| A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment I Schrauwen, S Helfmann, A Inagaki, F Predoehl, MA Tabatabaiefar, ... The American Journal of Human Genetics 91 (4), 636-645, 2012 | 128 | 2012 |
| Investigating of four main carbapenem-resistance mechanisms in high-level carbapenem resistant Pseudomonas aeruginosa isolated from burn patients S Rostami, AF Sheikh, S Shoja, A Farahani, MA Tabatabaiefar, A Jolodar, ... Journal of the Chinese Medical Association 81 (2), 127-132, 2018 | 78 | 2018 |
| Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform S De Keulenaer, J Hellemans, S Lefever, JP Renard, J De Schrijver, ... BMC medical genomics 5, 1-8, 2012 | 73 | 2012 |
| Genetic linkage analysis of 15 DFNB loci in a group of Iranian families with autosomal recessive hearing loss MA Tabatabaiefar, F Alasti, MM Zohour, L Shariati, E Farrokhi, DD Farhud, ... Iranian journal of public health 40 (2), 34, 2011 | 68 | 2011 |
| Detection of metallo-beta lactamases among carbapenem-resistant Pseudomonas aeruginosa AF Sheikh, S Rostami, A Jolodar, MA Tabatabaiefar, F Khorvash, A Saki, ... Jundishapur journal of microbiology 7 (11), 2014 | 58 | 2014 |
| Association of the TCF7L2 rs12255372 (G/T) variant with type 2 diabetes mellitus in an Iranian population FM Alami, M Ahmadi, H Bazrafshan, A Tabarraei, A Khosravi, ... Genetics and molecular biology 35, 413-417, 2012 | 53 | 2012 |
| Genetic disruption of the KLF1 gene to overexpress the γ‐globin gene using the CRISPR/Cas9 system L Shariati, H Khanahmad, M Salehi, Z Hejazi, I Rahimmanesh, ... The journal of gene medicine 18 (10), 294-301, 2016 | 50 | 2016 |
| Genotyping of carbapenem resistant Acinetobacter baumannii isolated from tracheal tube discharge of hospitalized patients in intensive care units, Ahvaz, Iran S Shoja, M Moosavian, A Peymani, MA Tabatabaiefar, S Rostami, ... Iranian journal of microbiology 5 (4), 315, 2013 | 43 | 2013 |
| DFNB93, a novel locus for autosomal recessive moderate‐to‐severe hearing impairment MA Tabatabaiefar, F Alasti, L Shariati, E Farrokhi, E Fransen, ... Clinical genetics 79 (6), 594-598, 2011 | 41 | 2011 |
| Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method FA Dehkordi, A Rashki, N Bagheri, MH Chaleshtori, E Memarzadeh, ... Acta cytologica 57 (6), 646-651, 2013 | 35 | 2013 |
| Characterization of oxacillinase and metallo-β-lactamas genes and molecular typing of clinical isolates of Acinetobacter baumannii in Ahvaz, South-West of Iran S Shoja, M Moosavian, S Rostami, F Abbasi, MA Tabatabaiefar, ... Jundishapur journal of microbiology 9 (5), 2016 | 32 | 2016 |
| Correlation between mucosal IL-6 mRNA expression level and virulence factors of Helicobacter pylori in Iranian adult patients with chronic gastritis F Azadegan-Dehkordi, N Bagheri, M Shirzad, MH Sanei, ... Jundishapur journal of microbiology 8 (8), 2015 | 32 | 2015 |
| Mutations in GJB2 as major causes of autosomal recessive non-syndromic hearing loss: first report of c. 299-300delAT mutation in Kurdish population of Iran F Azadegan-Dehkordi, T Bahrami, M Shirzad, G Karbasi, ... Journal of Audiology & Otology 23 (1), 20, 2019 | 31 | 2019 |
| GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants M Koohiyan, M Hashemzadeh-Chaleshtori, M Salehi, H Abtahi, S Reiisi, ... International Journal of Pediatric Otorhinolaryngology 107, 121-126, 2018 | 31 | 2018 |
| Post neurosurgical meningitis due to colistin heteroresistant Acinetobacter baumannii M Moosavian, S Shoja, R Nashibi, N Ebrahimi, MA Tabatabaiefar, ... Jundishapur journal of microbiology 7 (10), 2014 | 30 | 2014 |
| Comparison of Real-Time PCR with Disk Diffusion, Agar Screen and E-test Methods for Detection of Methicillin-Resistant Staphylococcus aureus L Shariati, M Validi, MA Tabatabaiefar, A Karimi, MR Nafisi Current microbiology 61, 520-524, 2010 | 30 | 2010 |
| Genetic study of the BRAF gene reveals new variants and high frequency of the V600E mutation among Iranian ameloblastoma patients M Soltani, MA Tabatabaiefar, Z Mohsenifar, MR Pourreza, A Moridnia, ... Journal of Oral Pathology & Medicine 47 (1), 86-90, 2018 | 29 | 2018 |
| Estrogen receptor alpha gene polymorphisms are associated with type 2 diabetes and fasting glucose in male subjects R Meshkani, H Saberi, N MohammadTaghvaei, MA Tabatabaiefar Molecular and cellular biochemistry 359, 225-233, 2012 | 29 | 2012 |
| A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect E Davoudi-Dehaghani, S Zeinali, N Mahdieh, A Shirkavand, H Bagherian, ... International Journal of Pediatric Otorhinolaryngology 77 (5), 821-826, 2013 | 28 | 2013 |
| Possible association of the CD4 gene polymorphism with vitiligo in an Iranian population M Zamani, MA Tabatabaiefar, S Mosayyebi, A Mashaghi, P Mansouri Clinical and experimental dermatology 35 (5), 521-524, 2010 | 28 | 2010 |
