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Roles of leptin and resistin in metabolism, reproduction, and leptin resistance

Domestic animal endocrinology, 2020-10, Vol.73, p.106472-106472, Article 106472

2020

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HEY2 , A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL

Heart rhythm, 2014-11, Vol.11 (11), p.2133-2133

2014

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Canola meal or soybean meal as protein source and the effect of microencapsulated sodium butyrate supplementation in calf starter mixture. II. Development of the gastrointestinal tract

Journal of dairy science, 2021-06, Vol.104 (6), p.6663-6676

2021

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Characterization of ketolactia in dairy cows during early lactation

Journal of dairy science, 2021-12, Vol.104 (12), p.12800-12815

2021

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Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death

Heart rhythm, 2013-11, Vol.10 (11), p.1743-1744

2013

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Modeling familial sinus node dysfunction with a large intergenic deletion between PITX2 and ANK2 using iPS cell-derived sinoatrial nodal-like cardiomyocytes

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

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GENECHOC study: genetic markers of arrhythmic risk in heart failure

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome

Archives of cardiovascular diseases, 2009, Vol.102, p.S70-S70

2009

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Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder

Archives of cardiovascular diseases supplements, 2023-01, Vol.15 (1), p.115-116

2023

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G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome

Archives of cardiovascular diseases, 2009, Vol.102, p.S70-S70

2009

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Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.261-261

2020

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Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.263-263

2020

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2014-A-31-CES - HEY2, A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL

Heart rhythm, 2014-11, Vol.11 (11), p.2133-2133

2014

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A mutation in CALM1 encoding calmodulin causes sudden cardiac death in childhood and adolescence

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2298-P2298

2013

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P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

Cardiovascular research, 2014-07, Vol.103 (suppl 1), p.S61-S61

2014

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Genechoc Study Genetic markers of arrhythmic risk in heart failure

Archives of Cardiovascular Diseases Supplements, 2020-10, Vol.12 (2-4), p.264-264

2020

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Novel HCN4 mutations in families with bradycardia and hypertrabeculation of the myocardium

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2297-P2297

2013

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Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2289-P2289

2013

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Genome-wide association studies: providers of candidate genes for identification of rare variants?

Europace (London, England), 2011-07, Vol.13 (7), p.911-912

2011

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P333HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy

Cardiovascular research, 2014-07, Vol.103 (suppl 1), p.S60-S60

2014

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371 - Risk stratification of arrhythmia and death in ARVC

Archives of Cardiovascular Diseases Supplements, 2017-04, Vol.9 (2), p.201-202

2017

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Roles of leptin and resistin in metabolism, reproduction, and leptin resistance

HEY2 , A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL

Canola meal or soybean meal as protein source and the effect of microencapsulated sodium butyrate supplementation in calf starter mixture. II. Development of the gastrointestinal tract

Characterization of ketolactia in dairy cows during early lactation

Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death

Modeling familial sinus node dysfunction with a large intergenic deletion between PITX2 and ANK2 using iPS cell-derived sinoatrial nodal-like cardiomyocytes

Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation

GENECHOC study: genetic markers of arrhythmic risk in heart failure

Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25

Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome

G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome

Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a syndromic cardiac disorder

G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome

Relevance and diagnostic performance of genes involved in arrhythmogenic cardiomyopathy

Identification by Whole Genome Sequencing of a New Gene Causing Hereditary Sinus Node and Atrioventricular Conduction Dysfunction

2014-A-31-CES - HEY2, A NOVEL SUSCEPTIBILITY GENE FOR BRUGADA SYNDROME, CONTROLS DEPOLARIZATION AND REPOLARIZATION GRADIENTS IN THE RVOT AND ACROSS THE VENTRICULAR WALL

A mutation in CALM1 encoding calmodulin causes sudden cardiac death in childhood and adolescence

P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

Genechoc Study Genetic markers of arrhythmic risk in heart failure

Novel HCN4 mutations in families with bradycardia and hypertrabeculation of the myocardium

Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder

Genome-wide association studies: providers of candidate genes for identification of rare variants?

P333HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy

371 - Risk stratification of arrhythmia and death in ARVC

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