Majid Maleki

发表

Effect of Intermediate-Dose vs Standard-Dose Prophylactic Anticoagulation on Thrombotic Events, Extracorporeal Membrane Oxygenation Treatment, or Mortality Among Patients With COVID-19 Admitted to the Intensive Care Unit: The INSPIRATION Randomized Clinical Trial.

S. Parikh, B. V. Van Tassell, M. Monreal, 2021, JAMA.

Arrhythmogenic left ventricular cardiomyopathy caused by a novel likely pathogenic DSP mutation, p.K1165Rfs*8, in a family with sudden cardiac death

G. Houshmand, Samira Kalayinia, Maryam Pourirahim, 2023, BMC Medical Genomics.

A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy

Niloofar Naderi, Samira Kalayinia, Y. Nilipour, 2023, BMC Cardiovascular Disorders.

Catecholaminergic polymorphic ventricular tachycardia (and seizure) caused by a novel homozygous likely pathogenic variant in CASQ2 gene.

Samira Kalayinia, Majid Maleki, Amir Askarinejad, 2023, Gene.

Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy

Samira Kalayinia, Serwa Ghasemi, Majid Maleki, 2023, BMC medical genomics.

Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysm.

F. Rafiee, Samira Kalayinia, Maryam Pourirahim, 2023, Laboratory medicine.

Polymorphism of rs599839 in the PSRC1 gene is associated with coronary artery disease in an Iranian population

Niloofar Naderi, G. Houshmand, M. Alemzadeh-Ansari, 2023, Journal of cardiovascular and thoracic research.

Exploring the role of non-coding RNAs in atrial septal defect pathogenesis: A systematic review

Z. Khajali, Akram Gholipour, Mahshid Malakootian, 2024, PloS one.

Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies

Niloofar Naderi, Samira Kalayinia, Maryam Hosseini Moghadam, 2024, Scientific reports.

A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features

Niloofar Naderi, Samira Kalayinia, Serwa Ghasemi, 2024, BMC cardiovascular disorders.

Copy number variations: The potential association genetic cause in severe cardiovascular diseases with unknown aetiology

Niloofar Naderi, Samira Kalayinia, Majid Maleki, 2024, Journal of Cellular and Molecular Medicine.

Combination of FLNC and JUP variants causing arrhythmogenic cardiomyopathy in an Iranian family with different clinical features

Samira Kalayinia, Sanaz Asadian, Mahdieh Soveizi, 2024, BMC cardiovascular disorders.

Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac death.

Samira Kalayinia, Mahdieh Soveizi, Alireza Salmanipour, 2024, ESC heart failure.

Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease

S. Mowla, H. Bakhshandeh, Farshad Shakerian, 2024, Scientific reports.

Short-term outcomes following total correction of tetralogy of fallot in adult patients

Z. Khajali, S. Saedi, Yaser Toloueitabar, 2023, Journal of Cardiothoracic Surgery.