مهری خاتمی

سمتهای علمی و اجرایی در دانشگاهها و مراکز علمی کشور

عضو هیات علمی دانشگاه یزد

سمتهای علمی و اجرایی در کنفرانس ها و نشستهای معتبر ایران

دبیر علمی کنفرانس بین المللی ژنتیک و ژنومیکس انسانی(1400)

مقالات بین المللی خارج از کشور

"Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis", Maad Rayan Publishing Company, (2020), Vol 12, No 3: 221-228
"Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease", Springer Science and Business Media LLC, (2020), Vol 191, No 3: 1326-1339
"Designing and Validation of One-Step T-ARMS-PCR for Genotyping the eNOS rs1799983 SNP", Armenian Green Publishing Co., (2017), Vol 15, No 3: 208-212
"Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects", Maad Rayan Publishing Company, (2018), Vol 10, No 1: 41-45
"Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease", Termedia Sp. z.o.o., (2016), Vol 1, No : 9-15
"Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis", CASRP: Center of Advanced Scientific Research and Publications, (2017), Vol 8, No 4: 279-284
"Relationship of the MTHFD1 (rs2236225), eNOS (rs1799983), CBS (rs2850144) and ACE (rs4343) gene polymorphisms in a population of Iranian pediatric patients with congenital heart defects", Wiley, (2017), Vol 33, No 9: 442-448
"Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients", Springer Science and Business Media LLC, (2019), Vol 190, No 3: 896-906
"Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome", VM Media SP. zo.o VM Group SK, (2018), Vol 25, No 1: 113-119
"The association of renin–angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss", Informa UK Limited, (2017), Vol 22, No 3: 164-170
"Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)", Wiley, (2021), Vol 35, No 5:
"Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome", VM Media SP. zo.o VM Group SK, (2018), Vol 25, No 1: 113-119
"Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease", MDPI AG, (2018), Vol 54, No 3: 46
"A novel heteroplasmic mutation in mitochondrial tRNAArg gene associated with non-dystrophic myotonias", Springer Science and Business Media LLC, (2018), Vol 120, No 3: 573-580
"Upregulation of miR-222 in both Helicobacter pylori-infected and noninfected gastric cancer patients", Springer Science and Business Media LLC, (2016), Vol 95, No 4: 991-995
"Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism", Walter de Gruyter GmbH, (2017), Vol 30, No 8:
"Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients", Medknow, (2015), Vol 5, No 1:
"A novel heteroplasmic mutation in mitochondrial tRNAArg gene associated with non-dystrophic myotonias", Springer Science and Business Media LLC, (2018), Vol 120, No 3: 573-580
"Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients", Springer Science and Business Media LLC, (2008), Vol 29, No 6: 489-493
"Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?", Elsevier BV, (2010), Vol 19, No 2: e21-e27
"A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia", Springer Science and Business Media LLC, (2008), Vol 29, No 2: 225-233
"Complex I and ATP Content Deficiency in Lymphocytes from Friedreich's Ataxia", Cambridge University Press (CUP), (2009), Vol 36, No 1: 26-31
"A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia", Springer Science and Business Media LLC, (2008), Vol 29, No 2: 225-233
"Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients", Springer Science and Business Media LLC, (2008), Vol 29, No 6: 489-493
"Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?", Elsevier BV, (2010), Vol 19, No 2: e21-e27
"Heterobimetallic PtII -AuI Complexes Comprising Unsymmetrical 1,1-Bis(diphenylphosphanyl)methane Bridges: Synthesis, Photophysical, and Cytotoxic Studies", Wiley, (2019), Vol 2019, No 10: 1360-1373
"The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study", Knowledge E, (2019), Vol , No :

مقالات کنفرانسهای داخلی

مقالات ژورنالهای تخصصی داخلی

خانم دکتر مهری خاتمی

Dr. Mehri Khatami