Cardiogenetics MDPI

Brian Xiangzhi Wang provides a comprehensive overview of the current understanding of the involvement of exosome-derived miRNAs in the pathogenesis and progression of HCM.

Check it here: https://brnw.ch/21x2W4l

Aino-Maija Vuorinen et al. indicate that the genetic testing of MELAS should be considered in new cases of HCM or sudden heart failure phenotypes of unknown etiology.

Check it here:

Cardiac Involvement in Patients with MELAS-Related mtDNA 3243A>G Variant Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare disease with variable clinical manifestations. MELAS is most often caused by the human mitochondrial DNA (mtDNA) m.3243A>G variant. We describe cardiac magnetic resonance (CMR) imaging findin...

Cameron J. Leong et al. summarize the utility of gene therapy for the treatment of inherited arrhythmia syndromes by exploring the current state of knowledge, limitations, and future directions in this review.

Check their work here: https://brnw.ch/21x2NOF

Sanjay Sivalokanathan published "Exploring the Role of Genetics in Sarcoidosis and Its Impact on the Development of Cardiac Sarcoidosis", Editor's Choice article in Cardiogenetics.

Check it here: https://brnw.ch/21x2Jp1

Tetiana A. Berezina et al. established that elevated levels of cf-nDNA, originating from NT-proBNP, were associated with heart failure in type 2 diabetes mellitus patients, in one of our Editor's Choice articles.

Check their work here: https://brnw.ch/21x2EVh

Gabriela Dostalova et al. published "Anderson–Fabry Disease Homozygosity: Rare Case of Late-Onset Variant", one of our Editor's Choice articles!

Check it here: https://brnw.ch/21x2ABU

Filippo Angelini et al. aim to identify independent clinical predictors of genotype positivity in hypertrophic cardiomyopathy and assess the incremental contribution of echocardiographic/clinical features.

Check it here: https://brnw.ch/21x2ueZ

Iftikhar Ali Ch et al. recently published "Whole-Genome Sequencing in Premature Coronary Artery Disease in South Asians: A Pilot Case–Control Study" in Cardiogenetics.

Check their work here: https://brnw.ch/21x2sDt

Natasha Trajkovska et al. benchmark the predictive PTM performance of three ML-based applications for phosphorylation, methylation, acetylation, and ubiquitination detection on a panel of sarcomeric proteins, commonly associated with HCM.

Check it here: https://brnw.ch/21x1Y0d

Antonio Concistrè et al. about their new review in Cardiogenetics: we propose a 3-category genetic framework for endocrine-related cardiomyopathies — from somatic mutations to pleiotropy & precision medicine.

https://brnw.ch/21x1pGr