| Polymorphisms of Antioxidant’ Genes as a Target for Diabetes Management MA Tabatabaei-Malazy O, Khodaeian M, Bitarafan F, Larijani B Int J Mol Cell Med. 6 (3), 2017 | 36 | 2017 |
| Isolated congenital anosmia and CNGA2 mutation MR Sailani, I Jingga, SH MirMazlomi, F Bitarafan, JA Bernstein, ... Scientific Reports 7 (1), 1-5, 2017 | 22 | 2017 |
| SLC34A3 intronic deletion in an Iranian kindred with hereditary hypophosphatemic rickets with hypercalciuria S Hasani-Ranjbar, HS Ejtahed, MM Amoli, F Bitarafan, M Qorbani, ... Journal of clinical research in pediatric endocrinology 10 (4), 343, 2018 | 17 | 2018 |
| A genotype-first approach for clinical and genetic evaluation of Wolcott-Rallison syndrome in a large cohort of Iranian children with neonatal diabetes F Abbasi, M Habibi, S Enayati, F Bitarafan, M Razzaghy-Azar, A Sotodeh, ... Canadian Journal of Diabetes 42 (3), 272-275, 2018 | 16 | 2018 |
| Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing F Bitarafan, SY Seyedena, M Mahmoudi, M Garshasbi J Clin Lab Anal., e23544, 2020 | 14 | 2020 |
| Influence of antioxidants' gene variants on risk of diabetes mellitus and its complications: a systematic review. F Bitarafan, M Khodaeian, O Tabatabaei-Malazy, MM Amoli Minerva endocrinologica 44 (3), 310-325, 2017 | 11 | 2017 |
| Prevalence and genotype distribution of human papillomavirus infection among 12 076 Iranian women F Bitarafan, MR Hekmat, M Khodaeian, E Razmara, T Ashrafganjoei, ... International Journal of Infectious Diseases 111, 295-302, 2021 | 10 | 2021 |
| Two novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive non-syndromic hearing loss S Zardadi, E Razmara, G Asgaritarghi, E Jafarinia, F Bitarafan, S Rayat, ... Molecular Genetics and Genomics Medicine, 2020 | 10 | 2020 |
| The first case of NSHL by direct impression on EYA1 gene and identification of one novel mutation in MYO7A in the Iranian families E Razmara, F Bitarafan, E Esmaeilzadeh-Gharehdaghi, N Almadani, ... Iranian journal of basic medical sciences 21 (3), 333, 2018 | 10 | 2018 |
| Identification of a novel MICU1 nonsense variant causes myopathy with extrapyramidal signs in an Iranian consanguineous family F Bitarafan, K Mehrnoosh, E Amjadi Sardehaei, DF Zahra, N Almadani, ... Molecular and Cellular Pediatrics, 2021 | 9 | 2021 |
| Molecular genetic analysis of polycystic kidney disease 1 and polycystic kidney disease 2 mutations in pedigrees with autosomal dominant polycystic kidney disease F Bitarafan, M Garshasbi Journal of Research in Medical Sciences 24 (1), 44, 2019 | 8 | 2019 |
| A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family A Sepahvand, E Razmara, F Bitarafan, M Galehdari, AR Tavasoli, ... Molecular Genetics & Genomic Medicine, e1413, 2020 | 6 | 2020 |
| Kabuki Syndrome: Identification of Two Novel Variants in KMT2D and KDM6A M Khodaeian, E Jafarinia, F Bitarafan, S Shafeii, N Almadani, ... Molecular Syndromology, 2021 | 5 | 2021 |
| Molecular investigation of WFS1 gene exon 8 in Iranian patients with Wolfram syndrome R Abbasi, F Bitarafan, M Khodaeian, A Ebrahim-Habibi, F Abbasi, ... International Journal of Diabetes in Developing Countries 36, 75-80, 2016 | 5 | 2016 |
| Molecular Genetic Analysis of PKHD1 Mutations in Pedigrees With Autosomal Recessive Polycystic Kidney Disease. F Bitarafan, G Masoud Iran J Kidney Dis. 12 (6), 350-358, 2018 | 4 | 2018 |
| Compound Heterozygous Mutations in PNKP Gene in an Iranian Child with Microcephaly, Seizures, and Developmental Delay F Bitarafan, M Khodaeian, N Almadani, A Kalhor, EA Sardehaei, ... Fetal and Pediatric Pathology 40 (2), 174-180, 2021 | 3 | 2021 |
| Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome F Bitarafan, E Razmara, M Khodaeian, M Keramatipour, A Kalhor, ... Molecular Genetics & Genomic Medicine 8 (8), e1274, 2020 | 3 | 2020 |
| Fertility assessment and mating type analysis reveal the absence of sexual stage in Magnaporthe oryzae populations in Iran V Zarrinnia, MJ Nikkhah, HRZ Zadeh, F Bitarafan, E Sedaghatfar Sci Series Data Rep 4, 123-32, 2012 | 3 | 2012 |
| Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia E Jamali, R Khalesi, F Bitarafan, N Almadani, M Garshasbi Iranian Biomedical Journal, 2020 | 2 | 2020 |
| Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report F Bitarafan, M Khodaeian, F Garrousi, R Khalesi, D Ghazi Nader, B Karimi, ... BMC Endocrine Disorders 23 (1), 155, 2023 | 1 | 2023 |
Masoud GarshasbiAssociate Professor of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares UniversityVerified email at modares.ac.ir
