Pegah Ghandil

6PUBLICATIONS
10CO-AUTHORS
Immunogenetics (incl. genetic immunology)Epigenetics (incl. genome methylation and epigenomics)Gene mappingMedical mycologyNeurology and neuromuscular diseases
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Publications (6)

|Mar 10, 2025
Association study of <i>interleukin-10</i> and <i>P53</i> polymorphisms and their influence on Iranian women with recurrent abortion.

Nastaran Rezaee Bakhtiar, Kobra Shojaei, Fariba Sharifnia

|Dec 13, 2021
Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management.

Fatemeh Davoudi, Majid Aminzadeh, Hajiye Bibi Shahbazian

|Oct 29, 2020
Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men.

Mahzad Nasirshalal, Maryam Tahmasebi-Birgani, Mohammadreza Dadfar

|Oct 24, 2020
Identification of Cytochrome b-245, beta-chain gene mutations, and clinical presentations in Iranian patients with X-linked chronic granulomatous disease.

Atefeh Heydari, Farhad Abolnezhadian, Mahnaz Sadeghi-Shabestari

|Oct 20, 2020
A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4.

Malihe Mohamadian, Pegah Ghandil, Mohsen Naseri

|Sep 01, 2020
The first report of two homozygous sequence variants in FKRP and SELENON genes associated with syndromic congenital muscular dystrophy in Iran: Further expansion of the clinical phenotypes.

Malihe Mohamadian, Mohsen Naseri, Pegah Ghandil

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Frequent Collaborators

2 joint publications

Malihe Mohamadian

2 joint publications

Mohsen Naseri

1 joint publications

Mahzad Nasirshalal

1 joint publications

Maryam Tahmasebi-Birgani