Samira Kalayinia

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 24

Top Topics

Duchenne Muscular Dystrophy

Dna Methylation

Congenital Heart Disease

Aortic Aneurysm

Top Venues

ESC heart failure

European journal of medical research

Laboratory medicine

Journal of cardiovascular and thoracic research

This page only lists publications with an associated author ORCID identifier.

Publications

MohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, Golnaz Houshmand, Mohamad Mahdavi, Majid Maleki, Samira Kalayinia
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness. ESC heart failure 11 (3) (2024)
Parham Sadeghipour, Marzieh Valuian, Serwa Ghasemi, Farnaz Rafiee, Maryam Pourirahim, Mehran Mahmoodian, Majid Maleki, Samira Kalayinia
Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysm. Laboratory medicine 55 (4) (2024)
MohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, Golnaz Houshmand, Mohamad Mahdavi, Majid Maleki, Samira Kalayinia
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness. ESC heart failure 11 (3) (2024)
MohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, Golnaz Houshmand, Mohamad Mahdavi, Majid Maleki, Samira Kalayinia
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness. ESC heart failure 11 (3) (2024)
MohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, Golnaz Houshmand, Mohamad Mahdavi, Majid Maleki, Samira Kalayinia
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness. ESC heart failure (2024)
MohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, Golnaz Houshmand, Mohamad Mahdavi, Majid Maleki, Samira Kalayinia
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weakness. ESC heart failure 11 (3) (2024)
Amir Azimi, Mahdieh Soveizi, Alireza Salmanipour, Mohammadhossein Mozafarybazargany, Amir Ghaffari Jolfayi, Majid Maleki, Samira Kalayinia
Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac death. ESC heart failure (2024)
Golnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, Niloofar Naderi, Maryam Pourirahim, Katayoun Heshmatzad, Majid Maleki, Samira Kalayinia
Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population. Journal of cardiovascular and thoracic research 15 (3) (2023)
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, Serwa Ghasemi, Avisa Tabib, Golnaz Houshmand, Niloofar Naderi, Tannaz Masoumi, Hamidreza Pouraliakbar, Samira Kalayinia
Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathy. Laboratory medicine (2023)
Parham Sadeghipour, Marzieh Valuian, Serwa Ghasemi, Farnaz Rafiee, Maryam Pourirahim, Mehran Mahmoodian, Majid Maleki, Samira Kalayinia
Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysm. Laboratory medicine (2023)
Taravat Talebi, Tannaz Masoumi, Katayoun Heshmatzad, Mahshid Hesami, Majid Maleki, Samira Kalayinia
Genetic Variations in the Human Angiotensin-ConvertingEnzyme 2 and Susceptibility to Coronavirus Disease-19. Genetics research 2023 (2023)
Amir Farjam Fazelifar, Maryam Pourirahim, Tannaz Masoumi, Alireza Biglari, Majid Maleki, Samira Kalayinia
Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole-exome sequencing. Journal of arrhythmia 39 (3) (2023)
Katayoun Heshmatzad, Niloofar Naderi, Majid Maleki, Shiva Abbasi, Serwa Ghasemi, Nooshin Ashrafi, Amir Farjam Fazelifar, Mohammad Mahdavi, Samira Kalayinia
Role of non-coding variants in cardiovascular disease. Journal of cellular and molecular medicine (2023)
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European journal of medical research 27 (1) (2022)
Neda Mohsen-Pour, Niloofar Naderi, Serwa Ghasemi, Mahshid Hesami, Majid Maleki, Samira Kalayinia
Whole-Exome Sequencing Revealed a Pathogenic Nonsense Variant in the SLC19A2 Gene in an Iranian Family with Thiamine-Responsive Megaloblastic Anemia. Laboratory medicine 53 (6) (2022)
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European journal of medical research 27 (1) (2022)
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European journal of medical research 27 (1) (2022)
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European journal of medical research 27 (1) (2022)
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects. European journal of medical research 27 (1) (2022)
Samira Kalayinia, Saeed Talebi, Mohammad Miryounesi, Peymaneh Sarkhail, Nejat Mahdieh
An Iranian Congenital Adrenal Hypoplasia Patient with Elevated Testosterone in Infancy due to a Novel Pathogenic Frameshift Variant in NR0B1 . International journal of endocrinology 2021 (2021)
Shiva Abbasi, Neda Mohsen-Pour, Niloofar Naderi, Shahin Rahimi, Majid Maleki, Samira Kalayinia
In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease. Journal of cardiovascular and thoracic research 13 (4) (2021)
Mohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, Mahshid Hesami, Niloofar Naderi, Golnaz Houshmand, Hamid R Rasouli Jazi, Hossein Shahzadi, Samira Kalayinia
Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian family. Cardiology in the young (2021)
Samira Kalayinia, Majid Maleki, Mohammad Mahdavi, Nejat Mahdieh
A novel de novo dominant mutation of NOTCH1 gene in an Iranian family with non-syndromic congenital heart disease. Journal of clinical laboratory analysis 34 (4) (2019)
Samira Kalayinia, Majid Maleki, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Hassan Ahangar, Alireza Biglari, Tina Shahani, Nejat Mahdieh
GATA4 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 GATA4 mutation in a family with autosomal dominant congenital heart disease. Journal of clinical laboratory analysis 33 (7) (2019)