Consultation +98 313 626 95 86
Last Update : June. 18, 2022
Curriculum Vitae (C.V)
DR MAJID KHEIROLLAHI is Associate professor of Medical Genetics, Division of Genetics and Molecular Biology, Medical School, Isfahan University of Medical Sciences, Isfahan (http://www.mui.ac.ir), 81746-73461 IRAN, Tel: +98(311)792 2486 (18 Years). He is also Founder and technical responsible of Gene Azma Medical Genetics laboratory (5 Years) and Head of Pediatric Infectious Diseases Research Center, Institute of Primary Prevention of Non-communicable Diseases, Isfahan University of Medical Sciences, Isfahan (8 Years).
PERSONAL DATA
- Date of Birth: 1973
- Place of Birth: Isfahan, Iran
- Marital Status: Married
RESEARCH FIELDS
- GENETICS & HEREDITY
- Identifiers
- Web of Science ResearcherID: W-1912-2017
- ORCID 0000-0003-1981-1340
- Scopus H-index: 12
- Google Scholar H-index: 14
TITLE OF Ph.D. THESIS
Alterations in Telomere Length, Telomerase Activity and Cell Cycle Genes
Expression in Human Brain Tumors (astrocytoma, meningioma), Executive Supervisor: Dr. Mehipour, P.
EDUCATION
- 2010- 2011 (Jan.) Short-term Exchange in Proteomics of Brain Tumors; Erasmus MC, Rotterdam, the Netherlands
- 2005 – 2011 (Jan.) Ph.D. in Medical Genetics; Tehran University of Medical Sciences
- 1997 – 1999 (Nov.) M.Sc. in Human Genetics; Tehran university of Medical sciences
- 1992 – 1996 B.Sc. in Biology; Isfahan University
SOCIETY MEMBERSHIP
Iranian Medical Genetics Society (5 years)
EMPLOYMENT HISTORY
- Expert of Genetic consulting center, Welfare Organization, Isfahan; from 1999 to 2000.
- Expert & Responsible Person of Genetic Consulting Center, Welfare Organization, Shahrekord; 2001-2005
PUBLICATIONS
- Expert of Genetic consulting center, Welfare Organization, Isfahan; from 1999 to 2000.
- Expert & Responsible Person of Genetic Consulting Center, Welfare Organization, Shahrekord; 2001-2005
HONORS, PRIZES AND AWARDS
- 2010 Top researcher in the field of Medical genetics (From Head of Tehran University of Medical School)
- 2000 Appreciation of the responsible of genetic counseling center (From Head of State Welfare Organization)
PUBLICATIONS
A ) BOOKS
- Kheirollahi M., Genetic (Basic and Medical), Tehran, Jahad Daneshgahi – Press, Dec. 2009.
- Kheirollahi M. & Rashidinejad A., IQB of GENETICS, 1st ed. Tehran; Behandishan – Press, 2009.
B ) JOURNAL PAPERS
No | TITLE | YEAR |
1 | A novel signal amplification tag to develop rapid and sensitive aptamer-based biosensors S Radfar, R Ghanbari, AA Isfahani, H Rezaei, M Kheirollahi Bioelectrochemistry 145, 108087 | 2022 |
2 | M Mirsafaie, L Moghaddam-Banaem, M Kheirollahi International Journal of Preventive Medicine 13 (1), 81 | 2022 |
3 | Methylation and polymorphism in CDH1 gene promoter among patients with diffuse gastric cancer MN Vishteh, M Zeinalian, M Kheirollahi, AJ Mamaghani, MA Zolfaghari International Journal of Preventive Medicine 13 | 2022 |
4 | M Khorrami, E Khorram, O Yaghini, M Rezaei, A Hejazifar, O Iravani Journal of Molecular Neuroscience 71 (11), 2405-2414 | 2021 |
5 | M Kheirollahi, M Saneipour, A Moridnia Journal of Cancer Research and Therapeutics 17 (6), 1434 | 2021 |
6 | M Khorrami, MA Tabatabaiefar, E Khorram, O Yaghini, M Rezaei, … Journal of Human Genetics 66 (10), 973-981 | 2021 |
7 | SZH Imani, Z Hojati, S Khalilian, F Dehghanian, M Kheirollahi, … Scientific reports 11 (1), 1-10 | 2021 |
8 | B Khademi, M Khorrami, H Ayromlou, R Rikhtegar, EA Moghadam, … Journal of Neuroimmunology 353, 577507 | 2021 |
9 | S Khalilian, Z Hojati, F Dehghanian, V Shaygannejad, SZH Imani, … Scientific reports 11 (1), 1-10 | 2021 |
10 | R Meamar, S Sabbagh, M Khorrami, MA Ghahfarokhi, A Chitsaz, … Neurology Asia 26 (1) | 2021 |
11 | FH Soureshjani, M Kheirollahi, P Yaghmaei, S Fattahjadnematalahi International Journal of Preventive Medicine 12 | 2021 |
12 | Novel somatic variants in CTNNA1 gene in Iranian patients with diffuse gastric cancer MN Vishteh, TA Salmani, AJ Mamaghani Gastroenterology and Hepatology From Bed to Bench 14 (1), 17 | 2021 |
13 | New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer M Kheirollahi, M Saneipour, MA Tabatabaiefar, M Zeinalian, M Minakari Middle East Journal of Cancer 11 (4), 493-501 | 2020 |
14 | A Gheissari, R Meamar, M Kheirollahi, A Abedini Iranian Journal of Kidney Diseases 14 (5), 348-357 | 2020 |
15 | Effect of Donepezil and Hyoscyamoside on Improving Spatial Memory in Rats With Alzheimer’s Disease F Heidari Soureshjani, M Kheirollahi, P Yaghmaei, … Journal of Arak University of Medical Sciences 23 (4), 524-539 | 2020 |
16 | M Mahdavi, SM Sharafi, SS Daniali, R Riahi, M Kheirollahi Global Medical Genetics 7 (01), 014-021 | 2020 |
17 | Meta-Analysis on the Association of C-Reactive Protein Polymorphisms with Metabolic Syndrome SM Sharafi, M Mahdavi, R Riahi, M Kheirollahi, R Kelishadi Global Medical Genetics 7 (01), 008-013 | 2020 |
18 | M Rasoolian, SY Hosseini, H Khanahmad, J Sarvari, F Rahbarizadeh, … FABAD Journal of Pharmaceutical Sciences 45 (1), 19-27 | 2020 |
19 | F Ahmadi, M Peymani Journal of Isfahan Medical School 37 (541), 1040-1046 | 2019 |
20 | A Moridnia, MA Tabatabaiefar, M Zeinalian, M Minakari, M Kheirollahi, … Journal of Gastrointestinal Cancer 50 (3), 420-427 | 2019 |
21 | NB Mohsenian, A Shanei, SJ Alavi, M Kheirollahi, AH Nia, MB Tavakoli IET nanobiotechnology 13 (4), 387-391 | 2019 |
22 | M Rasoolian, M Kheirollahi, SY Hosseini Expert Opinion on Biological Therapy 19 (3), 211-223 | 2019 |
23 | M Khorrami, M Mahdavi, F Fakhr, M Kheirollahi Iranian Journal of Child Neurology 13 (4), 173 | 2019 |
24 | M Khorrami, M Mahdavi, F Fakhr, M Kheirollahi Iranian Journal of Child Neurology 13 (4), 173-183 | 2019 |
25 | Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian Patients P Karimzadeh, M Kheirollahi, SM Houshmand, S Dadgar, O Aryani, … Iranian Journal of Child Neurology 13 (4), 37 | 2019 |
26 | Targeting MCF-7 Cell Line by Listeriolysin O Pore Forming Toxin Fusion with AHNP Targeted Peptide. Fotoohi-Ardakani G, Kheirollahi M, Zarei Jaliani H, Noorian M, Ansariniyia H. Adv Biomed Res. 2019 May 27;8:33. doi: 10.4103/abr.abr_18_19. eCollection 2019. | 2019 |
27 | Mohsenian NB, Shanei A, Alavi SJ, Kheirollahi M, Nia AH, Tavakoli MB. IET Nanobiotechnol. 2019 Jun;13(4):387-391. doi: 10.1049/iet-nbt.2018.5387. | 2019 |
28 | Mottaghi T, Khorvash F, Kheirollahi M, Maracy M, Askari G. J Res Med Sci. 2019 Apr 26; 24:36. doi: 10.4103/jrms.JRMS_774_18. eCollection 2019. | 2019 |
29 | Correlations between the expression of hTERT and α and β splice variants in human brain tumors. Khajehgoodari R, Khorvash F, Kheirollahi M, Mirsafaie M, Salehi M. Adv Clin Exp Med. 2019 Apr; 28(4):507-513. doi: 10.17219/acem/81934 | 2019 |
30 | Variants in Human Prostacyclin Receptor Gene in Patients with Migraine Headache. Khorvash F, Kheirollahi M, Kazemi M, Amini G, Khorrami M, Mirsafaie M, Mohammadi MR. Iran J Psychiatry. 2018 Oct; 13(4):239-243. | 2019 |
31 | Rasoolian M, Kheirollahi M, Hosseini SY. Expert Opin Biol Ther. 2019 Mar; 19(3):211-223. doi: 10.1080/14712598.2019.1566453. Epub 2019 Jan 21. Review | 2019 |
32 | TRPC6 Mutational Analysis in Iranian Children With Focal Segmental Glomerulosclerosis. Gheissari A, Meamar R, Kheirollahi M, Rouigari M, Dehbashi M, Dehghani L, Abedini A. Iran J Kidney Dis. 2018 Nov; 12(6):341-349. | 2019 |
33 | In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria. Mahdavi M, Koulivand L, Khorrami M, Mirsafaie M, Kheirollahi M. Mol Biol Rep. 2018 Oct; 45(5):1165-1173. doi: 10.1007/s11033-018-4269-6. Epub 2018 Aug 1. | 2018 |
34 | In silico analysis of A novel pathogenic variant in an Iranian Mucopolysaccharidosis IIIB patient identified by targeted next-generation sequencing Mehdi Khorrami, Manijeh Mahdavi, Fatemeh Fakhr, Majid Kheirollahi Iranain Journal of Child Neurology | 2018 |
35 | In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria M Mahdavi, L Koulivand, M Khorrami, M Mirsafaie, M Kheirollahi Molecular Biology Reports 45 (5), 1165-1173 | 2018 |
36 | Variants in Human Prostacyclin Receptor Gene in Patients with Migraine Headache F Khorvash, M Kheirollahi, M Kazemi, G Amini, M Khorrami, M Mirsafaie, … Iranian Journal of Psychiatry 13 (4), 239-243 | 2018 |
37 | Meta-Analysis of the Association between GABA Receptor Polymorphisms and Autism Spectrum Disorder (ASD) M Mahdavi, M Kheirollahi, R Riahi, F Khorvash, M Khorrami, M Mirsafaie Journal of Molecular Neuroscience 65 (1), 1-9 | 2018 |
38 | Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer A Moridnia, MA Tabatabaiefar, M Zeinalian, M Minakari, M Kheirollahi, … Journal of gastrointestinal cancer, 1-8 | 2018 |
39 | Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene M Hashemipour, M Khorrami, M Mahdavi, MH Khujin, M Kheirollahi Iranian Journal of Pediatrics 28 (1) | 2018 |
40 | Identification of B and T cell epitope based peptide vaccine from IGF-1 receptor in breast cancer M Mahdavi, V Moreau, M Kheirollahi Journal of Molecular Graphics and Modelling 75, 316-321 | 2017 |
41 | A report of a novel mutation in human prostacyclin receptor gene in patients affected with migraine M Kheirollahi, MR Pourreza, F Khorvash, M Kazemi, G Amini Iranian journal of psychiatry 12 (3), 219 | 2017 |
42 | A novel mutation in SLC7A9 gene in Cystinuria S Fazaeli, S Ashouri, M Kheirolahi, M Mohammadi, M Fazilati Iranian journal of kidney diseases 11 (2), 138 | 2017 |
43 | Comparative study on mutations in CDH1 gene in Iranian patients with hereditary diffuse gastric cancer (HDGC) and sporadic diffuse gastric cancer (SDGC) A Moridnia, M Kheirollahi, MA Tabatabaeifar, M Zeinalian Journal of Isfahan Medical School 35 (432), 622-628 | 2017 |
44 | Evaluation of miR-362 expression in astrocytoma of human brain tumors M Kheirollahi, M Moodi, S Ashouri, P Nikpour, M Kazemi Advanced biomedical research 6 | 2017 |
45 | Capillary versus Venous Blood Glucose in Patients with Coma V Wiwanitkit Advanced biomedical research 6 | 2017 |
46 | Assessment Effects of Resveratrol on Human Telomerase Reverse Transcriptase Messenger Ribonucleic Acid Transcript in Human Glioblastoma A Mirzazadeh, M Kheirollahi, E Farashahi, F Sadeghian-Nodoushan, … Advanced biomedical research 6 | 2017 |
47 | Simple and easy to perform preimplantation genetic diagnosis for β-thalassemia major using combination of conventional and fluorescent polymerase chain reaction R Salehi, S Khosravi, M Salehi, M Kheirollahi, H Khanahmad Advanced biomedical research | 2017 |
48 | MeDIP real-time qPCR has the potential for noninvasive prenatal screening of fetal trisomy 21 M Kazemi, M Salehi, M Kheirollahi International journal of molecular and cellular medicine 6 (1), 13 | 2017 |
49 | Report of SLC3A1/rBAT gene mutations in Iranian cystinuria patients: A direct sequencing study S Markazi, M Kheirollahi, A Doosti, M Mohammadi Journal of research in medical sciences: the official journal of Isfahan … | 2017 |
50 | Prevalence of high‐risk human papillomavirus infection in women with ovarian endometriosis M Heidarpour, M Derakhshan, M Derakhshan‐Horeh, M Kheirollahi, … Journal of Obstetrics and Gynaecology Research 43 (1), 135-139 | 2017 |
51 | miR-145 and miR20a-5p Potentially mediate pleiotropic effects of interferon-beta through mitogen-activated protein kinase signaling pathway in multiple sclerosis patients N Ehtesham, F Khorvash, M Kheirollahi Journal of Molecular Neuroscience 61 (1), 16-24 | 2017 |
52 | Comparison of the Frequency of Y-short Tandem Repeats Markers between Sadat and Non-Sadat Populations in Isfahan Province of Iran R Seyedebrahimi, E Esfandiari, B Rashidi, R Salehi, AG Dahghi, S Dabiri, … Advanced biomedical research | 2017 |
53 | MiR-182-5p inhibition with locked nucleic acid induces apoptosis, necrosis and reduces cell proliferation in human acute promyelocytic leukemia A Moridnia, M Sharifi, RM FASIHI, A Najafi, M Kheirollahi | 2016 |
54 | Ligustilide is a major component of Radix Angelica Sinensis and reported to have anti-inflammatory and anti-nociceptive effects. Toll-like receptor 4 (TLR4) has been shown to … M Kheirollahi, E Kazemi, S Ashouri Cellular and Molecular Neurobiology 36 (1), 143-149 | 2016 |
55 | Next-generation sequencing and its applications M MOSALLAYI, H MIRZAEI, M SIMONIAN, M KHEIROLLAHI JOURNAL OF ISFAHAN MEDICAL SCHOOL (IUMS) 33 (368), 2469-2480 | 2016 |
56 | The effect of beta interferon on the expression of miR-145 in patients with multiple sclerosis N EHTESHAM, MR SHARIFI, F KHORVASH, M KHEIROLLAHI JOURNAL OF ISFAHAN MEDICAL SCHOOL (IUMS) 34 (396), 1013-1018 | 2016 |
57 | Down syndrome: Current status, challenges and future perspectives M Kazemi, M Salehi, M Kheirollahi International journal of molecular and cellular medicine 5 (3), 125 | 2016 |
58 | Effect of teicoplanin on the expression of c-myc and c-fos proto-oncogenes in MCF-7 breast cancer cell line S Ashouri, MH Khujin, M Kazemi, M Kheirollahi Advanced biomedical research | 2016 |
59 | Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria B Ezatpour, M Kheirollahi, L Koulivand, M Mohammadi, R Salehi, … Urolithiasis | 2016 |
60 | Existence of mutations in the homeodomain-encoding region of NKX2. 5 gene in Iranian patients with tetralogy of Fallot M Kheirollahi, F Khosravi, S Ashouri, A Ahmadi Journal of research in medical sciences: the official journal of Isfahan … | 2016 |
61 | Genetic analysis of Iranian family with hereditary cardiac arrhythmias by next generation sequencing M Asadi, R Foo, MR Samienasab, AR Salehi, M Kheirollahi, … Advanced biomedical research | 2016 |
62 | A novel mutation in SLC3A1 gene in patients with cystinuria S Markazi, M Kheirollahi, A Doosti, M Mohammadi, L Koulivand Iranian journal of kidney diseases 10 (1), 44 | 2016 |
63 | Brain-derived neurotrophic factor gene Val66Met polymorphism and risk of schizophrenia: a meta-analysis of case–control studies M Kheirollahi, E Kazemi, S Ashouri Cellular and molecular neurobiology 36 (1), 1-10 | 2016 |
64 | Cystinuria in a Patient With a Novel Mutation in SLC7A9 Gene M Kheirollahi, L Koulivand, M Mohammadi, B Ezatpour Iranian Journal of Kidney Diseases | 2015 |
65 | Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria L Koulivand, M Mohammadi, B Ezatpour, R Salehi, S Markazi, S Dashti, … Urolithiasis 43 (5), 447-453 | 2015 |
66 | Comparison of TERRA expression in human brain tumors S Dashti, F Khorvash, R Salehi, P Mahzouni, L Koulivand, M Kheirollahi European Journal of Oncology 20 (1), 25-31 | 2015 |
67 | Knocking down the DRD2 by shRNA expressing plasmids in the nucleus accumbens prevented the disrupting effect of apomorphine on prepulse inhibition in rat MR Noori-Daloii, A Shahbazi, S Alizadeh Zendehrood, A Shayan Nia, … Journal of Sciences, Islamic Republic of Iran 26 (3), 205-212 | 2015 |
68 | Cystinuria in a patient with a novel mutation in SLC7A9 gene L Koulivand, M Mohammadi, B Ezatpour, M Kheirollahi Iranian journal of kidney diseases 9 (1), 63-66 | 2015 |
69 | Telomeric repeat-containing RNA (TERRA) and human diseases S Dashti, M Kheirollahi Journal of Isfahan Medical School 33 (330) | 2015 |
70 | Retinal cell regeneration by stem cells F Nazem-Roaya, R Heidari, M Kheirollahi Journal of Isfahan Medical School 33 (321), 54-69 | 2015 |
71 | Plant expression of human proinsulin using the plasmid viral university of Tehran (pVUT) vector M Kheirollahi, AA Shahnejat-Bushehri, F Abooei-Mehrizi, H Alizade Journal of Isfahan Medical School 33 (327) | 2015 |
72 | The role of transcription factors in regulating the development and differentiation of neural retina cells R Heidari, F Nazemroaya, M Kheirollahi Journal of Isfahan Medical School 33 (351) | 2015 |
73 | Expression of mir-148a in human meningioma tumors M Moodi, M Kheirollahi Journal of Isfahan Medical School 33 (325), 252-527 | 2015 |
74 | Expression of TERRA in different grades of astrocytoma S DASHTI, S ASHOURI, M KHEIROLLAHI JOURNAL OF ISFAHAN MEDICAL SCHOOL (IUMS) 32 (317), 2333-2342 | 2015 |
75 | Expression of ZFX gene correlated with the central features of the neoplastic phenotype in human brain tumors with distinct phenotypes A Afzali, M Emadi-Baygi, P Nikpour, F Nazemroaya, M Kheirollahi Advanced biomedical research 4 | 2015 |
76 | Annexin V FITC conjugated as a radiation toxicity indicator in lymphocytes following radiation overexposure in radiotherapy programs MB Tavakoli, M Kheirollahi, A Kiani, M Kazemi, SH Javanmard, … Advanced biomedical research 4 | 2015 |
77 | Expression of prostaglandin I2 (prostacyclin) receptor in blood of migraine patients: A potential biomarker M Kheirollahi, M Kazemi, G Amini, F Khorvash, F Ahangari, M Kolahdouz, Advanced biomedical research 4 | 2015 |
78 | Brain tumors: Special characters for research and banking M Kheirollahi, S Dashti, Z Khalaj, F Nazemroaia, P Mahzouni Advanced biomedical research 4 | 2015 |
79 | Comparison of Inserted Mouse IP-10 Gene Copy Number in Helper-Dependent and Independent System Based on PiggyBac Transposition in Human Embryonic Kidney Cells. H Mirzapour, A Karamzade, H Khanahmad, R Salehi, M Kheirollahi Journal of Isfahan Medical School 32 (275) | 2014 |
80 | An Overview of Peptide Nucleic Acids: Structure, Properties, and Applications. A Farrokhifard, M Kheirollahi Journal of Isfahan Medical School 31 (270) | 2014 |
81 | An Overview of Peptide Nucleic Acids: Structure, Properties, and Applications. A Farrokhifard, M Kheirollahi Journal of Isfahan Medical School 31 (270) | 2014 |
82 | Telomerase and Therapy of Brain Tumors. M Kheirollahi, R Khajeh-Goodari, R Ghavimi Journal of Isfahan Medical School 31 (267) | 2014 |
83 | Detection of Mutation in Exons 3 and 8 of SLC3A1 and Exons 4 and 10 of SLC7A9 Genes in Patients Affected by Cystinuria in Iran L Koulivand, M Mohammadi, R Salehi, B Ezatpour, … JOURNAL OF ISFAHAN MEDICAL SCHOOL (IUMS) 32 (293), 1-8 | 2014 |
84 | miRNA, Biogenesis and Mechanisms of Regulations N Ehtesham, M Modi, M Kheirollahi Journal of Isfahan Medical School (IUMS) 32 (296), 0-0 | 2014 |
85 | Evaluation of Measuring Radiation-Induced Apoptosis in Human T-Lymphocytes by Flow Cytometry as a Biological Dosimetry System MB Tavakkoli, M Kheirollahi, A Kiani, M Kazemi, L Mohebat, Journal of Isfahan Medical School Received: 27.02.2014 Vol. 32, No. 284, 1st Week, July 2014 | 2014 |
86 | Genetics Aspects of Male Infertility. A Karamzade, H Mirzapour, M Kheirollahi Journal of Isfahan Medical School 31 (246) | 2013 |
87 | Establishing a Tumor Bank and Challenges. M Kheirollahi, Z Khalaj, F Nazem-Roaia, S Dashti, F Khorvash, M Kazemi Journal of Isfahan Medical School 31 (245) | 2013 |
88 | Telomerase activity in human brain tumors: astrocytoma and meningioma M Kheirollahi, M Mehrazin, N Kamalian, J Mohammadi-asl, P Mehdipour Cellular and molecular neurobiology 33 (4), 569-574 | 2013 |
89 | The Role of Telomere in Cell; Telomere Dysfunction and Tumorigenesis. M Kheirollahi, M Kolahdouz, F Ahangari, L Koulivand, F Khorvash Journal of Isfahan Medical School 30 (222) | 2013 |
90 | The Role of Telomere in Cell; Telomere Dysfunction and Tumorigenesis. M Kheirollahi, M Kolahdouz, F Ahangari, L Koulivand, F Khorvash Journal of Isfahan Medical School 30 (222) | 2013 |
91 | Telomere, Regulation and Tumorigenesis M Kheirollahi Telomere Territory and Cancer, 55-98 | 2013 |
92 | Telomere Structure and Its Role in DNA Damage and Genetic Disorders. M Kheirollahi, L Koulivand Journal of Isfahan Medical School 30 (210) | 2012 |
93 | Glioma Biomarker Discovery by Mass Spectrometry (P06. 001) L Dekker, M Kheirollahi, G Stockhammer, T Luider, PS Smitt Neurology 78 (1 Supplement), P06. 001-P06. 001 | 2012 |
94 | Glioma biomarker discovery by mass spectrometry L Dekker, M Kheirollahi, G Stockhammer, T Luider, PS Smitt Cancer Research 72 (8 Supplement), 1266-1266 | 2012 |
95 | Use of siRNA in knocking down of dopamine receptors, a possible therapeutic option in neuropsychiatric disorders MR Noori-Daloii, M Mojarrad, A Rashidi-nezhad, M Kheirollahi, … Molecular biology reports 39 (2), 2003-2010 | 2012 |
96 | Qualitative and quantitative promoter hypermethylation patterns of the P16, TSHR, RASSF1A and RARβ2 genes in papillary thyroid carcinoma J Mohammadi-asl, B Larijani, Z Khorgami, SM Tavangar, V Haghpanah, … Medical oncology 28 (4), 1123-1128 | 2011 |
97 | Evolutionary hypothesis of telomere length in primary breast cancer and brain tumour patients: a tracer for genomic—tumour heterogeneity and instability P Mehdipour, M Kheirollahi, M Mehrazin, N Kamalian, M Atri Cell biology international 35 (9), 915-925 | 2011 |
98 | Alterations of telomere length in human brain tumors M Kheirollahi, M Mehrazin, N Kamalian, P Mehdipour Medical Oncology 28 (3), 864-870 | 2011 |
99 | Expression of cyclin D2, P53, Rb and ATM cell cycle genes in brain tumors M Kheirollahi, M Mehr-Azin, N Kamalian, P Mehdipour Medical Oncology 28 (1), 7-14 | 2011 |
100 | Androgen Receptor Gene CAG Repeat Polymorphism and Breast Cancer Risk in Iranian Women: A Case‐Control Study P Mehdipour, S Pirouzpanah, M Kheirollahi, M Atri The breast journal 17 (1), 39-46 | 2011 |
101 | Alpha-and beta-synucleins mRNA expression in lymphocytes of schizophrenia patients MR Noori-Daloii, M Kheirollahi, P Mahbod, F Mohammadi, AN Astaneh, … Genetic testing and molecular biomarkers 14 (5), 725-729 | 2010 |
102 | Mining the Common Facts in Cancer: Reliability of Protein Expression in Breast Cancer and Brain Tumor P Mehdipour, M Kheirollahi, M Mehrazin, M Atri Proceedings of the World Medical Conference. p.226-230 | 2010 |
103 | The spectrum of β-thalassemia mutations in Isfahan Province of Iran P Derakhshandeh-Peykar, H Hourfar, M Heidari, M Kheirollahi, … Iranian Journal of Public Health 37 (2), 106-111 | 2008 |
C) PRESENTATION AT CONFERENCES
1- Mutations in SLC3A1 and SLC7A9 Genes in Iranian Patients with Cystinuria
Conference:PCS Wolrd Conference of Reproductive Health-2017
Authors: Kheirollahi M., Mahdavi M., Koulivand L., Markazi S., Fazaeli S., Mohammadi M., Mirsafaie, M
2- Telomerase Activity in Human Brain Tumors, accepted by the ICG-6 conference committee.
Conference: The 6th International Conference on Genomics (ICG-6), Nov. 12-15, 2011
Authors: Kheirollahi M., Mehrazin M., Kamalian N., Mohammadi J., Mehdipour p.
3- A rare case of Fibula aplasia and complex brachydactyly
Conference: European Congress of Human Genetics, May 25 – 29, 2002, Strasbourg,
France Programme.
Authors: Kheirollahi M., Azadeh B.
4- Mining the Common Facts in Cancer: Reliability of Protein Expression in Breast Cancer and Brain Tumor
Conference: Proceedings of the World Medical Conference. Sep. 15-17, 2010, North
Atlantic University Union, Malta
Authors: Mehdipour P, Kheirollahi M, Mehrazin M, Atri M
5- Proteomics of CSF, Cyst and serum samples of patients affected with Glioblastoma
Conference: The second Iranian society of Medical Genetics congress. June 20-21,
2011; (Speech).
Authors: Luider T., Kheirollahi M., Dekker L., Mehdipour P.
6- A rare case of Fibula aplasia and complex brachydactyly
Conference: The 8th Iranian Genetics Congress. May 20- 23, 2003; (Speech).
Authors: Kheirollahi M., Azadeh B.
7- Identification of mutations in exons 5 and 8 of the P53 gene in patients affected with colorectal cancer
Conference: The First International Congress of Cancer Genetics, under the Auspices of the UICC. 13-16 December 2003; (Poster).
Authors: Kheirollahi, M., Mehdipour, P., Atri M.
8- Prevalence of the Connexin 26 gene Mutations in non-syndromic hearing loss in Iran
Conference: The 9th Iranian Genetics Congress. May 19- 22, 2006; (Speech).
Authors: Hashemzadeh M., Kheirollahi M.
9- Report of a case of Chediak Higashi syndrome
Conference: The first Congress of Genetic Disorder & Disabilities in Iran. April 12-
14, 1999; (Poster).
Authors: Farhoud D., Kheirollahi, M.
10- Report of a Case of Multiple Cartilaginous Exostoses
Conference: The 2nd Iranian Congress of Genetic Disorder & Disabilities. 7–11 Dec., 2002; (Speech).
Authors: Kheirollahi M., Razavi M.
11- Susceptibility genes in an Iranian Breast Cancer population: BRAC1, BRCA2, ATM and AR
Conference: The 2nd International Congress of Cancer Genetics. Nov. 30-Dec. 2, 2006;
(Speech)
Authors: Mehdipour, P., Mohammadi M., Habibi L., Pirouzpanah S., Kheirollahi, M,
Hosseini SS., Atri, M.
PROJECTS
1- Associations study between genetic variations, rs6721763 of ITGA4 gene with multiple sclerosis severity
Shaygannejad V, Kheirollahi M, Khorrami M
2- Study of phenolalanine hydroxylase gene mutations in children with phenylketonuria in Isfahan province
Executive Supervisor: Dr. Kheirollahi M
3- Evaluation of coding sequences in three individuals of one family with diagnosis of Ig A Nephropathy by whole exome sequencing
Executive Supervisor: Dr. Kheirollahi M
4- Evaluation of the relationship between gene expression and FHIT gene polymorphism of rs760316 locus and serum IL-17 level with response to interferon beta treatment in patients with RRMS
Executive Supervisor: Dr. Kheirollahi M
5- PTGIR gene polymorphisms and expression in migraine patients
Executive Supervisor: Dr. Kheirollahi M, Members: Kheirollahi M, Salehi R, Saadatnia M, Kazemi M, Amini G, Karamzadeh A, Authority: Isfahan University of Medical
Sciences
6- Study of Molecular function of SiRNA at gene Therapy in Patients Affected with Schizophrenia, Executive Supervisor: Dr. Noori Daloii, M.R.
7- Analysis of P53, ATM, PTEN, P14ARF, P16ink4a , Cycline D2 , Rb proteins and detection of ATM-gene-mutation in Brain tumors, Executive Supervisor: Dr. Mehipour, P.
EXECUTIVE RESPONSIBILITIES & PROFESSIONAL EXPERIENCES
- Editorial Board; Journal of Medical School, Isfahan University of Medical Sciences.
- Scientific Secretary of Genetics of Human Brain Tumors (at EDC), Nov. 10, 2011, Isfahan University of Medical Sciences.
- Co-Executive of the 1st international congress of biomedical sciences, August 29-31, 2012, Isfahan University of Medical Sciences.
CONGRESS & WORKSHOPS
(The most important cases)
- Dec. 21-25, 2009 Teaching skills (40 hours), Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- Oct. 11, 2011 PMDR and Electronic Databases, Isfahan University of Medical Sciences, Isfahan, Iran
- Jan. 12-17, 2001 Genetic counseling training course, University of Social Welfare and Rehabilitation, Tehran, Iran
- Oct. 6-7, 2011 Multi-targeted and general unknown screening with identification in LC/MS/MS
NH Leeuwenhorst, Noordwijkhout, Netherlands - Dec. 13-16, 2003 The 1st International Congress of Cancer Genetics, Imam-Khomeini Hospital, Tehran, Iran.
- Nov. 30-Dec. 30, 2006 The 2nd International Congress of Cancer Genetics, Imam-Khomeini Hospital, Tehran, Iran.
- Nov.19-14, 2006 Hybrid Course in Genetic Counseling in Practice, European, School of Genetic Medicine, Medical Genetics Department, Tehran University of Medical, Sciences, Poursina St., Tehran,Iran
- May 5-11, 2007 Hybrid Course in Medical Genetics, European School of Genetic Medicine, Medical Genetics Department, Tehran University of Medical, Sciences, Poursina St., Tehran,Iran
- May 1-3, 2006 New Thoughts of Cancer Cell Biology & Genetics Symposium, Tehran, Iran
- June 20-21, 2011 Seminar of Medical Genetics in Iran, Imam-Khomeini Hospital, Tehran
- July 21, 2011 Survival analysis, Isfahan University of Medical Sciences
- April 29 – May 1, 2007 Symposium of Molecular Aspects of Cancer Diseases, Cancer Institute, Imam-Khomeini Hospital, Tehran, Iran
- Nov. 24- 26, 2007 The 1st International Congress on Health Genomics & Biotechnology and 4th Iranian Congress of Genetic Disorder & Disabilities, Summit Meeting Conference Hall, Tehran, Iran
- May 6-8, 2007 The 2nd Iranian Congress of Genetic Disorder, Imam-Khomeini Hospital, Tehran, Iran
- Apr. 15-17, 2006 The 2nd Reviewing Seminar of Genetic diseases, Imam-Khomeini Hospital, Tehran, Iran
- Nov. 27-Dec. 1, 2004 The 3rd Iranian Congress of Genetic Disorder & Disabilities, University of Social Welfare and Rehabilitation, Tehran, Iran
- Jan. 9-11, 2004 The 3rd Reviewing Seminar of Genetic Diseases for Genetic Counselors, Yazd University of Medical Sciences, Yazd, Iran
- May 20- 23, 2003 The 8th Iranian Genetic congress, Milad Hospital, Tehran, Iran
- May 19- 22, 2006 The 9th Iranian Genetics Congress, Milad Hospital, Tehran, Iran
- Jan. 6-8, 2004 The Training Course of Genetic Diseases for Genetic Counselors, University of Social Welfare and Rehabilitation, Tehran, Iran
- Nov. 27-29, 2007 Two Dimensional Electrophoresis and Proteomics, Pasture Institute of Iran
- June 24-27, 2007 Workshop of Bioinformatics, Theoretical and practical, Pasture Institute of Iran
- Sep.15-17, 2007 Workshop of Cancer Genetics, Imam-Khomeini Hospital, Tehran, Iran
- 4-5 March, 2009 Workshop of Cell culture, Anatomy Department, Iran University of Medical Sciences, Tehran, Iran
- Dec. 20, 2005 Workshop of Mental Retardation, University of Social Welfare and Rehabilitation, Tehran, Iran
- Nov. 12-13, 2004 Workshop of Molecular Genetic Methods, Genetic & Biotechnology Research Center, Tehran, Iran
- Dec. 28, 2005 Workshop of Ovarian Hereditary Cancer Genetics, Imam-Khomeini Hospital, Tehran, Iran
- July 21- Aug. 18, 2011 Workshop of Photoshop (4 session), Isfahan University of Medical Sciences
- April 27-28, 2004 Workshop of prevention of Genetic diseases, Welfare Organization, Tehran, Iran
- Jul. 5, 2007 Workshop of Reference Management, Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- May 17, 2007 Workshop of Scientific Writing (Advanced), Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- May 3, 2007 Workshop of Scientific Writing (Elementary), Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- Sep. 20, 2007 Workshop of Searching (Advanced), Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- May 3, 2007 Workshop of Searching (Elementary), Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- Aug. 18, 2007 Workshop of Searching (Intermediate), Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- Jul. 19 & 26, 2007 Workshop of SPSS, Tehran University of Medical Sciences, Poursina St., Tehran,Iran
- Jun. 14, 2007 Workshop of Systematic Searching, Tehran University of Medical Sciences, Poursina St., Tehran,Iran
COMPUTER COURSES
1. General Courses: Windows: 30 h., Internet: 30 h.
2. Special Courses (Microsoft office): Word: 26 h., Excel: 26 h., Power point: 20 h.,
Access: 26 h.
CLINICAL EXPERIENCES
About 9 years.
COLLABORATION AT OTHER PROJECTS
1. Identification and functional analysis of MGP gene variations associated with coronary artery disease.
2. Production of Stem Cell Specific Marker for Detection of Mesenshymal Stem
Cell.
3. Prevention of Mental Retardation Because of Hyperthyroidism.
4. Prevalence of the Connexin 26 Gene Mutation 35delG in non-syndromic hearing loss in Iran (unpublished)
OTHER
Workshops lecturer of Chaharmahal-Bakhtiari Heath Services (about 100 h.)