    h-index

  3. PubMed

    Repository · 103 publications · 3.6K citations

    33

    h-index

  4. British Journal of Haematology

    BJH · 60 publications · 3.7K citations

    32

    h-index

  5. Journal of Thrombosis and Haemostasis

    JTH · 44 publications · 1.9K citations

    29

    h-index

1–5