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مقالات انگلیسی منتشر شده توسط مرکز تحقیقات بیماریهای ارثی

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.