Education 

 Ph.D. in Medical genetics, Tehran University of Medical Sciences, Tehran, Iran, 2021

Thesis title: Genetic analysis of 10 pedigrees with dilated cardiomyopathy by whole exome sequencing and molecular validation of findings in pedigree scale. July.2021

 M.Sc. in Cell & Molecular Biology, Human genetics research department, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran, 2012

Thesis title: Assessing gene expression of the Th1/Th2-associated cytokines and transcription factors in patients with Graves’ disease. Sep.2012

B.Sc. in biology, Tarbiat Moallem University, Sabzevar, Iran, 2008 

Journal Publications

 Eshaghkhani Y, Sanati MH, Nakhjavani M, Safari R, Khajavi A, Ataei M, Jadali Z. Disturbed Th1 and Th2 balance in patients with Graves' disease. Minerva endocrinologica. 2015 Sep 22;41(1):28-36

Saberi M, Golchehre Z, Karamzade A, Entezam M, Eshaghkhani Y, Alavinejad E, Jafari HK, Keramatipour M. CRB1-related leber congenital amaurosis: reporting novel pathogenic variants and a brief review on mutations spectrum. Iranian biomedical journal. 2019 Sep;23(5):362

 Ghadami S and Eshaghkhani Y. ARX: A Small Gene with a Crucial Role in X-Linked Intellectual Disability. Journal of Genetics and Cell Biology. 2020 April 3(1): 135-139

Hesami S, Sayar M, Sayyar F, Eshaghkhani Y, Pirhoushiaran M, Erfan MB, Abdollahzadeh R, Azarnezhad A. Expression and Clinicopathological Significances of lncRNAs: Could ARA and ZEB2NAT be the Potential Breast Cancer-Related Biomarkers? Archives of Medical Research. 2020 Nov 1;51(8):851-9. 

Mehrabi S, Pirhoushiaran M, Eshaghkhani Y, Teimourzadeh Baboli A, Mahmoudi A, Zarifian Yeganeh R, Abdollahzadeh R, Sadeghi Rad H, Mokhtari V, Mokhtarinejad M, Shakoori Farahani A. Molecular Analysis of EGFR and PIK3CA Genetic Mutations in Iranian Patients with Head and Neck Squamous Cell Carcinoma. International Journal of Pharmaceutical and Phytopharmacological Research (eIJPPR). 2020 December 10(6):222-229

Taghizadeh M, Derakhshan SM, Khaniani MS, Eshaghkhani Y, Golchehre Z, Taheri SR, Nourmohammadi P, Keramatipour M. Identifi cation of multi-exon deletion in the COL7A1 gene underlying dystrophic epidermolysis bullosa by whole-exome sequencing. Our Dermatology Online/Nasza Dermatologia Online. 2021 Oct 1;12(4).

 Eshaghkhani Y, Mohamadifar A, Asadollahi M, Taghizadeh M, Karamzade A, Saberi M, Nourmohammadi P, Golchehre Z, Amin A, Keramatipour M. Whole-Exome Sequencing Identified a Novel Variant (C. 405_422+ 39del) in DSP Gene in an Iranian Pedigree with Familial Dilated Cardiomyopathy. Reports of Biochemistry & Molecular Biology. 2021 Jul;10(2):280.

 Karamzade A, Babaei M, Saberi M, Golchin N, Khalil Nejad Sani Banaei A, Eshaghkhani Y, Golchehre Z, Keramatipour M. Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum. Molecular biology reports. 2021 Jun;48(6):5339-45.

 Nourmohammadi P, Asadollahi M, Karamzade A, Eshaghkhani Y, Babaei M, Golchehre Z, Taheri Sr, Hasani S, Taghizadeh M and Keramatipour M. A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature. Journal of genetics. 2023. Waiting for publish.

 Persian rewiew articles

 Noori-Daloii MR, Eshaghkhani Y. lncRNAs: significance and function mechanisms. Medical Sciences Journal of Islamic Azad University. 2015;25(2).

 Noori-Daloii MR, Eshaghkhani Y. lncRNAs roles in cancer occurrence. Medical Science Journal of Islamic Azad Univesity-Tehran Medical Branch. 2015 Sep 10;25(3):163-82.

 Noori-Daloii MR, Eshaghkhani Y. LncRNAs: new approach in cancer therapy. Medical Science Journal of Islamic Azad Univesity-Tehran Medical Branch. 2015 Dec 10;25(4):249-56.

 Books

 Compilation (In Persian): Cell signaling processes and crossover talk pathways in induction of breast cancer and treatment of disease by intervention in these pathways. 2014. Tehran university-jahad daneshgahi publication

Translation (English to persian): Thompson & Thompson Genetics in Medicine, 8e 8th Edition. 2016. Ebne-sina publication

work experiences

 National Institute of Genetic Engineering and Biotechnology

 Farabi hospital

 Imam Khomeini hospital

 Watson genetics laboratory Tehranlab pathobiology and genetics laborator