Concepedia
Author
Samira Kalayinia
Also Known As
62
Publications
503
Citations
11
H-Index
0
Concepts
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7
114
A novel de novo dominant mutation of <i>NOTCH1</i> gene in an Iranian family with non‐syndromic congenital heart disease
Samira Kalayinia, Majid Maleki, Mohammad Mahdavi, +1
Journal of Clinical Laboratory Analysis
2019
24
Prediction of Parkinson’s disease pathogenic variants using hybrid Machine learning systems and radiomic features
Ghasem Hajianfar, Samira Kalayinia, Mahdi Hosseinzadeh, +5
Physica Medica
2023
21
Development of a patients’ satisfaction analysis system using machine learning and lexicon-based methods
Shiva Khaleghparast, Majid Maleki, Ghasem Hajianfar, +9
BMC Health Services Research
18
<i>GATA4</i> screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous <i>GATA4</i> mutation in a family with autosomal dominant congenital heart disease
Samira Kalayinia, Majid Maleki, Hassan Rokni‐Zadeh, +5
16
A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease
Samira Kalayinia, Serwa Ghasemi, Nejat Mahdieh
Journal of Cardiovascular and Thoracic Research
13
Association between the atrial natriuretic peptide rs5065 gene polymorphism and the presence and severity of coronary artery disease in an Iranian population
Shayan Ziaee, Samira Kalayinia, Mohammad Ali Boroumand, +4
Coronary Artery Disease
2014
Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation
Mahshid Malakootian, Masoumeh Jalilian, Samira Kalayinia, +3
BMC Cardiovascular Disorders
2022
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