Mohammad Miryounesi

14PUBLICATIONS
123CO-AUTHORS
Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Molecular targets
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Publications (14)

|Apr 19, 2025
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet-Biedl Syndrome.

Mohammad Reza Seyedtaghia, Mohsen Habibi, Farzad Hashemi-Gorji

|Jan 21, 2025
Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype-Genotype Correlations From 175 Previous Cases and Identification of a Novel Variant.

Mohammad-Reza Ghasemi, Zahra Esmaeilizadeh, Sahand Tehrani Fateh

|Nov 20, 2024
Novel TECPR2 variant in two cases of hereditary sensory and autonomic neuropathy type 9: insights from genetic characterization and comprehensive literature review.

Aysan Moeinafshar, Sahand Tehrani Fateh, Farzad Hashemi-Gorji

|Nov 18, 2024
A Case Report of Parental Germline Mosaicism in the PCDH19 Gene of Two Iranian Siblings.

Sahar Alijanpour, Soudeh Ghafouri-Fard, Seyed Hassan Tonekaboni

|Apr 15, 2024
Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort.

Parinaz Moghimi, Farzad Hashemi-Gorji, Sanaz Jamshidi

|Feb 29, 2024
The first Iranian patient with You-Hoover-Fong syndrome and a review of the literature on 27 cases: expanding the genotypic and phenotypic spectrum.

Nima Shokrollahi, Sahand Tehrani Fateh, Mohammad Nouri

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Frequent Collaborators

10 joint publications

Mohammad-Reza Ghasemi

10 joint publications

Hossein Sadeghi

9 joint publications

Sahand Tehrani-Fateh

8 joint publications

Reza Mirfakhraie