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Genotype-Phenotype Associations with Restrictive Cardiomyopathy Induced by Pathogenic Genetic Mutations

Reviews in cardiovascular medicine, 2022-05, Vol.23 (6), p.185

2022

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Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

Orphanet journal of rare diseases, 2022-05, Vol.17 (1), p.183-183, Article 183

2022

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Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation

Orphanet journal of rare diseases, 2021-11, Vol.16 (1), p.496-496, Article 496

2021

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Bacteroides fragilis Supplementation Deteriorated Metabolic Dysfunction, Inflammation, and Aorta Atherosclerosis by Inducing Gut Microbiota Dysbiosis in Animal Model

Nutrients, 2022-05, Vol.14 (11), p.2199

2022

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Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel

Orphanet journal of rare diseases, 2022-10, Vol.17 (1), p.1-394, Article 394

2022

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Young and early‐onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations

Annals of noninvasive electrocardiology, 2021-07, Vol.26 (4), p.e12840-n/a

2021

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GW28-e0737 Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death

Journal of the American College of Cardiology, 2017-10, Vol.70 (16), p.C27-C27

Lin, Yubi

2017

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GW28-e0738 Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy involving both Ventricles

Journal of the American College of Cardiology, 2017-10, Vol.70 (16), p.C27-C27

Lin, Yubi

2017

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GW28-e0741 SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syndrome, and Progressive Conduction Disease

Journal of the American College of Cardiology, 2017-10, Vol.70 (16), p.C28-C28

Lin, Yubi

2017

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GW28-e0739 Familial Sudden Cardiac Death Caused by DSG2 Mutation as Genetic Backgrounds: Whole Exome Sequencing and Valid Therapy of Catheter Ablation

Journal of the American College of Cardiology, 2017-10, Vol.70 (16), p.C27-C27

Lin, Yubi

2017

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Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early‐onset long QT syndrome and sinoatrial node dysfunction

Annals of noninvasive electrocardiology, 2022-01, Vol.27 (1), p.e12889-n/a

2022

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Reactivation of PPARα alleviates myocardial lipid accumulation and cardiac dysfunction by improving fatty acid β-oxidation in Dsg2-deficient arrhythmogenic cardiomyopathy

Acta pharmaceutica Sinica. B, 2023-01, Vol.13 (1), p.192-203

2023

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Mechanism of and Therapeutic Strategy for Atrial Fibrillation Associated with Diabetes Mellitus

TheScientificWorld, 2013-01, Vol.2013 (1), p.209428-209428

2013

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Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation

BMC medical genetics, 2018-08, Vol.19 (1), p.148-148, Article 148

2018

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Identification of rare heterozygous linkage R965C‐R1309H mutations in the pore‐forming region of SCN5A gene associated with complex arrhythmia

Molecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1613-n/a

2021

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Interleukin-27 decreases ghrelin production through signal transducer and activator of transcription 3—mechanistic target of rapamycin signaling

Acta pharmaceutica Sinica. B, 2020-05, Vol.10 (5), p.837-849

2020

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Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles

Cardiology, 2017, Vol.138 (1), p.41-54

2017

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Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death

Journal of electrocardiology, 2018-03, Vol.51 (2), p.309-315

2018

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Effect of Epicardial Fat Pad Ablation on Acute Atrial Electrical Remodeling and Inducibility of Atrial Fibrillation

Circulation Journal, 2010, Vol.74(5), pp.885-894

2010

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SGLT2 inhibitor dapagliflozin attenuates cardiac fibrosis and inflammation by reverting the HIF‐2α signaling pathway in arrhythmogenic cardiomyopathy

The FASEB journal, 2022-07, Vol.36 (7), p.e22410-n/a

2022

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Effects of Low-Level Autonomic Stimulation on Prevention of Atrial Fibrillation Induced by Acute Electrical Remodeling

TheScientificWorld, 2013-01, Vol.2013 (1), p.781084-781084

2013

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Indicators and prediction models for the severity of Covid‐19

International journal of clinical practice (Esher), 2021-10, Vol.75 (10), p.e14571-n/a

2021

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IBacteroides fragilis/I Supplementation Deteriorated Metabolic Dysfunction, Inflammation, and Aorta Atherosclerosis by Inducing Gut Microbiota Dysbiosis in Animal Model

Nutrients, 2022-05, Vol.14 (11)

2022

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Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes

Annals of noninvasive electrocardiology, 2020-01, Vol.25 (1), p.e12694-n/a

2020

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GW28-e0736 Digoxin-induced Anemia among Patients with Atrial Fibrillation and Heart Failure: Clinical Data Analysis and Drug-gene Interaction Network

Journal of the American College of Cardiology, 2017-10, Vol.70 (16), p.C26-C27

2017

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Genotype-Phenotype Associations with Restrictive Cardiomyopathy Induced by Pathogenic Genetic Mutations

Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

Overlap phenotypes of the left ventricular noncompaction and hypertrophic cardiomyopathy with complex arrhythmias and heart failure induced by the novel truncated DSC2 mutation

Bacteroides fragilis Supplementation Deteriorated Metabolic Dysfunction, Inflammation, and Aorta Atherosclerosis by Inducing Gut Microbiota Dysbiosis in Animal Model

Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel

Young and early‐onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations

GW28-e0737 Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death

GW28-e0738 Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy involving both Ventricles

GW28-e0741 SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syndrome, and Progressive Conduction Disease

GW28-e0739 Familial Sudden Cardiac Death Caused by DSG2 Mutation as Genetic Backgrounds: Whole Exome Sequencing and Valid Therapy of Catheter Ablation

Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early‐onset long QT syndrome and sinoatrial node dysfunction

Reactivation of PPARα alleviates myocardial lipid accumulation and cardiac dysfunction by improving fatty acid β-oxidation in Dsg2-deficient arrhythmogenic cardiomyopathy

Mechanism of and Therapeutic Strategy for Atrial Fibrillation Associated with Diabetes Mellitus

Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation

Identification of rare heterozygous linkage R965C‐R1309H mutations in the pore‐forming region of SCN5A gene associated with complex arrhythmia

Interleukin-27 decreases ghrelin production through signal transducer and activator of transcription 3—mechanistic target of rapamycin signaling

Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles

Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death

Effect of Epicardial Fat Pad Ablation on Acute Atrial Electrical Remodeling and Inducibility of Atrial Fibrillation

SGLT2 inhibitor dapagliflozin attenuates cardiac fibrosis and inflammation by reverting the HIF‐2α signaling pathway in arrhythmogenic cardiomyopathy

Effects of Low-Level Autonomic Stimulation on Prevention of Atrial Fibrillation Induced by Acute Electrical Remodeling

Indicators and prediction models for the severity of Covid‐19

IBacteroides fragilis/I Supplementation Deteriorated Metabolic Dysfunction, Inflammation, and Aorta Atherosclerosis by Inducing Gut Microbiota Dysbiosis in Animal Model

Compound and heterozygous mutations of KCNQ1 in long QT syndrome with familial history of unexplained sudden death: Identified by analysis of whole exome sequencing and predisposing genes

GW28-e0736 Digoxin-induced Anemia among Patients with Atrial Fibrillation and Heart Failure: Clinical Data Analysis and Drug-gene Interaction Network

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