| COL18A1 is a candidate eye iridocorneal angle-closure gene in humans F Suri, S Yazdani, M Chapi, I Safari, P Rasooli, N Daftarian, ... Human molecular genetics 27 (21), 3772-3786, 2018 | 41 | 2018 |
| Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy M Chapi, H Sabbaghi, F Suri, E Alehabib, S Rahimi-Aliabadi, F Jamali, ... Ophthalmic Genetics 40 (3), 259-266, 2019 | 19 | 2019 |
| Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes H Darvish, LJ Azcona, A Tafakhori, R Mesias, A Ahmadifard, E Sanchez, ... Scientific reports 10 (1), 968, 2020 | 15 | 2020 |
| Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder F Mattioli, H Darvish, SA Paracha, A Tafakhori, SG Firouzabadi, M Chapi, ... NPJ Genomic Medicine 6 (1), 94, 2021 | 13 | 2021 |
| A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome J Jamshidi, S Abdollahi, H Ghaedi, E Alehabib, A Tafakhori, S Alinaghi, ... European Journal of Medical Genetics 60 (11), 578-582, 2017 | 12 | 2017 |
| A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome Z Bahmanpour, Y Daneshmandpour, S Kazeminasab, S Khalil Khalili, ... International Ophthalmology 41, 389-397, 2021 | 7 | 2021 |
| Homozygous mutation in TWNK cases ataxia, sensorineural hearing loss and optic nerve atrophy F Jamali, H Ghaedi, A Tafakhori, E Alehabib, M Chapi, N Daftarian, ... Archives of Iranian Medicine 22 (12), 728-730, 2019 | 7 | 2019 |
| A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis Y Daneshmandpour, Z Bahmanpour, S Kazeminasab, ... Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24 (1-2), 148-151, 2023 | 3 | 2023 |
| The rs1986112 Variant is Associated with Increased RAB8B Gene Expression in Schizophrenic Patients. AH Johari, FR Nejad, N Mansoori, F Vafaei, S Salehi, E Alehabib, ... Clinical Laboratory 65 (4), 2019 | 1 | 2019 |
| Hossein Darvish1, 2, Luis J. Azcona3, 4, Abbas Tafakhori5, Roxana Mesias3, 6, Azadeh Ahmadifard7, Elena Sanchez3, Arman Habibi5, Elham Alehabib7, Amir Hossein Johari7 B Emamalizadeh, F Jamali, M Chapi, J Jamshidi, Y Kajiwara11, ... | | |
Hossein Darvishmedical geneticsAdresse e-mail validée de sbmu.ac.ir
