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Mitochondria, contractile apparatus, and ion channels in the failing myocardium: Special relationships or dangerous liaisons?

Heart rhythm, 2016-05, Vol.13 (5), p.1140-1141

Vatta, Matteo, PhD

2016

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Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

Journal of cardiac failure, 2018-05, Vol.24 (5), p.281-302

2018

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Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2018-09, Vol.20 (9), p.899-909

2018

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MY APPROACH to genetic testing in cardiology practice

Trends in cardiovascular medicine, 2016-01, Vol.26 (1), p.97-98

Vatta, Matteo, PhD, FACMG

2016

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Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199

Clinical cancer research, 2015-11, Vol.21 (22), p.5082-5091

2015

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Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (27), p.9355-9360

2008

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Editorial commentary: Genetic testing for congenital heart disease: The future is now

Trends in cardiovascular medicine, 2022-07, Vol.32 (5), p.320-321

Vatta, Matteo

2022

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Telethonin variants found in Brugada syndrome, J‐wave pattern ECG, and ARVC reduce peak Nav1.5 currents in HEK‐293 cells

Pacing and clinical electrophysiology, 2020-08, Vol.43 (8), p.838-846

2020

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ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

Journal of the American College of Cardiology, 2009-07, Vol.54 (4), p.325-333

2009

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Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy

Journal of the American College of Cardiology, 2010-02, Vol.55 (6), p.587-597

2010

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A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG

PloS one, 2016-08, Vol.11 (8), p.e0161872-e0161872

2016

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Use of genetic testing to identify sudden cardiac death syndromes

Trends in cardiovascular medicine, 2015-11, Vol.25 (8), p.738-748

2015

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Genetic variants and ECG pattern variability in long QT syndrome: How far are we?

Heart rhythm, 2010-07, Vol.7 (7), p.904-905

Vatta, Matteo, PhD

2010

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Novel mechanism for sudden infant death syndrome: Persistent late sodium current secondary to mutations in caveolin-3

Heart rhythm, 2007-02, Vol.4 (2), p.161-166

2007

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

Frontiers in cardiovascular medicine, 2023-06, Vol.10, p.1170460

2023

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Intronic variants and splicing errors in cardiovascular diseases

Heart rhythm, 2009-02, Vol.6 (2), p.219-220

Vatta, Matteo, PhD

2009

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Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function

Physiological reports, 2021-11, Vol.9 (22), p.n/a

2021

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Editorial: Current Challenges in Cardiovascular Molecular Diagnostics

Frontiers in cardiovascular medicine, 2017-09, Vol.4, p.54-54

2017

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Editorial commentary: Targeting TYMP for cardiovascular disease: How far are we?

Trends in cardiovascular medicine, 2018-04, Vol.28 (3), p.172-173

Vatta, Matteo

2018

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ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscle

PloS one, 2014-03, Vol.9 (3), p.e92259-e92259

2014

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Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya

PloS one, 2017-09, Vol.12 (9), p.e0185204-e0185204

2017

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Coronary artery disease: The magnificent fifty?

Trends in cardiovascular medicine, 2015-04, Vol.25 (3), p.179-180

2015

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Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

Journal of the American College of Cardiology, 2010-10, Vol.56 (18), p.1493-1502

2010

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P222: TTN truncating variants are enriched in cardiomyopathy/arrhythmia and neuromuscular cases and M-band exon 358 contributes to primary cardiomyopathy/arrhythmia

Genetics in Medicine Open, 2024, Vol.2, p.101119, Article 101119

2024

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14-3-3ε Plays a Role in Cardiac Ventricular Compaction by Regulating the Cardiomyocyte Cell Cycle

Molecular and Cellular Biology, 2012-12, Vol.32 (24), p.5089-5102

2012

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Mitochondria, contractile apparatus, and ion channels in the failing myocardium: Special relationships or dangerous liaisons?

Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

MY APPROACH to genetic testing in cardiology practice

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Editorial commentary: Genetic testing for congenital heart disease: The future is now

Telethonin variants found in Brugada syndrome, J‐wave pattern ECG, and ARVC reduce peak Nav1.5 currents in HEK‐293 cells

ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy

A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG

Use of genetic testing to identify sudden cardiac death syndromes

Genetic variants and ECG pattern variability in long QT syndrome: How far are we?

Novel mechanism for sudden infant death syndrome: Persistent late sodium current secondary to mutations in caveolin-3

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

Intronic variants and splicing errors in cardiovascular diseases

Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function

Editorial: Current Challenges in Cardiovascular Molecular Diagnostics

Editorial commentary: Targeting TYMP for cardiovascular disease: How far are we?

ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscle

Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya

Coronary artery disease: The magnificent fifty?

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

P222: TTN truncating variants are enriched in cardiomyopathy/arrhythmia and neuromuscular cases and M-band exon 358 contributes to primary cardiomyopathy/arrhythmia

14-3-3ε Plays a Role in Cardiac Ventricular Compaction by Regulating the Cardiomyocyte Cell Cycle

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