Mehdi Khorrami
5PUBLICATIONS
18CO-AUTHORS
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Publications (5)
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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
|Apr 08, 2023
Developmental and epileptic encephalopathy 89: A novel bi-allelic variant, molecular dynamics simulation, and a comprehensive clinical and molecular profile.Erfan Khorram, Masoomeh Amini, Mehdi Khorrami
|Aug 01, 2022
Interdependency of NINJ2 gene expression and polymorphism with susceptibility and response to interferon beta in patients with multiple sclerosis.Mehdi Khorrami, Maryam Saneipour, Abbas Moridnia
|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
Erfan Khorram
3 joint publications
Omid Yaghini
3 joint publications
Majid Kheirollahi
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 Saneipour
