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Lista de obras de Jodie Ingles

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

scientific article published on 09 May 2019

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary

scientific article published on 01 November 2019

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

artículo científico publicado en 2021

A Control Theory-Based Pilot Intervention toIncrease Physical Activity in Patients WithHypertrophic Cardiomyopathy

scientific article published on 08 June 2018

A Cost-effectiveness Analysis of Genetic Testing in the Evaluation of Families with Hypertrophic Cardiomyopathy

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

artículo científico publicado en 2016

A Validated Model for Sudden Cardiac Death Risk Prediction in Pediatric Hypertrophic Cardiomyopathy

artículo científico publicado en 2020

A balanced translocation disrupting SCN5A in a family with Brugada syndrome and sudden cardiac death

scientific article published on 28 August 2018

A clinical approach to genetic testing for non-specialists

scientific article published on 28 September 2017

A cost-effectiveness model of genetic testing for the evaluation of families with hypertrophic cardiomyopathy

article

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

artículo científico publicado en 2016

A prospective longitudinal study of health-related quality of life and psychological wellbeing after an implantable cardioverter-defibrillator in patients with genetic heart diseases

artículo científico publicado en 2022

Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel

artículo científico publicado en 2018

An International Multi-Center Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2- Catecholaminergic Polymorphic Ventricular Tachycardia

artículo científico publicado en 2020

An Unexpected FLNC Phenotype: Expanding the Clinical Spectrum or a Second-Hit Disease Mechanism?

artículo científico publicado en 2019

Application of Genetic Testing in Hypertrophic Cardiomyopathy for Preclinical Disease Detection.

artículo científico

Association of Race With Disease Expression and Clinical Outcomes Among Patients With Hypertrophic Cardiomyopathy

scientific article published on 04 December 2019

Associations Between Female Sex, Sarcomere Variants and Clinical Outcomes in Hypertrophic Cardiomyopathy

artículo científico publicado en 2020

Attitudes, knowledge and consequences of uncertain genetic findings in hypertrophic cardiomyopathy.

artículo científico publicado en 2017

Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic Cardiomyopathy.

artículo científico publicado en 2017

Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.

artículo científico publicado en 2005

Cardiovascular Effects of Energy Drinks in Familial Long QT Syndrome: A Randomized Cross-Over Study

artículo científico publicado en 2017

Challenges of exercise recommendations and sports participation in genetic heart disease patients

artículo científico publicado en 2015

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

scientific article published on 25 September 2020

Clinical Profile and Health Disparities in a Multiethnic Cohort of Patients With Hypertrophic Cardiomyopathy

artículo científico publicado en 2021

Clinical and genetic features of Australian families with long QT syndrome: A registry-based study.

artículo científico publicado en 2016

Clinical characteristics and outcomes in childhood-onset hypertrophic cardiomyopathy

artículo científico publicado en 2021

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy

artículo científico publicado en 2013

Communication of genetic information to families with inherited rhythm disorders.

artículo científico publicado en 2017

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

artículo científico publicado en 2005

Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation

artículo científico publicado en 2021

Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events

scientific article published on 01 November 2018

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

artículo científico publicado en 2014

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

scientific article published on 01 May 2019

Daily Step Count as a Simple Marker of Disease Severity in Hypertrophic Cardiomyopathy.

artículo científico publicado en 2018

Delay to diagnosis amongst patients with catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2014

Determining pathogenicity in cardiac genetic testing: Filling in the blank spaces

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Development of a communication aid for explaining hypertrophic cardiomyopathy genetic test results.

artículo científico publicado en 2017

Discordant clinical features of identical hypertrophic cardiomyopathy twins

artículo científico publicado en 2021

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

artículo científico publicado en 2020

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

artículo científico publicado en 2020

Editorial commentary: Genetic contributions to cardiovascular disease: The blurred lines between monogenic and polygenic traits

scientific article published on 11 April 2017

Epidemiology and clinical characteristics of atrial fibrillation in patients with inherited heart diseases

artículo científico publicado en 2020

Establishment of an Australian National Genetic Heart Disease Registry.

artículo científico publicado en 2008

Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial

Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes

article

Evaluation of Psychological Wellbeing in Patients with Hypertrophic Cardiomyopathy

article published in 2007

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

artículo científico publicado en 2021

Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest

artículo científico publicado en 2015

Exome sequencing-based molecular autopsy of formalin-fixed paraffin-embedded tissue after sudden death.

artículo científico publicado en 2017

Expanding the genetic spectrum of hypertrophic cardiomyopathy: X marks the spot.

artículo científico publicado en 2013

Factors influencing uptake of familial long QT syndrome genetic testing

artículo científico publicado en 2015

Family Matters: Outcomes of Hypertrophic Cardiomyopathy Family Screening

artículo científico publicado en 2018

Genetic Testing for Cardiomyopathies in Clinical Practice.

artículo científico publicado en 2018

Genetic Testing for Inherited Heart Diseases: Longitudinal Impact on Health-Related Quality of Life

article

Genetic Testing in Inherited Heart Diseases

artículo científico publicado en 2019

Genetic architecture of left ventricular noncompaction in adults

scientific article published on 15 October 2020

Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy

article

Genetic testing for inherited heart diseases: longitudinal impact on health-related quality of life

artículo científico publicado en 2012

Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent

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

artículo científico publicado en 2018

Global approaches to cardiogenetic evaluation after sudden cardiac death in the young: A survey among health care professionals

artículo científico publicado en 2021

Guidelines for genetic testing of inherited cardiac disorders

artículo científico publicado en 2011

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

artículo científico publicado en 2021

Health Status of Cardiac Genetic Disease Patients and Their At-risk Relatives

article

Health status of cardiac genetic disease patients and their at-risk relatives

artículo científico publicado en 2011

Higher rates but similar causes of young out‐of‐hospital cardiac arrest in rural Australian patients

artículo científico publicado en 2022

Homozygous mutation in the cardiac troponin I gene: clinical heterogeneity in hypertrophic cardiomyopathy

scientific article published on 25 December 2012

How Patient Perceptions Shape Responses and Outcomes in Inherited Cardiac Conditions

scientific article published on 18 December 2019

Hypertrophic Cardiomyopathy with Left Ventricular Systolic Dysfunction: Insights from the SHaRe Registry

scientific article published on 31 March 2020

Hypertrophic Cardiomyopathy: Genetic Testing and Risk Stratification

artículo científico publicado en 2021

Impact of the implantable cardioverter defibrillator on confidence to undertake physical activity in inherited heart disease: A cross-sectional study.

artículo científico publicado en 2017

Implantable cardioverter-defibrillator therapy in Australia, 2002-2015

artículo científico publicado en 2018

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest

scientific article published on 1 September 2019

Inconsistent discharge diagnoses for young cardiac arrest episodes: insights from a statewide registry

artículo científico publicado en 2022

Interdisciplinary psychosocial care for families with inherited cardiovascular diseases

artículo científico publicado en 2016

Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic Cardiomyopathy

scientific article published on 01 January 2019

LAMP2 shines a light on cardiomyopathy in an athlete

artículo científico publicado en 2017

Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants

scientific article published on 11 May 2018

Letter by Semsarian and Ingles regarding article, "A randomized trial of social media from Circulation".

artículo científico publicado en 2015

Long-term follow-up of implantable cardioverter defibrillator therapy for hypertrophic cardiomyopathy.

artículo científico publicado en 2004

Long-term follow-up of patients with obstructive hypertrophic cardiomyopathy treated with dual-chamber pacing.

artículo científico publicado en 2005

Making the case for cascade screening among families with inherited heart disease

artículo científico publicado en 2019

Minding the Genes: a Multidisciplinary Approach towards Genetic Assessment of Cardiovascular Disease.

artículo científico publicado en 2016

Molecular autopsy in victims of inherited arrhythmias

artículo científico publicado en 2016

Molecular diagnostics of cardiomyopathies: the future is here.

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Mutation analysis of the natriuretic peptide precursor B (NPPB) gene in patients with hypertrophic cardiomyopathy

artículo científico publicado en 2006

Mutations in alpha-actinin-2 cause hypertrophic cardiomyopathy: a genome-wide analysis

artículo científico publicado en 2010

NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy

artículo científico publicado en 2015

Natural history of genotype positive-phenotype negative patients with hypertrophic cardiomyopathy

artículo científico publicado en 2011

Needs analysis of parents following sudden cardiac death in the young

scientific article published on 01 July 2020

New perspectives on the prevalence of hypertrophic cardiomyopathy

artículo científico publicado en 2015

Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.

artículo científico publicado en 2017

Obesity in young sudden cardiac death: Rates, clinical features, and insights into people with body mass index >50kg/m2

artículo científico publicado en 2022

Participation in thrill-seeking activities by patients with hypertrophic cardiomyopathy: Individual preferences, adverse events and physician attitude

artículo científico publicado en 2019

Pathogenicity of Hypertrophic Cardiomyopathy Variants: A Path Forward Together.

artículo científico publicado en 2017

Patients with Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement

artículo científico publicado en 2020

Perceptions of genetic variant reclassification in patients with inherited cardiac disease

artículo científico publicado en 2019

Physical activity in hypertrophic cardiomyopathy: prevalence of inactivity and perceived barriers

artículo científico publicado en 2016

Poor psychological wellbeing particularly in mothers following sudden cardiac death in the young.

artículo científico publicado en 2013

Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians

artículo científico publicado en 2007

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

artículo científico publicado en 2016

Precision Medicine in Cardiovascular Disease: Genetics and Impact on Phenotypes

artículo científico publicado en 2021

Predictors and outcomes of in-hospital referrals for forensic investigation after young sudden cardiac death

artículo científico publicado en 2022

Prevalence of Anderson-Fabry disease in a cohort with unexplained late gadolinium enhancement on cardiac MRI

scientific article published on 30 December 2019

Prevalence of Coronary Artery Anomalies in Young and Middle-Aged Sudden Cardiac Death Victims (from a Prospective State-Wide Registry)

artículo científico publicado en 2022

Preventing sudden cardiac death in athletes

artículo científico publicado en 2016

Progression of left ventricular hypertrophy and the angiotensin-converting enzyme gene polymorphism in hypertrophic cardiomyopathy

artículo científico publicado en 2004

Prolongation of the QTc interval predicts appropriate implantable cardioverter-defibrillator therapies in hypertrophic cardiomyopathy.

artículo científico publicado en 2013

Psychological Issues in Managing Families with Inherited Cardiovascular Diseases

scientific article published on 23 September 2019

Psychological adaptation to molecular autopsy findings following sudden cardiac death in the young

scientific article published on 16 October 2018

Psychological wellbeing and posttraumatic stress associated with implantable cardioverter defibrillator therapy in young adults with genetic heart disease

artículo científico publicado en 2013

Psychosocial Impact of a Positive Gene Result for Asymptomatic Relatives at Risk of Hypertrophic Cardiomyopathy

artículo científico publicado en 2018

Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood

artículo científico publicado en 2017

Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy.

artículo científico publicado en 2008

Rare desmin variant causing penetrant life-threatening arrhythmic cardiomyopathy.

artículo científico publicado en 2018

Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen–Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT)

Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy

scientific article published on 01 March 2019

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

artículo científico publicado en 2018

Reply: What Is the True Prevalence of Hypertrophic Cardiomyopathy?

scientific article published on 01 October 2015

Response by Ingles and Semsarian to Letter Regarding Article, "Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events"

scientific article published on 01 March 2019

Response to Brodehl et al

scientific article published on 28 September 2018

Revisiting Genome Sequencing Data in Light of Novel Disease Gene Associations

artículo científico publicado en 2019

Revisiting the Diagnostic Yield of Hypertrophic Cardiomyopathy Genetic Testing

scientific article published on 21 April 2020

Role of Genetic Testing in Inherited Cardiovascular Disease: A Review.

artículo científico publicado en 2017

Routinely collected health data to study inherited heart disease: a systematic review (2000-2016).

artículo científico publicado en 2017

Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients

article

Social determinants of health in the setting of hypertrophic cardiomyopathy.

artículo científico publicado en 2015

Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients with Hypertrophic Cardiomyopathy

scientific article published on 25 August 2020

Sudden Cardiac Death in People With Schizophrenia

artículo científico publicado en 2023

Sudden cardiac death in the young: a clinical genetic approach.

artículo científico publicado en 2007

Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.

artículo científico

Sudden cardiac death rates in an Australian population: a data linkage study.

artículo científico publicado en 2015

Sudden death in athletes: preventable or inevitable?

artículo científico publicado en 2014

Sudden deaths during the largest community running event in Australia: A 25-year review.

artículo científico publicado en 2015

Temporal Trends in Sudden Cardiac Death From 1997 to 2010: A Data Linkage Study

artículo científico publicado en 2017

The Australian Genetic Heart Disease Registry

artículo científico publicado en 2013

The Dynamic and Multifaceted Nature of Cardiovascular Disease and Using Genetic Testing to Inform Clinical Care: An International Perspective

artículo científico publicado en 2020

The End Unexplained Cardiac Death (EndUCD) Registry for Young Australian Sudden Cardiac Arrest

scientific article published on 13 November 2020

The emerging role of the cardiac genetic counselor

artículo científico publicado en 2011

The genetic architecture of Plakophilin 2 cardiomyopathy

The social gradient of taking a family history.

artículo científico publicado en 2014

The value of cardiac genetic testing.

artículo científico publicado en 2014

Time to Rethink the Genetic Architecture of Long QT Syndrome

artículo científico publicado en 2020

Transcriptome Sequencing of Patients With Hypertrophic Cardiomyopathy Reveals Novel Splice-Altering Variants in <i>MYBPC3</i>

artículo científico publicado en 2021

Tweeting our way to cardiovascular health

artículo científico publicado en 2013

What Is the Risk of Sudden Cardiac Arrest in Inherited Cardiac Conditions?

artículo científico publicado en 2020

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

artículo científico publicado en 2020

Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy

scientific article published on 01 July 2018

Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy

artículo científico publicado en 2022

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