Samira Kalayinia

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 et al. · Journal of Clinical Laboratory Analysis · 2019 · 24 citations · Full text

Prediction of Parkinson’s disease pathogenic variants using hybrid Machine learning systems and radiomic features

Ghasem Hajianfar, Samira Kalayinia, Mahdi Hosseinzadeh et al. · Physica Medica · 2023 · 21 citations · Full text

Development of a patients’ satisfaction analysis system using machine learning and lexicon-based methods

Shiva Khaleghparast, Majid Maleki, Ghasem Hajianfar et al. · BMC Health Services Research · 2023 · 18 citations · Full text

<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 et al. · Journal of Clinical Laboratory Analysis · 2019 · 16 citations · Full text

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 · 2019 · 13 citations · Full text