1 Curriculum vitae Name: Morteza Hashemzadeh Chaleshtori Address: Cellular & Molecular Research Center, Shahrekord University of Medical Sciences, Rahmatieh, Shahrekord, Iran Tel: 0098 38- 33346692, 33331471 Fax: Fax: 0098 38- 33330709, 33334911 & 33334588 E-Mail: [email protected]& [email protected]Homepage: http://mail.skums.ac.ir Birth Place: Shahrekord - Iran Birth Date: 23/07/1960 Marital Status: Married http://www.scopus.com/authid/detail.url?authorId=55663265400 B.Sc Plant Pathology, Tehran University, 1985, Iran. M.Sc medical Entomology & vectors control , Tehran University of Medical Sciences,1989, Iran 1 PERSONAL EDUCATION
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Curriculum vitae
Name: Morteza Hashemzadeh Chaleshtori
Address: Cellular & Molecular Research Center, Shahrekord University of
•1989-1994 Instructor, Department of Medical Parasitology, Shahrekord University of Medical Sciences, Shahrekord, Iran.
•1989-1994 Vice Chancellor for student affairs, Shahrekord University of Medical Sciences, Shahrekord, Iran.
•1997-2000 Assistant Professor, Department of Biochemistry and Genetics, Shahrekord University of Medical Sciences, Shahrekord, Iran.
•1997-2001 Chancellor of Shahrekord University of Medical Sciences, Shahrekord, Iran.
•2000)June)-2003(Sept) Assistant professor, Department of Human Genetics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
•2003(Sept)-2004(Aug) Assistant professor, Department of Biochemistry & Genetics, Medical School, Shahrekord University of Medical Sciences, Shahrekord, Iran.
•2004(Aug)-2008(Dec) Associate Professor, Dept of Biochemistry & Genetics, Medical School, Shahrekord University of Medical Sciences, Shahrekord, Iran.
•2005(Sept present Head of Cellular & Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran.
•2008)Dec) present Professor, Dept of Biochemistry & Genetics, Medical School, Shahrekord University of Medical Sciences, Shahrekord, Iran.
*2010(nov) present Head of Department of Biochemistry and Genetics
•2013 Chancellor of Shahrekord University of Medical Sciences, Shahrekord, Iran
• Human Genetics
• Medical Genetics
• Molecular Genetics
• Genetic Engineering
• Advanced Molecular biology
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POSITIONS HELD
TEACHING
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• Cell and Molecular Biology
•1997 present, Supervisor and Advisor of up to 100 MSc and PhD students.
•1999 present, Chairman of Shahrekord University of Medical Sciences Journal.
•2005 Superior Researcher of shahrekord University of Medical Sciences, Shahrekord, Iran.
•2005 present, Member of the Shahrekord University of Medical Sciences research council.
•2007 Superior Lecturer of shahrekord University of Medical Sciences, Shahrekord, Iran.
•2007 present, Referee of Iranian Scientific Razi Festival.
•2007 present, Member of Iranian global scientific mapping: Committee of molecular medicine fore sighting.
•2009 ( February) present, member of scientific board of medical biotechnology and Molecullar medicine
•2010 Superior Researcher of shahrekord University of Medical Sciences, Shahrekord, Iran.
•2011 Superior Researcher of shahrekord University of Medical Sciences, Shahrekord, Iran
2015 Superior Researcher of shahrekord University of Medical Sciences, Shahrekord, Iran
•2016 Superior Researcher of shahrekord University of Medical Sciences, Shahrekord, Iran
Farsi (Mother Language), English (Well (
Microsoft Word, Internet, Windows.
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RESEARCH PROJECTS
HONORS, DISTINCTIONS AND SCIENTIFIC SOCIETY MEMBERSHIPS
LANGUAGE SKILLS
COMPUTER KNOWLEDGE AND SKILLS
LANGUAGE SKILLS
LANGUAGE SKILLS
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- Study of Connexin 26 gene (GJB2) mutations associated with deafness in different population of Iranian deaf pupils.
- Genetic analysis of hearing loss in different populations of Iranian deaf pupils.
- Study of genomic diversity on four VNTR loci ( D1S80, D17S5, D19S20 and APOB) in different Iranian ethnic groups.
-RT-PCR analysis of Prostate Specific Antigen (PSA) and ProstateSpecific Membrane ( PSM) in peripheral blood of prostate cancerpatients referred to hospitals of Tehran University of Medical Sciences.
- Study of LDL receptor gene mutations in patients with familial hypercholesterolemia
in Chaharmahal va Bakhtiari province.
- Study of -629C/A and 1405V polymorphism in cholesteryl ester transfer proteingene and -514C/T polymorphism of hepatic lipase gene in patients with coronary artery stenosis.
- Study of SCN1A mutation in severe myoclonic epilepsy of infancy (SMEI) and generalized epilepsy With febrile seizure plus (GEFS+) by PCR-SSCP in Cheharmahal va Bakhtiari province.
- Pathogenic role of 6 novel deafness-related Connexcin 26 gene( GJB2) mutations.
- Genetic linkage analysis of the frequent loci: DFNB3, DFNB9 and DFNB59 in theIranian patients with autosomal recessive non-syndromic hearing loss (ARNSHL)
- Genetic linkage analysis of the frequent loci:DFNB4, DFNB7/11 and DFNB21
- Genetic of hearing loss in Chaharmahal va Bakhtiari province.
- Study of DFNB59 gene (pejvakin) mutations associated with deafness in different population of Iranian deaf pupils.
- Study of mutations of 3 mitochondrial genes (MTRNR1, MTTL1 and MTTS1) in Iranian deaf individuals.
- study of LDLreceptor gene mutatios promoter and exexons 1 ,3, 5. 11, 13, 15, 16, 17 and 18 in patients with familial hypercholesterolemia in chaharmahal va bakhtiari province.
- study of mitochondrial gene mutation and Founder of common GJB2 gene mutation Iranian deaf with 35 delG.
- investigating of Double Heterozygosity in 7 member of the connexin gene family in patients with autosomal recessive hearing loss cases with one GJB2 mutant allele in iran.
- Screening of SLC26A4 gene mutations in Iranian probands with autosomal recessive non syndromic hearing loss using.
- Detection of Helicobacter pylori in samples from drinking water sources in Chaharmahal va Bakhtiary province using PCR.
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-The production of high titer of polycistronic lentiviral vector containing Nanog, Oct3/4, Sox2 and c-myc for induction of IPSs.
- Association of 3 polymorphisms of IL-18 gene (137G/C,-607C/A,-133C/G) in patient with allergic rhinitis in shahrekord.
- The production of induced pluripotent stem cells (IPSc) from foreskin fibroblasts using lentiviral vector.
-Analysis of CaBP2 mutations in affected families with autosomal recessive non-syndromic hearing loss (ARNSHL) using linkage analysis and sequencing.
- Analysis of TMC1 mutations in affected families with autosomal recessive non-syndromic hearing loss (ARNSHL) using linkage analysis and sequencing.
-The production of high titer of polycistronic lentiviral vector containing Nanog, Oct3/4, Sox2 and c - myc for induction of IPSs.
-The study of VSX1 mutations in patients with keratoconous in Cheharmahal va provinces using PCR-SSCP and Sequencing.
- Immunologic study of Toll like receptors types TLR2 and Micro RNAs regulatory roles in multiple sclerosis.
-Immunologic study of Toll like receptors types TLR4 and Micro RNAs regulatory roles in multiple sclerosis.
-Analysis of expression different Isoforms of HIFs genes compare with Tsga10 expression in cell lines Hela ، MCF7 & MDA-MB-231.
-study of (ccttt)n polymorphism of nos2 gene promoter invernal keratoconjunctivitis patient in chaharmahal va bakhtiari provinc.
-Study of RHO gene mutations associated with retinitis pigmentosa in population of Chaharmahal va Bakhtiari provivce.
- Study Of Exons 4,10,12 Mutations In TMPRSS3 Gene In Patients With Autosomal Recessive non-Syndromic Hearing Loss From Chaharmahal Va Bakhtiari and kohgilouyeh Va Boirahmad Provinces.
-Mutations screening in exon 7 and 13 of TMC1 gene on DFNB7/11 locous in Iranian probands affected wit autosomal recessive non-syndromic hearing loss using PCR-SSCP/HA
-Serum and stromal cell free Differentiation of ESCs to HSCs by HOXB4 overexpression.
-detection of RHO gene mutations associated with retinitis pigmentosa in population of Chaharmahal va Bakhtiari provivce.
- Study of gene expression deviations of TLR4 and two related Micro RNAs (hsa-mir-103 and hsa-mir-217)in multiple sclerosis patients in MS clinic of Esfahan kashani hospital.
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- Screening of LRTOMT gene mutations exon 1, 3, 5 and 8 (DFNB63) in Iranian patients affected with genetic hearing loss using PCR-SSCP/HA.
- Study of Possible Founder Effect for The Frequent 35delG GJB2 Gene Mutation in Iranian Patients With Hearing Impairment.
-Microsattellite Instability (MSI) testing and Immunohistochemistry of mismatch repair proteins (MMRs) in the patients suspected to Lynch Syndrome in Isfahan and Chahar mahal va Bakhtiari Provinces.
-Mutation analysis of MSH2 and MSH6 genes (DNA-MMRs) in the families suspected to Lynch Syndrome with MSI-H state or abnormal immunohistochemistry of MMR proteins within Isfahan and Chahar mahal va Bakhtiari Provinces.
•Mutation analysis of MLH1 and PMS2 genes in the families suspected to Lynch Syndrome with MSI-H state or abnormal immunohistochemistry of MMR proteins within Isfahan and Chahar mahal va Bakhtiari Provinces.
*Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province
*Genetic linkage analysis of DFNB98 and DFNB48 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Khouzestan province
*Genetic linkage analysis of DFNB1,DFNB13 and DFNB22 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Khuzestan province
*Genetic manipulation of stem cells to investigate differentiation potency into auditory hair cells
*Genetic linkage study and analysis of two loci DFNB53 and DFNB39 involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in khuzestan province
*Genetic linkage analysis of DFNB12 & DFNB42 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Khuzestan province
*Human stem cells differentiation into auditory hair cell-like cells via in vitro co-culturing by means of cell therapy
*Investigation of stem cells reprogramming process into auditory hair cells by genetic manipulation of feeder cells in order to expression of necessary factors
*Association Study of rs833061and rs2010963 Variants of VEGF Gene and Susceptibility to Colorectal Cancer in Iranian patients
*Association of 2 polymorphisms (1102C/T, 1058C/T) of Myocilin gene in patients with Primary open angle Glaucoma in Chaharmahal va Bakhtiari provin
*Differentiation of umbilical cord stem cells into Germ cells
*Linkage analysis of 4 genes (RPGR , RP1, PRPF31, CRB1) in patients in Families with retinitis pigmentosa
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*Linkage analysis of 4 genes (RP2 ,USH2A,RHO, RDS in Families with retinitis pigmentosa
*Investigating of Double heterozygosity in 7 members of Connexin gene family members in patients with autosomal recessive nonsyndromic hearing loss with one GJB2 mutant allele in Iran
*Linkage analysis of 4 genes (RP2 ,USH2A,RHO, RDS in Families with retinitis pigmentosa
*Analysis of TMC1 mutations in affected families with autosomal recessive non-syndromic hearing loss (ARNSHL) using linkage analysis and sequencing
*BRAF gene analysis and associated Microsatellite Instability in colorectal cancer patients with Amsterdam II criteria resident in Isfahan and Chahar Mahal va Bakhtiari Provinces
*Genetic linkage analysis of DFNB59 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Hamedan and yasuj provinces
*The assessment of effect of mesenchymal stem cells (MSCs) and their conditional media in recovery of ischemic liver failure
*Differentiation of ESCs to HSCs by HOXB4 overexpression and Tgfβ R2 signaling inhibition
*Analysis of expression different Isoforms of HIFs genes and it's comparison withTsga10 expression in cell lines ( Hela & MCF7 & MDA-MB-231) in cancer
*Association Study of rs833061and rs2010963 Variants of VEGF Gene and Susceptibility to Colorectal Cancer in Iranian patients
*Analysis of CIB2 gene sequencing exons in the family suspected link to the DFNB48 loci
*Evaluation of the expression of auditory neuron differentiation markers including beta-III tubulin , GATA3, Peripherin upon transient overexpression of miR-124a in neural crest-derived stem cells in hair follicle
*study of three families with Maturity Onset Diabetes of Young (MODY) to identify the genetic etiology profile of using NGS in Isfahan population
*The assessment of changes in expression levels of miR-451 and miR-21 in the plasma of recurrent and nonrecurrent breast cancer patients comparing to healthy controls
*Genomic study (exome sequencing) of the parent and deafness children of Ahv-14 family samples in order to identify the genetic etiologic profile
*Genomic study of the Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) samples in order to identify the geneic etiologic profile in Khuzestan province of Iran
*Genomic study of the autosomal recessive nonsyndromic hearing loss samples in order to identify the genetic etiologic profile in Kohgiluyeh & Boyer Ahmad province
*Genetic linkage analysis of the loci DFNB1 ,DFNB2 ,DFNB3 ,DFNB4 ,DFNB12, DFNB104 in the group of autosomal recessive non-syndromic hearing loss families in Kurdistan
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*Evaluation of the expression of auditory neuron differentiation markers including beta-III tubulin , GATA3, Peripherin upon elevation of miR-124a level in human embryonic stem cells
*Survey of human Mesenchymal Stem Cells differentiation (obtained by MEEM method from Umbilical Cord) into Male Germ cell using sheep testis natural scaffold
*Study of PALB2 gene mutations (exons 3, 4, 7 and 10) in patients with breast cancer using PCR-SSCP/HA technique and DNA sequencing
*Genetic manipulation of stem cells to investigate differentiation potency into auditory hair cells
*Differentiataion of human dental stem cells twoard auditory sensory neurons
*Genetic linkage analyse of GCK and HNF1A genes in patients suspected with Maturity-Onset Diabetes of the Young (MODY) in Chaharmahal va Bakhtiari and Esfahan province
*Evaluation of simultaneous expression of NUDCD1 gene and lnc-HMGA1-2:4 in colorectal adenocarcinoma tissue specimens using Real time RT- PCR
*Evaluation of simultaneous expression of PLXNA1 gene and LncRNA BAIAP2-AS1 in colorectal adenocarcinoma tissue specimens using Real Time RT-PCR
*Survey of human Mesenchymal Stem Cells differentiation (obtained by MEEM method from Umbilical Cord) into Male Germ cell using sheep testis natural scaffold
*Evaluation of the expression of auditory neuron differentiation markers including beta-III tubulin , GATA3, Peripherin upon elevation of miR-124a level in human embryonic stem cells
*Investigation of stem cells reprogramming process into auditory hair cells by genetic manipulation of feeder cells in order to expression of necessary factors
*Achieving the practical capability of stem cells reprograming into auditory hair cells using growth factors
*Genetic linkage study and analysis of two loci DFNB53 and DFNB39 involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in khuzestan province
*Genetic linkage analysis of DFNB1,DFNB22 and DFNB24 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Khuzestan province
*Genetic linkage analysis of DFNB98 and DFNB48 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Khouzestan province
*Genetic linkage analysis of DFNB35 & DFNB42 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Khuzestan province
*Genetic linkage analysis of DFNB59 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Hamedan and yasuj provinces
*Genetic linkage analysis of DFNB63 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in Hamedan and yasouj provinces
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*The assessment of effect of mesenchymal stem cells (MSCs) and their conditional media in recovery of ischemic liver failure
*Mutations screening in 7 and 13 exons of TMC1 gene on DFNB7/11 locous in Iranian probands affected wit autosomal recessive non-syndromic hearing loss using PCR-SSCP/HA
*Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province
*detection of RHO gene mutations associated with retinitis pigmentosa in population of Chaharmahal va Bakhtiyari provivce
PAPERS:
1. Jenkins GJS, Hashemzadeh Chaleshtori M, Song H, Parry JM. Mutation analysis using the Restriction Site Mutation (RSM) assay.Journal Mutation Research 1998; 405: 209-20.
2. Hashemzadeh Chaleshtori M, Farhud DD, Taylor R, Hadavi V, Patton MA, Afzal AR. Deafness-associated connexin 26 gene (GJB2) mutations in Iranian population. Iranian J Public Health 2002; 31(3-4): 75-9.
3. Pourjafari H, Farhud DD, Yazdani A, Hashemzadeh Chaleshtori M. Dermatoglyphics in patients with eczema, psoriasis and alopecia areata. J Skin Res Technol 2003; 9: 240-4.
4. Pourjafari H, Farhud DD, Hashemzadeh Chaleshtori M. Fetal death and congenital malformations in progenies of Iranian chemical victims. J Res Health Sci 2003; 3: 18-21.
5. Oshaghi MA, Ghalandari R, Vatandoost H, Shayeghi M, Kamali-nejad M, Tourabi-khaledi H, Abolhassani M, Hashemzadeh M. Repellent effect of extracts and essential oils of Citrus limon (Rutaceae) and Melissa officinalis (labiatae) against main malaria vector, Anopheles stephensi (Diptera: culicidae). Iranian J Public Health 2003; 32(4): 47-52.
6. Hadavi V, Sanati MH, Farhud DD, Houshmand M, Hashemzadeh Chaleshtori M, Nabavi SM, Younesian M, Seyedian M. Association of Apolipoprotein E polymorphism with susceptibility to multiple sclerosis. Iranian J Biotechnol 2004; 2:49-54.
7. Hashemzadeh Chaleshtori M, Dowlati M, Farhud DD, Hoghooghi Rad L, Sasanfar R, Hoseinipour A, Montazer Zohour M, Tolooi A, Ghadami M, Poujafari H, Oshaghi MA, Patton MA (2004). Two novel mutations and predominant 35delG mutation in the connexin 26 gene (GJB2) in Iranian populations. Iranian J Public Health 33(2): 14-9.
8. Sasanfar R, Tolouei A, Hoseinipour A, Farhud DD, Dolati M, Hoghooghi Rad L, Montazer Zohour M, Ghadami M, Pourjafari H, Hashemzadeh Chaleshtori M. Frequency of a very rare 35delG mutation in two ethnic groups of Iranian populations. Iranian J Public Health 2004; 33(4): 26-30.
9. Oshaghi MA, Chavshin AR, Vatandoost H, Yaghoobi F, Mohtarami F, Hashemzadeh M, Noorjah N, Modaresi MH. Effect of post ingestion and physical conditions on PCR
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ENGLISH PUBLICATIONS
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amplification of host blood meal DNA in mosquitoes. Iranian J Public Health 2005; 34(3): 12-9.
10. Andonian L, Khorramizadeh MR, Farhud DD, Hashemzadeh Chaleshtori M, Holakouie Naieni K, Razi A, sanadizadeh J, Pourmand G, Nouraie M, Rezaie S, Saadat F, Yepiskoposyan L, Norouzi M, Soleimanpour H, Berahme A, Alizadeh N. Molecular detection of Prostate specific antigen in patients with prostate cancer or benign prostate hyperplasia the first investigation from Iran. Iranian J Public Health 2005; 34(3): 20-6.
11. Pour-Jafari H, Hashemzadeh Chaleshtori M, Farhud DD. Dermatoglyphics in patients with oligo/azospermia. Iranian J Public Health 2005; 34(3): 56-61.
12. Hashemzadeh Chaleshtori M, Hoghooghi Rad L, Dolati M, Sasanfar R, Hoseinipour A, montazer Zohour M, Pourjafari H, Tolooi A, Ghadami M, Farhud DD, Patton MA. Frequencies of mutations in the connexin 26 gene (GJB2) in two populations of Iran (Tehran and Tabriz). Iranian J Public Health 2005; 34(1): 1-7.
13. Hosseinipour A, Hashemzadeh Chaleshtori M, Sasanfar R, Farhud DD, Tolooi A, Doulati M, Hoghooghi Rad L, Montazer Zohour M, Ghadami M. Report of a new mutation and frequency of connexin 26 gene (GJB2) mutations in patients from three provinces of Iran. Iranian J Public Health 2005; 34(1): 47-50.
14. Sadeghi AR, Sanati MH, Alasti F, Hashemzadeh Chaleshtori M, Ataei M. Mutation Analysis of Connexin 26 gene and del (GJB6-D1351830) in patients with hereditary deafness from two provinces in Iran. Iranian J Biotechnol 3(4): 2005; 255-258.
15. Hashemzadeh Chaleshtori M, Montazer Zohour M, Hoghooghi Rad L, Poujafari H, Farhud DD, Dolati M, Safa Chaleshtori K, Sasanfar R, Hoseinipour A, Andonian L, Tolouei A, Ghadami M, Patton MA. Autosomal recessive and sporadic non syndromic hearing loss and the incidence of Cx26 mutations in a province of Iran. Iranian J Public Health 2006; 35(1): 88-91.
16. Hashemzadeh Chaleshtori M, Farhud DD, Patton MA. Familial and sporadic GJB2-related deafness in Iran: review of gene mutations. Iranian J Public Health 2007; 36(1): 1-14.
17. Hashemzadeh Chaleshtori M, Farrokhi E, Shahrani M, Kheiri S, Dolati M, Hoghooghi Rad L, Poujafari H, Ghatreh Samani K, Safa Chaleshtori K, Crosby AH. High carrier frequency of the GJB2 mutation (35delG) in the north of Iran. Int J Pediatric Otorhinolaryngol 2007; 71: 863-7.
18. Hashemzadeh Chaleshtori M, Simpson MA, Farrokhi E, Dolati M, Hoghooghi Rad L, Amani Geshnigani S, Crosby AH. Novel mutations in the Pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. Clin Genet 2007; 72(3): 261-3.
19. Banoei MM, Hashemzadeh Chaleshtori M, Sanati MH, Shafa Shariat Panahi M, Majidzadeh T, Rostami M, Dehghan Manshadi M, Golalipour M. Diversity and relationship between Iranian ethnic groups: Human Dopamine Transporter gene (DAT1) VNTR genotyping. Am J Hum Biol 2007; 19: 821-6.
20. Banoei MM, Hashemzadeh Chaleshtori M, Sanati MH, Shariati p, Houshmand M, Majidizadeh T, Jahangir Soltani N, Golalipour M. Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus region. Human Biology 2008; 80(1): 73-81.
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21. Hashemzadeh Chaleshtori M, Farhud DD, Crosby AH, Farrokhi E, Pour-Jafari H, Ghatreh Samani K, Safa Chaleshtori K, Kasiri M, Shahrani M, Bani talebi M, Mansouri M, Modarresinia D, Jafari M. Molecular pathology of 6 novel GJB2 allelic variants detected in familial and sporadic Iranian non syndromic hearing loss cases. Iranian J Public Health 2008; 37(3): 1-9.
22. Farhud D, Lotfi AS, Hashemzadeh Chaleshtori M, Akhondi M, Sadighi H (2009). Progress of education, research and services in medical genetics in some institutions of Iran. Iranian J Public Health 38(Suppl. 1): 115-118.
23. Ghatreh Samani K, Noori M, Rohbani Nobar M, Hashemzadeh Chaleshtori M, Farrokhi E, Darabi Amin M. 1405V and -629C/A polymorphisms of the cholesteryl ester transfer protein gene in patients with coronary artery disease. Iranian Biomed J 2009; 13(2): 103-8.
24. Tabatabaiefar MA, Alasti F, Peeters N, Wuyts W, Nooridaloii MR, Chaleshtori MH, Van Camp G. Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome. Hum Genet 2010; 127(4): 468-9.
25. Ghatreh Samani K, Darabi Amin M, Rohbani Nobar M, Hashemzadeh Chaleshtori M, Farrokhi E, Noori M, (2009). Combined hepatic lipase -514C/T and cholesteryl ester transfer protein 1405V polymorphisms are associated with the risk of coronary artery disease. Genet Test Mol Biomarkers 13(6): 1-7.
26. Sadeghi AR, sanati MH, Alasti F, Hashemzadeh Chaleshtori M, Mahmoudian S, Ataei M (2009). Contribution of GJB2 mutations and four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran. Iranian J Biotechnol 7(2): 108-14.
27. Hamid M, Karimipoor M, Chaleshtori MH, Akbari MT. A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. J Genet 2009; 88(3): 359-62.
28. Manouchehri Naeini K, Asadi M, Hashemzadeh Chaleshtori M. Detection and Molecular Characterization of Cryptosporidium species in Recreational Waters of Chaharmahal and Bakhtiyari Province of Iran using nested-PCR-RFLP. Iranian J Parasitol 2010; 6(1): 20-7.
29. Tabatabaiefar MA, Montazer Zohour M, Shariati L, Chaleshtori SA, Saffari Chaleshtori J, Ashrafi K, Gholami A, Farrokhi E, Hashemzadeh Chaleshtori M, Noori-Daloii MR. Mutation analysis of GJB2 and GJB6 genes and the genetic linkage analysis of five common DFNB loci in the Iranian families with autosomal recessive non-syndromic hearing loss. J Sci IR Iran 2010; 21(2): 105-12.
30. Farrokhi E, Shayesteh Mobarakeh F, Asadi Dehkordi S, Roghani Samani F, Ghatreh K, Hashemzadeh Chaleshtori M. Molecular Characterization of Iranian Patients with Possible Familial Hypercholesterolemia. Indian J Clin Biochem 2011; 26; 244-48.
31. Tabatabaiefar MA, Alasti F, Montazer Zohour M, Shariati L, Farrokhi E, Farhud DD, Camp GV, Noori-Daloii MR, Hashemzadeh Chaleshtori M. Genetic linkage Analysis of 15 DFNB Loci in A group of Iranian families with Autosomal recessive hearing loss. Iran J Public Health 2011; 40(2): 34-48.
32. Saee-Rad S, Hashemi H, Miraftab M, Noori-Daloii MR, Hashemzadeh Chaleshtori M, Raoofian R, Jafari F, Greene W, Fakhraie G, Rezvan F, Heidari M. Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus. Mol Vis 2011; 17: 3128-36.
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33. Vanwesemael M, Schrauwen I, Ceuppens R, Alasti F, Jorssen E, Farrokhi E, Hashemzadeh Chaleshtori M, Van Camp G. A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame. Am J Med Genet A 2011; 155A(8): 2021-3.
34. Tabatabaiefar MA, Alasti F, Shariati L, Farrokhi E, Fransen E, Nooridaloii MR, Chaleshtori MH, Van Camp G. DFNB93, a novel locus for autosomal recessive moderate‐to‐severe hearing impairment. J Clin J Genet 2011; 79(6): 594-8.
35. Ghatreh Samani K, Noori M, Rohbani Nobar M, Hashemzadeh Chaleshtory M, Farrokhi E, Darabi Amin M. The -514C/T Polymorphism of Hepatic Lipase Gene amongIranian Patients with Coronary Heart Disease. Iranian J Publ Health, 2012; 41(1): 59-65.
36. Montazer Zohour M, Tabatabaiefar MA, Azadegan Dehkordi F, Farrokhi E, Akbari MT, Hashemzadeh Chaleshtori M. Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment. Genet Test Mol Biomarkers 2012; 16(4): 271-8.
37. Yazdanpanahi N, Hashemzadeh Chaleshtori M, Tabatabaiefar MA, Noormohammadi Z, Farrokhi E, Najmabadi H, Shahbazi S, Hosseinipour A. Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss. Int J Pediatr Otorhinolaryngol 2012; 76(6): 845-50.
38. Zohour MM, Akbari MT, MH Chaleshtori. Frequency of the mitochondrial A1555G mutation in Iranian patients with non-syndromic hearing impairment. Indian J Sci Technol 2012; 5: 3378-83.
39. Schrauwen I, Helfmann S, Inagaki A, Predoehl F, Tabatabaiefar MA, Picher MM, Sommen M, Seco CZ, Oostrik J, Kremer H, Dheedene A, Claes C, Fransen E, Hashemzadeh Chaleshtori M, Coucke P, Lee A, Moser T, Van Camp G. A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. Am J Hum Genet 2012; 91(4): 636-45.
40. Kooshavar D, Tabatabaiefar MA, Farrokhi E, Abolhasani M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M. Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: assessment of GJB4, GJA1, and GJC3. Int J Pediatr Otorhinolaryngol 2012; 77(2):189-93.
41. Teimori H, Ashoori S, Akbari MT, Mojtabavi Naeini M, Hashemzade Chaleshtori M. FISH Analysis for del6q21 and del17p13 in B-cell Chronic Lymphocytic Leukemia in Iranians. Iran Red Crescent Med J 2013; 15(2): 107-12.
42. Taghizadeh SH, Kazeminezhad SR, Sefidgar SA, Yazdanpanahi N, Tabatabaeifar MA, Yousefi A, Lesani SM, Abolhasani M, Hashemzadeh Chaleshtori M. Investigation of LRTOMT gene (locus DFNB63)mutations in Iranian patients with autosomal recessive non syndromic hearing loss. Int J Mol Cell Med 2013; 2(1): 41-5.
43. Zeinalian M, Nobari RF, Moafi A, Salehi M, Hashemzade Chaleshtori M. Two decades of pre-marital screening for beta-thalassemia in central Iran. J Community Genet 2013; 4(4): 517-22.
44. Azadegan Dehkordi F, Rashki A, Bagheri N, Hashemzadeh Chaleshtori M, Memarzadeh E, Salehi A, Ghatreh H, Zandi F, Yazdanpanahie N, Tabatabaiefar MA, Hashemzadeh Chaleshtori M. Study of VSX1 mutations in patients with keratoconus in southwest Iran using
45. Yazdanpanahi N, Tabatabaiefar MA, Farrokhi E, Abdian N, Bagheri N, Shahbazi S, Noormohammadi Z, Hashemzadeh Chaleshtori M. Compound heterozygosity for two novel SLC26A4 mutations in a large Iranian pedigree with Pendred syndrome. Clin Exp Otorhinolaryngol 2013; 6(4): 201-8.
46. Jafarzadeh L, Danesh A, Sadeghi M, Heybati F, Hashemzadeh Chaleshtori M. Analysis of relationship between tumor necrosis factor alpha gene (G308A Polymorphism) with Preterm Labor. Int J Prev Med 2013; 4(8): 896-901.
47. Bagheri N, Taghikhani A, Rahimian G, Salimzadeh L, Azadegan Dehkordi F, Zandi F, Hashemzadeh Chaleshtori M, Rafieian-Kopaei M, Shirzad H. Association between virulence factors of helicobacter pylori andgastric mucosal interleukin-18 mRNA expression in dyspeptic patients. Microb Pathog 65: 7-13.
48. Allahbakhshian-Farsani M, Abdian N, Ghasemi-Dehkordi P, Sadeghiani M, Saffari-Chaleshtori J, Hashemzadeh-Chaleshtori M, Khosravi-Farsani S. Cytogenetic analysis of human dermal fibroblasts (HDFs) in early and late passages using both karyotyping and comet assay techniques. Cytotechnol 2014; 66: 815-22.
49. Rahimian G, Sanei MH, Shirzad H, Azadegan-Dehkordi F, Taghikhani A, Salimzadeh L, Hashemzadeh-Chaleshtori M, Rafieian-Kopaei M, Bagheri N. Virulence factors of Helicobacter pylori vacA increase markedly gastricmucosal TGF-b1 mRNA expression in gastritis patients. Microb Pathog 2014; 67:1-7.
50. Zeinalian M, Merghati-Khoei E, Azin SA, Hashemzadeh-Chaleshtori M. Help-seeking Behaviours among Haemophilia Community in Central Iran: A Qualitative Study. J Blood Disorders Transf 2014; 5(6).
51. Rajabpour FV, Raoofian R, Youssefian L, Vahidnezhad H, Shahshahani MM, Fathi H, Noormohammadpour P, Hesari KK, Hashemzadeh-Chaleshtori M, Tabrizi M. BMI1 and TWIST1 downregulated mRNA expression in basal cell carcinoma. Asian Pac J Cancer Prev 2014; 15(8): 3797-800.
52. Farrokhi E, Samani KG, Chaleshtori MH . Oxidized low-density lipoprotein and upregulated expression of osteonectin and bone sialoprotein in vascular smooth muscle cells. Lab Med 2014; 45(4): 297-301.
53. Mojtabavi Naeini M, Mesrian Tanha H, Hashemzadeh Chaleshtori M, Vallian S. Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population. Genet Test Mol Biomarkers 2014; 18(12): 820-5.
54. Abdian N, Ghasemi-Dehkordi P, Hashemzadeh-Chaleshtori M, Ganji-Arjenaki M, Doosti A, Amiri B. Comparison of human dermal fibroblasts (HDFs) growth rate in culture media supplemented with or without basic fibroblast growth factor (bFGF). Cell and Tissue Banking 2015; 10.1007/s10561-015-9494-9.
55. Zeinalian M, Emami MH, Naimi A, Salehi R, Hashemzadeh-Chaleshtori M. Immunohistochemical analysis of mismatch repair proteins in Iranian colorectal cancer patients at risk for lynch syndrome. Iran J Cancer Prev. 2015; 8(1): 11-7.
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56. Sedighi M, Karimnejad S, Farhadi B, Chaleshtori MH, Amiri A, Miraj S. Influence of the CYP1B1 gene polymorphisms and uterine leiomyoma risk in Iranian women. Int J Biosci 2015; 6(4): 118-23.
57. Zeinalian M, Emami MH, Salehi R, Naimi A, Kazemi M, Hashemzadeh-Chaleshtori M. Molecular analysis of Iranian colorectal cancer patients at risk for lynch syndrome: a new molecular, clinicopathological feature. J Gastrointest Cancer 2015; 46(2): 118-25.
58. Salimzadeh L, Bagheri N, Zamanzad B, Azadegan-Dehkordi F, Rahimian G, Hashemzadeh-Chaleshtori M, Rafieian-Kopaei M, Sanei MH, Shirzad H. Frequency of virulence factors in Helicobacter pylori-infected patients with gastritis. Microb Pathog 2015; 80: 67-72.
59. Abdian N, Allahbakhshian-Farsani M, Ghasemi-Dehkordi P, Mirzaeian A, Saffari-Chaleshtori J, Sadeghiani M, Hashemzadeh-Chaleshtori M. Effects of lentiviral vectors on DNA damage of human dermal fibroblasts (HDFs). J Pure and Applied Microbiol 2015; 9(1): 307-17.
60. Zeinalian M, Hashemzadeh-Chaleshtori M, Salehi R, Kazemi M, Emami MH. Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome. J Res Med Sci 2015; 20(2): 154-60.
61. Abdian N, Allahbakhshian-Farsani M, Khosravi-Farsani S, Ghasemi-Dehkordi P, Kazemi-Sheykhshabani S, Ganji-Arjenaki M, Hashemzadeh-Chaleshtori M. Generation of HSC-Like Cells from Human Embryonic Stem Cells by Inhibition of TGF-βR2 Signaling. Proceedings of the National Academy of Sciences, India Section B: Biological Sciences, 2015; 10.1007/s40011-015-0504-2.
62. Mahvi A, Mardani G, Ghasemi-Dehkordi P, Saffari-Chaleshtori J, Hashemzadeh-Chaleshtori M, Allahbakhshian-Farsani M, Abdian N. Effects of Phenanthrene and Pyrene on Cytogenetic Stability of Human Dermal Fibroblasts Using Alkaline Comet Assay Technique. Proceedings of the National Academy of Sciences, India Section B: Biological Sciences, 2015; 10.1007/s40011-015-0514-0.
63 Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Mohammad Javad kbarpour, Mohammad Hassan Emami. Epidemioclinical Feature of Early-Onset Colorectal Cancer at-Risk for Lynch Syndrome in Central Iran. Asian Pacific Journal of Cancer Prevention2015, Vol 16, /10.7314/APJCP.2015.16.11.4647
64Hamideh Jafari-Ghahfarokhi, Maryam Moradi-Chaleshtori, Thomas Liehr1,MortezaHashemzadeh - Chaleshtori .Hossein Teimori, Payam Ghasemi-Dehkordi . Small supernumerary marker chromosomes and theircorrelation with specific syndromes2015.Advanced Biomedical ResearchIP: 31.184.153.237
65-Ali Karimi, Marziyeh Abolhasani, Morteza Hashemzadeh-Chaleshtori . Batoul Pourgheysari. A preliminary study of inherited thrombophilic risk factors indifferent clinical manifestations of venous thromboembolismin central Iran. 2015. Indian J Med Res 142, July 2015, pp 46-52
with Uterine Fibroid, A Case- Control Study. BIOSCIENCES BIOTECHNOLOGY RESEARCH ASIA, April 2015. Vol. 12(1), 341-345
67Mehrdad Zeinalian,1,2 Mohammad Hassan Emami,2,3 Azar Naimi,2,3 Rasoul Salehi,2 and Morteza Hashemzadeh-Chaleshtori1. Immunohistochemical Analysis of Mismatch Repair Proteins in Iranian Colorectal Cancer Patients at Risk for Lynch Syndrome. Iran J Cancer 2015 Jan-Feb; 8(1): 11–17.
68Payam Ghasemi-Dehkordi1 & Mehdi Allahbakhshian-Farsani2 & Narges Abdian1 Amin Mirzaeian1 & Javad Saffari-Chaleshtori3 & Fatemeh Heybati1 &Gashtasb Mardani 3 & Alireza Karimi-Taghanaki1 & Abbas Doosti.Mohammad-Saeid Jami1 & Marziyeh Abolhasani 1 & Morteza Hashemzadeh-Chaleshtori . Comparison between the cultures of stem cells (hiPSCs) on feeder-and serum-free system (Matrigelmatrix), MEF and HDF feeder cell lines. J. Cell Commun. Signal. (2015) 9:233–246DOI 10.1007/s12079-015-0289-3
69Mohammad-Saeid Jami d, Zahra Salehi-Najafabadi Fereshteh Ahmadinejad, esthelle Hoedt, Morteza Hashemzadeh Chaleshtori Mahdi Ghatrehsamani Thomas A. Neubert b, Jan Petter Larsen, Simon Geir Møller. Edaravone leads to proteome changes indicative of neuronal cellprotection in response to oxidative stress. 2015Neurochemistry International 90 (2015) 134e141
70 Negar Moradipour, Payam Ghasemi-Dehkordi, Fatemeh Heibati, Shahrbanuo Parchami-Barjui, Marziyeh Abolhasani Ahmad Rashki, and Morteza Hashemzadeh-Chaleshtori. Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran.2016 Iran Red Crescent Med J. 2016 February; 18(2): e22076.
71Nader Bagher, Fatemeh Azadegan-Dehkordi, Ghorbanali Rahimian,MortezaHashemzadeh-Chaleshtori, Mahmoud Rafieian-Kopae, Soleyman KheirAbolfazl Gholipourb, and Hedayatollah Shirzad. Altered Th17 Cytokine Expression in Helicobacter pyloriPatients with TLR4 (D299G) Polymorphism. 2016A Journal of Molecular and Cellular ImmunologyISSN: 0882-0139 (Print) 1532-4311 (Online) Journal. homepagehttp://www.tandfonline.com/loi/iimm20
72AliMomeni, MortezaHashemzadehChaleshtori, Saeed Saadatmand, Soleiman Kheiri. Correlation of Endothelial Nitric Oxide Synthase Gene Polymorphism (GG, TT and GT Genotype) with Proteinuria and Retinopathy in Type 2 Diabetic Patients. Journal of Clinical and Diagnostic Research. 2016 Feb, Vol-10(2): OC32-OC35
73Effat Farrokhi, Keihan Ghatreh Samani, Morteza HashemzadehChaleshtoriand Mohammad Amin Tabatabaiefar. Effect of Oxidized Low Density Lipoprotein on the Expression ofRunx2 and SPARC Genes in Vascular Smooth Muscle Cells. Iranian Biomedical Journal 19 (3): 160-164 (July 2015)
74Nasim Sadrizade, Shahrbanu Parchami-Barjui2, Somayeh Reiisi3, Morteza Hashemzadeh-Chaleshtori, Maryam Hajhashemi. Screening BRCA1 and BRCA2 mutation frequencies in breastcancer patients of west Iran reveals a novel polymorphism inBRCA1 geneEUR. J. ONCOL.; Vol. 20, n. 2, pp. 94-99, 2015
75 Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour1,15
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Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori. Genetic Linkage Analysis of DFNB40 and DFNB48 loci in Families withAutosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) from WesternProvinces of Iran. Journal of Isfahan Medical School Vol. 34, No. 374, 2nd Week, May 2016
76Korosh Ashrafi Dehkordi1• Morteza Hashemzadeh Chaleshtori2Mohamadreza Sharifi3• Ali Jalil• Fardin Fathi4• Daem Roshani5Bahram Nikkhoo6• Mohammad Saeed Hakhamaneshi4Mohammad Reza Mahmoodian Sani7• Mahboue Ganji-Arjenaki. Inhibition of MicroRNA miR-222 with LNA Inhibitor Can ReduceCell Proliferation in B Chronic Lymphoblastic Leukemia)2016(Indian J Hematol Blood TransfusDOI 10.1007/s12288-016-0694-7
77Mehdi Banitalebi Dehkordi, Zahra Madjd,† Morteza Hashemzadeh Chaleshtori, Reza Meshkani,Laleh Nikfarjam, and Abdol-Mohammad Kajbafzadeh.. A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem CellsFrom the Entire Umbilical Cord. )2016(. Cell Transplantation, Vol. 25, pp. 1287–1297, 2016
78. Somayeh Reiisi1, Mohammad Amin Tabatabaiefar, Mohammad Hosein Sanati, Morteza Hashemzadeh Chaleshtori. Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family)2016(.Iran J Basic Med Sci, Vol. 19, No. 7, Jul 2016
79 Samira ASGHARZADE1, Morteza HASHEMZADE CHALESHTORI2, Mohammad Amin TABATABAIFAR3, Somayeh REISI 4, Mohammad Hossein MODARESSI)2016(. MUTATION IN SECOND EXON OF MYO15A GENE CAUSE OF NONSYNDROMIC HEARING LOSS AND ITS ASSOCIATION IN THE ARAB POPULATION IN IRAN. GENETIKA, Vol. 48, No.2,587 -596, 2016
80Samira Asgharzade, e, Mohammad Amin Tabatabaiefar. Mohammad Hossein Modarressi, Mohammad Hossein Ghahremani, Somayeh Reiisi,Parisa Tahmasebi,FatemehAbdollahnejad, Morteza Hashemzadeh Chaleshtori, A novel TECTA mutation causes ARNSHL)2016)International Journal of Pediatric Otorhinolaryngology 92 (2017) 88e93 (
81Mohammad Reza Mahmoudian sani., Morteza Hashemzadeh-ChaleshtoriAmeneh Mehri-Ghahfarrokhi, Payam Ghasemi-Dehkordi,Massoud Saidijam, , and Mohammad-Saeid Jami3MicroRNA-183 Family in Inner Ear:Hair Cell Development and Deafness)2016) J Audiol Otol 2016;20(3):131-138
82 Gashtasb MARDANI, Amir Hossein MAHVI, , Morteza HASHEMZADEH-CHALESHTORI, Simin NASSERI1Mohammad Hadi DEHGHANI, Payam GHASEMI-DEHKORDI DEGRADATION OF PHENANTHRENE AND PYRENE USING GENETICALLY ENGINEERED DIOXYGENASE PRODUCING Pseudomonas putida IN SOIL)2016) GENETIKA, Vol. 48, No3, 837-858, 2016
83Mohammad Reza Mahmoudian sani Morteza Hashemzadeh-Chaleshtori,Ameneh Mehri-Ghahfarrokhi, Payam Ghasemi-Dehkordi,Massoud Saidijam , and Mohammad-Saeid Jami. )2016(MicroRNA-183 Family in Inner Ear:Hair Cell Development and Deafness3J Audiol Otol 2016;20(3):131-138
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84 Samira Motamedi, Mohammad Teimouri, Marjan Mojtabavi-Naeini, Morteza Hashemzadeh-Chaleshtori, Hossein Teimor Study And Molecular Investigation Of Transmembrane Channel-Like1 Gene RelatedPolymorphic Markers In Iranian Population. INTERNATIONAL JOURNAL OF SCIENTIFIC & TECHNOLOGY RESEARCH VOLUME 5, ISSUE 11, NOVEMBER 2016
85 Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, *Morteza HASHEMZADEH CHALESHTORI) 2017(. Screening of Myo7A Mutations in Iranian Patients withAutosomal Recessive Hearing Loss from West of IranIran. J Public Health, Vol. 46, No.1, Jan 2017, pp.76-82
87 Javad SAFFARI-CHALESHTORI, Mohammad-Amin TABATABAIEFAR,Payam GHASEMI-DEHKORDI, Effat FAROKHI3, Mohammad-Taghi MORADI,Morteza HASHEMZADEH-CHALESHTORI (2017) THE LACK OF CORRELATION BETWEEN TP53 MUTATIONS AND GASTRIC CANCER: A REPORT FROM A PROVINCE OF IRANGENETIKA, Vol. 49, No.1, 235-246, 2017
•PAPERS:
•1Pourjafari H, Hashemzadeh M, Razi N (2002). Sex ratio in Iran during a period of ten years. Journal of Research in Health Sciences 2(1): 28-31.
•2Pourjafari H, Hashemzadeh Chaleshtori M (2003). Study of some probable reasons for occurrence of congenital facial dysmorphy and hydrocephaly in an infant with maternal hyperthyroidism and treated with methimazoleand propyl thiouracil. Journal of Medical Council of IRI 21(3): 228-230.
•3Pourjafari H, Hashemzadeh M (2003). A case of outistic boy with heteromorphism of maternal number 15 chromosome. Urmia Medical Journal 13(4): 322-328.
•4Hadavi V, Hashemzadeh Chaleshtori M (2003). Techniques of clone formation (cloning). Pezeshk va Azmayeshgah 2: 12-20.
•5Hadavi v, Hashemzadeh Chaleshtori M (2003). Down's Syndrome and diagnostic methods (with emphasis on QF-PCR method). Pezeshk va Azmayeshgah 1: 16-24.
•6Pourjafari M, Hashemzadeh Chaleshtori M, Imani MR (2003). Frequencies of ABO gene and Rh blood groups in Hamadan, Iran. Journal of Research in Health Sciences 2(2): 33-37.
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FARSI PUBLICATIONS
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•7Pourjafari H, Hashemzadeh Chaleshtori M (2003). Different types of the coagulation disorders in Hamadan and a comparison of the ABo Rh blood group distribution in the patients and the control group. Scientific Journal of Hamadan University of Medical Sciences & Health Services 10(3): 51-54.
•8Pourjafari H, Hashemzadeh M, Arab M (2004). Frequencies of antigens and their alleles from ABO & RH blood types in a group of Women with two or more abortions. Scientific Journal of Hamadan University of Medical Sciences & Health Services 10(supl 4): 43-46.
•9Pourjafari H, Hashemzadeh Chaleshtori M (2004). Pedigree patterns of families having at least one member with sensorineural deafness in Hamadan. Journal of Shahrekord University of Medical Sciences 5(4): 1-4.
•10Sadeghi A, Sanati MH, Alasti F, Hashemzadeh Chaleshtori M (2006). Accessing genetic and environmental factors of hearing loss in 354 families in Qom and Markazi provinces. Journal of Rehabilitation 6(2): 7-10.
•11Shahrani M, Rafieian M, Shirzad H, Hashemzadeh M, Yousofi H, Khadivi R, Amini SA, Moradi M, Moghadasi j, Rahmani MR, Rahimi M, Shahrani D (2006). Effect of Allium sativum L. extract on acid and pepsin secretion in rat. Journal of Feiz 10(4): 8-13.
•12Yousofi H, Hashemzadeh M, Kohansal K, Zabardast N, Shirzad H, Shahabi G (2006). A survey about protective effect of Echinococcus granulosus protoscolices surface antigens in preventing secondary hydatid cyst. Armaghane-danesh 11(3): 37-44.
•13Shahrani M, Rafieian M, Pilevarian AA, Shirzad H, Hashemzadeh M, Yousofi H, Moradi M, Ebrahimzadeh A, Hasanpoor A, Sadeghi M, Imani R, Ganji F, Moghadasi J (2006). The effect of Amirkabiria odoratissima extract on gastric acid and pepsin secretion level in rat. Journal of Shahrekord University of Medical Sciences 8(4): 88-95.
•14Yousofi H, Hashemzadeh M, Aliyari Z, Farrokhi E, Zabardast N (2007). Molecular Characterization of the strains cause sheep-hydatid cyst, in Chaharmahal va Bakhtiary province using restriction fragment length polymorphism. Journal of Shahrekord University of Medical Sciences 9(2): 28-33.
•15Shahrani M, Rafieian M, Shirzad H, Hashemzadeh M, Yousofi H, Khadivi R, Amini SA, Dehghan M, Khayri S, Moradi M, Rahimian G, Gheitasi I (2007). Effect of Allium sativum L. extract on acid and pepsin secretion in basal condition and stimulated with Vag stimulate in rat. Journal of Medicinal Plants 6(24): 28-38.
•16Shahrani M, Nabavi-zadeh F, Rafieian M, Shirzad H, Hashemzadeh M, Yoosefi H, Khadivi R, Amini SA, Khalili B, Rahimian GH, Moradi MT Etemadi-far SH (2007). Effect of Allium sativum extract on acid and pepsin secretion in basal condition and stimulated with Pentagastrin in rat. Journal of Arak University of Medical Sciences Rahavard Danesh 10(3): 48-57.
•17Ghatreh Samani K, Noori M, Rohbani Nobar M, Hashemzadeh Chaleshtori M, Farrokhi E, Darabi Amin M (2008). Investigating two polymorphisms effective in HDL-C concentration in the patients with coronary artery disease. Journal of Shahrekord University of Medical Sciences 10(2): 1-12.
•18Farrokhi E, Shirmardi A, Khoshdel A, Amani S, Soleimani M, Kasiri M, Rahbarian J, Parvin N, Shahinfard N, Noparast Z, Salehifard AZ, Afzal M, Tabatabaiefar MA, Shirani M, Hashemzadeh
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Chaleshtori M (2009). Genetic study of 45 big hearing loss pedigrees and GJB2 gene mutations frequency in Cheharmahal va Bakhtiari province, Iran, 2008. Journal of Shahrekord University of Medical Sciences 10(4): 16-21.
•19Saffari Chaleshtori J, Moradi MT, Farrokhi E, Tabatabaiefar MA, Taherzadeh Farrokhshahri M, Shayesteh F, Mobini GR, Banitalebi M, Khademi S, Mardani G, Shahrani M, Parvin N, Shahinfard N, Rahimian GA, Nazem HA, Hashemzadeh Chaleshtori M (2009). Study of two common P53 gene mutations in gastric cancer using PCR-RFLP in Cheharmahal va Bakhtiari province, Iran, 2003. Journal of Shahrekord University of Medical Sciences 10(4): 43-50.
•20Taherzadeh Farrokhshahri M, Farrokhi E, Saffari Chaleshtori J, Khademi S, Moradi MT, Shirmardi A, Mobini GR, Parvin N, Banitalebi M, Hajihoseini Baghdadabadi R, Nazem H, Noorbakhsh M, Hashemzadeh Chaleshtori M (2009). Study of DFNB59 gene mutations in exon 2 and 4 in association with deafness using PCR-RFLP in Cheharmahal va Bakhtiari, Iran. Journal of Shahrekord University of Medical Sciences 10(4): 77-82.
•21Shayesteh F, Ghatreh Samani K, Shirani M, Parvin N, Saffari Chaleshtori J, Taherzadeh Farrokhshahri M, Mobini GR, Banitalebi M, modarresi M, Hashemzadeh Chaleshtori M (2009). Study of three common ApoB gene mutations in possible familial hypercholesterolemia patients in Cheharmahal va Bakhtiari province, Iran, 2003. Journal of Shahrekord University of Medical Sciences 10(4): 105-111.
•23Saffari Chaleshtori J, Moradi MT, Farrokhi E, Tabatabaiefar MA, Taherzadeh M, Shayesteh F, Mobini GR, Banitalebi M, Mardani G, Shahrani M, Parvin N, Shahinfard N, Rahimian GA, Nazem HA, Hashemzadeh Chaleshtori M (2009). Detection of mutations in exons 5-8 of the p53 gene in gastric cancer samples using PCR-SSCP in Chaharmahal va Bakhtiari province, 2006-2007. Journal of Shahrekord University of Medical Sciences 11(3): 61-69.
•24Parvin N, Shahinfard N, Farrokhi E, Kasiri M, Khoshdel A, Amani S, Hosseinzadeh SH, Shirmardi A, Noparast Z, Akbarian A, Sedaei M, Hashemzadeh Chaleshtori M (2009). The frequency of hearing loss etiology among deaf students in Chaharmahal va Bakhtiari province, Iran, 2008-2009. Journal of Shahrekord University of Medical Sciences 11(3): 93-99.
•25Taherzadeh Ghahfarrokhi M, Banitalebi M, Mobini GH, Saffari Chaleshtori J, Farrokhi E, Shirmardi SA, Asadi S, Ghatreh Samani K, Abolhasani M, Azadegan F, Reisi S, Reisi M, Banitalebi GA, Parvin N, Hajihoseini R, Hashemzadeh Chaleshtori M (2010). DFNB59 gene mutations screening in non syndromic deaf subjects in Chaharmahal va Bakhtiari province. Journal of Shahrekord University of Medical Sciences 11(4): 76-83.
•26Asadi S, Ghatreh Samani K, Shirani M, Parvin N, Saffari Chaleshtori J, Taherzadeh Ghahfarrokhi M, Shayesteh F, Nazem H, Hajihosseini Baghdadabadi R, Roghani F, Hashemzadeh Chaleshtori M (2010). Study of LDL receptor gene mutations in patients with familial hypercholesterolemia in Cheharmahal va Bakhtiari province. Journal of Shahrekord University of Medical Sciences 11(4): 27-34.
•27E Farrokhi, K Ghatreh Samani, SA Amini, M Hashemzadeh Chaleshtori, MT Moradi, H Amini Najafabadi.2010- Study of -629C/A polymorphism of cholesteryl ester transfer protein gene in statin effects on plasma high density lipoprotein cholesterol level. Shahrekord University of Medical Sciences Journal ;12(2): 35-43.
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•28Taherzadeh Ghahfarrokhi M, Farrokhi E, Shirmardi A, Ghasemi S, Abolhasani M, Azadegan F,Reisi S, Reeisi M, Banitalebi G, Hashemzadeh Chaleshtori M.2010- DFNB59 Gene Mutations and its Association with Deafness in Schoolchildren in Kohgilooyeh & Boyerahmad Province. Armaghane-danesh, Journal of Yasuj University of Medical Sciences;14(4): 31-39.
•29M Abolhasani, E Farrokhi, M Noorbakhsh, M Taherzadeh, F Azadegan, A Asgari, M Hashmzadeh.(2010)- The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin). Zahedan Journal of Research in Medical Sciences, Journal of Zahedan University of Medical Sciences (Tabib-e-shargh;12(3): 19-23.
•30A NozarI , AM Foroghmand , AM Ahadi, A Khoshdel, Sh Salehian, H Bagheri, M Hashemzadeh-Chaleshtori.( 2010)- Assosiation study between IL1RA gene polymorphism with febrile convulsion in Shahrekord children. Shahrekord University of Medical Sciences Journal ;12(3).29-35.
•31Tabatabaiefar MA, Shariati L, Montazer-Zohour M, Ashrafi K, Saffari-Chaleshtori J Ghasemikhah R, Farrokhi E, Noori-Daloii ,M HashemzadehChaleshtori.(2010.( Mutation screening of GJB2 and GJB6 and genetic linkage study of three prevalent DFNB loci in Iranian families with autosomal recessive non-syndromic hearing loss. Shahrekord University of Medical Sciences Journal;12(3):65-75.
•32Moradi MT, Farrokhi E, Azadegan F , Bani-Mehdi M ,Doulati M, Keshavarz S, Farhood D, HosseinIpoor A, Mansouri Sh, Hashemzadeh Chaleshtori M .( 2010) Frequency of 35delG mutation in GJB2 gene in non-syndromic prelingual hearing loss in 3 provinces of Iran. University of Medical Sciences Journal;12(3:6067.
•33F. Azadegan Dehkordi, E. Farrokhi, M. Montazerozohori, J. Saffari, G. Mobini, M. Taherzadeh, M. Abolhasani, M. Reisi, G. Banitalebi, S. Reisi, M. Banitalebi, A. Asgari, F. Taje, A. Shirmardi, M. Soleimani, M. kasiri, M. Hashemzadeh Chaleshtori.(2010) DFNB59 gene mutation screening using PCR-SSCP/HA technique in non-syndromic genetic hearing loss in Booshehr province. Booshehr University of Medical Sciences Journal;13(3); 163-170.
•34S. Reissi E. Farokhi, M. Taherzadeh ghahfarohki, F. Azadegan, M. Abolhasani, M. reisi, G. Banitalebi, A. Esmaieli, R. Zaker, M. Hashemzadeh Chaleshtori .(2010) Study of deafness associated with DFNB59 gene (pejvakin) mutation in Fars . Qom University of Medical Sciences Journal, (Issue 4) .10-15.
•35Shayesteh F, Farrokhi E, Shirani M, Modarresi M, Roghani F,Hashemzadeh M.(2011) The study of mutations of the 9 exons of LDLR gene patients with familial hypercholesterolemia in Cheharmahal va Bakhtiari province Arak Medical University Journal (AMUJ) Original Article; 13(4): 30-3.
,•36Taji F, Montazer Zohouri, Farrokhei E, Bani talebi dehkordi , Hosseini pour, A-Keshavarz , S-Asgari A-Hashemzadeh Chaleshtori M.(2011) Screening of Mitochondria Mutations of A1555G,A3243G,and A7445G in MTRNR1,MTTL1 AND MTTS1 Genes in Subjects with Nonsyndromic sensorineural Hearing Loss.Journal of Guilan University of medical Sciences ,winter,vol 15,no;76,pages;15-21.
•37Heydari S, Montazer Zohouri M, Farrokhi E, Shirmardi A, Banitalebi G, Reisi S, Atai Z,
Abolhasani M, Kasiri M, Akbari MT, Ghatreh K, Hashemzadeh Chaleshtori M.(2011).Molecular investigation of mtDNA A1555G, A3243G and A7445Gmutations among the non syndromic hearing
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loss cases in Fars, Iran Journal of KashanUniversity of Medical Sciences,; Vol. 14, No 4, Pages 447-452.
•38A, Asghari, M. Montazer Zohori, E. Farrokhi, G. Banitalebi Dehkordi, M. Abolhasani, F. Azadeghan, M. Saedi Morghmaleki, A. Hoseinipor, . Keshavarz,K. Ashrafi, F. Taji, M. Hashemzadeh Chaleshtori,.(2011)- Mitochondrial gene mutation screening in hearing loss patients, Hormozgan, Iran Journal of hormozgan University of Medical Sciences, spril,; Vol. 15, No 1, Pages 1-7
•39Fatemeh Azadegan-Dehkordi, Mostafa Montazer-Zohouri, Effat Farrokhi, Abolfateh Shirmardi, Mojtaba Saedi-Marghmaleki, Zohreh Ataei, Somayeh Reisi, Marzieh Abolhasani, Hamid Khazraei, Mohammad Taghi Akbari, Morteza Hashmzadeh Chaleshtori.(2011)- Screening of three common mtDNA mutations among subjects with autosomal recessive non-syndromic hearing loss in Sistan va Baluchestan province, Iran . Zahedan J Res Med Sci(ZJRMS; 13(5): 17-22.
•40solmaz Khademi, alimohamad Ahadi, jafar Mehvari, hoda Ayat, effat Farokhi, mohamadtaghi Moradi, mortaza Hashemzadeh-Chaleshtori.(2011) Detection of A1430G mutation in SCN1A gene in a patient affected by GEFS-Like epilepsy in Chaharmahal va Bakhtiari Province. Shahrekord University of Medical Sciences Journal ;13(4): 60-66.
•41Montazer-Zohour M, Hashemzadeh Chaleshtori M , Akbari MT .(2012) Frequency of the common mitochondrial DNA (mtDNA) mutations in non-syndromic hearing impairment in southwest subpopulations of .IranJournal of Shahrekord University of Medical Sciences..July, Aug; 14(3): 81-91.
•42Golandam Banitalebi, Mostafa Montazerzohor, Efat Farokhi, Marzeyeh Abolhasani, Somayeh Reissi, Soraya Heydari, Zohreh Ataii, Fatemeh Azadegan, Azam Hoseinipoor , Morteza Hashemzadeh Chaleshtori.(2012) Study of three common mitochondrial mutations in Arab patients with nonsyndromic hearing loss in Khuzestan province, I.R.Iran Journal of Shahrekord University of Medical Sciences(J Shahrekord Univ Med Sci), 14(3): 30-39.
•43Fatemeh Taghizade-Mortezaee, Morteza Hashemzadeh Chaleshtori, Soleiman Kheiri, Neda Parvin,4 Mahbubeh Norbakhsh, Sima Etemadi, Shahla Taherian, Sepideh Miraj.(2012) Association of Interleukin-1β (IL-1β) Gene Polymorphisms with Uterin Leiomyoma .Zahedan Journal of Research in Medical SciencesJ Sep; 14(7): 53-56.
•44 Javad Saffari Chaleshtori , Mohammad taghi Moradi, Effat Farrokhi, Mohammad Amin Tabatabaiefar, Maryam taherzadeh, Fatemeh Azadegan, Gholamreza Mobini, Mehdi Banitalebi, Ghorban Ali Rahimian, Morteza Hashemzadeh Chaleshtary.(2012)-Study of P53 gene mutations in promoter and exons 2-4 and 9-11 in patient with gastric cancer by PCR-SSCP in Chaharmahal Va Bakhtiari province .Iranian South Medical Journal ;14(4): 220-229.
•45 Keyhan Ghatreh Samani, Effat Farrokhi, Mortaza Hashemzadeh Chaleshtori, Masoud Sadeghi.(2012) Study the relationship between Q192R paraoxonase gene polymorphism and high density lipoprotein composition after Lovastatin Trapy. Shahrekord University of Medical Sciences Journal ;14(5): 1-12.
•46 Keyhan Ghatreh Samani, Effat Farrokhi, Morteza Hashemzadeh Chaleshtory, Fatemeh Azadegan. (2012) Paraoxonase-1 L55M polymorphism with fatty acid composition of phospholipids in high-density lipoproteins. Tehran University Medical Journal;70(1): 7-14
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•47 Kyehan Ghatreh-Samani, Effat Farrokhi, Mortaza Hashemzadeh-Chaleshtori, Mortaza Nikookar, Zahra Noormohammadian.(2012)- Study of I405V polymorphism of cholesterol ester transfer protein gene in efficacy of statins on plasma level of high density lipoprotein cholesterol. Shahrekord University of Medical Sciences Journal ;14(2): 1-10.
48* Taghizade-Mortezaee F, Farrokhi E, Shahinfard N, Ashoori S, Gatreh-Samani K, Hashemzadeh-Chaleshtori M et al . Association of (Ile462Val in genetic polymorphisms CYP1A1) and uterine leiomyoma risk in women in Charmahal va Bakhtiari, I.R. Iran . J Shahrekord Univ Med Sci. 2012; 14 (2) :74-81
•49 Daniz Kooshavar, Effat Farrokhi, Marziye Abolhasani, Mohammad Amin Tabatabaiefar, Mohammad Reza Noori Daloii, Mortaza Hashemzadeh Chaleshtori.(2013) Digenic inheritance of GJB4 gene in autosomal recessive Non-syndromic hearing loss patients with one mutant GJB2 allele. Shahrekord University of Medical Sciences Journal 14(6): 89-100.
•50 Soraya Heydari, Razieh Pourahmad, Arsalan Khaledifar, Morteza Hashemzadeh, Zeinab Amini, Soheila Badfar, Nariman Khosravi Farsani.2013- Investigation of Mutations in Exons 12-15 MYH7 Gene in Hypertrophi Cardiomyopathie Patients Using PCR-SSCP Technique. Zahedan J Res Med Sci Sep; 15: 10-14.
•51F. Taghizade Mortezaee, S. Miraj, G. Bani Talebi, M. Hashemzadeh Chaleshtori, F. Sedgh Azar, M. Haj Hashemi.(2013) Association of estrogen receptor α-351 and -397 polymorphisms with uterine leiomyoma in Chaharmahal & Bakhtiari women. ISMJ; 16(3): 198-206
52*Marjan Mojtabavi Naeini, Sadeq Vallian Borujeni, Morteza Hashemzadeh Chaleshtori.(2013) Genetic Variation of D7S2420 Marker in Five EthnicGroups of the Iranian Population: A Highly InformativeMarker for Molecular Diagnosis of ARNSHL.JGenetics in the Third MillenniumJourna.1(11):2698-2707
53*Mojtabavi Naeini M, Vallian S, Hashemzadeh Chaleshtori M.(2013) Study of Alleles Characteristics and Informativeness of D7S2459 Marker inFive Ethnic Groups of the Iranian Population. Arak Medical University Journal. 2013; 16(76): 55-65
54*Heydari S, Khaledifar A, Pourahmad R, Hashemzadeh-Chaleshtori M, Heydari S, Bagheri N, et al . (2013) Investigation of mutations in exons 19-23 MYH7 gene in hypertrophic cardiomyopathy patients using PCR-SSCP/HA technique in Chaharmahal va Bakhtiari province. J Shahrekord Univ Med Sci; 15 (4) :35-44
55* norbahksh S, kasiri K, jalil A, hashem zade M.( 2013) Determining the frequency of glucose-6-phosphate dehydrogenase deficiency in newborn infants in Shahrekord. J Shahrekord Univ Med Sci.; 15 (5) :30-37
56*Nader Bagheri, Afshin Taghikhani, Ghorbanali Rahimian, Loghman Salimzadeh,Fatemeh Azadegan Dehkordi, Farid Zandi, Morteza Hashemzadeh Chaleshtori,Mahmoud Rafieian-Kopaei, Hedayatollah Shirzad.(2013). Association between virulence factors of helicobacter pylori andgastric mucosal interleukin-18 mRNA expression in dyspeptic patients. journa Microbial Pathogenesis. 12 September . 1/7
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57* Lobat Jafarzadeh, Azar Danesh, Marzieh Sadeghi, Fateme Heybati, Morteza Hashemzadeh. .(2013) Analysis of Relationship between Tumor Necrosis Factor Alpha Gene (G308A olymorphism) with Preterm Labor. International Journal of Preventive Medicine, Vol 4, No 8, August
58* Dehkordi F ,Rashki A ,Bagheri N,Chaleshtori M ,Memarzadeh E ,Salehi A,Ghatreh H, Hydari S, Yazdanpanahi N,Ghalehnoo Z, Merzaeyan A, Chaleshtori M.(2013) Studying VSX1 Gene Mutations in Patients with Keratoconus of Chaharmahal and BakhtiariProvince, IranJournal of Kerman University of Medical Sciences,; 20(6): 546-554
59*A.R. Salehi Chaleshtori, F. Fattahi, M.A. Tabatabaiefar, A. Hoseinipour, H.R. Salehi Chaleshtori, F. Rezaian, M. Hashemzadeh Chaleshtori .(2014) Analysis of CABP2 c.637+1G>T Mutation in Iranian Families with Autosomal Recessive Non-Syndromic Hearing Loss. J Babol Univ Med Sci; 16(1); Jan 2014; pp: 70-76
60*Bagheri N, Salimzadeh L, Azadegan-Dehkordi F, Hashemzadeh M,Heydari S, Rahimian R, Rahimian Gh, Taghikhani A, Rafieian-Koupaee M, Kheiri S, Shirzad H.(2014) Expression levels of mRNA cytokines of IL-17 and IL-23 iepithelialfiber of stomach inpatients with Helicobacter pylori usingReal-Time PCR in Chahar Mahal and Bakhtiari province. (J Shahrekord Univ Med Sci) 2014 Feb, March; 15(6): 124-131
61*Marjan Mojtabavi Naeini, Sadeq Vallian, Morteza Hashmzadeh Chaleshtor .(2014)Investigation of D7S496 marker characteristics in five Iranian ethnic groups for linkage analysis of autosomal recessive non syndromic hearing loss. J Shahrekord Univ Med Sci. Volume 15, Number 7
62* Mehdi Allahbakhshian-Farsani, Payam Ghasemi-Dehkordi, Narges Abdian, Somayeh Khosravi-Farsani, Amin Mirzaeian, Masoud Nasri, Alireza Karimi-Taghanaki, Gashtasb Mardani, Seyedeh Amiri, Dr. Morteza Hashemzadeh.(2014) The assessment of lentiviral vectors application for gene transformation in human dermal fibroblasts (HDFs) . J Shahrekord Univ Med Sci Volume 15, Number 763*Soleimani A, Mobedi Z, Hashemzadeh M, Alerasoul M, Sadeghi B, Kazemi-Vardanjani AR, Sharifi-Faradonbeh.(2014) The effect of HLADRB1 subtypes, on clinical diseases activity index inrheumatoid arthritis patients referred to rheumatology clinic ofShahrekord University . J Shahrekord Univ Med Sci 2014 Apr, May; 16(1): 81-90
64*Seyed Javad Hasheminia, Sayyed Hamid Zarkesh-Esfahani, SepideTolouei, Vahid Shaygannejad, Hedaiatallah Shirzad, Morteza HashemzadehChaleshtory.(2014) Toll Like Receptor 2 and 4 Expression inPeripheral Blood Mononuclear Cells ofMultiple Sclerosis Patients. Iran.J.Immunol. VOL.11 NO.2 June 2014
65*Shahrbanoo Parchami-Barjui, Somayeh Reiisi .Fatemeh Rezaiean,Fatemeh Heybati, Morteza Hashemzadeh-Chaleshtori .(2014) Screening LRTOMT Gene (DFNB63 locus) in Patients with RecessiveNonsyndromic Hearing Loss in Hormozgan Province by UsingSSCP-PCR, HA-PCR and DNA Sequencing. Journal of Isfahan Medical School. Vol. 32, No. 298, 3rd Week, October 2014
66*Somayeh Reiisi, Mohammad Hossein Sanati, Mohammad Amin Tabatabaiefar,Hamid Reza Pourjafari, Zarrin Minuchehr, Afsaneh Shavarzi, Mitra Ataie Mahbobeh Kasiri, Morteza Hashemzadeh-Chaleshtori .(2014) Study of the Association of DFNB3 Locus with Autosomal RecessiveNon-Syndromic Hearing Loss in Iranian Deaf Population UsingGenetic Linkage Analysis.Journal of Isfahan Medical School.Vol. 32, No. 285, 2nd Week, July 2014
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67*Marjan Mojtabavi Naeini, Sadeq Vallian BoroujeniMorteza Hashemzadeh Chaleshtori. Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL.(2014). Journal of Kerman University of Medical Sciences, 2014; 21(6): 540-550
68*Rezaeian F, Tabatabaiefar MA, Heybati F, Reiisi S, Parchami Sh, Abolhasani M,Amiri B, Salehi AR, Hashemzadeh-Chaleshtori M. Genetic linkage analysis of DFNB93 locus in a group of families withautosomal recessive non-syndromic hearing loss in Chahar Mahal &Bakhtiari and Kohkiluyeh & Boyer Ahmad provinces of Iran.(2014). (J Shahrekord Univ Med Sci) 2014 Oct, Nov; 16(4):62-70.
69*Ramazi SH, Motovalibashi M, Hashemzade Chaloshtari M, Khazraei HR. Introduction of Interleukin-18 genotype as a risk factor for allergicrhinitis in Chaharmahal va Bakhtiari province. .(2014) J Shahrekord Univ Med Sci) 2014 Dec, Jan; 16(5): 76-83
70*N. Bagheri, Gh. Rahimian, L. Salimzadeh, A. Taghikhani, M. Mahsa . M. Hashemzadeh, F. Azadegan-Dehkordi, N. Solimani, H. Shirzad. .(2014). Expression of IL-18 cytokine mRNA in gastric mucosa tissue of patients with H. pylori infection in Chahar Mahal and Bakhtiari. ISMJ 2014; 17(4): 533-541
71**Ramazi ShahinMotovalibashi Majid.,Abolfazl Rad.,Khazrai HamidReza.,Hashemzade chaleshtori Morteza..(2014). Association between Interleukin-18 -607A/C gene polymorphism and the concentration of serum IgE as a risk factor for allergic rhinitis. Quarterly Journal of Sabzevar University of Medical Sciences, Volume 21, Number 5, November & December 2014
72*Motamedi S, Hashemzadeh-Chaleshtori M, Mojtabavi-Naeini M, Teimori H. Genetic variation of D9S1837 Marker located at TMC1 gene in Iranian.population. (J Shahrekord Univ Med Sci) 2015 Feb, Mar; 16(6): 75-83
73* Zohreh Hojati; Behnam Zamanzad Morteza Hashemzadeh; Razieh Molaie; Abolfazl Gholipour.( 2015.) Detection of FimH Gene in Uropathogenic Escherichia coli Strains Isolated From Patients With Urinary Tract Infection. Jundishapur J Microbiol. 2015;8(2):e17520.
74*Motamedi S, Hashemzadeh-Chaleshtori M, Mojtabavi-Naeini M, Teimori H 2015 Genetic variation of D9S1837 Marker located at TMC1 gene in Iranianpopulation. J Shahrekord Univ Med Sci) 2015 Feb, Mar; 16(6): 75-83.
75*Motamedi S, Hashemzadeh chaleshtori M, Mojtabavi Naeini M, Teimori H. Informativeness of D9S1876 Marker Located within the TMC1 Gene in Iranian Population. 2015ZUMS Journal. 2015; 23 (97) :61-71
76*Shahpari A, Dehghan M*, Pourahmad R, Hashemzadeh-Chaleshtori M Amiri M, Kazemi -Sheikhshabani S.(2015) Association of ApaI and Taq1 polymorphic site of vitamin D receptorgene with bone mineral density in women aged 45 years and older. (J Shahrekord Univ Med Sci) 2015 Jun, Jul; 17(2):17-25.
77*arghampour F, Pourahmad R*,Dehghan M, Hashemzadeh-Chaleshtori M.Association of Taq1 restriction site of Calcitonine gene and Alu1(rs1801197) polymorphism of Calcitonin receptor gene with bone mineraldensity in 200 women over 45 years in Shahrekord city. J Shahrekord Univ Med Sci) 2015 Aug, Sep; 17(3): 112-120
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78*Arbabi M, Hashemzadeh- Chaleshtori M, Mardani G, Sadeghi M,Najafi-Chaleshtori A, Shakeri K. Survey of the residual polycyclic aromatic hydrocarbons in petroleumcontaminated soils in Shahrekord in 2013. (J Shahrekord Univ Med Sci) 2015 Aug, Sep; 17(3): 102-111
79*- Fatemeh Azadegan-Dehkordi; Nader Bagheri; Mahsa Shirzad; Mohammad Hossein Sanei; Morteza Hashemzadeh-Chaleshtori; Mahmoud Rafieian-Kopaei; Mohammad Amin Tabatabaiefar; Hedayatollah Shirzad. Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis. Jundishapur J Microbiol. 2015;8(8):e21701
80 Fatemeh Azadegan-Dehkordi . Nader Bagheri . Mahsa Shirzad . Mohammad Hossein Sanei . Morteza Hashemzadeh-Chaleshtori . Mahmoud Rafieian-Kopaei ..ohammadAminTabatabaiefar . Hedayatollah Shirzad . Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis. Jundishapur J Microbiol. 2015 August; 8(8): e21701.
81ouladi B, Yadegari M, Rajabibazl M, Fazaeli A, Hashemzadehchaleshtari M.. Identification of Candida Species in Patients with Vulvovaginitis Presenting Different ClinicalSymptoms. J . ZUMS Journal. 2015; 23 (98 and 3) :53-67
82Behnaz Sadat Abedi, Seyedeh Zohreh kiyani, Morteza Hashemzadeh Chaleshtori,Shahrbanoo Parchami, Abbas Doosti. Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene inHypertrophic Cardiomyopathy Patients. 2015Arak Medical University Journal (AMUJ) Original Article2015; 18(98): 59-67
83Fattahi N, Tabatabaie Far MA, Reiisi S, Alipour P, Pourahmadian A., Hashemzadeh-Chaleshtori M. Genetic linkage analysis of DFNB59 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in 3 western provinces of Iran. (J Shahrekord Univ Med Sci) 2015 Oct, Nov; 17(4): 39-46. Original article
84Najmeh Farahani, Parvaneh Nikpour .Mohammad Hassan Emami,Morteza Hashemzadeh 4, Mehrdad Zeinalian MSc5, Rasoul Salehi MT1XT20 Single Quasi-Monomorphic Mononucleotide Marker for Detection ofMicrosatellite Instability in Iranian Patients with Hereditary NonpolyposisColorectal Cancer (HNPCC). Journal of Isfahan Medical SchoolVol. 33, No. 362, 2nd Week, Februaty 2016
85Saeidi E, Hashemzadeh Chaleshtori M, Doosti A, Parchami Bajue S. The study of mutations presence in exons 27 and 29 of MYBPC3 gene by PCR-SSCP/HA method in patients with hypertrophy cardiomyopathy in Chaharmahal and Bakhtiari province.2016. (J Shahrekord Univ Med Sci) 2016; 18(1): 27-35
86 .Shahin Ramazi, , Ali Fasihi, Maryam Godarziyan, Morteza Hashemzadeh-Chaleshtori, Expandable DNA Repeat and Human Hereditary Disorders.2016 Journal of Kerman University of Medical Sciences, 2016; 23(2): 234-249
87Sheikhshahrokh A, Hashemzadeh Chaleshteri M, Doosti A, Parchami Barjoui S. Study the presence of mutations in exons 30 and 33 MYBPC3 gene in patients with hypertrophic
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cardiomyopathy by PCR-SSCP/HA method in Chaharmahal and Bakhtiari. (J Shahrekord Univ Med Sci) 2016; 18(2): 10-20
87Pourahmadiyan A, Tabatabaiefar MA, Reiisi S, Alipour P, Fattahi N, Hashemzadeh-Chaleshtori M2016Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province2016(J Shahrekord Univ Med Sci) 2016; 18(3): 8-18.
.89 Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour,Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori)2016(.Genetic Linkage Analysis of DFNB40 and DFNB48 loci in Families withAutosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) from WesternProvinces of IranJournal of Isfahan Medical School. Vol. 34, No. 374, 2nd Week, May 2016
90Karami-Eshkaftaki R, Farrokhi E, Zia N, Hashemzadeh-Chaleshtori. )2016(.Study of rs6050307 polymorphism of VSX1 gene in patient with keratoconus in Chaharmahal and Bakhtiari. (J Shahrekord Univ Med Sci) 2016; 18(4): 1-8.
91Azimeh Danesh Shahraki, Shahram Tahmasebian, Hamid Habibi Ghahfarokhi, Morteza Hashemzadeh Chaleshtori. )2016(.Recognition of Congenital Deafness Main Cause Using Datamining Techniques. Iranian Journal of Medical Informatics (2016), Vol 5, Issue 3
92Bakhshian Dehkordi E, Hashemadeh Chaleshtori M.Haerian BS, Mohammadinejad P. )2016(.. Correlation study of rs833061, rs2010963 polymorphisms in VEGF-A gene in Iranian colorectal cancer patients. )2016(.J Shahrekord Univ Med Sci 2016; 18(5): 128-139
93Taghipour Sheshdeh A, Tabatabaiefar MA, Nemati Zargaran F, Moradi FZarepour N1, Hashemzadeh Chaleshtori M2017Genetic linkage analysis of the DFNB48 and DFNB98 loci in familieswith Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL)from Khouzestan province. Journal of Shahrekord University of Medical Science 2017; 18(6): 6-17.
94Nemati-Zargaran F, Tabatabaiefar MA, Taghipour-Sheshdeh A, Moradi F,Zarepour N, Hashemzadeh-Chaleshtori M.2017Genetic linkage analysis of the DFNB35 and DFNB42 loci in familieswith autosomal recessive non-syndromic hearing loss from KhuzestanprovinceJournal of Shahrekord University of Medical Sciences(J Shahrekord Univ Med Sci) 2017; 19(1): 1-9.
•Hashemzadeh Chaleshtori M, Myers B, Jenkins GJS, Parry JM (15-17 July 1996). Genotypic analysis of 4-Nitroquinoline 1-oxide induced mutation using the Restriction Site Mutation assay (RSM) at
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codon 247-250 of the human P53 gene. UK Environmental Mutagen Society (UKEMS), University of Birmingham, UK. P: 16.
•Farhud DD, Sadighi H, Hashemzadeh M, Hadavi V, Saadat M (12-15Aug 2001). ABO blood groups and red cell enzymes in various ethnic groups of Iran.9th Southern African Society of Human Genetics Congress, Kruger National Park, South Africa.
•Pourjafari H, Sarihi A, Hashemzadeh M (6-11Jul 2003). Dermatoglyphic observations in an Iranian girl affected with congenital cutis laxa (autosomal recessive). XIX International Congress of Genetics, Melbourne, Australia.
•Pourjafari H, Farhud DD, Hashemzadeh Chaleshtori M (8-10Sept 2003). Genetic consequences of war chemical agents. 8th Conference on Environmental science & technology, Lemon Island, Greece.
•Mojarrad M, Yazdanpanahi N, Derakhshandeh Peykar P, Rafiee M, Mirfakhraie R, Jalali M, Rahmani M, Farhud D, Hashemzadeh M, Mirzajani F (26-30 Oct 2004). Mutation detection of CFTR gene using SSCP methods in Iran. The American Society of Human Genetics (54th Annual Meeting), Metropolitan Toronto Convention Center, Toronto, Canada. P: 489.
•Hashemzadeh M, Farhud DD, Hoghooghi rad L, Dolati M, Sasanfar R, Hoseinipour A, Tolooi A, Ghadami M, Montazer Zohour M, Andonian L, Poujafari H, Patton MA (26-30 Oct 2004). Connexin 26 (GJB2) gene mutations in different populations of Iran. The American Society of Human Genetics (54th Annual Meeting), Metropolitan Toronto, Convention Center, Toronto, Canada. P: 478.
•Banoei MM, Bayat B, Mahianeh A, Dehghan Menshadi M, Rostami M, Majdizadeh T, Houshiar Kashani B, Jahangir Soltani N, Sanati MH, Hashemzadeh Chaleshtori M, Patton MA (12-14Sept 2005). Genetic variation of the 3' VNTR region of human dopamine transporter gene (DAT1) in the Iranian population. British Human genetics Conference, University of York, York, UK. P: S103.
•Bayat B, Banoei MM, Mahianeh A, Jahangir Soltani N, Sanati MH, Hashemzadeh Chaleshtori M, Patton MA (12-14Sept 2005). Genetic variation of Apo B3' hyper variable region polymorphism among five ethnic groups of Iranian population. British Human genetics Conference, University of York, York, UK. P: S103.
•Banoei MM, Bayat B, Mahianeh A, Jahangir Soltani N, Sanati MH, Hashemzadeh Chaleshtori M, Patton MA (12-14Sept 2005). Allele frequency distribution of D17S5, D1S80 and D19S20 VNTRs in 5 ethnic groups of Iranian population.British Human genetics Conference, University of York, York, UK. P: S50.
•Ataei Kachoei Z, Andonian L, Akbari MT, Khorramizadeh MR, Patton MA, Hashemzadeh Chaleshtori M (25-29 Oct 2005). Molecular diagnosis of CML (RT-PCR for bcr-abl gene) compared with cytogenetic diagnosis. The American Society of Human Genetics (55th Annual Meeting), salt Lake City, USA.
•Hashemzadeh Chaleshtori M, Poujafari H, Farhud DD (16-18 May 2007). Deafness in Iran: review of GJB2 gene mutations and DFNB59 gene mutation analysis. Regional Seminar on Genetics in Clinical medicine, Hamadan, Iran. P: 32.
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•Hamid M, Hashemzadeh Chaleshtori M, Zare S, Mahjoubi F, Akbari MT (16-19 June 2007). A novel 355-356delGA frameshift mutation and frequency of connexin 26(GJB2) mutation in Iranian patients. European Human Genetics Conference, Nice, France. P: 54.
•Hamid M, Hashemzadeh Chaleshtori M, Akbari MT (24-26 November 2007). Two novel frame-shift mutations in the connexin 26 gene (GJB2) in Iranian HHL patients.The First International Congress on Health Genomics and Biotechnology, Tehran, Iran. P: 150.
•Ghatreh Samani K, Noori M, Rohbani Nobar M, Hashemzadeh Chaleshtori M, Farrokhi E (11-15 Nov 2008). The -514C/T polymorphism of hepatic lipase gene among Iranian patients with coronary heart disease.The American Society of Human Genetics (58th Annual Meeting), Philadelphia, Pennsylvania, USA.
•Noori M, Ghatreh Samani K, Rohbani Nobar M, Hashemzadeh Chaleshtori M, Farrokhi E, Aslanabad N (11-15 Nov 2008). Association of I405V and -629C/A polymorphisms of cholesteryl ester transfer protein gene with high density lipoprotein cholesterol levels in coronary artery disease. The American Society of Human Genetics (58th Annual Meeting), Philadelphia, Pennsylvania, USA.
•Pourjafari H, Farimani M, Ghahremani S, Hashemzadeh M, Pourjafari B (12-17 July 2008). Genetic counceling in carriers of reciprocal chromosomal translocations involving two autosomes.XX international congress of genetics, Berlin, Germany.
•Tabatabaiefar MA, Alasti F, Farrokhi E, Peeters N, Wuyts W, Nooridaloii MR, Hashemzadeh Chaleshtori M, Van Camp G (23-26 May 2009). Genetic Analysis of 31 Iranian families segregating autosomal recessive hearing impairment. European society of human genetics, Viena, Austria
•Hashemzadeh Chaleshtori M, Parry JM (15-17 Aug 2000) Sensitive diagnosis of Helicobacter Pylori infection by PCR: (comparison with histological examination and detection of flagellin (flaA) gene in gastric biopsy specimens. National Congress on Human Genetics, Shahrekord University of Medical Sciences, Shahrekord, Iran. P: 1.
•Hashemzadeh Chaleshtori M, Parry JM (15-17 Aug 2000). Analysis of P53 mutations in human oral and oesophageal tumours by the use of the Polymerase Chain Reaction and Direct Sequencing.National Congress on Human Genetics, Shahrekord University of Medical, Sciences Shahrekord, Iran. P: 32.
•Pourjafari H, Hashemzadeh Chaleshtori M, Arab M. (13-15 May 2003). Frequencies of antigens and their alleles from ABO & Rh blood types in a group of women with recurrent abortions. The First Congress of Early Detection Of Diseases. Hamadan university of medical sciences, Hamadan, Iran. P: 234.
•Hashemzadeh Chaleshtori M, Kheirollahi M (20-22 May 2006). B-thalassemia mutation spectrum in the Iranian province of Chaharmahal va Bakhtiari. 9th Iranian genetics congress, Millad hospital hall center, Tehran, Iran. P: 363.
•Sadeghi A, Sanati MH, Alasti F, Hashemzadeh Chaleshtori M (20-22 May 2006). Linkage analysis of some of the DFNB loci in non-syndromic autosomal recessive hearing loss in two provinces of Iran. 9th Iranian genetics congress, Millad hospital hall center, Tehran, Iran. P: 271.
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•Foroughmand, A. Nozari, A. Ahadi, A. Khoshdel, S. Saleheian, H. Bagheri, M. Hashem Zadeh Chaleshtori, E. Farrokhi. Assosiation study between IL1RA gene polymorphism and Febrile Convulsion in Iranian children. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden P08.24.
•M. Noorbakhsh, M. Abolhasani, E. Farrokhi, M. Hashemzadeh Chaleshtori . Study of DFNB59 gene (Pejvakin) promoter mutations associated with deafness in deaf subjects of Chaharmahal va Bakhtiari province in Iran. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden P10.14 .
•M. A. Tabatabaiefar, F. Alasti L. Shariati, E. Farrokhi, M. R. Nooridaloii, M. Hashemzadeh Chaleshtori, Genetic linkage analysis in a cohort of Iranian families with autosomal recessive non-syndromic hearing impairment. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden, p12.010.
•Asadi mobarake, e. farrokhe, G. Mobini, M. Banitaleby, J. Saffari Chaleshtori, M. Taherzadeh, F. Shayesteh, H. Nazem, R. Haji Hosini, f. Roghani, M. Hashemzadeh Chaleshtor.;Study of LDL receptor gene mutations in patients with familial hypercholesterolemia in Chaharmahal va Bakhtiari. province. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden P12.072.
•D. Kooshavar, E. Farrokhi, M. Hashemzade chaleshtori Study of two deletions in GJB6 gene as the second mutant allele in GJB2 heterozygous autosomal recessive nonsyndromic hearing loss subjects in Iran. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden P12.091.
•F. Shayesteh, E. Farrokhi, M. Modarresi, M. Hashemzadeh Study of mutations in 9 exons of LDLR gene in possible familial hypercholesterolemia patlents in a province of Iran. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden P13.20.
•Ghasemi, m. taherzadeh, E. Farokhi, M. Hashemzadeh. Survey of DFNB59 gene mutations in exon 2 association with deafness children in Kohkeloiye va BoerAhmad. European Human Genetics Conference 2010 June 12 – 15, 2010 Gothenburg, Sweden P02.065 .
•Mohammad Amin Tabatabaiefar ،Fatemeh Alasti ،Laleh Shariati ،Effat Farrokhi ،Mohammad Reza Nooridaloii ،Guy Van Camp ،Morteza Hashemzadeh Chaleshtori. SNP array-based whole genome scan of Iranian families with autosomal recessive nonsyndromic hearing impairment gives an overview of the most frequent genes and identifies a novel locus. 11th Iranin Gentics Congress May22-24, 2010.
•Dr Mohammad Amin Tabatabaiefar , Mr Mostafa Montaer Zohour , Prof Mohammad Reza Noori-Daloii , Prof Morteza Hashemzadeh Chaleshtori. Hearing loss research: an overview of the 15 years of progress toward solving the dilemma. 11th Iranin Gentics Congress May22-24, 2010.
•Montazer-zohor M, Farokhi E, Shirmardi A, Banitalebi GH, Heydari S, Reisi S, Atai Z, Abolhasani M, Akbari T, Hashemzadeh Chaleshtori M. Investigation of mtDNA A1555G, A3243G and A7445G mutations in non-syndromic hearing loss patients in Fars province in Iran. 11th Iranin Gentics Congress May22-24, 2010.
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•Montazer-zohor M, Tabatabaiefar MA, Abolhasani M, Farokhi E, Reisi S, Saedi M, Akbari T, Hashemzadeh Chaleshtori M. Overview of Mitochondrial Genetics in Hearing Loss : Research Progress in Iran. 11th Iranin Gentics Congress May22-24, 2010.
•Azadeghan F, Farokhi E, Montazer-zohor M, Taherzadeh M, Safari J, Banitalebi GH, Moradi M, Asgari A, Ashrafi K, Hashemzadeh Chaleshtori M. DFNB59 gene mutation screening using PCR-SSCP/HA technique in non-syndromic genetic hearing loss in Booshehr province.11th Iranin Gentics Congress May22-24, 2010.
•Montazer-zohor M, Farokhi E, Saedi M, Azadeghan F, Atai Z, Heydari S, Reisi S, Akbari M, Hashemzadeh Chaleshtori M. Screening of three common mutation of mtDNA among subjects with pre-lingual deafness in Zahedan province in south.11th Iranin Gentics Congress May22-24, 2010.
•Banitalebi GH, Montazer-zohor M, Farokhi E, Reisi S, Abolhasani M, Heydari S, Atai Z, Azadeghan F, FArhod D, Hashemzadeh Chaleshtori M. study of the mtDNA A1555G, A3243G and A7445G mutations frequency in patients with nonsyndromic hearing loss in Khuzestan province. 11th Iranin Gentics Congress May22-24, 2010.
•Azadeghan F, Farokhi E, Montazer-zohor M,TAherzadeh M, Safari J, Banitalebi GH, Moradi M, Asgari A, Ashrafi K, Hashemzadeh Chaleshtori M. DFNB59 gene mutation screening using PCR-SSCP/HA technique in non-syndromic genetic hearing loss in Booshehr province. 11th Iranin Gentics Congress May22-24, 2010.
•Montazer-zohor M, Tabatabaiefar M, Reisi S, Azadeghan F, Saedi M, Banitalebi GH, Farokhi E,Akbari M, Hashemzadeh Chaleshtori M. prevalence of mtDNA A1555G, A3243G and A7445G mutations among postlingual hearing impaired subjects in Iran. 11th Iranin Gentics Congress May22-24, 2010.
•Abolhasani M, Farokhi E, Farhod D, Norbakhsh M, Taherzade M, Shirmardi A, Azadeghan F, Amiri B, Asgari M, Hashemzadeh Chaleshtori M. Deafness- associated DFNB599 gene (Pejvakin) mutations in Sistsn va Bluchestan province. 11th Iranin Gentics Congress May22-24, 2010.
•Asgari A, Montazer-zohor M, Farokhi E, Azadeghan F, Azadeghan F,Banitalebi GH, Taji F, Abolhasani M, Hashemzadeh Chaleshtori M. Mitochondrial mutations screening (A1555G, A7445G and A3243G) in Patients with nonsyndromic Sensorineural hearing loss in Hormozgan province. 11th Iranin Gentics Congress May22-24, 2010.
•Taji F, Montazer-zohor M, Farokhi E, Hoseinpour A, Keshavarz S, Reisi S, Banitalebi G, Asgari A, Azadeghan F, Hashemzadeh Chaleshtori M. Mutation analysis of the mtDNA A1555G,a3243G,and A7445G mutations in nonsyndromic sensorineural subjects in north Iran. 11th Iranin Gentics Congress May22-24, 2010.
•Reissi M, Montazer-zohor M, Reisi S, Frokhi E, Taherzadeh M, Banitalebi G, Azadeghan F, Mobini GH, Hashemzadeh Chaleshtori M. DFNB59 gene (Pejvaking) mutation screening in Autosomal recessive nonsyndromic hearing loss subjects using PCR-SSCP and Heteroduplex analysis protocol in two Iranian populations . 11th Iranin Gentics Congress May22-24, 2010.
•Safari J, Farokhi E, Moradi M, Tabatabaiefar M, Banitalebi M, Taherzadeh M, Mobini GH, Nazem H, Hashemzadeh Chaleshtori M. Study of P53 gene mutations in exons 5-8 in gastric cancer samples using PCR-SSCP in Chaharmahal Va Bakhtiari Province. 11th Iranin Gentics Congress May22-24, 2010.
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•D.Kooshavar E.farrokhi M.R.Noori-Daloli.M.Heahemzadeh Chaleshtori.. Double heterozgosity in GJB2 heterozygots of autosomal recessive non – syndromic hearing impairment:assessment of GJB6 genThe 12th International Congress of Human Genetics and the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada
•E.Farokhe. N yazdanpanpanahi , F. Teghizade, D.Kooshavar, H.Taghizade ,R.Heshmatifar ,S .Ashoori. Screening of LRTOMT gene mutations (D:NB63 Locus) in granian patients wih aurosomai recessive nonsyndromic hearing loss the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada
• safari Chaleshtori,M. Moradi, E.Farrokhi , M.A. Tabatabaieefar, M.Taherzadeh Ghahfarokhi G. Mobini ,F. Shayesteh, F. Azadegan, G. Rahimian ,H. Nazen,M. Heshemzadeh Chaleshtori Study of P53 gene mutations in promoter and exons 2-11 in gastric cancer by PCR-SSCP in a province of Iran the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada.
•F.taghizade mortezai,S Miraj,v E Farroki,M.Hashemzade Chaleshtori,S Kheyri Association of Estrogen receptor a-351 Xbal A>G and-397 Pvull T>C Polymorhisms with uterine Ieiomyoma in women from chaharmahal va Bakhtiari Province;Iran the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada
•M.Montazer Zohouri ,M.A Tabatabaeefar, M Rais, F.Azadegan, S.Raisi, E farrokhi, M.T.Akbari. M. Hashemzade Chaleshtori An overview of Mitochondrial Genetics in Hearing Loss: Research Progress in Iran the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada.
•َI A.Asgari.M . Montazer Zohouri , E. Farroki, M.Abolhasani. M.Akbari, F Azadegan Denkordi ,M . Hashemzade Chaleshtori-Mitochondrial gene mutation Screening related whit hearing loss in Hormozgan Province in Iran-The the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada.
• E. Farroki ,M. Taherzadeh,F.azadegan,A Asgani, E. Farroki ,S.Raisi.Z .Noeparasi, G.Bani Talebi, M.Abolhasani ,M . Hashemzade Chaleshtori- Deafiness-associated DFNB599 Gene (Pejvakin) mutations in sistsn va Bluchestan Province.the American Society of Human Genetics 61st Annual Meeting October 11-15,2011 Montreal,Canada
•G.Banitalebi, M . Hashemzade Chaleshtori , E. Farroki, M.Abolhasani , ,S.Raisi , S Keshavarz, A. Hosseinipor - Prevalence of the A1555G, A3243G and A744G mitochondrial mutations in non-syndromic hearing impairment in Khuzestan Province of the Iran. the American Society of Human Genetics 61st Annial Meeting October 11-15,2011 Montreal,Canada.
•M. A. Tabatabaiefar, F. Alasti, L. Shariati, E. Farrokhi, E. Fransen, M. R.Noori-Daloii, M. Hashemzadeh Chaleshtori, G. Van Camp- DFNB93, a novel locus for autosomal recessive moderate-toseverehearing impairment UROPEAN Human Genetics CONFERENCE 2011Amsterdam RAI Congress Centre Amsterdam, The Netherlands May 28 –31, 2011
•F. Azadegan-Dehkordi, M. Montazer-Zohouri, E. Farrokhi, A. Shirmardi,M. Saedi-Marghmaleki, Z. Ataei, S. Reisi, M. Abolhasani, H. Khazraei, M.Akbari, M. Hashmzadeh-Chaleshtori- Screening of three mtDNA mutations using PCR-RFLP UROPEANHumanGeneticsCONFERENCE 2011Amsterdam RAI Congress CentreAmsterdam, The NetherlandsSaturday, May 28 – Tuesday, May 31, 2011
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•F. Taji, M. Zohoor, F. arrokhi, M. Hashemzadeh - Chaleshtori- Mutation analysis of the mtDNA A1555G,a3243G,and A7445Gmutations in nonsyndromic sensorineural subjects in north Iran. UROPEAN Human Genetics CONFERENCE 2011 Amsterdam RAI ongress CentreAmsterdam, The NetherlandsSaturday, May 28 – Tuesday, May 31, 2011
*S. Parchami Barjui, N. Sadrizade, A. Salehi, N. Abdian, F. Heibati Goojani, M. Hashemzadeh Chaleshtori, M. Hajhashemi;- Screening of BRCA1 (5382insC, 185deAG) and BRCA2 (6174delT)mutations in Breast cancer patients in Iran by MultiplexMutagenically Separated PCR. European Human GeneticsConference 2013 June 8 - 11, 2013Paris, France
*M. Allahbakhshian Farsani, M. Hashemzadeh Chaleshtori, N. Abdian, P. GhasemiDehkordi, A. Mirzaeian;- Reprogramming of HDF cells to iPSc using polycistronic lentiviralvectors delivering the OSKM. European Human GeneticsConference 2013 June 8 - 11, 2013Paris, France
*M. Zeinalian, , A. Moafi, M. Hashemzadeh Chaleshtori;- Two decades of Pre-marital Screening for Beta-thalassaemia in central Iran European Human GeneticsConference 2013 June 8 - 11, 2013Paris, France
* M. Hashemzadeh Chaleshtori, M. Allahbakhshian Farsani, N. Abdian, P. Ghasemi- Cytogenetic analysis of Human dermal fibroblasts (HDF) cells usingkaryotyping test. European Human GeneticsConference 2013 June 8 - 11, 2013Paris, France
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* Ghasemi-Dehkordi P, Allahbakhshian-Farsani M, Abdian 1, Khosravi-Farsani S.and hashemzadeh-Chaleshtori M.(2013) CULTURES OF HUMAN INDUCED PLURIPOTENT STEM (HIPS)CELLS ON MATRIGEL MATRIX WITH CONDITIONAL MEDIA. Vox Sanguinis (2013) 105 (Suppl. 2), 1–132
* Allahbakhshian-Farsani M, Ghasemi Dehkordi P, Abdian N, Sadeghiani M,Saffari Chaleshtori J, Hashemzadeh Chaleshtor M and Khosravi-Farsani S. CYTOGENTIC ANALYSIS OF HUMAN DERMAL FIBROBLASTS(HDFS) CELLS IN EARLY AND LATE PASSAGES USING BOTHKARYOTYPING AND COMET ASSAY TECHNIQUES. Vox Sanguinis (2013) 105 (Suppl. 2), 1–132
*Ramazi S1*, Fasihi A2, Motovali bashi M, 1 khazrai H3, Hashemzade chaleshtori M4. Association between the concentration of serum immunoglobulin E and allergic rhinitisinChaharmahal va Bakhtiari province . 112th International Congress of Immunology & Allergy of Iran2th International Congress of Immunology & Allergy of Iran
*Hasheminia S.J1, 2*,Tolouei S3,HashemZadehChaloshtory M1,Zarkesh-Esfahani S.H2,4,Shaygannejad V5. Cytokine profile in new cases patients with Multiple Sclerosis
* Mohammad-Saeid Jami, Payam Ghasemi Dehkordi, Fereshteh Ahmadinejad and Morteza Hashemzadeh Chaleshtori. Comparison of three strategies to differentiate mechanosensory cells from human mesenchymal stem cells (HMSCS) and hair follicle pluripotent stem cells International Conference and Exhibition on. Cell and Gene TherapyMay 19-21, 2016 San Antonio, USA
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*Payam Ghasemi-Dehkordi, Azar Jaafari, ShahrbanuoParchami-Barjui, Somayeh Reiisi,Morteza Hashemzadeh-Chaleshtori, Sepideh Miraj. Evaluation of Serum Level Parametersand C677T Polymorphism of MTHFR Gene inPreeclampsia PatientsThe 2016 Annual Meeting of the International Genetic EpidemiologySociety
Akram Sarmadi, Mohammad Amin Tabatabiefar, Fatemeh Tabatabaei, Morteza Hashemzade chaleshtori* Diagnosis of patients with Maturity Onset Diabetes of Young (MODY) in a large population of diabetic patients
The 11th International Congress of Endocrine Disorders As speaker From 2nd to 4th November, 2016 In Shahid Beheshti International Convention Center, Tehran, Iran
