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Abdulghani Msalati, Abdulla Bashein, Murad Ghrew, Ibtesam Khalil, Khaled Sedaa, Abushawashi Ali & Ahmed Zaid. (2021) Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients. Libyan Journal of Medicine 16:1.
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Minerva Codruta Badescu, Lăcrămioara Ionela Butnariu, Alexandru Dan Costache, Liliana Gheorghe, Petronela Nicoleta Seritean Isac, Adriana Chetran, Sabina Andreea Leancă, Irina Afrăsânie, Ștefania-Teodora Duca, Eusebiu Vlad Gorduza, Irina Iuliana Costache & Ciprian Rezus. (2023) Acute Myocardial Infarction in Patients with Hereditary Thrombophilia—A Focus on Factor V Leiden and Prothrombin G20210A. Life 13:6, pages 1371.
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Salma Younes, Zumin Shi & Hatem Zayed. (2020) Genetic variations associated with coronary artery disease and myocardial infarction in the Arab world: a systematic review and meta-analysis. Highlights in BioScience.
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Amal Ahmed Abd El-Fattah, Nermin Abdel hamid Sadik, Heba Sedrak, Ahmed Battah & Mai Nabil. (2018) Association of genetic variants of hemostatic genes with myocardial infarction in Egyptian patients. Gene 641, pages 212-219.
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Wiam Hmimech, Brehima Diakite, Hind Hassani Idrissi, Khalil Hamzi, Farah Korchi, Dalila Baghdadi, Rachida Habbal & Sellama Nadifi. (2016) G2691A and C2491T mutations of factor V gene and pre-disposition to myocardial infarction in Morocco. Biomedical Reports 5:5, pages 618-622.
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Wael Alkhiary, Hanan Azzam, Mahmoud Mohammed Abdo Yossof, Salah Aref, Maha Othman & Solafa El-Sharawy. (2016) Association of Hemostatic Gene Polymorphisms With Early-Onset Ischemic Heart Disease in Egyptian Patients. Clinical and Applied Thrombosis/Hemostasis 22:6, pages 535-542.
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Liang Tang & Yu Hu. (2017) Ethnic diversity in the genetics of venous thromboembolism. Thrombosis and Haemostasis 114:11, pages 901-909.
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Hamdia Ezzat, Fatma A. Attia, Amal Mokhtar, Hanan M. El-Tokhy, Mohamed N. Alalfy & Nashwa Y. Elkhouly. (2014) Prevalence of thrombophilic gene polymorphisms (FVL G1691A and MTHFR C677T) in patients with myocardial infarction. Egyptian Journal of Medical Human Genetics 15:2, pages 113-123.
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Jeremy S. C. Clark, Grażyna Adler, Nermin N. Salkic & Andrzej Ciechanowicz. (2013) Allele frequency distribution of 1691G>A F5 (which confers Factor V Leiden) across Europe, including Slavic populations. Journal of Applied Genetics 54:4, pages 441-446.
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Ayman S. Hussein. (2012) High prevalence of three prothrombotic polymorphisms among Palestinians: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T. Journal of Thrombosis and Thrombolysis 34:3, pages 383-387.
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Alexander Gonchar, Maxim Ameliyanovich, Kristina Zhur, Irma Mosse & Konstantin Mosse. 2012. Radiobiology and Environmental Security. Radiobiology and Environmental Security
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Ali A. Dashti, Mehrez M. Jadaon, Abdulsamad M. Abdulsamad, Mohammad H. Dashti & Hend L. Lewis. (2011) Thrombosis risk in carriers of the factor V Leiden mutation: Is it associated with a defined skin color?. Pathology - Research and Practice 207:11, pages 671-673.
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Mehrez M. Jadaon, Ali A. Dashti & Hend L. Lewis. (2010) High Prevalence of Activated Protein C Resistance and Factor V Leiden Mutation in an Arab Population and Patients With Venous Thrombosis in Kuwait. Diagnostic Molecular Pathology 19:3, pages 180-183.
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Benjamin Sussman & B. Brent Simmons. (2010) Antiphospholipid antibody syndrome causing acute myocardial infarction in a young adult. Osteopathic Family Physician 2:5, pages 139-143.
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Moataz DowaidarAhmad Settin. (2010) Risk of Myocardial Infarction Related to Factor V Leiden Mutation: A Meta-Analysis. Genetic Testing and Molecular Biomarkers 14:4, pages 493-498.
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Ali A Dashti, Mehrez M Jadaon & Hend L Lewis. (2010) Factor V Leiden mutation in Arabs in Kuwait by real-time PCR: different values for different Arabs. Journal of Human Genetics 55:4, pages 232-235.
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G. A Chumakova, A. P Momot, A. A Kozarenko & N. G Veselovskaya. (2010) Genetic predisposition to atherothromboses in patients with severe angina pectoris. CardioSomatics 1:1, pages 80-83.
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