SK
Samira Kalayinia
Research areas: Biochemistry, Genetics and Molecular Biology · Genetics · Genomics and Rare Diseases · Cardiac electrophysiology and arrhythmias · Cardiomyopathy and Myosin Studies
0000-0002-3499-044X
About
PhD in Molecular Medicine
Cardigenetic Research Center, Rajaie Cardiovascular Medical and Research Center
Employment
Employment history is unavailable.
Education
Education history is unavailable.
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Publications (41)
- From Genomics to Precision Cardiology: A Comprehensive Review of Clinical Applications and Challenges in Cardiovascular Diseases Save
- Exome Sequencing Identifies Variants in MLH1 and ERBB2 as Potential Cancer‐Predisposing Factors in Familial Early‐Onset Colorectal Cancer Save
- From Genotype to Phenotype: Investigating SLC22A5 Variants and Their Significance in Carnitine Deficiency: A Systematic Review Study Save
- MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia Save
- Potential Contribution of DES (p.Leu88Met) and MYH7 (p.Arg787His) Variants to Familial Restrictive Cardiomyopathy Save
- The Trace of c.3747_3748insGG Variation of the MYBPC3 Gene in the Family With Atrioventricular Canal Defect Save
- Pharmacogenomics in cardiac therapy: Personalizing treatment for heart health Save
- 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 Save
- Beyond the Beat, Next‐Generation Sequencing Discovery of Novel RYR2 Gene Variant in Long QT Syndrome Save
- Unlocking the Secrets of Andersen–Tawil Syndrome: The Role of Next‐Generation Sequencing in a Family With Long QT Syndrome Save
- Identification of a Novel Likely Pathogenic TPM1 Variant Linked to Hypertrophic Cardiomyopathy in a Family with Sudden Cardiac Death Save
- Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysm Save
- A Novel Likely Pathogenic Homozygous RBCK1 Variant in Dilated Cardiomyopathy with Muscle Weakness Save
- Copy number variations: The potential association genetic cause in severe cardiovascular diseases with unknown aetiology Save
- Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy Save
- Genetic Variations in the Human Angiotensin-ConvertingEnzyme 2 and Susceptibility to Coronavirus Disease-19 Save
- Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population Save
- Prediction of Parkinson’s disease pathogenic variants using hybrid Machine learning systems and radiomic features Save
- Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing Save
- Role of non‐coding variants in cardiovascular disease Save