Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Global prevalence of prothrombin gene mutation G20210A and implications in women's health: a systematic review.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jul 2016

Dziadosz Margaret, Baxi Laxmi V

Abstract excerpt

Distribution of hereditary thrombophilic gene mutations differs globally. Prothrombin gene mutation G20210A is a common prothrombotic single-nucleotide polymorphism. In this systematic review, we provide a comprehensive report of the prevalence of prothrombin G20210A across the globe. Databases [Pubmed, Web of Science, Embase] were interrogated from their inception through December 2015 for articles reporting...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Black People
Share to Global Health

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation Rate

Share to Prothrombin

Share to Thrombophilia

Share to Venous Thromboembolism

Share to White People

Share to Women's Health

Source

Identifiers

PMID: 27058219
DOI: 10.1097/MBC.0000000000000562

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Global prevalence of prothrombin gene mutation G20210A and implications in women's health: a systematic review.PMID 27058219Read ↗

Clinical and laboratory management of the prothrombin G20210A mutation.Semantic proximity Read ↗

Inherited thrombophilia: an update.Semantic proximity Read ↗

Management of antithrombin deficiency: an update for cliniciansSemantic proximity Read ↗

Genetic Testing for Thrombophilia-Related Genes: Observations of Testing Patterns for Factor V Leiden (G1691A) and Prothrombin Gene “Mutation” (G20210A)Semantic proximity Read ↗

Management of inherited thrombophilia: guide for genetics professionals.Semantic proximity Read ↗

The first homozygous family for prothrombin G20210A polymorphism reported in Latin America.Semantic proximity Read ↗

Clinical and Molecular Study of Common Thrombophilia Mutation Prothrombin G20210A.Semantic proximity Read ↗

[Frequently associated genotypes to thrombophilia].Semantic proximity Read ↗

Evolving paradigm in thrombophilia screeningSemantic proximity Read ↗

Prothrombin gene 20210A mutation in Slovak population.Semantic proximity Read ↗

Thrombophilia, risk factors and preventionSemantic proximity Read ↗

Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.