Get started
Author

Meriem Mrad

The Effect of ACE I/D Polymorphisms Alone and With Concomitant Risk Factors on Coronary Artery Disease
2016 · Ahmed Amara, Meriem Mrad, et al. · Clinical and Applied Thrombosis/Hemostasis · 53
PDF
Methylenetetrahydrofolate Reductase (C677T and A1298C) Polymorphisms, Hyperhomocysteinemia, and Ischemic Stroke in Tunisian Patients
2013 · Najiba Fekih-Mrissa, Meriem Mrad, et al. · Journal of Stroke and Cerebrovascular Diseases · 52
Methylenetetrahydrofolate Reductase (MTHFR) (C677T and A1298C) Polymorphisms and Vascular Complications in Patients with Type 2 Diabetes
2017 · Najiba Fekih-Mrissa, Meriem Mrad, et al. · Canadian Journal of Diabetes · 34
Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients
2013 · Najiba Fekih Mrissa, Meriem Mrad, et al. · Clinical Neurology and Neurosurgery · 29
Association of HLA-DR/DQ polymorphisms with Guillain–Barré syndrome in Tunisian patients
2014 · Najiba Fekih-Mrissa, Meriem Mrad, et al. · Clinical Neurology and Neurosurgery · 27
Association of HLA-DR-DQ polymorphisms with diabetes in Tunisian patients
2013 · Najiba Fekih Mrissa, Meriem Mrad, et al. · Transfusion and Apheresis Science · 26
Association of HLA-DR/DQ polymorphism with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in Tunisian patients
2013 · Meriem Mrad, Najiba Fekih-Mrissa, et al. · Transfusion and Apheresis Science · 19
Association between an angiotensin-converting enzyme gene polymorphism and Alzheimer’s disease in a Tunisian population
2017 · Najiba Fekih-Mrissa, Ines Bedoui, et al. · Annals of General Psychiatry · 14
PDF
HLA DRB1*03 as a possible common etiology of schizophrenia, Graves’ disease, and type 2 diabetes
2017 · Aicha Sayeh, Cheker Ben Cheikh, et al. · Annals of General Psychiatry · 13
PDF
Association of HLA-DR/DQ polymorphisms with schizophrenia in Tunisian patients
2014 · Aicha Sayeh, Cheker Ben Cheikh, et al. · Annals of Saudi Medicine · 13
Association of methylenetetrahydrofolate reductase (A1298C and C677T) polymorphisms with retinal vein occlusion in Tunisian patients
2014 · Meriem Mrad, Cheima Wathek, et al. · Transfusion and Apheresis Science · 13
Apolipoprotein E Genotypes Associated with Alzheimer Disease and Concomitant Stroke
2013 · Najiba Fekih-Mrissa, Sarra Klai, et al. · Journal of Stroke and Cerebrovascular Diseases · 13
Association of FV G1691A Polymorphism but not A4070G With Coronary Artery Disease
2017 · Ahmed Amara, Meriem Mrad, et al. · Clinical and Applied Thrombosis/Hemostasis · 11
PDF
The Plasminogen Activator Inhibitor 1 4G/5G Polymorphism and the Risk of Alzheimer’s Disease
2017 · Najiba Fekih-Mrissa, Malek Mansour, et al. · American Journal of Alzheimer s Disease & Other Dementias® · 10
Association Between Thrombophilic Gene Mutations and the Risk of Vascular Access Thrombosis in Hemodialysis Patients
2016 · Najiba Fekih‐Mrissa, Aycha Sayeh, et al. · Therapeutic Apheresis and Dialysis · 10
Thrombophilic Risk Factors in Different Types of Retinal Vein Occlusion in Tunisian Patients
2014 · Meriem Mrad, Najiba Fekih-Mrissa, et al. · Journal of Stroke and Cerebrovascular Diseases · 10
Role of methylenetetrahydrofolate reductase A1298C polymorphism in cerebral venous thrombosis
2013 · Najiba Fekih-Mrissa, Sarra Klai, et al. · Blood Coagulation & Fibrinolysis · 9
Role of the Apolipoprotein E Polymorphisms in the Development of Retinal Vein Occlusion in a Tunisian Population: A Case–Control Study
2016 · Meriem Mrad, Najiba Fekih-Mrissa, et al. · Clinical and Applied Thrombosis/Hemostasis · 6
Diabetes - experimental models
2013 · V. Blanco-Gozalo, A. Blazquez-Medela, et al. · Nephrology Dialysis Transplantation · 2
Mthfr (c677t and a1298c) polymorphisms and coronary heart disease
2014 · N. Fekih-Mrissa, M. Mrad, et al. · Atherosclerosis · 1
Inherited thrombophilia-related complications in the treatment of a biatrial thrombus
2012 · Issam Jalouli, Meriem Mrad, et al. · Blood Coagulation & Fibrinolysis · 1
Non-arteritic ischemic optic neuropathy reveals Marchiafava–Micheli disease: a case report
2016 · Cheima Wathek, Rym Maamouri, et al. · Research
Prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms in peripheral capillary nonperfusion: a case report
2015 · Chaima Wathek, Meriem Mrad, et al. · Blood Coagulation & Fibrinolysis
Genetic polymorphisms and their association with central retinal vein occlusion combined with cilioretinal artery occlusion
2014 · Meriem Mrad, Chaima Wathek, et al. · Comparative Clinical Pathology
Works count: 25
Citation count: 366
H-index: 12
I10-index: 16
Year
Topic
Type