Original Research

Published on 24 Jun 2024

RNAseq of INOCA patients identifies innate, invariant, and acquired immune changes: potential autoimmune microvascular dysfunction

in Cardiovascular Genetics and Systems Medicine

Kevin Jaatinen
Palak Shah
Ramesh Mazhari
Zane Hayden
Richard Wargowsky
Tisha Jepson
Ian Toma
John Perkins
Timothy A. McCaffrey

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1385457

1,541 views

Case Report

Published on 13 Jun 2024

TTN novel splice variant in familial dilated cardiomyopathy and splice variants review: a case report

in Cardiovascular Genetics and Systems Medicine

Paul León
Paula Franco
Nicole Hinojosa
Kevin Torres
Andrés Moreano
Vanessa I. Romero

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1387063

1,472 views
1 citation

Original Research

Published on 03 Jun 2024

Identifying molecular subgroups of patients with preeclampsia through bioinformatics

in Cardiovascular Genetics and Systems Medicine

Huijie Zhang
Jianglei Ma
Xueli Gao

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1367578

927 views

Original Research

Published on 23 May 2024

A Lifelike guided journey through the pathophysiology of pulmonary hypertension—from measured metabolites to the mechanism of action of drugs

in Cardiovascular Genetics and Systems Medicine

Nathan Weinstein
Jørn Carlsen
Sebastian Schulz
Timothy Stapleton
Hanne H. Henriksen
Evelyn Travnik
Pär Ingemar Johansson

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1341145

1,571 views

Original Research

Published on 22 May 2024

Low expression of Notch1 may be associated with acute myocardial infarction

in Cardiovascular Genetics and Systems Medicine

Qing Zhang
Heyu Meng
Xue Wang
Yanqiu Chen
Zhaohan Yan
Jianjun Ruan
Fanbo Meng

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1367675

1,061 views

Case Report

Published on 22 May 2024

Case Report: A rare transthyretin mutation p.D58Y in a Chinese case of transthyretin amyloid cardiomyopathy

in Cardiovascular Genetics and Systems Medicine

Jibin Lin
Jiangtong Peng
Bingjie Lv
Zheng Cao
Zhijian Chen

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1374241

1,023 views

Original Research

Published on 25 Apr 2024

Genome-wide association studies reveal differences in genetic susceptibility between single events vs. recurrent events of atrial fibrillation and myocardial infarction: the HUNT study

in Cardiovascular Genetics and Systems Medicine

Martina Hall
Anne Heidi Skogholt
Ida Surakka
Haavard Dalen
Eivind Almaas

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1372107

1,279 views

Editorial

Published on 17 Apr 2024

Editorial: Multi-omics in cardiomyopathies causing heart failure: from mechanism to treatment

in Cardiovascular Genetics and Systems Medicine

Chen Yao

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1405813

697 views

Editorial

Published on 16 Apr 2024

Editorial: Community series in epigenetic regulation in cardiovascular diseases, volume III

in Cardiovascular Genetics and Systems Medicine

Zhihua Wang
Qing Robert Miao
Suowen Xu
Indulekha C. L. Pillai
Christoph D. Rau

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1406370

789 views

Original Research

Published on 11 Apr 2024

A causal association between amyotrophic lateral sclerosis and atrial fibrillation: a two-sample Mendelian randomization study

in Cardiovascular Genetics and Systems Medicine

Yiren Yao
Hongyang Liu
Yang Gu
Xiaojin Xu
Xiwen Zhang

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1351495

2,002 views

Original Research

Published on 09 Apr 2024

Serum albumin levels and risk of atrial fibrillation: a Mendelian randomization study

in Cardiovascular Genetics and Systems Medicine

Bohang Chen
Chuqiao Wang
Wenjie Li

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1385223

2,221 views

Review

Published on 08 Apr 2024

Research progress on the improvement of cardiovascular diseases through the autonomic nervous system regulation of the NLRP3 inflammasome pathway

in Cardiovascular Genetics and Systems Medicine

Yuchi Hu
Songyuan Dai
Lulu Zhao
Ling Zhao

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1369343

1,566 views
1 citation

Case Report

Published on 28 Mar 2024

Case Report: Multiple types of arrhythmias in a late-confirmed Danon disease

in Cardiovascular Genetics and Systems Medicine

Nan Wang
Yu Cao
Jie Wang
Qing Zhang

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1369680

1,650 views
1 citation

Original Research

Published on 18 Mar 2024

Cardiac defects of hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders: a retrospective cohort study

in Cardiovascular Genetics and Systems Medicine

Dacre R. T. Knight
Katelyn A. Bruno
Ayush Singh
Bala Munipalli
Shilpa Gajarawala
Mahima Solomon
S. Christian Kocsis
Ashley A. Darakjian
Angita Jain
Emily R. Whelan

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1332508

8,060 views
3 citations

Review

Published on 11 Mar 2024

Gender-specific genetic and epigenetic signatures in cardiovascular disease

in Cardiovascular Genetics and Systems Medicine

Justin Bridges
Jose A. Ramirez-Guerrero
Manuel Rosa-Garrido

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1355980

3,182 views

Systematic Review

Published on 26 Feb 2024

Impact of the MIF -173G/C variant on cardiovascular disease risk: a meta-analysis of 9,047 participants

in Cardiovascular Genetics and Systems Medicine

Hamas Fouda
Wisam N. Ibrahim
Zumin Shi
Fahad Alahmadi
Yousef Almohammadi
Amal Al-Haidose
Atiyeh M. Abdallah

Frontiers in Cardiovascular Medicine

doi 10.3389/fcvm.2024.1323423

1,693 views

Navigation group

Articles

RNAseq of INOCA patients identifies innate, invariant, and acquired immune changes: potential autoimmune microvascular dysfunction

TTN novel splice variant in familial dilated cardiomyopathy and splice variants review: a case report

Identifying molecular subgroups of patients with preeclampsia through bioinformatics

A Lifelike guided journey through the pathophysiology of pulmonary hypertension—from measured metabolites to the mechanism of action of drugs

Low expression of Notch1 may be associated with acute myocardial infarction

Case Report: A rare transthyretin mutation p.D58Y in a Chinese case of transthyretin amyloid cardiomyopathy

Genome-wide association studies reveal differences in genetic susceptibility between single events vs. recurrent events of atrial fibrillation and myocardial infarction: the HUNT study

Editorial: Multi-omics in cardiomyopathies causing heart failure: from mechanism to treatment

Editorial: Community series in epigenetic regulation in cardiovascular diseases, volume III

A causal association between amyotrophic lateral sclerosis and atrial fibrillation: a two-sample Mendelian randomization study

Serum albumin levels and risk of atrial fibrillation: a Mendelian randomization study

Research progress on the improvement of cardiovascular diseases through the autonomic nervous system regulation of the NLRP3 inflammasome pathway

Case Report: Multiple types of arrhythmias in a late-confirmed Danon disease

Cardiac defects of hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorders: a retrospective cohort study

Gender-specific genetic and epigenetic signatures in cardiovascular disease

Impact of the MIF -173G/C variant on cardiovascular disease risk: a meta-analysis of 9,047 participants