| Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss O Diaz-Horta, D Duman, J Foster, A Sırmacı, M Gonzalez, N Mahdieh, ... PloS one 7 (11), e50628, 2012 | 170 | 2012 |
| Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran MJ Bonyadi, N Fotouhi, M Esmaeili International journal of pediatric otorhinolaryngology 78 (4), 637-640, 2014 | 27 | 2014 |
| Prevalence of IVS1+ 1G> A mutation among Iranian Azeri Turkish patients with autosomal recessive non-syndromic hearing loss (ARNSHL) M Bonyadi, N Fotouhi, M Esmaeili International Journal of Pediatric Otorhinolaryngology 75 (12), 1612-1615, 2011 | 21 | 2011 |
| Evaluation of CC‐cytokine ligand 2 and complementary factor H Y402H polymorphisms and their interactional association with age‐related macular degeneration M Bonyadi, Z Foruzandeh, T Mohammadian, N Fotouhi, M Soheilian, ... Acta ophthalmologica 94 (8), e779-e785, 2016 | 19 | 2016 |
| ACA pumps maintain leaf excitability during herbivore onslaught N Fotouhi, M Fischer-Stettler, G Lenzoni, S Stolz, G Glauser, SC Zeeman, ... Current Biology 32, 2517–2528, 2022 | 16 | 2022 |
| Association of polymorphisms in complement component 3 with age-related macular degeneration in an Iranian population M Bonyadi, T Mohammadian, MH Jabbarpoor Bonyadi, N Fotouhi, ... Ophthalmic genetics 38 (1), 61-66, 2017 | 16 | 2017 |
| R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome a preliminary study N Fotouhi, M Ardalan, MJ Bonyadi, R Abdolmohammadi, A Kamalifar, ... Iranian journal of kidney diseases 7 (5), 399-403, 2013 | 14 | 2013 |
| Association between proto-oncogene mutations and clinicopathologic characteristics and overall survival in colorectal cancer in East Azerbaijan, Iran R Dolatkhah, MH Somi, I Asvadi Kermani, M Bonyadi, B Sepehri, ... OncoTargets and therapy, 7385-7395, 2016 | 9 | 2016 |
| Joint association of complement component 3 and CC-cytokine ligand2 (CCL2) or complement component 3 and CFH polymorphisms in age-related macular … M Bonyadi, MH Jabbarpoor Bonyadi, M Yaseri, T Mohammadian, ... Ophthalmic Genetics 38 (4), 365-370, 2017 | 7 | 2017 |
| Tumour necrosis factor-alpha gene polymorphisms in Iranian patients with biliary atresia N Fotouhi, M Bonyadi, Z Jahanafrooz, N Ahmadian, ... African Journal of Paediatric Surgery 11 (3), 233-237, 2014 | 4 | 2014 |
| Common KRAS and BRAF mutations in colorectal cancer patients R Dolatkhah, S Dastgiri, MH Somi, MJ Bonyadi, S Gherami, N Fotouhi, ... Govaresh 20 (1), 27-33, 2015 | 3 | 2015 |
| Early detection of dark-affected plant mechanical responses using enhanced electrical signals H Li, N Fotouhi, F Liu, H Ji, Q Wu Plant Methods 20 (1), 49, 2024 | | 2024 |
| Disruption of putative Ca2+ transporters and jasmonate pathway regulation in Arabidopsis EF Nikou Fotouhi Regulatory Oxylipins- VIB conference series, 2019 | | 2019 |
| CORRELATION BETWEEN ANTI-PHOSPHOLIPASE A2 RECEPTOR AND ANTI-SOLUBLE PHOSPHOLIPASE A2 ANTIBODIES IN IDIOPATHIC MEMBRANOUS NEPHROPATHY N Fotouhi, A Ghaffari, F Hamzavi, H Nasri, M Ardalan 50th European-Renal-Association-European-Dialysis-and-Transplant-Association …, 2013 | | 2013 |
| POSTER PRESENTATIONS: P-20: GENETIC ANALYSIS OF HEARING LOSS AMONG AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS PATIENTS FROM IRANIAN AZERI TURK ETHNIC GROUP M BONYADI, N FOTOUHI, M ESMAEILI CELL JOURNAL (YAKHTEH) 13 (2), 33-33, 2011 | | 2011 |
Mortaza Bonyadi, Mortaza Jabbarpour...University of TabrizVerified email at tabrizu.ac.ir
