Ehsan Razmara

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 19

Top Venues

Molecular genetics & genomic medicine

European journal of clinical investigation

Annals of the New York Academy of Sciences

Journal of clinical laboratory analysis

Monash University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Monash University

Australia

PHD :: Faculty of Medicine, Nursing and Health Sciences

Publications

Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation 53 (4) (2023)
Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation 53 (4) (2023)
Fatemeh Bitarafan, Ehsan Razmara, Ehsan Jafarinia, Navid Almadani, Masoud Garshasbi
A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. European journal of clinical investigation (2022)
Mohadeseh Mirzaee Godarzee, Bashdar Mahmud Hussen, Ehsan Razmara, Benyamin Hakak-Zargar, Fatemeh Mohajerani, Hamed Dabiri, Mohammed Fatih Rasul, Mohammad Hossein Ghazimoradi, Sadegh Babashah, Majid Sadeghizadeh
Strategies to overcome the side effects of chimeric antigen receptor T cell therapy. Annals of the New York Academy of Sciences 1510 (1) (2022)
Maryam Jalessi, Mohammad Saeed Gholami, Ehsan Razmara, Sajad Hassanzadeh, Alireza Sadeghipour, Amin Jahanbakhshi, Alireza Tabibkhooei, Eshagh Bahrami, Masoumeh Falah
Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T-ARMS-PCR assay. Journal of clinical laboratory analysis (2021)
Mohammad Farhadi, Ehsan Razmara, Maryam Balali, Yeganeh Hajabbas Farshchi, Masoumeh Falah
How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us. Journal of cellular and molecular medicine (2021)
Amirreza Bitaraf, Ehsan Razmara, Babak Bakhshinejad, Hassan Yousefi, Mousa Vatanmakanian, Masoud Garshasbi, William Chi Shing Cho, Sadegh Babashah
The oncogenic and tumor suppressive roles of RNA-binding proteins in human cancers. Journal of cellular physiology 236 (9) (2021)
Ehsan Razmara, Amirreza Bitaraf, Behnaz Karimi, Sadegh Babashah
Functions of the SNAI family in chondrocyte-to-osteocyte development. Annals of the New York Academy of Sciences 1503 (1) (2021)
Mojdeh Mahmoudian, Ehsan Razmara, Bashdar Mahmud Hussen, Mandana Simiyari, Nazanin Lotfizadeh, Hoda Motaghed, Arefeh Khazraei Monfared, Maryam Montazeri, Sadegh Babashah
Identification of a six-microRNA signature as a potential diagnostic biomarker in breast cancer tissues. Journal of clinical laboratory analysis 35 (11) (2021)
Fatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, Mohammad Keramatipour, Alireza Kalhor, Ehsan Jafarinia, Masoud Garshasbi
Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome. Molecular genetics & genomic medicine 8 (8) (2020)
Ehsan Razmara, Homeyra Azimi, Amirreza Bitaraf, Mohammad Ali Daneshmand, Mohammad Galehdari, Maryam Dokhanchi, Elika Esmaeilzadeh-Gharehdaghi, Masoud Garshasbi
Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis. Molecular genetics & genomic medicine 8 (3) (2020)
Erfan Heidari, Ehsan Razmara, Sareh Hosseinpour, Ali Reza Tavasoli, Masoud Garshasbi
Homozygous in-frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family. Annals of human genetics 84 (4) (2020)
Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi
Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss. Molecular genetics & genomic medicine 8 (12) (2020)
Zahra Farajollahi, Ehsan Razmara, Erfan Heidari, Ehsan Jafarinia, Masoud Garshasbi
A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients. The journal of gene medicine 22 (11) (2020)
Afrooz Sepahvand, Ehsan Razmara, Fatemeh Bitarafan, Mohammad Galehdari, Ali Reza Tavasoli, Navid Almadani, Masoud Garshasbi
A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family. Molecular genetics & genomic medicine 8 (10) (2020)
Elika Esmaeilzadeh-Gharehdaghi, Ehsan Razmara, Amirreza Bitaraf, Ahmadreza Jamshidi, Mahdi Mahmoudi, Masoud Garshasbi
Functional Analysis of RELN S2486G Mutation and its Contribution to Pathogenesis of Ankylosing Spondylitis. Archives of Iranian medicine 23 (10) (2020)
Fatemeh Tahmouresi, Ehsan Razmara, Katayoon Pakravan, Majid Mossahebi-Mohammadi, Fatemeh Rouhollah, Maryam Montazeri, Alireza Sarrafzadeh, Hossein Fahimi, Sadegh Babashah
Upregulation of the long noncoding RNAs DSCAM-AS1 and MANCR is a potential diagnostic marker for breast carcinoma. Biotechnology and applied biochemistry (2020)
Masoud Garshasbi, Mahdi Mahmoudi, Ehsan Razmara, Mahdi Vojdanian, Saeed Aslani, Elham Farhadi, Lars Riff Jensen, Seyed Masoud Arzaghi, Shiva Poursani, Amirreza Bitaraf, Milad Eidi, Elika Esmaeilzadeh Gharehdaghi, Andreas Walter Kuss, Ahmadreza Jamshidi
Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS. European journal of human genetics : EJHG 28 (6) (2020)
Ehsan Razmara, Amirreza Bitaraf, Hassan Yousefi, Tina H Nguyen, Masoud Garshasbi, William Chi Shing Cho, Sadegh Babashah
Non-Coding RNAs in Cartilage Development: An Updated Review. International journal of molecular sciences 20 (18) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ehsan Razmara