Nejat Mahdieh

25PUBLICATIONS
19CO-AUTHORS
Genetic immunologyNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Anthropological geneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (25)

|Jul 30, 2026
Unveiling New Insights: Reinterpreting DES Mutation, p.Arg383His, Through a Study of an Iranian Family With Isolated Hypertrophic Cardiomyopathy, Implication for Phenotype-Genotype Correlation Analysis.

|Jun 08, 2026
MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia.

|Mar 09, 2026
A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.

Maryam Arefzadeh, Bahareh Rabbani, Saeideh Abdolahpour

|Nov 11, 2025
An Intronic Variant in CDKN1C Gene Causing IMAGe Syndrome in an Iranian Girl.

Setila Dalili, Seyyedeh Azade Hoseini Nouri, Ameneh Sharifi

|Jun 10, 2025
Association of Obstructive Sleep Apnea Syndrome with Leptin Receptor Gene Q223R and K109R Single Nucleotide Polymorphisms in the Iranian Kurdish Population.

Ali Alizadeh Severi, Sharareh Rasouli, Mohammad Abdolsamadi

|Feb 11, 2025
Reevaluation of the Impact of the Novel Likely Pathogenic Variant c.1286_1288delAGA in the ATP8A2 Gene: A 7-Year Follow-Up With Clinical, Genetic, and ACMG Insights in an Iranian Family.

Samira Kalayinia, Hamed Hesami, Reza Shervin Badv

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Frequent Collaborators

7 joint publications

Bahareh Rabbani

5 joint publications

Samira Kalayinia

4 joint publications

Bahman Akbari

3 joint publications

Pouria Mohammadi