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Samira Kalayinia

20PUBLICATIONS
23CO-AUTHORS
Neurology and neuromuscular diseasesCancer geneticsNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)
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Journal

Publications (20)

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

|Jan 02, 2026
Exome Sequencing Identifies Variants in MLH1 and ERBB2 as Potential Cancer-Predisposing Factors in Familial Early-Onset Colorectal Cancer.

Behnaz Bagheri, Neda Mohsen-Pour, Najmeh Salehi

|Nov 19, 2025
Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT Syndrome.

Mansoor Namazi, Niloofar Naderi, Amir Askarinejad

|Sep 05, 2025
Beyond the Beat, Next-Generation Sequencing Discovery of Novel <i>RYR2</i> Gene Variant in Long QT Syndrome.

Samira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili

|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

|Jun 14, 2024
Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac death.

Amir Azimi, Mahdieh Soveizi, Alireza Salmanipour

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Frequent Collaborators

5 joint publications

Nejat Mahdieh

2 joint publications

Mohammad Dalili

2 joint publications

Majid Maleki

1 joint publications

Shiva Abbasi

1 joint publications

Golnaz Houshmand

1 joint publications

Mohammad Javad Alemzadeh-Ansari

1 joint publications

Saeideh Mazloumzadeh

1 joint publications

Taravat Talebi

1 joint publications

Amirreza Taherkhani

1 joint publications

Katayoun Heshmatzad

Frequent Collaborators

5 joint publications

Nejat Mahdieh

2 joint publications

Mohammad Dalili

2 joint publications

Majid Maleki

1 joint publications

Shiva Abbasi