| Molecular basis of α-thalassemia S Farashi, CL Harteveld Blood Cells, Molecules, and Diseases 70, 43-53, 2018 | 235 | 2018 |
| Post-GWAS in prostate cancer: from genetic association to biological contribution S Farashi, T Kryza, J Clements, J Batra Nature Reviews Cancer 19 (1), 46-59, 2019 | 97 | 2019 |
| The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients M Banan, H Bayat, A Azarkeivan, S Mohammadparast, K Kamali, ... Hemoglobin 36 (4), 371-380, 2012 | 48 | 2012 |
| Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma M Zarif Yeganeh, S Sheikholeslami, G Dehbashi Behbahani, S Farashi, ... Tumor Biology 36, 5225-5231, 2015 | 34 | 2015 |
| Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia S Farashi, N Bayat, N Faramarzi Garous, M Ashki, M Montajabi Niat, ... Hemoglobin 39 (3), 201-206, 2015 | 33 | 2015 |
| Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder R Bonelli, VE Jackson, A Prasad, JE Munro, S Farashi, TFC Heeren, ... Communications biology 4 (1), 274, 2021 | 28 | 2021 |
| Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans A Heidari, ZNS Fam, E Esmaeilzadeh-Gharehdaghi, M Banan, ... Gene 492 (1), 195-198, 2012 | 24 | 2012 |
| Diagnostic pitfalls of less well recognized HbH disease S Farashi, H Najmabadi Blood Cells, Molecules, and Diseases 55 (4), 387-395, 2015 | 18 | 2015 |
| Novel mutations responsible for α-thalassemia in Iranian families N Bayat, S Farashi, N Hafezi-Nejad, N Faramarzi, M Ashki, S Vakili, ... Hemoglobin 37 (2), 148-159, 2013 | 18 | 2013 |
| Support for down-tuning of the calreticulin gene in the process of human evolution E Esmaeilzadeh-Gharehdaghi, M Banan, S Farashi, A Mirabzadeh, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 35 (7), 1770-1773, 2011 | 17 | 2011 |
| Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes S Farashi, S Vakili, N Faramarzi Garous, M Ashki, H Imanian, ... Expert Review of Hematology 8 (5), 693-698, 2015 | 11 | 2015 |
| Point mutations which should not be overlooked in Hb H disease S Farashi, N Bayat, S Vakili, N Faramarzi Garous, M Ashki, H Imanian, ... Expert review of hematology 9 (1), 107-113, 2016 | 10 | 2016 |
| c AMP response element‐binding protein 1 is required for hydroxyurea‐mediated induction of γ‐globin expression in K 562 cells M Banan, E Esmaeilzadeh‐Gharehdaghi, M Nezami, Z Deilami, S Farashi, ... Clinical and Experimental Pharmacology and Physiology 39 (6), 510-517, 2012 | 10 | 2012 |
| Homozygosity for the AATAAA > AATA– – Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian … S Farashi, NF Garous, M Ashki, S Vakili, F Zeinali, H Imanian, ... Hemoglobin 39 (5), 355-358, 2015 | 8 | 2015 |
| Frequency of α-globin gene triplications and coinheritance with β-globin gene mutations in the Iranian population SS Abedini, F Forouzesh Pour, K Karimi, Z Ghaderi, S Farashi, ... Hemoglobin 42 (4), 252-256, 2018 | 7 | 2018 |
| Point mutations in ret proto-oncogene exon 10 in Patients with medullary thyroid carcinoma M Zarif-Yeganeh, S Sheikholeslami, G Dehbashi-Behbahani, S Farashi, ... Journal of Kerman University of Medical Sciences 22 (3), 249-260, 2015 | 7 | 2015 |
| Pathway analysis of genes identified through post-GWAS to underpin prostate cancer aetiology S Farashi, T Kryza, J Batra Genes 11 (5), 526, 2020 | 6 | 2020 |
| Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient S Farashi, N Faramarzi Garous, M Ashki, S Vakili, F Zeinali, H Imanian, ... Hemoglobin 39 (3), 152-155, 2015 | 6 | 2015 |
| First report of a dominantly inherited β-thalassemia caused by a novel elongated β-globin chain S Farashi, F Rad, B Shahmohammadi, H Imanian, A Azarkeivan, ... Hemoglobin 40 (2), 102-107, 2016 | 4 | 2016 |
| Severe COVID-19 May Impact Hepatic Fibrosis/Hepatic Stellate Cells Activation as Indicated by a Pathway and Population Genetic Study L Moya, S Farashi, P Suravajhala, P Janaththani, J Batra Genes 14 (1), 22, 2022 | 3 | 2022 |
