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Samira Kalayinia

Showing results (11-20 of 53) with videos related to

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BMC Medical Genomics|November 7, 2022
A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencingSerwa Ghasemi, Mohammad Mahdavi, Majid Maleki, et al.
BMC Medical Genomics|December 22, 2023
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathySerwa Ghasemi, Mohammad Mahdavi, Majid Maleki, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 6, 2020
MicroRNAs: roles in cardiovascular development and diseaseSamira Kalayinia, Fateme Arjmand, Majid Maleki, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|August 3, 2025
Pharmacogenomics in cardiac therapy: Personalizing treatment for heart healthNiloofar Naderi, Amir Ghaffari Jolfayi, Amir Azimi, et al.
BMC Medical Genomics|May 7, 2024
Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencingErfan Kohansal, Niloofar Naderi, Amir Farjam Fazelifar, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 8, 2021
The association between in vitro fertilization and intracytoplasmic sperm injection treatment and the risk of congenital heart defectsTaravat Talebi, Neda Mohsen-Pour, Mahshid Hesami, et al.
BMC Medical Genomics|October 27, 2023
Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac deathAmir Azimi, Maryam Pourirahim, Golnaz Houshmand, et al.
BMC Cardiovascular Disorders|August 6, 2022
Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathySamira Kalayinia, Mohammad Mahdavi, Golnaz Houshmand, et al.
Cardiology Research and Practice|November 19, 2025
Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT SyndromeMansoor Namazi, Niloofar Naderi, Amir Askarinejad, et al.
Genetics Research|December 11, 2023
Genetic Variations in the Human Angiotensin-ConvertingEnzyme 2 and Susceptibility to Coronavirus Disease-19Taravat Talebi, Tannaz Masoumi, Katayoun Heshmatzad, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
BMC Medical Genomics|November 7, 2022
A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencingSerwa Ghasemi, Mohammad Mahdavi, Majid Maleki, et al.
BMC Medical Genomics|December 22, 2023
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathySerwa Ghasemi, Mohammad Mahdavi, Majid Maleki, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 6, 2020
MicroRNAs: roles in cardiovascular development and diseaseSamira Kalayinia, Fateme Arjmand, Majid Maleki, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|August 3, 2025
Pharmacogenomics in cardiac therapy: Personalizing treatment for heart healthNiloofar Naderi, Amir Ghaffari Jolfayi, Amir Azimi, et al.
BMC Medical Genomics|May 7, 2024
Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencingErfan Kohansal, Niloofar Naderi, Amir Farjam Fazelifar, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|July 8, 2021
The association between in vitro fertilization and intracytoplasmic sperm injection treatment and the risk of congenital heart defectsTaravat Talebi, Neda Mohsen-Pour, Mahshid Hesami, et al.
BMC Medical Genomics|October 27, 2023
Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac deathAmir Azimi, Maryam Pourirahim, Golnaz Houshmand, et al.
BMC Cardiovascular Disorders|August 6, 2022
Novel homozygous stop-gain pathogenic variant of PPP1R13L gene leads to arrhythmogenic cardiomyopathySamira Kalayinia, Mohammad Mahdavi, Golnaz Houshmand, et al.
Cardiology Research and Practice|November 19, 2025
Unlocking the Secrets of Andersen-Tawil Syndrome: The Role of Next-Generation Sequencing in a Family With Long QT SyndromeMansoor Namazi, Niloofar Naderi, Amir Askarinejad, et al.
Genetics Research|December 11, 2023
Genetic Variations in the Human Angiotensin-ConvertingEnzyme 2 and Susceptibility to Coronavirus Disease-19Taravat Talebi, Tannaz Masoumi, Katayoun Heshmatzad, et al.
Pageof 6