Varaico: Literature-Extracted Genetic Variants

Gene:F5
Variant:p.W152*
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F5

NM_000130.5:p.W152*

Associated Papers

Genetic landscape of thrombophilia in recurrent miscarriages.

Athar A et al.

Obstetrics & Gynecology Science, 2024

Impact of pharmacogenetics on aspirin resistance: a systematic review.

Silva GFD et al.

Arquivos De Neuro-psiquiatria, 2023

Genetic Markers for Thrombophilia and Cardiovascular Disease Associated with Multiple Sclerosis.

Hadjiagapiou MS et al.

Biomedicines, 2022

Association of polymorphisms in genes encoding prothrombotic and cardiovascular risk factors with disease severity in COVID-19 patients: A pilot study.

Lapić I et al.

Journal of Medical Virology, 2022

Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.

Quintero-Ronderos P et al.

Reproductive Sciences (thousand Oaks, Calif.), 2020

The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease.

Yalım Z et al.

Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2020

Association of Polymorphisms in Coagulation Factor Genes and Enzymes of Homocysteine Metabolism With Arterial Ischemic Stroke in Children.

Coen Herak D et al.

Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2017

Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.

Fawzy MS et al.

Bmc Cardiovascular Disorders, 2017

Association of Hemostatic Gene Polymorphisms With Early-Onset Ischemic Heart Disease in Egyptian Patients.

Alkhiary W et al.

Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2016

Combination of thrombophilic gene polymorphisms as a cause of increased the risk of recurrent pregnancy loss.

Torabi R et al.

Journal of Reproduction & Infertility, 2012

Genetic cardiovascular risk factors and age-related macular degeneration.

Haas P et al.

Acta Ophthalmologica, 2011

A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.

Yenicesu GI et al.

American Journal of Reproductive Immunology (new York, N.y. : 1989), 2010

Fibrinogen Aalpha Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension.

Suntharalingam J et al.

The European Respiratory Journal, 2008

Clinical applications of bioinformatics, genomics, and pharmacogenomics.

Iqbal O et al.

Methods in Molecular Biology (clifton, N.j.), 2006

Genetic factors contribute to bleeding after cardiac surgery.

Welsby IJ et al.

Journal of Thrombosis and Haemostasis : Jth, 2005

Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.

Marchetti G et al.

British Journal of Haematology, 2003

Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester.

Pihusch R et al.

American Journal of Reproductive Immunology (new York, N.y. : 1989), 2001

Genetics and ischaemic stroke.

Hassan A et al.

Brain : a Journal of Neurology, 2000

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."