Bahareh Rabbani

10PUBLICATIONS
11CO-AUTHORS
Genetic immunologyEpigenetics (incl. genome methylation and epigenomics)Chemical engineering designGene expression (incl. microarray and other genome-wide approaches)Autonomic nervous system
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Publications (10)

|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.

|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

|Aug 13, 2024
Expanding the Phenotype of Congenital Glucocorticoid Deficiency: An Iranian Patient with Cholestasis due to Pathogenic Variants in the MC2R Gene.

Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi

|Jun 28, 2024
Pancreatitis as a Main Consequence of APOC2-Related Hypertriglyceridemia: The Role of Nonsense and Frameshift Variants.

Bahareh Rabbani, Mohadeseh Aghli Moghadam, Shiva Esmaeili

|Aug 20, 2021
Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome.

Bahareh Rabbani, Mohammadrafi Khorgami, Mohammad Dalili

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Frequent Collaborators

7 joint publications

Nejat Mahdieh

2 joint publications

Reza Bayat

1 joint publications

Majid Maleki

1 joint publications

Ali Rabbani