| Molecular biomarkers in diabetes mellitus (DM) SM Aghaei Zarch, M Dehghan Tezerjani, M Talebi, MY Vahidi Mehrjardi Medical Journal of The Islamic Republic of Iran (MJIRI) 34 (1), 196-203, 2020 | 30* | 2020 |
| Application of nanoparticles in cancer therapy with an emphasis on cell cycle HG Almanghadim, Z Nourollahzadeh, NS Khademi, M Dehghan Tezerjani, ... Cell biology international, 2021 | 24 | 2021 |
| Deficient Expression of DGCR8 in Human Testis is Related to Spermatogenesis Dysfunction, Especially in Meiosis I A Babakhanzadeh, Emad, Khodadadian, M Nazari, M Dehghan Tezerjani, ... International Journal of General Medicine 13, 185-192, 2020 | 20 | 2020 |
| Association of GSTP1, GSTT1 and GSTM1 Gene Variants with Coronary Artery Disease in Iranian Population: A Case–Control Study A Pourkeramati, E Zare Mehrjardi, M Dehghan Tezerjani, SM Seifati International Journal of General Medicine 13, 249-259, 2020 | 20 | 2020 |
| Circulating MiR-15a and MiR-222 as potential biomarkers of type 2 diabetes S Sadeghzadeh, M Dehghani Ashkezari, SM Seifati, MY Vahidi Mehrjardi, ... Diabetes, Metabolic Syndrome and Obesity, 3461-3469, 2020 | 19 | 2020 |
| Tumor Necrosis Factor Alpha -308 G/A Single Nucleotide Polymorphism and Risk of Sperm Abnormalities in Iranian Males M Khademi Bami, M Dehghan Tezerjani, F Montazeri, ... International Journal of Fertility and Sterility 11 (2), 112-116, 2017 | 18 | 2017 |
| Frequency of TNFR1 36 A/G gene polymorphism in azoospermic infertile men: A case-control study HR Ashrafzadeh, T Nazari, MD Tezerjani, MK Bami, ... International Journal of Reproductive BioMedicine 15 (8), 521, 2017 | 13 | 2017 |
| A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II) M Dehghan Tezerjani, MY Vahidi Mehrjardi, H Hozhabri, M Rahmanian Frontiers in Pediatrics 8, 340, 2020 | 9 | 2020 |
| A novel mutation in the OFD1 gene in a family with oral-facial-digital syndrome type 1: A case report MD Tezerjani, R Maroofian, MYV Mehrjardi, BA Chioza, S Zamaninejad, ... Iranian Journal of Public Health 45 (10), 1359, 2016 | 9 | 2016 |
| A novel missense mutation in the ALDH13 gene causes anophthalmia in two unrelated iranian consanguineous families M Dehghani, MD Tezerjani, Z Metanat, MYV Mehrjardi International Journal of Molecular and Cellular Medicine 6 (2), 131, 2017 | 7 | 2017 |
| Association of HLA-DRB1 Alleles with Juvenile-onset Systemic Lupus Erythematosus (SLE) in Iranian Children S Farivar, M Dehghan Tezerjani, R Shiari International Journal of Pediatrics 3, 555-560, 2015 | 4 | 2015 |
| Association of 1661A/G cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism with a clinical subset of Iranian children with systemic lupus erythematosus S Farivar, MD Tezerjani, N Parvini, R Shiari Thrita 3 (1), 2014 | 4 | 2014 |
| Genetic susceptibility to transient and permanent neonatal diabetes mellitus M Dehghan Tezerjani, MY Vahidi Mehrjardi, SM Kalantar, M Dehghani International Journal of Pediatrics 3 (6), 1073-1081, 2015 | 3 | 2015 |
| Association study of ESR1 rs9340799, rs2234693, and MMP2 rs243865 variants in Iranian women with premature ovarian insufficiency: A case-control study FS Eshaghi, M Dehghan Tezerjani, N Ghasemi, M Dehghani International Journal of Reproductive BioMedicine (IJRM), 841–850-841–850, 2022 | 2 | 2022 |
| Unraveling the dark matter, long non-coding RNAs, in male reproductive diseases: A narrative review M Dehghan Tezerjani, SM Kalantar International Journal of Reproductive Biomedicine 18 (11), 921-934, 2020 | 2 | 2020 |
| Transforming growth factor Beta leucine10 proline variation and breast cancer risk in Iranian women MD Tezerjani, B Mahdi, SM Kalantar, A Rasti, SM Kalantar, SM Shiryazdi Iranian journal of public health 44 (3), 427, 2015 | 2 | 2015 |
| Genetic variants of IL-10, TGFβ, FGF1, ESR1, MMP1 and WNT4 genes and their association with endometriosis in Iranian women EZ Mehrjardi, M Dehghan Tezerjani, BD Mahmoodabadi, F Mirjalili, ... Human Gene, 201169, 2023 | 1 | 2023 |
| Evaluation of miR-146a (rs2910164) polymorphism in coronary artery disease: Case-control and silico analysis E Zare Mehrjardi, M Dehghan Tezerjani, F Shemshad Ghad, SM Seifati Gene Reports, 101687, 2022 | 1 | 2022 |
| GLUTATHIONE S-TRANSFERASE M1 - T1 NULL GENOTYPES AND SUSCEPTIBILITY TO HODGKIN’S LYMPHOMA A Moosavi, M Forat Yazdi, M Dehghan Tezerjani, et al. GENETIKA 49 (3), 911-920, 2017 | 1 | 2017 |
| Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22-A Case Report MYV Mehrjardi, MD Tezerjani, NS Mahmoud, SM Kalantar, M Dehghani Iranian Journal of Public Health 45 (3), 376, 2016 | 1 | 2016 |
Mohammad Yahya Vahidi MehrjardiAssistant Professor in Molecular Genetics, Shahid Sadoughi University of Medical SciencesVerified email at ssu.ac.ir
