Case Report

Published on 12 Jun 2023

De novo heterozygous pathogenic FBN1 variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case report

in Cardiovascular Genetics and Systems Medicine

Taylor MacGowan
Taylor McClinchey
Vibhu Parcha
Matteo Vatta
Silvio Litovsky
Pankaj Arora
Paul V. Benson

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1170460

1,399 views
1 citation

Case Report

Published on 08 Jun 2023

Case report: Mutation in NPPA gene as a cause of fibrotic atrial myopathy

in Cardiovascular Genetics and Systems Medicine

Pedro Silva Cunha
Diana Oliveira Antunes
Sérgio Laranjo
Ana Coutinho
João Abecasis
Mário Martins Oliveira

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1149717

2,070 views
3 citations

Systematic Review

Published on 07 Jun 2023

The diagnostic value of electrocardiogram-based machine learning in long QT syndrome: a systematic review and meta-analysis

in Cardiovascular Genetics and Systems Medicine

Min-Juan Wu
Wen-Qin Wang
Wei Zhang
Jun-Hua Li
Xing-Wei Zhang

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1172451

3,764 views
2 citations

Mini Review

Published on 26 May 2023

Perivascular adipose tissue in vascular pathologies—a novel therapeutic target for atherosclerotic disease?

in Cardiovascular Genetics and Systems Medicine

Yusuke Adachi
Kazutaka Ueda
Eiki Takimoto

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1151717

3,788 views
8 citations

Original Research

Published on 26 May 2023

Genome-wide detection of m6A-associated SNPs in atrial fibrillation pathogenesis

in Cardiovascular Genetics and Systems Medicine

Yan Huang
Yuqian Tan
Yuan Yao
Linglong Gu
Liusong Huang
Tao Song

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1152851

2,576 views
5 citations

Original Research

Published on 26 May 2023

Identification of mitophagy-related genes with potential clinical utility in myocardial infarction at transcriptional level

in Cardiovascular Genetics and Systems Medicine

Zhikai Yang
Liang Sun
Hua Wang

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1166324

2,963 views
2 citations

Original Research

Published on 24 May 2023

Genetic landscape in Russian patients with familial left ventricular noncompaction

in Cardiovascular Genetics and Systems Medicine

Alexey N. Meshkov
Roman P. Myasnikov
Anna V. Kiseleva
Olga V. Kulikova
Evgeniia A. Sotnikova
Maria M. Kudryavtseva
Anastasia A. Zharikova
Sergey N. Koretskiy
Elena A. Mershina
Vasily E. Ramensky

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1205787

2,534 views
6 citations

Mini Review

Published on 23 May 2023

VEGF-A related SNPs: a cardiovascular context

in Cardiovascular Genetics and Systems Medicine

J. C. Meza-Alvarado
R. A. Page
B. Mallard
C. Bromhead
B. R. Palmer

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1190513

2,712 views
3 citations

Original Research

Published on 23 May 2023

Transcriptome data analysis of primary cardiomyopathies reveals perturbations in arachidonic acid metabolism

in Cardiovascular Genetics and Systems Medicine

Pankaj Kumar Chauhan
Ramanathan Sowdhamini

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1110119

1,977 views
2 citations

Case Report

Published on 23 May 2023

Misdiagnosed myocarditis in arrhythmogenic cardiomyopathy induced by a homozygous variant of DSG2: a case report

in Cardiovascular Genetics and Systems Medicine

Xuwei Liu
Yue Zhang
Wenjuan Li
Qian Zhang
Letao Zhou
Yimin Hua
Hongyu Duan
Yifei Li

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1150657

1,906 views
4 citations

Review

Published on 22 May 2023

The role of noncoding genetic variants in cardiomyopathy

in Cardiovascular Genetics and Systems Medicine

Myo Htet
Shunyao Lei
Sheetal Bajpayi
Asimina Zoitou
Myrsini Chamakioti
Emmanouil Tampakakis

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1116925

2,545 views
3 citations

Review

Published on 19 May 2023

Critical roles of m6A methylation in cardiovascular diseases

in Cardiovascular Genetics and Systems Medicine

Xinmin Zhang
He Cai
He Xu
Su Dong
Haichun Ma

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1187514

2,994 views
3 citations

Original Research

Published on 19 May 2023

Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing

in Cardiovascular Genetics and Systems Medicine

Greta Marie Pohl
Manuel Göz
Anna Gaertner
Andreas Brodehl
Tolga Cimen
Ardan M. Saguner
Eric Schulze-Bahr
Volker Walhorn
Dario Anselmetti
Hendrik Milting

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1127261

2,259 views
2 citations

Original Research

Published on 15 May 2023

Perceived self-efficacy and empowerment in patients at increased risk of sudden cardiac arrest

in Cardiovascular Genetics and Systems Medicine

Brianna Davies
Katherine S. Allan
Sandra L. Carroll
Karen Gibbs
Jason D. Roberts
Ciorsti MacIntyre
Christian Steinberg
Rafik Tadros
Paul Dorian
Jeff S. Healey

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.955060

2,233 views
1 citation

Original Research

Published on 03 May 2023

Association between ACE I/D genetic polymorphism and the severity of coronary artery disease in Vietnamese patients with acute myocardial infarction

in Cardiovascular Genetics and Systems Medicine

Duy Cong Tran
Linh Hoang Gia Le
Truc Thanh Thai
Sy Van Hoang
Minh Duc Do
Binh Quang Truong

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1091612

2,540 views
3 citations

Systematic Review

Published on 28 Apr 2023

Identification of microRNAs as diagnostic biomarkers for atrial fibrillation: a systematic review and meta-analysis

in Cardiovascular Genetics and Systems Medicine

Ardian Rizal
Yoga Waranugraha
Adhika Prastya Wikananda
Yoga Yuniadi

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2023.1128708

2,650 views
7 citations

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Articles

De novo heterozygous pathogenic FBN1 variant in an autopsy case of multiple aneurysms and right renal artery dissection: a case report

Case report: Mutation in NPPA gene as a cause of fibrotic atrial myopathy

The diagnostic value of electrocardiogram-based machine learning in long QT syndrome: a systematic review and meta-analysis

Perivascular adipose tissue in vascular pathologies—a novel therapeutic target for atherosclerotic disease?

Genome-wide detection of m6A-associated SNPs in atrial fibrillation pathogenesis

Identification of mitophagy-related genes with potential clinical utility in myocardial infarction at transcriptional level

Genetic landscape in Russian patients with familial left ventricular noncompaction

VEGF-A related SNPs: a cardiovascular context

Transcriptome data analysis of primary cardiomyopathies reveals perturbations in arachidonic acid metabolism

Misdiagnosed myocarditis in arrhythmogenic cardiomyopathy induced by a homozygous variant of DSG2: a case report

The role of noncoding genetic variants in cardiomyopathy

Critical roles of m6A methylation in cardiovascular diseases

Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing

Perceived self-efficacy and empowerment in patients at increased risk of sudden cardiac arrest

Association between ACE I/D genetic polymorphism and the severity of coronary artery disease in Vietnamese patients with acute myocardial infarction

Identification of microRNAs as diagnostic biomarkers for atrial fibrillation: a systematic review and meta-analysis