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Bahareh Rabbani

9PUBLICATIONS

10CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyChemical engineering designGene expression (incl. microarray and other genome-wide approaches)Autonomic nervous system

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Publications (9)

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|Mar 09, 2026

A Novel Homozygous <i>CUL7</i> 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 <i>MC2R</i> Gene.

Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi

|Jun 28, 2024

Pancreatitis as a Main Consequence of <i>APOC2</i>-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

|Oct 22, 2020

A novel pathogenic variant of <i>SRD5A2</i> in an Iranian psuedohermaphrodite male.

Setilla Dalili, Bahareh Rabbani, Afagh Hassanzadeh Rad

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Frequent Collaborators

6 joint publications

Nejat Mahdieh

2 joint publications

Reza Bayat

1 joint publications

Majid Maleki

1 joint publications

Ali Rabbani

1 joint publications

Shiva Esmaeili

1 joint publications

Bahman Akbari

1 joint publications

Shohreh Maleknejad

1 joint publications

Setila Dalili

1 joint publications

Ameneh Sharifi

1 joint publications

Afagh Hassanzadeh Rad

Frequent Collaborators

6 joint publications

Nejat Mahdieh

2 joint publications

Reza Bayat

1 joint publications

Majid Maleki

1 joint publications

Ali Rabbani

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