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New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2015-03, Vol.65 (12), p.1249-1254

2015

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Time to Rethink the Genetic Architecture of Long QT Syndrome

Circulation (New York, N.Y.), 2020-02, Vol.141 (6), p.440-443

2020

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Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study

European journal of human genetics : EJHG, 2022-02, Vol.30 (2), p.187-193

2022

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A Prospective Study of Sudden Cardiac Death among Children and Young Adults

The New England journal of medicine, 2016-06, Vol.374 (25), p.2441-2452

2016

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What do we do and how do we do it? Assessing genetic counselling in the modern era

European journal of human genetics : EJHG, 2020-09, Vol.28 (9), p.1137-1138

2020

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Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing

Circulation. Cardiovascular genetics, 2017-08, Vol.10 (4)

2017

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Posttraumatic Stress and Prolonged Grief After the Sudden Cardiac Death of a Young Relative

JAMA internal medicine, 2016-03, Vol.176 (3), p.402

2016

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Conveying a probabilistic genetic test result to families with an inherited heart disease

Heart rhythm, 2014-06, Vol.11 (6), p.1073-1078

2014

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Molecular autopsy in victims of inherited arrhythmias

Journal of arrhythmia, 2016-10, Vol.32 (5), p.359-365

2016

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Hypertrophic Cardiomyopathy: Genetic Testing and Risk Stratification

Current cardiology reports, 2021-02, Vol.23 (2), p.9-9, Article 9

2021

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Recommendations for clinical interpretation of variants found in non-coding regions of the genome

Genome medicine, 2022-07, Vol.14 (1), p.73-19, Article 73

2022

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Genetic architecture of left ventricular noncompaction in adults

Human genome variation, 2020-10, Vol.7 (1), p.33-33, Article 33

2020

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Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes

Circulation. Genomic and precision medicine, 2019-02, Vol.12 (2), p.e002460-e002460

2019

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The emerging role of the cardiac genetic counselor

Heart rhythm, 2011-12, Vol.8 (12), p.1958-1962

2011

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Perceptions of genetic variant reclassification in patients with inherited cardiac disease

European journal of human genetics : EJHG, 2019-07, Vol.27 (7), p.1134-1142

2019

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Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death

Genetics in medicine, 2021-01, Vol.23 (1), p.86-93

2021

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Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy

Genetics in medicine, 2013-12, Vol.15 (12), p.972-977

2013

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Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

Genetics in medicine, 2014-04, Vol.16 (4), p.286-293

2014

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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

Genetics in medicine, 2019-03, Vol.21 (3), p.650-662

2019

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Doctor-patient care relationship in genetic cardiomyopathies: An exploratory study on clinical consultations

PloS one, 2020-08, Vol.15 (8), p.e0236814-e0236814

2020

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Psychological Issues in Managing Families with Inherited Cardiovascular Diseases

Cold Spring Harbor perspectives in medicine, 2020-09, Vol.10 (9), p.a036558

Ingles, Jodie

2020

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Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young

BMJ open, 2022-08, Vol.12 (8), p.e053785

2022

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A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

Heart rhythm, 2016-08, Vol.13 (8), p.1652-1660

2016

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Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome

PloS one, 2018-04, Vol.13 (4), p.e0195594-e0195594

2018

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New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy

Time to Rethink the Genetic Architecture of Long QT Syndrome

Decision-making and experiences of preimplantation genetic diagnosis in inherited heart diseases: a qualitative study

A Prospective Study of Sudden Cardiac Death among Children and Young Adults

What do we do and how do we do it? Assessing genetic counselling in the modern era

Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing

Posttraumatic Stress and Prolonged Grief After the Sudden Cardiac Death of a Young Relative

Conveying a probabilistic genetic test result to families with an inherited heart disease

Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions

Molecular autopsy in victims of inherited arrhythmias

Hypertrophic Cardiomyopathy: Genetic Testing and Risk Stratification

Recommendations for clinical interpretation of variants found in non-coding regions of the genome

Genetic architecture of left ventricular noncompaction in adults

Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes

The emerging role of the cardiac genetic counselor

Perceptions of genetic variant reclassification in patients with inherited cardiac disease

Characterization of clinically relevant copy-number variants from exomes of patients with inherited heart disease and unexplained sudden cardiac death

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy

Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

Doctor-patient care relationship in genetic cardiomyopathies: An exploratory study on clinical consultations

Psychological Issues in Managing Families with Inherited Cardiovascular Diseases

Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome

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