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Rami A. Jarjour

Observed names: Jarjour R, Jarjour, Rami A., R. A. Jarjour, Rami Jarjour
ORCID: 0000-0003-3688-8809
Observed ORCID: 0000-0003-3688-8809
OpenAlex ID: A5081243307
Familial Mediterranean fever in Syrian patients: MEFV gene mutations and genotype–phenotype correlation
2009 · Rami A. Jarjour · Molecular Biology Reports · 47
Arthritis patterns in familial Mediterranean fever patients and association with M694V mutation
2010 · Rami A. Jarjour, Reem Dodaki · Molecular Biology Reports · 38
Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations
2014 · Rami A. Jarjour, Hossam Murad, et al. · Hemoglobin · 33
Geographical distribution of β-globin gene mutations in Syria
2018 · Hossam Murad, Faten Moasses, et al. · Hematology · 29
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Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women
2017 · Walid Al-Achkar, Abdulsamad Wafa, et al. · Reproductive Sciences · 28
Familial Mediterranean fever in Syrian children: phenotype–genotype correlation
2014 · Rami A. Jarjour, Sumaya Al-Berrawi · Rheumatology International · 25
Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population
2014 · Hossam Murad, Faten Moassas, et al. · Hemoglobin · 21
Combination of conventional multiplex PCR and quantitative real-time PCR detects large rearrangements in the dystrophin gene in 59% of Syrian DMD/BMD patients
2010 · Ammar Madania, Hana Zarzour, et al. · Clinical Biochemistry · 16
Spectrum of cystic fibrosis mutations in Syrian patients
2018 · Rami A. Jarjour, Sumaya Al-Berrawi, et al. · Minerva Pediatrics · 12
Mutations of familial Mediterranean fever in Syrian patients and controls: Evidence for high carrier rate
2016 · Rami A. Jarjour, Rami Abou Jamra · Gene Reports · 8
Frequency of three prothrombotic polymorphisms among Syrian population: factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T
2015 · Rami A. Jarjour, Samer Ammar, et al. · Annals of Human Biology · 8
Free-Standing Porous Silicon Film Produced by a Pulsed Anodic Etching of n+-Silicon Substrate in an HF: HCl: C2H5 OH: H2O2:H2O Electrolyte: Characterization and Adsorption of Colchicine
2020 · M. Naddaf, R. A. Jarjour · Silicon · 5
A new case of de novo translocation (12;17;18)(q21.2;q22;q21.1) and cranio‐cerebello‐cardiac (3C) syndrome
2011 · Walid Al‐Achkar, Abdulsamad Wafa, et al. · American Journal of Medical Genetics Part A · 3
Syrian females with congenital adrenal hyperplasia: a case series
2022 · Nada Dehneh, Rami Jarjour, et al. · Journal of Medical Case Reports · 2
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A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome
2020 · Abdulsamad Wafa, Rami A. Jarjour, et al. · Molecular Cytogenetics · 2
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An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case
2020 · Abdulsamad Wafa, Rami A. Jarjour, et al. · Molecular Cytogenetics · 2
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Review of: "Effect of Supplementation with Moringa oleifera on Antioxidant and Oxidative Stress Biomarkers of Infertile Women: A Pilot Open-Label Randomized Clinical Trial"
2024 · Rami Jarjour · Qeios
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The Prognostic Role of Apelin in the Assessment of Cardiac Outcomes in Patients with Chronic Kidney Disease: A Case-Control Study
2023 · Janet Ali, Rami A. Jarjour, et al. · International Journal of Medical Science
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Syrian females with congenital adrenal hyperplasia: a case series
2023 · Dehneh N, Jarjour R, et al. · Yearbook of pediatric endocrinology
Strong association between acute phase reactants (high-sensitivity C-reactive protein and erythrocyte sedimentation rate) and the familial Mediterranean fever (FMF) in patients but not with the MEFV genotype
2022 · Rami A. Jarjour, Wafika Zarzour · Human Gene
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A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome
2020 · Atomic Energy Commission of Syria, Abdulsamad Wafa, et al. · RESEARCH RESULTS IN BIOMEDICINE
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Works count: 23
Citation count: 278
H-index: 9
I10-index: 9
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