Exploring the role of non-coding RNAs in atrial septal defect pathogenesis: A systematic review von AmiRsardari, Zahra, Gholipour, Akram, Khajali, Zahra, Maleki, Majid, Malakootian, Mahshid

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Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy von Pourirahim, Maryam, Houshmand, Golnaz, Abdolkarimi, Leyla, Maleki, Majid, Kalayinia, Samira

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Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy von Ghasemi, Serwa, Mahdavi, Mohammad, Maleki, Majid, Salahshourifar, Iman, Kalayinia, Samira

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Development of a patients' satisfaction analysis system using machine learning and lexicon-based methods von Khaleghparast, Shiva, Maleki, Majid, Hajianfar, Ghasem, Soumari, Esmaeil, Oveisi, Mehrdad, Golandouz, Hassan Maleki, Noohi, Feridoun, Dehaki, Maziar Gholampour, Golpira, Reza, Mazloomzadeh, Saeideh, Arabian, Maedeh, Kalayinia, Samira

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Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease von Taheri Bajgan, Elham, Zahedmehr, Ali, Shakerian, Farshad, Maleki, Majid, Bakhshandeh, Hooman, Mowla, Seyed Javad, Malakootian, Mahshid

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A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing von Ghasemi, Serwa, Mahdavi, Mohammad, Maleki, Majid, Salahshourifar, Iman, Kalayinia, Samira

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A novel stop-gain pathogenic variant in the KCNQ1 gene causing long QT syndrome 1 von Kalayinia, Samira, Dalili, Mohammad, Pourirahim, Maryam, Maleki, Majid, Mahdieh, Nejat

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Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exome sequencing von Kohansal, Erfan, Naderi, Niloofar, Fazelifar, Amir Farjam, Maleki, Majid, Kalayinia, Samira

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Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs8, in a family with sudden cardiac death von Azimi, Amir, Pourirahim, Maryam, Houshmand, Golnaz, Adimi, Sara, Maleki, Majid, Kalayinia, Samira

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A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case report von Hesami, Hamed, Ghasemi, Serwa, Houshmand, Golnaz, Nilipour, Yalda, Hesami, Mahshid, Biglari, Alireza, Nafissi, Shahriar, Maleki, Majid, Kalayinia, Samira

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Small Molecules with Big Impacts on Cardiovascular Diseases von Mirzadeh Azad, Fatemeh, Arabian, Maedeh, Maleki, Majid, Malakootian, Mahshid

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Left main and three vessels spontaneous coronary artery dissection as an incidental finding in young man with history of Hodgkin's lymphoma-a case report von Kavyani, Raheleh, Salari, Soheila, Norozi, Zeinab, Hosseini, Saeid, Abdi, Saifullah, Rai, Alireza, Maleki, Majid

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A novel stop-gain pathogenic variant in FLT4 and a nonsynonymous pathogenic variant in PTPN11 associated with congenital heart defects von Tabib, Avisa, Talebi, Taravat, Ghasemi, Serwa, Pourirahim, Maryam, Naderi, Niloofar, Maleki, Majid, Kalayinia, Samira

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A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy von Naderi, Niloofar, Mohsen-Pour, Neda, Nilipour, Yalda, Pourirahim, Maryam, Maleki, Majid, Kalayinia, Samira

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Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies von Jolfayi, Amir Ghaffari, Kohansal, Erfan, Ghasemi, Serwa, Naderi, Niloofar, Hesami, Mahshid, MozafaryBazargany, MohammadHossein, Moghadam, Maryam Hosseini, Fazelifar, Amir Farjam, Maleki, Majid, Kalayinia, Samira

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Prevention of anthracycline-induced cardiotoxicity: a systematic review and network meta-analysis von Alizadehasl, Azin, Ghadimi, Nashmil, Kaveh, Sara, Maleki, Majid, Ghavamzadeh, Ardeshir, Noohi, Feridoun, Hosseinifard, Hossein

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Deep COVID DeteCT: an international experience on COVID-19 lung detection and prognosis using chest CT von Lee, Edward H., Zheng, Jimmy, Colak, Errol, Mohammadzadeh, Maryam, Houshmand, Golnaz, Bevins, Nicholas, Kitamura, Felipe, Altinmakas, Emre, Reis, Eduardo Pontes, Kim, Jae-Kwang, Klochko, Chad, Han, Michelle, Moradian, Sadegh, Mohammadzadeh, Ali, Sharifian, Hashem, Hashemi, Hassan, Firouznia, Kavous, Ghanaati, Hossien, Gity, Masoumeh, Doğan, Hakan, Salehinejad, Hojjat, Alves, Henrique, Seekins, Jayne, Abdala, Nitamar, Atasoy, Çetin, Pouraliakbar, Hamidreza, Maleki, Majid, Wong, S. Simon, Yeom, Kristen W.

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Microvascular and structural analysis of the retina and choroid in heart failure patients with reduced ejection fraction von Khalilipur, Ehsan, Mahdizad, Zahra, Molazadeh, Negin, Faghihi, Hooshang, Naderi, Nasim, Mehrabi Bahar, Mohammadreza, Firouzi, Ata, Sadeghipour, Parham, Maleki, Majid, Soltani Shahgoli, Sahel, Khalili Pour, Elias, Riazi-Esfahani, Hamid

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Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features von Mehdizadeh, Kasra, Soveizi, Mahdieh, Askarinejad, Amir, Elahifar, Amin, Masoumi, Tannaz, Fazelifar, Amir Farjam, Asadian, Sanaz, Maleki, Majid, Kalayinia, Samira

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Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing von Fazelifar, Amir Farjam, Pourirahim, Maryam, Masoumi, Tannaz, Biglari, Alireza, Maleki, Majid, Kalayinia, Samira

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