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Journal of Cardiovascular and Thoracic Research|January 20, 2022
In silico analysis of GATA4 variants demonstrates main contribution to congenital heart diseaseShiva Abbasi, Neda Mohsen-Pour, Niloofar Naderi, et al.
European Journal of Medical Research|December 10, 2022
A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defectsAvisa Tabib, Taravat Talebi, Serwa Ghasemi, et al.
Current Molecular Medicine|August 9, 2021
Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical ReportsNeda Mohsen-Pour, Taravat Talebi, Niloofar Naderi, et al.
BMC Cardiovascular Disorders|January 3, 2024
A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy featuresAmir Ghaffari Jolfayi, Niloofar Naderi, Serwa Ghasemi, et al.
Journal of Cellular and Molecular Medicine|July 21, 2026
From Genotype to Phenotype: Investigating SLC22A5 Variants and Their Significance in Carnitine Deficiency: A Systematic Review StudyAmir Ghaffari Jolfayi, Mahdieh Soveizi, Niloofar Naderi, et al.
Archives of Virology|December 22, 2016
Merkel cell polyomavirus IgG antibody levels are associated with progression to AIDS among HIV-infected individualsRouhollah Vahabpour, Maryam Nasimi, Niloofar Naderi, et al.
Journal of Cardiovascular and Thoracic Research|November 29, 2023
Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian populationGolnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, et al.
Journal of Cellular and Molecular Medicine|May 15, 2023
Role of non-coding variants in cardiovascular diseaseKatayoun Heshmatzad, Niloofar Naderi, Majid Maleki, et al.
Cardiology in the Young|November 16, 2021
Whole-exome sequencing identified compound heterozygous variants in the TTN gene causing Salih myopathy with dilated cardiomyopathy in an Iranian familyMohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, et al.
Laboratory Medicine|May 29, 2023
Whole-exome sequencing reveals a likely pathogenic LMNA variant causing hypertrophic cardiomyopathyMohammad Mahdavi, Neda Mohsen-Pour, Majid Maleki, et al.
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