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.
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2017–2026
74
Variants
F2 Gene Mutation
Parents
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Malignancies, Prothrombotic Mutations, and the Risk of Venous Thrombosis
Jeanet W. Blom · JAMA · 2005 · 2K citations
Medicine, Genetics, Hematology +14
Geographic Distribution of the 20210 G to A Prothrombin Variant
Carine J.M. Doggen, Ariella Zivelin, Valder R. Arruda et al. · Thrombosis and Haemostasis · 1998 · 702 citations · Full text
Ethnic Distribution of Factor V Leiden in 4047 Men and Women
Paul M. Ridker · JAMA · 1997 · 642 citations
Medicine, Genetics, Hematology +17
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Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Italy
20 publications · 3.1K citations
19
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17
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Leiden University Medical Center
Leiden, The Netherlands
31 h-index
152 publications
23.5K citations

University of Milan
Milan, Italy
25 h-index
109 publications
11.1K citations
Inserm
Paris, France
23 h-index
173 publications
11K citations

Lund University
Lund, Sweden
19 h-index
58 publications
4.5K citations

Ankara University
Ankara, Türkiye
18 h-index
75 publications
2.5K citations
Harvard University
Cambridge, United States
17 h-index
60 publications
4.6K citations

Amsterdam UMC Location University of Amsterdam
Amsterdam, The Netherlands
17 h-index
78 publications
7.9K citations

Casa Sollievo della Sofferenza
San Giovanni Rotondo, Italy
16 h-index
69 publications
7.2K citations
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137 publications · 8.7K citations
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96 publications · 9.6K citations
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Repository · 103 publications · 3.6K citations
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BJH · 60 publications · 3.7K citations
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JTH · 44 publications · 1.9K citations
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