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Majid Kheirollahi

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 10

Top Venues

Molecular genetics and genomics : MGG

Journal of orthopaedic surgery and research

Molecular biology reports

Journal of gastrointestinal cancer

Isfahan University of Medical Sciences

Tehran University of Medical Sciences (PHD)

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

Affiliation History

Isfahan University of Medical Sciences

Iran

Dr. :: Department of Genetics and Molecular Biology

Education History

Tehran University of Medical Sciences Feb 12o 2006 - Jan 17o 2011

Iran

PHD :: Genetics Department

Publications

Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini, Mehdi Khorrami, Vida Yazdani, Fatemeh Fakhr, Masoomeh Amini, Majid Kheirollahi
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature. Molecular genetics and genomics : MGG 298 (2) (2023)
Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini, Mehdi Khorrami, Vida Yazdani, Fatemeh Fakhr, Masoomeh Amini, Majid Kheirollahi
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature. Molecular genetics and genomics : MGG 298 (2) (2023)
Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini, Mehdi Khorrami, Vida Yazdani, Fatemeh Fakhr, Masoomeh Amini, Majid Kheirollahi
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature. Molecular genetics and genomics : MGG (2023)
Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini, Mehdi Khorrami, Vida Yazdani, Fatemeh Fakhr, Masoomeh Amini, Majid Kheirollahi
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature. Molecular genetics and genomics : MGG 298 (2) (2023)
Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini, Mehdi Khorrami, Vida Yazdani, Fatemeh Fakhr, Masoomeh Amini, Majid Kheirollahi
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature. Molecular genetics and genomics : MGG 298 (2) (2023)
Seyed Peyman Mirghaderi, Maryam Salimi, Majid Kheirollahi, Seyed Mohammad Javad Mortazavi, Hossein Akbari Aghdam
Anterior cruciate ligament injury and its postoperative outcomes are not associated with polymorphism in COL1A1 rs1107946 (G/T): a case-control study in the Middle East elite athletes. Journal of orthopaedic surgery and research 17 (1) (2022)
Mehdi Khorrami, Erfan Khorram, Omid Yaghini, Mojgan Rezaei, Arash Hejazifar, Omid Iravani, Vida Yazdani, Maryam Riahinezhad, Majid Kheirollahi
Identification of a Missense Variant in the EIF2B3 Gene Causing Vanishing White Matter Disease with Antenatal-Onset but Mild Symptoms and Long-Term Survival. Journal of molecular neuroscience : MN 71 (11) (2021)
Mehdi Khorrami, Mohammad Amin Tabatabaiefar, Erfan Khorram, Omid Yaghini, Mojgan Rezaei, Arash Hejazifar, Maryam Riahinezhad, Majid Kheirollahi
Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature. Journal of human genetics 66 (10) (2021)
Abbas Moridnia, Mohammad Amin Tabatabaiefar, Mehrdad Zeinalian, Mohammad Minakari, Majid Kheirollahi, Noushin Afshar Moghaddam
Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer. Journal of gastrointestinal cancer 50 (3) (2020)
Manijeh Mahdavi, Leila Koulivand, Mehdi Khorrami, Maryam Mirsafaie, Majid Kheirollahi
In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria. Molecular biology reports 45 (5) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Majid Kheirollahi