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Bahareh Rabbani
Bahareh Rabbani
Iran University of Medical Sciences
Verified email at modares.ac.ir
Title
Cited by
Cited by
Year
The promise of whole-exome sequencing in medical genetics
B Rabbani, M Tekin, N Mahdieh
Journal of human genetics 59 (1), 5-15, 2014
6722014
Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders
B Rabbani, N Mahdieh, K Hosomichi, H Nakaoka, I Inoue
Journal of human genetics 57 (10), 621-632, 2012
2782012
An overview of mutation detection methods in genetic disorders
N Mahdieh, B Rabbani
Iranian journal of pediatrics 23 (4), 375, 2013
1622013
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations
N Mahdieh, B Rabbani, S Wiley, MT Akbari, S Zeinali
Journal of human genetics 55 (10), 639-648, 2010
1202010
Next generation sequencing: implications in personalized medicine and pharmacogenomics
B Rabbani, H Nakaoka, S Akhondzadeh, M Tekin, N Mahdieh
Molecular biosystems 12 (6), 1818-1830, 2016
1192016
Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency
N Mahdieh, B Rabbani
International journal of audiology 48 (6), 363-370, 2009
1112009
Vitamin D insufficiency among children and adolescents living in Tehran, Iran
A Rabbani, SM Alavian, ME Motlagh, MTH Ashtiani, G Ardalan, A Salavati, ...
Journal of tropical pediatrics 55 (3), 189-191, 2009
932009
Beta thalassemia in 31,734 cases with HBB gene mutations: pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East
N Mahdieh, B Rabbani
Blood reviews 30 (6), 493-508, 2016
452016
Screening of OTOF mutations in Iran: a novel mutation and review
N Mahdieh, A Shirkavand, B Rabbani, M Tekin, B Akbari, MT Akbari, ...
International journal of pediatric otorhinolaryngology 76 (11), 1610-1615, 2012
422012
Mutation Analysis of the CYP21A2 Gene in the Iranian Population
B Rabbani, N Mahdieh, MTH Ashtiani, B Larijani, MT Akbari, M New, ...
Genetic Testing and Molecular Biomarkers 16 (2), 82-90, 2012
352012
Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant
N Mahdieh, B Rabbani, A Shirkavand, H Bagherian, ZS Movahed, ...
Genetic testing and molecular biomarkers 15 (7-8), 489-493, 2011
352011
In silico structural, functional and pathogenicity evaluation of a novel mutation: an overview of HSD3B2 gene mutations
B Rabbani, N Mahdieh, MTH Ashtiani, A Setoodeh, A Rabbani
Gene 503 (2), 215-221, 2012
312012
Molecular diagnosis of congenital adrenal hyperplasia in Iran: focusing on CYP21A2 gene
B Rabbani, N Mahdieh, MTH Ashtiani, MT Akbari, A Rabbani
Iranian journal of pediatrics 21 (2), 139, 2011
312011
Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants
N Mahdieh, M Soveizi, AR Tavasoli, A Rabbani, MR Ashrafi, ...
Scientific reports 11 (1), 3231, 2021
192021
The frequency of HBB mutations among β-thalassemia patients in Hamadan Province, Iran
M Jalilian, F Azizi Jalilian, L Ahmadi, R Amini, H Esfehani, M Sosanian, ...
Hemoglobin 41 (1), 61-64, 2017
192017
A novel single step double positive double negative selection strategy for β-globin gene replacement
H Khanahmad, MRN Daloii, MA Shokrgozar, K Azadmanesh, ...
Biochemical and biophysical research communications 345 (1), 14-20, 2006
172006
A novel single step double positive double negative selection strategy for β-globin gene replacement
H Khanahmad, MRN Daloii, MA Shokrgozar, K Azadmanesh, ...
Biochemical and biophysical research communications 345 (1), 14-20, 2006
172006
HLA‐DRB,‐DQA, and DQB alleles and haplotypes in Iranian patients with diabetes mellitus type I
A Rabbani, F Abbasi, M Taghvaei, B Rabbani, B Moradi, Y Shakiba, ...
Pediatric diabetes 14 (5), 366-371, 2013
162013
Clopidogrel pharmacogenetics in Iranian patients undergoing percutaneous coronary intervention
N Mahdieh, A Rabbani, A Firouzi, A Zahedmehr, M Hoseinimoghaddam, ...
Cardiovascular Toxicology 18, 482-491, 2018
102018
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular …
B Rabbani, M Khorgami, M Dalili, N Zamani, N Mahdieh, MH Gollob
American Journal of Medical Genetics Part A 185 (11), 3433-3445, 2021
92021
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