Samira Kalayinia

22PUBLICATIONS
28CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Cancer geneticsNeurology and neuromuscular diseasesNeurogeneticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (22)

|Sep 16, 2026
Potential Contribution of DES (p.Leu88Met) and MYH7 (p.Arg787His) Variants to Familial Restrictive Cardiomyopathy.

|Jul 21, 2026
From Genotype to Phenotype: Investigating SLC22A5 Variants and Their Significance in Carnitine Deficiency: A Systematic Review Study.

|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 RYR2 Gene Variant in Long QT Syndrome.

Samira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili

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Frequent Collaborators

5 joint publications

Nejat Mahdieh

3 joint publications

Majid Maleki

2 joint publications

Mohammad Dalili

1 joint publications

Shiva Abbasi