۱. Ranjbar M, Salehi R, Haghjooy Javanmard S, Rafiee L, Faraji H, jafarpor S, et al. The dysbiosis signature of Fusobacterium nucleatum in colorectal cancer-cause or consequences? A systematic review. Cancer Cell Int. 2021;21(1).
۲. Pourahmadiyan A, Alipour P, Golchin N, Tabatabaiefar MA. Next-generation sequencing reveals a novel pathogenic variant in the ATM gene. Int J Neurosci. 2021.
۳. Norouzi M, Shafiei M, Abdollahi Z, Miar P, Galehdari H, Emami MH, et al. WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family. Front Oncol. 2021;11.
۴. Norouzi M, Miar P, Norouzi S, Nikpour P. Nervous System Involvement in COVID-19: a Review of the Current Knowledge. Mol Neurobiol. 2021;58(7):3561-74.
۵. Manian M, Sohrabi E, Eskandari N, Assarehzadegan MA, Ferns GA, Nourbakhsh M, et al. An integrated bioinformatics analysis of the potential regulatory effects of mir-21 on t-cell related target genes in multiple sclerosis. Avicenna J Med Biotechnol. 2021;13(3):149-65.
۶. Koohiyan M, Hashemzadeh-Chaleshtori M, Tabatabaiefar MA. Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran. Intractable Rare Dis Res. 2021;10(1):23-30.
۷. Keshvari M, Nedaeinia R, Nedaeinia M, Ferns GA, Nia SN, Asgary S. Assessment of heavy metal contamination in herbal medicinal products consumed in the Iranian market. Environ Sci Pollut Res. 2021;28(25):33208-18.
۸. Jafarpour S, Khosravi S, Janghorbani M, Mansourian M, Karimi R, Ghiasi MR, et al. Association of serum and follicular fluid leptin and in vitro Fertilization/ ICSI outcome: A systematic review and meta-analysis. J Gynecol Obstet Hum Reprod. 2021;50(6).
۹. Fatemi A, Alipour R, Khanahmad H, Alsahebfosul F, Andalib A, Pourazar A. The impact of neutrophil extracellular trap from patients with systemic lupus erythematosus on the viability, CD11b expression and oxidative burst of healthy neutrophils. BMC Immunol. 2021;22(1).
۱۰. Esmaeilzadeh E, Saghi M, Hassani M, Davar S, Alani B, Pakzad B, et al. Strong association of common variants in the miRNA-binding site of NOD2 gene with clinicopathological characteristics and disease activity of systemic lupus erythematosus. Clin Rheumatol. 2021.
۱۱. Emami Nejad A, Najafgholian S, Rostami A, Sistani A, Shojaeifar S, Esparvarinha M, et al. The role of hypoxia in the tumor microenvironment and development of cancer stem cell: a novel approach to developing treatment. Cancer Cell Int. 2021;21(1).
۱۲. Ehtesham N, Zare Rafie M, Esmaeilzadeh E, Dehani M, Davar S, Mosallaei M, et al. Three functional variants in the NLRP3 gene are associated with susceptibility and clinical characteristics of systemic lupus erythematosus. Lupus. 2021;30(8):1273-82.
۱۳. Ehtesham N, Alani B, Mortazavi D, Azhdari S, Kenarangi T, Esmaeilzadeh E, et al. Association of rs3135500 and rs3135499 Polymorphisms in the MicroRNA-binding Site of Nucleotide-binding Oligomerization Domain 2 (NOD2) Gene with Susceptibility to Rheumatoid Arthritis. Iran J Allergy Asthma Immunol. 2021;20(2):178-87.
۱۴. Sobhani M, Tabatabaiefar MA, Ghafouri-Fard S, Rajab A, Hojjat A, Kajbafzadeh AM, et al. Erratum: Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: A case report (BMC Medical Genetics (2020) 21 (13) DOI: 10.1186/s12881-020-0950-4). BMC Med Genet. 2020;21(1).
۱۵. Sobhani M, Tabatabaiefar MA, Ghafouri-Fard S, Rajab A, Hojat A, Kajbafzadeh AM, et al. Clinical and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: A case report. BMC Med Genet. 2020;21(1).
۱۶. Sayyari M, Salehzadeh A, Tabatabaiefar MA, Abbasi A. Genetic polymorphisms of Y-chromosome short tandem repeats (Y-STRs) in a male population from Golestan province, Iran. Mol Biol Res Commun. 2020;9(1):11-6.
۱۷. Sarmadi A, Nasrniya S, Soleimani Farsani M, Narrei S, Nouri Z, Sepehrnejad M, et al. A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. BMC Med Genet. 2020;21(1).
۱۸. Sarmadi A, Nasrniya S, Narrei S, Nouri Z, Abtahi H, Tabatabaiefar MA. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss. Mol Biol Rep. 2020;47(7):5355-64.
۱۹. Sarhadi V, Lahti L, Saberi F, Youssef O, Kokkola A, Karla T, et al. Gut microbiota and host gene mutations in colorectal cancer patients and controls of Iranian and finnish origin. Anticancer Res. 2020;40(3):1325-34.
۲۰. Rahimmanesh I, Totonchi M, Khanahmad H. The challenging nature of primary T lymphocytes for transfection: Effect of protamine sulfate on the transfection efficiency of chemical transfection reagents. Res Pharm Sci. 2020;15(5):437-46.
۲۱. Pourreza MR, Sobhani M, Rahimi A, Aramideh M, Kajbafzadeh AM, Noori-Daloii MR, et al. Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family. Acta Diabetol. 2020;57(1):81-7.
۲۲. Pakzad B, Shirpour R, Mousavi M, Karimzadeh H, Salehi A, Kazemi M, et al. C1QTNF4 gene p.His198Gln mutation is correlated with early-onset systemic lupus erythematosus in Iranian patients. Int J Rheum Dis. 2020;23(11):1594-8.
۲۳. Nourmohammadi E, Hosseinkhani S, Nedaeinia R, Khoshdel-Sarkarizi H, Nedaeinia M, Ranjbar M, et al. Construction of a sensitive and specific lead biosensor using a genetically engineered bacterial system with a luciferase gene reporter controlled by pbr and cadA promoters. Biomed Eng Online. 2020;19(1).
۲۴. Mohammadi A, Shadmehri AA, Taghavi M, Yaghoobi G, Pourreza MR, Tabatabaiefar MA. A pathogenic variant in the transforming growth factor beta I (TGFBI) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review. Iran J Basic Med Sci. 2020;23(8):1020-7.
۲۵. Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Noori-Daloii MR, Tabatabaiefar MA. A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23. Audiol Neurotol. 2020;25(5):258-62.
۲۶. Kheirollahi M, Saneipour M, Tabatabaiefar MA, Zeinalian M, Minakari M, Moridnia A. New variants in the cdh1 gene in iranian families with hereditary diffuse gastric cancer. Middle East J Cancer. 2020;11(4):493-501.
۲۷. Jazayeri MH, Barzaman K, Nedaeinia R, Aghaie T, Motallebnezhad M. Human placental extract attenuates neurological symptoms in the experimental autoimmune encephalomyelitis model of multiple sclerosis-A putative approach in MS disease? Autoimmun Highlights. 2020;11(1).
۲۸. Jazayeri MH, Aghaie T, Nedaeinia R, Manian M, Nickho H. Rapid noninvasive detection of bladder cancer using survivin antibody-conjugated gold nanoparticles (GNPs) based on localized surface plasmon resonance (LSPR). Cancer Immunol Immunother. 2020;69(9):1833-40.
۲۹. Javanmard SH, Vaseghi G, Ghasemi A, Rafiee L, Ferns GA, Esfahani HN, et al. Therapeutic inhibition of microRNA-21 (miR-21) using locked-nucleic acid (LNA)-anti-miR and its effects on the biological behaviors of melanoma cancer cells in preclinical studies. Cancer Cell Int. 2020;20(1).
۳۰. Ghiasi MR, Mohammadi H, Symonds ME, Tabei SMB, Salehi AR, Jafarpour S, et al. Efficacy of insulin targeted gene therapy for type 1 diabetes mellitus: A systematic review and meta-analysis of rodent studies. Iran J Basic Med Sci. 2020;23(4):406-15.
۳۱. Gheissari A, Meamar R, Kheirollahi M, Abedini A. The effect of parental consanguinity on clinical course and outcome of children with focal segmental glomerulosclerosis, a report from Isfahan, Iran. Iran J Kidney Dis. 2020;14(5):348-57.
۳۲. Fazel F, Oliya B, Mirmohammadkhani M, Fazel M, Yadegarfar G, Pourazizi M. Intravitreal injections of bevacizumab plus methotrexate versus bevacizumab alone for the treatment of diabetic macular edema: A randomized, sham-controlled trial. J Curr Ophthalmol. 2020;32(2):164-9.
۳۳. Fazel F, Nikpour H, Pourazizi M. Combination of Intravitreal Bevacizumab and Topical Dorzolamide versus Intravitreal Bevacizumab Alone for Diabetic Macular Edema: A Randomized Contralateral Clinical Trial. BioMed Res Int. 2020;2020.
۳۴. Alizadehmohajer N, Shojaeifar S, Nedaeinia R, Esparvarinha M, Mohammadi F, Ferns GA, et al. Association between the microbiota and women's cancers – Cause or consequences? Biomed Pharmacother. 2020;127.
۳۵. Akhlaghi M, Zarei M, Ziaei M, Pourazizi M. Sensitivity, Specificity, and Accuracy of Color Doppler Ultrasonography for Diagnosis of Retinal Detachment. J Ophthalmic Vis Res. 2020;15(2):166-71.
۳۶. Akbarian F, Tabatabaiefar MA, Shaygannejad V, Shahpouri MM, Badihian N, Sajjadi R, et al. Upregulation of MTOR, RPS6KB1, and EIF4EBP1 in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls. Metab Brain Dis. 2020;35(8):1309-16.
۳۷. Zarepour N, Koohiyan M, Taghipour-Sheshdeh A, Nemati-Zargaran F, Saki N, Mohammadi-Asl J, et al. Identification and clinical implications of a novel MyO15A variant in a consanguineous Iranian family by targeted exome sequencing. Audiol Neurotol. 2019;24(1):25-31.
۳۸. Taghipour-Sheshdeh A, Nemati-Zargaran F, Zarepour N, Tahmasebi P, Saki N, Tabatabaiefar MA, et al. A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family. Genomics. 2019;111(4):840-8.
۳۹. Tabatabaiefar MA, Sajjadi RS, Narrei S. Epigenetics and Common Non Communicable Disease. Advances in Experimental Medicine and Biology: Springer New York LLC; 2019. p. 7-20.
۴۰. Sobhani M, Tahmasebi P, Nasiri F, Rahnama M, Karimi-Nejad R, Tabatabaiefar MA. The first report of a patient with trisomy 4p and monosomy 10q. Arch Iran Med. 2019;22(7):414-7.
۴۱. Sobhani M, Amin Tabatabaiefar M, Ghafouri-Fard S, Rajab A, Mozafarpour S, Nasrniya S, et al. Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome. Endocrine. 2019;66(2):185-91.
۴۲. Shariati L, Modarressi MH, Tabatabaiefar MA, Kouhpayeh S, Hejazi Z, Shahbazi M, et al. Engineered zinc-finger nuclease to generate site-directed modification in the KLF1 gene for fetal hemoglobin induction. J Cell Biochem. 2019;120(5):8438-46.
۴۳. Shadmehri AA, Fattahi N, Pourreza MR, Koohiyan M, Zarifi S, Darbouy M, et al. Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation. J Cell Biochem. 2019;120(3):3367-72.
۴۴. Sayyari M, Salehzadeh A, Tabatabaiefar MA, Abbasi A. Profiling of 17 y-str loci in mazandaran and gilan provinces of ira. Turk J Med Sci. 2019;49(5):1277-86.
۴۵. Sadeghian L, Tabatabaiefar MA, Fattahi N, Pourreza MR, Tahmasebi P, Alavi Z, et al. Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred. Int J Pediatr Otorhinolaryngol. 2019;124:99-105.
۴۶. Pourahmadiyan A, Alipour P, Fattahi N, Kasiri M, Rezaeian F, Taghipour-Sheshdeh A, et al. A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family. Int J Audiol. 2019;58(10):628-34.
۴۷. Mottaghi T, Khorvash F, Kheirollahi M, Maracy M, Askari G. The MTHFR C677T polymorphism influences the efficacy of folic acid supplementation on the nerve conduction studies in patients with diabetic polyneuropathy; A randomized, double blind, placebo-controlled study. J Res Med Sci. 2019;24(1).
۴۸. Moridnia A, Tabatabaiefar MA, Zeinalian M, Minakari M, Kheirollahi M, Moghaddam NA. Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. J Gastrointest Cancer. 2019;50(3):420-7.
۴۹. Mohammadi Z, Karamzadeh A, Tabatabaiefar MA, Khanahmad H, Shariati L. Evidence for expression of promoterless GFP cassette: Is GFP an ideal reporter gene in biotechnology science? Res Pharm Sci. 2019;14(4):351-8.
۵۰. Koohiyan M, Reiisi S, Azadegan-Dehkordi F, Salehi M, Abtahi H, Hashemzadeh-Chaleshtori M, et al. Screening of 10 DFNB loci causing autosomal recessive non-syndromic hearing loss in two Iranian populations negative for GJB2 mutations. Iran J Public Health. 2019;48(9):1704-13.
۵۱. Koohiyan M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Tabatabaiefar MA. A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family. Audiol Neurotol. 2019;24(5):258-63.
۵۲. Khorrami M, Mahdavi M, Fakhr F, Kheirollahi M. A novel pathogenic variant in NAGLU (N-Acetyl-alpha-glucosaminidase) gene identified by targeted next-generation sequencing followed by in silico analysis. Iran J Child Neurol. 2019;13(4):173-83.
۵۳. Karimzadeh P, Kheirollahi M, Houshmand SM, Dadgar S, Aryani O, Yaghini O. Clinical feature and genetics in rett syndrome: A report on Iranian patients. Iran J Child Neurol. 2019;13(4):37-51.
۵۴. Tabatabaiefar MA, Pourreza MR, Tahmasebi P, Saki N, Hashemzadeh Chaleshtori M, Salehi R, et al. A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss. Otolaryngol Head Neck Surg. 2018;158(6):1084-92.
۵۵. Soltani M, Tabatabaiefar MA, Mohsenifar Z, Pourreza MR, Moridnia A, Shariati L, et al. Genetic study of the BRAF gene reveals new variants and high frequency of the V600E mutation among Iranian ameloblastoma patients. J Oral Pathol Med. 2018;47(1):86-90.
۵۶. Salehi S, Emadi-Baygi M, Rezaei M, Kelishadi R, Nikpour P. Lack of evidence of the role of apoa5 3'utr polymorphisms in iranian children and adolescents with metabolic syndrome. Diabetes Metab J. 2018;42(1):74-81.
۵۷. Modares Sadeghi M, Shariati L, Hejazi Z, Shahbazi M, Tabatabaiefar MA, Khanahmad H. Inducing indel mutation in the SOX6 gene by zinc finger nuclease for gamma reactivation: An approach towards gene therapy of beta thalassemia. J Cell Biochem. 2018;119(3):2512-9.
۵۸. Mahdavi M, Koulivand L, Khorrami M, Mirsafaie M, Kheirollahi M. In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria. Mol Biol Rep. 2018;45(5):1165-73.
۵۹. Mahdavi M, Kheirollahi M, Riahi R, Khorvash F, Khorrami M, Mirsafaie M. Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD). J Mol Neurosci. 2018;65(1).
۶۰. Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Reiisi S, Pourreza MR, et al. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. Int J Pediatr Otorhinolaryngol. 2018;107:121-6.
۶۱. Khorvash F, Kheirollahi M, Kazemi M, Amini G, Khorrami M, Mirsafaie M, et al. Variants in human prostacyclin receptor gene in patients with migraine headache. Iran J Psychiatry. 2018;13(4):239-43.
۶۲. Kazemi M, Khosravian F, Sameti AA, Moafi A, Merasi MR, Salehi M, et al. Association between (GT)n repeats in heme oxygenase-1 gene promoter and 3-year survival of patients with acute leukemia: A controlled, cross-sectional study. Int J Hematol Oncol Stem Cell Res. 2018;12(1):49-56.
۶۳. Jalilian N, Tabatabaiefar MA, Yazdanpanah M, Darabi E, Bahrami T, Zekri A, et al. A comprehensive genetic and clinical evaluation of Waardenburg syndrome type II in a set of Iranian patients. Int J Mol Cell Med. 2018;7(1).
۶۴. Hashemipour M, Khorrami M, Mahdavi M, Khujin MH, Kheirollahi M. Allgrove syndrome in Iranian patients and report on a novel mutation in AAAS gene. Iran J Pediatr. 2018;28(1).
۶۵. Gheissari A, Meamar R, Kheirollahi M, Rouigari M, Dehbashi M, Dehghani L, et al. TRPC6 mutational analysis in iranian children with focal segmental glomerulosclerosis. Iran J Kidney Dis. 2018;12(6):341-9.
۶۶. Ghadiri N, Emamnia N, Ganjalikhani-Hakemi M, Ghaedi K, Etemadifar M, Salehi M, et al. Analysis of the expression of mir-34a, mir-199a, mir-30c and mir-19a in peripheral blood CD4+T lymphocytes of relapsing-remitting multiple sclerosis patients. Gene. 2018;659:109-17.
۶۷. Cheraghipour K, Shariati L, Khanahmad H, Ganjalikhani-Hakemi M, Moridnia A, Mirian M, et al. Induction of apoptosis in Toxoplasma gondii infected hela cells by cisplatin and sodium azide and isolation of apoptotic bodies and potential use for vaccination against Toxoplasma gondii. Iran J Parasitol. 2018;13(3):406-15.
۶۸. Asgharzade S, Tabatabaiefar MA, Mohammadi-asl J, Chaleshtori MH. A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing. Int J Pediatr Otorhinolaryngol. 2018;108:8-11.
۶۹. Tabatabaiefar MA, Alipour P, Pourahmadiyan A, Fattahi N, Shariati L, Golchin N, et al. A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. J Neurol Sci. 2017;379:212-6.
۷۰. Mohammadi-asl J, Pourreza MR, Mohammadi A, Eskandari A, Mozafar-Jalali S, Tabatabaiefar MA. A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred. J Dermatol Sci. 2017;88(1):134-8.
۷۱. Markazi S, Kheirollahi M, Doosti A, Mohammadi M. Report of SLC3A1/rBAT gene mutations in Iranian cystinuria patients: A direct sequencing study. J Res Med Sci. 2017;22(1).
۷۲. Mahdavi M, Moreau V, Kheirollahi M. Identification of B and T cell epitope based peptide vaccine from IGF-1 receptor in breast cancer. J Mol Graph Model. 2017;75:316-21.
۷۳. Kouhpayeh S, Hejazi Z, Khanahmad H, Rezaei A. Real-time PCR: An appropriate approach to confirm ssDNA generation from PCR product in SELEX process. Iran J Biotechnol. 2017;15(2):143-8.
۷۴. Kheirollahi M, Pourreza MR, Khorvash F, Kazemi M, Amini G. A report of a novel mutation in human prostacyclin receptor gene in patients affected with migraine. Iran J Psychiatry. 2017;12(3):219-22.
۷۵. Kazemi M, Salehi M, Kheirollahi M. MeDIP real-time qPCR has the potential for noninvasive prenatal screening of fetal trisomy 21. Int J Mol Cell Med. 2017;6(1):13-21.
۷۶. Jalilian N, Tabatabaiefar MA, Bahrami T, Karbasi G, Bahramian MH, Salimpoor A, et al. A Novel Pathogenic Variant in the MITF Gene Segregating with a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred. Mol Syndr. 2017;8(4):195-200.
۷۷. Jalilian N, Tabatabaiefar MA, Alimadadi H, Noori-Daloii MR. SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis. Int J Pediatr Otorhinolaryngol. 2017;96:122-6.
۷۸. Heidarpour M, Derakhshan M, Derakhshan-Horeh M, Kheirollahi M, Dashti S. Prevalence of high-risk human papillomavirus infection in women with ovarian endometriosis. J Obstet Gynaecol Res. 2017;43(1):135-9.
۷۹. Fazaeli S, Ashouri S, Kheirolahi M, Mohammadi M, Fazilati M. A novel mutation in SLC7A9 gene in Cystinuria. Iran J Kidney Dis. 2017;11(2):138-41.
۸۰. Ehtesham N, Khorvash F, Kheirollahi M. miR-145 and miR20a-5p Potentially Mediate Pleiotropic Effects of Interferon-Beta Through Mitogen-Activated Protein Kinase Signaling Pathway in Multiple Sclerosis Patients. J Mol Neurosci. 2017;61(1):16-24.
۸۱. Darzi L, Boshtam M, Shariati L, Kouhpayeh S, Gheibi A, Mirian M, et al. The silencing effect of MIR-30a on ITGA4 gene expression in vitro: An approach for gene therapy. Res Pharm Sci. 2017;12(6):456-64.
۸۲. Shariati L, Modaress M, Khanahmad H, Hejazi Z, Tabatabaiefar MA, Salehi M, et al. Comparison of different methods for erythroid differentiation in the K562 cell line. Biotechnol Lett. 2016;38(8):1243-50.
۸۳. Shariati L, Khanahmad H, Salehi M, Hejazi Z, Rahimmanesh I, Tabatabaiefar MA, et al. Genetic disruption of the KLF1 gene to overexpress the γ-globin gene using the CRISPR/Cas9 system. J Gene Med. 2016;18(10):294-301.
۸۴. Sedghi M, Esfandiari E, Najafabadi EF, Salehi M, Salavaty A, Fattahpour S, et al. Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families. J Res Med Sci. 2016;21(7).
۸۵. Rezaei M, Emadi-Baygi M, Hoffmann MJ, Schulz WA, Nikpour P. Altered expression of LINC-ROR in cancer cell lines and tissues. Tumor Biol. 2016;37(2):1763-9.
۸۶. Pourzadegan F, Shariati L, Taghizadeh R, Khanahmad H, Mohammadi Z, Tabatabaiefar MA. Using intron splicing trick for preferential gene expression in transduced cells: An approach for suicide gene therapy. Cancer Gene Ther. 2016;23(1):7-12.
۸۷. Mosallayi M, Salehi R. Fetal nucleic acids in maternal circulation for noninvasive prenatal diagnosis. J Isfahan Med Sch. 2016;33(363):1-6.
۸۸. Mosallayi M, Mirzaei H, Simonian M, Kheirollahi M. Next-generation sequencing and its applications. J Isfahan Med Sch. 2016;33(368):2469-80.
۸۹. Markazi S, Kheirollahi M, Doosti A, Mohammadi M, Koulivand L. A novel mutation in SLC3A1 gene in patients with cystinuria. Iran J Kidney Dis. 2016;10(1):44-7.
۹۰. Khosravi S, Salehi M, Ramezanzadeh M, Mirzaei H, Salehi R. Novel Multiplex Fluorescent PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of β-Thalassemia. Arch Med Res. 2016;47(4):293-8.
۹۱. Kheirollahi M, Khosravi F, Ashouri S, Ahmadi A. Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of fallot. J Res Med Sci. 2016;21(2).
۹۲. Kheirollahi M, Kazemi E, Ashouri S. Brain-Derived Neurotrophic Factor Gene Val66Met Polymorphism and Risk of Schizophrenia: A Meta-analysis of Case–Control Studies. Cell Mol Neurobiol. 2016;36(1):1-10.
۹۳. Kazemi M, Salehi M, Kheirollahi M. Down syndrome: Current status, challenges and future perspectives. Int J Mol Cell Med. 2016;5(3):125-33.
۹۴. Heydari N, Shariati L, Khanahmad H, Hejazi Z, Shahbazi M, Salehi M. Gamma reactivation using the spongy effect of KLF1-binding site sequence: An approach in gene therapy for beta-thalassemia. Iran J Basic Med Sci. 2016;19(10):1063-9.
۹۵. Ehtesham N, Sharifi M, Khorvash F, Kheirollahi M. The effect of beta interferon on the expression of miR-145 in patients with multiple sclerosis. J Isfahan Med Sch. 2016;34(396):1013-8.
۹۶. Shariati L, Validi M, Hasheminia AM, Ghasemikhah R, Kianpour F, Karimi A, et al. Staphylococcus aureus isolates carrying panton-valentine leucocidin genes: Their frequency, antimicrobial patterns, and association with infectious disease in shahrekord city, southwest Iran. Jundishapur J Microbiol. 2015;9(1).
۹۷. Senniappan S, Sadeghizadeh A, Flanagan SE, Ellard S, Hashemipour M, Hosseinzadeh M, et al. Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia. BMC Res Notes. 2015;8(1).
۹۸. Mosallayi M, Salehi R. Fetal cells in maternal blood: Technical and clinical aspects. J Isfahan Med Sch. 2015;32(313):2165-73.
۹۹. Miranzadeh-Mahabadi H, Miranzadeh-Mahabadi H, Nikpour P, Emadi-Baygi M, Kelishadi R. Comparison of TaqMan real-time and tetra-primer ARMS PCR techniques for genotyping of Rs 8066560 variant in children and adolescents with metabolic syndrome. Adv Clin Exp Med. 2015;24(6):951-5.
۱۰۰. Koulivand L, Mohammadi M, Ezatpour B, Salehi R, Markazi S, Dashti S, et al. Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria. Urolithiasis. 2015;43(5):447-53.
۱۰۱. Jalilian N, Tabatabaiefar MA, Farhadi M, Bahrami T, Noori-Daloii MR. A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family. Int J Pediatr Otorhinolaryngol. 2015;79(10):1736-40.
۱۰۲. Jalilian N, Tabatabaiefar MA, Farhadi M, Bahrami T, Emamdjomeh H, Noori-Daloii MR. Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations. Gene. 2015;574(2):302-7.
۱۰۳. Jafary F, Nadeali Z, Salehi M, Hosseinzadeh M, Sedghi M, Gholamrezapour T, et al. Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population. Mol Biol. 2015;49(6):848-51.
۱۰۴. Heidari-Hafshejani N, Naderi S, Salehi R, Nikpour P, Modares-Sadeghi M, Hejazi Z, et al. Construction and characterization of recombinant HEK cell over-expressing TOSO/FAIM3 and evaluation of its expression. J Isfahan Med Sch. 2015;33(324):171-82.
۱۰۵. Fazel-Najafabadi E, Vahdat Ahar E, Fattahpour S, Sedghi M. Structural and functional impact of missense mutations in TPMT: An integrated computational approach. Comput Biol Chem. 2015;59:48-55.
۱۰۶. Dashti S, Khorvash F, Salehi R, Mahzouni P, Koulivand L, Kheirollahi M. Comparison of TERRA expression in human brain tumors. Eur J Oncol. 2015;20(1):25-31.
۱۰۷. Dashti S, Kheirollahi M. Telomeric repeat-containing RNA (TERRA) and human diseases. J Isfahan Med Sch. 2015;33(330).
۱۰۸. Dashti S, Ashouri S, Kheirollahi M. Expression of TERRA in different grades of astrocytoma. J Isfahan Med Sch. 2015;32(317):2333-42.
۱۰۹. Tavakkoli MB, Kheirollahi M, Kiani A, Kazemi M, Mohebat L, Haghjooy-Javanmard S, et al. Evaluation of measuring Radiation-Induced apoptosis in human T-Lymphocytes by flow cytometry as a biological dosimetry system. J Isfahan Med Sch. 2014;32(284):610-20.
۱۱۰. Savabi O, Kazemi M, Salehi R. Effects of biosurfactants derived from Lactobacillus casei and Lactobacillus reuteri on gene expression profile of gtfB/C and ftf genes in Lactobacillus mutans. J Isfahan Med Sch. 2014;31(260).
۱۱۱. Rahmati S, Emadi-Baygi M, Nikpour P, Emadi-Andani E. Expression profile of ZFX isoform3/variant 5 in gastric cancer tissues and its association with tumor size. Iran J Basic Med Sci. 2014;17(10):767-71.
۱۱۲. Nouri N, Fazel-Najafabadi E, Behnam M, Nouri N, Aryani O, Ghasemi M, et al. Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries. Gene. 2014;535(2):250-4.
۱۱۳. Nikpour P, Miranzadeh-Mahabadi H, Emadi-Baygi M, Kelishadi R. Association of rs8066560 variant in the sterol regulatory element-binding protein 1 (SREBP-1) and miR-33b genes with hyperglycemia and insulin resistance. J Pediatr Endocrinol Metab. 2014;27(7-8):611-5.
۱۱۴. Nikpour P, Emadi-Baygi M, Emadi-Andani E, Rahmati S. EYA1 expression in gastric carcinoma and its association with clinicopathological characteristics: A pilot study. Med Oncol. 2014;31(5).
۱۱۵. Nikpour M, Emadi-Baygi M, Fischer U, Niegisch G, Schulz WA, Nikpour P. MTDH/AEG-1 contributes to central features of the neoplastic phenotype in bladder cancer. Urol Oncol Semin Orig Invest. 2014;32(5):670-7.
۱۱۶. Karamzade A, Mirzapour H, Hoseinzade M, Asadi S, Gholamrezapour T, Tavakoli P, et al. Globin gene mutations in isfahan province, Iran. Hemoglobin. 2014;38(3):161-4.
۱۱۷. Fatemi SG, Emadi-Baygi M, Nikpour P, Kelishadi R, Hashemipour M. Absence of association between -1131T>C polymorphism in the apolipoprotein APOA5 gene and pediatric metabolic syndrome. Iran J Pediatr. 2014;24(3):319-22.
۱۱۸. Ehtesham N, Modi M, Kheirollahi M. miRNA, biogenesis and mechanisms of regulations. J Isfahan Med Sch. 2014;32(296):1259-68.
۱۱۹. Yazdanian M, Memarnejadian A, Shahreza HK, Soleimanjahi H, Motevali F, Roohvand F. Construction and evaluation of DNA vaccine encoding fusion protein of hepatitis C virus core protein and hepatitis B surface antigen as a vaccine candidate. J Isfahan Med Sch. 2013;31(226).
۱۲۰. Nouri N, Aryani O, Nouri N, Kamalidehghan B, Houshmand M. Cutis laxa type II with mutation in the pyrroline-5-carboxylate reductase 1 Gene. Pediatr Dermatol. 2013;30(6):e265-e7.
۱۲۱. Nikpour P, Mowla SJ, Forouzandeh-Moghaddam M, Ziaee SA. The stem cell self-renewal gene, Musashi 1, is highly expressed in tumor and non-tumor samples of human bladder. Indian J Cancer. 2013;50(3):214-8.
۱۲۲. Nikpour P, Emadi-Baygi M, Mohhamad-Hashem F, Maracy MR, Haghjooy-Javanmard S. MSI1 overexpression in diffuse type of gastric cancer. Pathol Res Pract. 2013;209(1):10-3.
۱۲۳. Mostofizade N, Nikpour P, Javanmard SH, Emadi-Baygi M, Miranzadeh-Mahabadi H, Hovsepian S, et al. The G395R mutation of the sodium/iodide symporter (NIS) gene in patients with dyshormonogenetic congenital hypothyroidism. Intl J Prev Med. 2013;4(1):57-62.
۱۲۴. Kheirollahi M, Kolahdouz M, Ahangari F, Koulivand L, Khorvash F. The role of telomere in cell; telomere dysfunction and tumorigenesis. J Isfahan Med Sch. 2013;30(222):2554-83.
۱۲۵. Karamzade A, Mirzapour H, Kheirollahi M. Genetics aspects of male infertility. J Isfahan Med Sch. 2013;31(246):1149-62.
۱۲۶. Emadi-Baygi M, Nikpour P, Mohammad-Hashem F, Maracy MR, Haghjooy-Javanmard S. MSI2 expression is decreased in grade II of gastric carcinoma. Pathol Res Pract. 2013;209(11):689-91.
۱۲۷. Nouri N, Karimi P, Nouri N, Izaditabar A, Salehi M, Noori-Daloii MR. Chromosomal abnormalities in regions 8q22 and 13q32 associated with different disorders in an Iranian family. J Sci Islam Repub Iran. 2012;23(3):213-7.
۱۲۸. Kheirollahi M, Koulivand L. Telomere structure and its role in DNA damage and genetic disorders. J Isfahan Med Sch. 2012;30(210).
۱۲۹. Baygi ME, Nikpour P. Deregulation of MTDH gene expression in gastric cancer. Asian Pac J Cancer Preven. 2012;13(6):2833-6.