| Analysis of virulence genes and accessory gene regulator (agr) types among methicillin-resistant Staphylococcus aureus strains in Iran S Cheraghi, L Pourgholi, M Shafaati, SH Fesharaki, A Jalali, R Nosrati, ... Journal of global antimicrobial resistance 10, 315-320, 2017 | 25 | 2017 |
| Improvement in the Production of L-Lysine by Over-expression of Aspartokinase (ASK) in C. glutamicum ATCC 21799 H Rastegari, M Chiani, A Akbarzadeh, S Cheraghi, Z Saffari, MR Mehrabi, ... Tropical Journal of Pharmaceutical Research 12 (1), 51-56, 2013 | 22 | 2013 |
| The Kalirin Gene rs9289231 Polymorphism as a Novel Predisposing Marker for Coronary Artery Disease M Boroumand, S Ziaee, N Zarghami, MS Anvari, S Cheraghi, SH Abbasi, ... Laboratory medicine 45 (4), 302-308, 2014 | 14 | 2014 |
| Association between the atrial natriuretic peptide rs5065 gene polymorphism and the presence and severity of coronary artery disease in an Iranian population S Ziaee, S Kalayinia, MA Boroumand, L Pourgholi, S Cheraghi, MS Anvari, ... Coronary artery disease 25 (3), 242-246, 2014 | 11 | 2014 |
| A systematic review of molecular alterations in invasive non-functioning pituitary adenoma NHMHZESCNHMME Khamseh Endocrine, 2022 | 5 | 2022 |
| A novel PTC mutation in the BTB domain of KLHL7 gene in two patients with Bohring-Opitz syndrome-like features S Cheraghi, S Moghbelinejad, H Najmabadi, K Kahrizi, R Najafipour European Journal of Medical Genetics 63 (4), 103849, 2020 | 4 | 2020 |
| Association between R353Q polymorphism for coagulative factor VII and severity of coronary artery disease in Iranian population S Cheraghi, S Shajiee, MA Boroumand, L Pourgholi, S Ziaee, MS Anvari, ... Cardiology Journal 20 (5), 533-538, 2013 | 4 | 2013 |
| The association of umbilical coiling and angiogenesis markers: Impact assessment of gestational diabetes L Najafi, M Honardoost, A Khajavi, S Cheraghi, M Kadivar, ME Khamseh Placenta 129, 70-76, 2022 | 3 | 2022 |
| Predictive inflammation-related microRNAs for cardiovascular events following early-onset coronary artery disease S Ziaee, M Hosseindokht, S Cheraghi, L Pourgholi, A Ahmadi, ... Archives of Medical Research 52 (1), 69-75, 2021 | 3 | 2021 |
| C1019T polymorphism in the connexin 37 gene and myocardial infarction risk in premature coronary artery disease M Sheikhvatan, M Boroumand, M Behmanesh, SH Abbasi, G Davoodi, ... The Journal of Tehran University Heart Center 12 (2), 72, 2017 | 3 | 2017 |
| Evaluation of a warfarin dosing algorithm including CYP2C9, VKORC1, and CYP4F2 polymorphisms and non-genetic determinants for the Iranian population M Farajzadeh-Dehkordi, F Samiee-Rad, SS Farzam, A Javadi, ... Pharmacological Reports 75 (3), 695-704, 2023 | 2 | 2023 |
| The PTRHD1 mutation in intellectual disability S Cheraghi, S Moghbelinejad, H Najmabadi, K Kahrizi, R Najafipour Archives of Iranian medicine 24 (10), 747-751, 2021 | 2 | 2021 |
| Bonepally, Chandrasekhar R.; Gandey, Sai Jyothsna; Bommineni, Krishnaveni; Gottumukkala, Krishna Mohan; Aukunuru, Jithan S Honary, H Barabadi, E Gharaei-Fathabad, F Naghibi, M Shivashankar, ... Sort 12, 01, 2013 | 2 | 2013 |
| Improved production of L-lysine by over-expression of Meso-diaminopimelate decarboxylase enzyme of Corynebacterium glutamicum in Escherichia coli. S Cheraghi, A Akbarzade, A Farhangi, M Chiani, Z Saffari, S Ghassemi, ... Pakistan Journal of Biological Sciences: PJBS 13 (10), 504-508, 2010 | 2 | 2010 |
| A Novel ARMC5 Germline Variant in Primary Macronodular Adrenal Hyperplasia Using Whole-Exome Sequencing M Eghbali, S Cheraghi, S Samanian, I Rad, J Meghdadi, H Akbari, ... Diagnostics 12 (12), 3028, 2022 | 1 | 2022 |
| Pathological Variants of Aminoacyl-tRNA-synthetase-Interacting Multifunctional Protein 1 Gene in an Iranian Consanguineous Family With Autosomal Recessive Intellectual Disability S Cheraghi, S Moghbelinejad, R Najafipour The Journal of Qazvin University of Medical Sciences 23 (6), 494-503, 2020 | | 2020 |
| Cloning of LysA gene in expression vector in order to increase the production rate of L-lysine S Cheraghi Modares Journal of Biotechnology 2 (1), 0-0, 2011 | | 2011 |
| Research Paper Pathological Variants of Aminoacyl-tRNA-synthetase-Interacting Multifunc-tional Protein 1 Gene in an Iranian Consanguineous Family With Autosomal Recessive … S Cheraghi, S Moghbelinejad, R Najafipour | | |
