Majid Kheirollahi
8PUBLICATIONS
21CO-AUTHORS

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Publications (8)
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|Dec 29, 2025
A Truncating Variant in the ERCC6 Gene With Three Different Phenotypes: Significant Effects of Modifier Genes.Mehdi Khorrami, Erfan Khorram, Mohammad Amin Tabatabaiefar
|Jan 18, 2023
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature.Erfan Khorram, Mohammad Amin Tabatabaiefar, Omid Yaghini
|Oct 22, 2022
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.Seyed Peyman Mirghaderi, Maryam Salimi, Majid Kheirollahi
|Mar 26, 2021
Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature.Mehdi Khorrami, Mohammad Amin Tabatabaiefar, Erfan Khorram
|Mar 09, 2021
Identification of a Missense Variant in the EIF2B3 Gene Causing Vanishing White Matter Disease with Antenatal-Onset but Mild Symptoms and Long-Term Survival.Mehdi Khorrami, Erfan Khorram, Omid Yaghini
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Frequent Collaborators
3 joint publications
Mehdi Khorrami
3 joint publications
Erfan Khorram
3 joint publications
Omid Yaghini
2 joint publications
Mojgan Rezaei
2 joint publications
Arash Hejazifar
2 joint publications
Omid Iravani
2 joint publications
Vida Yazdani
2 joint publications
Maryam Riahinezhad
2 joint publications
Mohammad Amin Tabatabaiefar
1 joint publications
Maryam Mirsafaie