| Familial Mediterranean fever in Syrian patients: MEFV gene mutations and genotype–phenotype correlation RA Jarjour Molecular biology reports 37, 1-5, 2010 | 77 | 2010 |
| Arthritis patterns in familial Mediterranean fever patients and association with M694V mutation RA Jarjour, R Dodaki Molecular biology reports 38, 2033-2036, 2011 | 53 | 2011 |
| Association of methylenetetrahydrofolate reductase C677T and A1298C gene polymorphisms with recurrent pregnancy loss in Syrian women W Al-Achkar, A Wafa, S Ammar, F Moassass, RA Jarjour Reproductive Sciences 24 (9), 1275-1279, 2017 | 43 | 2017 |
| Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutations RA Jarjour, H Murad, F Moasses, W Al-Achkar Hemoglobin 38 (4), 272-276, 2014 | 40 | 2014 |
| Familial Mediterranean fever in Syrian children: phenotype–genotype correlation RA Jarjour, S Al-Berrawi Rheumatology international 35, 629-634, 2015 | 35 | 2015 |
| Geographical distribution of β-globin gene mutations in Syria H Murad, F Moasses, A Dabboul, Y Mukhalalaty, AO Bakoor, W Al-Achkar, ... Hematology 23 (9), 697-704, 2018 | 34 | 2018 |
| Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population H Murad, F Moassas, R Jarjour, Y Mukhalalaty, W Al-Achkar Hemoglobin 38 (6), 390-393, 2014 | 28 | 2014 |
| Combination of conventional multiplex PCR and quantitative real-time PCR detects large rearrangements in the dystrophin gene in 59% of Syrian DMD/BMD patients A Madania, H Zarzour, RA Jarjour, I Ghoury Clinical biochemistry 43 (10-11), 836-842, 2010 | 18 | 2010 |
| Frequency of three prothrombotic polymorphisms among Syrian population: factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T RA Jarjour, S Ammar, R Majdalawi Annals of Human Biology 44 (1), 70-73, 2017 | 14 | 2017 |
| Spectrum of cystic fibrosis mutations in Syrian patients. RA Jarjour, S Al-Berrawi, S Ammar, R Majdalawi Minerva Pediatrica 70 (2), 159-164, 2015 | 14 | 2015 |
| Mutations of familial Mediterranean fever in Syrian patients and controls: evidence for high carrier rate RA Jarjour, R Abou Jamra Gene Reports 6, 87-92, 2017 | 9 | 2017 |
| 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 … MNRA Jarjour Silicon, 2020 | 5* | 2020 |
| A new case of de novo translocation (12; 17; 18)(q21. 2; q22; q21. 1) and cranio‐cerebello‐cardiac (3C) syndrome W Al‐Achkar, A Wafa, RA Jarjour American Journal of Medical Genetics Part A 155 (3), 648-651, 2011 | 5 | 2011 |
| Syrian females with congenital adrenal hyperplasia: a case series N Dehneh, R Jarjour, S Idelbi, A Alibrahem, S Al Fahoum Journal of Medical Case Reports 16 (1), 371, 2022 | 2 | 2022 |
| Distinct Mechanisms Downstream of the Repeat Expansion Are Implicated in the Molecular Basis of Myotonic Dystrophy Type 1 KJ Jouhnson, RA Jarjour | 2 | 2006 |
| Association Between Acute Phase Reactants (High Sensitivity C-Reactive Protein and Erythrocyte Sedimentation Rate) and the Genotype of Familial Mediterranean Fever (FMF) in … RA Jarjour, W Zarzour | 1 | 2021 |
| E148Q as a Familial Mediterranean Fever-causing Mutation: A Clinical-based Study RA Jarjour West Indian Med J 69 (5), 304, 2021 | 1 | 2021 |
| A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome A Wafa, RA Jarjour, D Alolabi, T Liehr, O Hamdan, JB Melo, IM Carreira, ... Molecular Cytogenetics 13, 1-6, 2020 | 1 | 2020 |
| An acquired stable variant of a dicentric dic (9; 20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case A Wafa, RA Jarjour, A Aljapawe, S ALmedania, T Liehr, JB Melo, ... Molecular Cytogenetics 13, 1-6, 2020 | 1 | 2020 |
| Identification of SIX5 binding site, target genes, and functional links with myotonic dysrtophy (DM1) symptoms RA Jarjour PQDT-Global, 2003 | 1 | 2003 |
Abou Jamra, RamiInstitute of Human Genetics, Leipzig在 medizin.uni-leipzig.de 的电子邮件经过验证
Abou Jamra, RamiInstitute of Human Genetics, Leipzig在 medizin.uni-leipzig.de 的电子邮件经过验证