Morteza Oladnabi

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 11

Top Venues

Molecular biology reports

Journal of cellular biochemistry

Journal of ophthalmic & vision research

Journal of molecular neuroscience : MN

Golestan University of Medical Sciences and Health Services Medical School

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

Affiliation History

Golestan University of Medical Sciences and Health Services Medical School Oct 12 2015

Iran

Faculty of Advanced Medical Science Technologies :: Department of Medical Genetics

Publications

Farzaneh Motallebi, Zainab M Al Sudani, Fatemeh Vaghefi, Teymoor Khosravi, Arian Rahimzadeh, Ali Kowsari, Morteza Oladnabi
A novel biallelic 19-bp deletion in the IL10RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and literature review. Molecular biology reports 51 (1) (2024)
Abdolazim Sarli, Zainab Mohammed Al Sudani, Fatemeh Vaghefi, Farzaneh Motallebi, Teymoor Khosravi, Nahid Rezaie, Morteza Oladnabi
Second report of TEDC1-related microcephaly caused by a novel biallelic mutation in an Iranian consanguineous family. Molecular biology reports 51 (1) (2024)
Farzaneh Motallebi, Zainab M Al Sudani, Fatemeh Vaghefi, Teymoor Khosravi, Arian Rahimzadeh, Ali Kowsari, Morteza Oladnabi
A novel biallelic 19-bp deletion in the IL10RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and literature review. Molecular biology reports 51 (1) (2024)
Farzaneh Motallebi, Zainab M Al Sudani, Fatemeh Vaghefi, Teymoor Khosravi, Arian Rahimzadeh, Ali Kowsari, Morteza Oladnabi
A novel biallelic 19-bp deletion in the IL10RB gene caused infant-onset inflammatory bowel disease in a consanguineous family: a molecular docking simulation study and literature review. Molecular biology reports 51 (1) (2024)
Nahid Rezaie, Nader Mansour Samaei, Morteza Oladnabi
Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing. Molecular biology reports 51 (1) (2024)
Abdolazim Sarli, Zainab Mohammed Al Sudani, Fatemeh Vaghefi, Farzaneh Motallebi, Teymoor Khosravi, Nahid Rezaie, Morteza Oladnabi
Second report of TEDC1-related microcephaly caused by a novel biallelic mutation in an Iranian consanguineous family. Molecular biology reports 51 (1) (2024)
Karim Naghipoor, Teymoor Khosravi, Morteza Oladnabi
Whole exome sequencing identifies a novel variant in the COL12A1 gene in a family with Ullrich congenital muscular dystrophy 2. Molecular biology reports (2023)
Teymoor Khosravi, Morteza Oladnabi
The role of miRNAs and lncRNAs in neurofibromatosis type 1. Journal of cellular biochemistry (2022)
Morteza Oladnabi, Mohammad Amir Mishan, Mozhgan Rezaeikanavi, Mehryar Zargari, Rouhallah Najjar Sadeghi, Abouzar Bagheri
Correlation between ELF-PEMF exposure and Human RPE Cell Proliferation, Apoptosis and Gene Expression. Journal of ophthalmic & vision research 16 (2) (2021)
Amin Tadayoni Nia, Zahra Bazi, Ayyoob Khosravi, Morteza Oladnabi
WDR81 Gene Silencing Can Reduce Exosome Levels in Human U87-MG Glioblastoma Cells. Journal of molecular neuroscience : MN 71 (8) (2021)
Saeed Dorgaleleh, Karim Naghipoor, Ahmad Barahouie, Farzad Dastaviz, Morteza Oladnabi
Molecular and biochemical mechanisms of human iris color: A comprehensive review. Journal of cellular physiology 235 (12) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Morteza Oladnabi