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List of works by Laura Yeates

"Concealed cardiomyopathy" as a cause of previously unexplained sudden cardiac arrest

scientific article published on 12 September 2020

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

scientific article published in June 2016

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

scientific article published on 28 August 2018

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

scientific article published on 08 February 2022

Analysis of the Z-disc genes PDLIM3 and MYPN in patients with hypertrophic cardiomyopathy.

scientific article

Assessment of myocardial oxygenation, strain, and diastology in MYBPC3-related hypertrophic cardiomyopathy: a cardiovascular magnetic resonance and echocardiography study

scientific article published on 01 August 2019

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

scientific article published on 03 May 2017

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

article

Clinical challenges of genotype positive (+)-phenotype negative (-) family members in hypertrophic cardiomyopathy

scientific article published on 22 December 2010

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy

scientific article

Comparison of conventional autopsy and magnetic resonance imaging in determining the cause of sudden death in the young

scientific article

Concealed Arrhythmogenic Right Ventricular Cardiomyopathy in Sudden Unexplained Cardiac Death Events

scientific article published on 01 November 2018

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

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

scientific article published on 23 March 2017

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

scientific article published on 3 May 2012

Guidelines for genetic testing of inherited cardiac disorders

scientific article

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

scientific article published on 17 September 2011

Holt-Oram syndrome in two families diagnosed with left ventricular noncompaction and conduction disease.

scientific article published on 13 February 2018

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

scientific article published on 25 December 2012

Interdisciplinary psychosocial care for families with inherited cardiovascular diseases

scientific article published on 28 April 2016

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

scientific article

Needs analysis of parents following sudden cardiac death in the young

scientific article published on 01 July 2020

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

scientific article published on April 2017

Perceptions of genetic variant reclassification in patients with inherited cardiac disease

scientific article published on 21 March 2019

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

scientific article published on 8 April 2013

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

scientific article published on 25 January 2016

Preclinical alterations in cardiac energetics amongst sarcomere mutation carriers in hypertrophic cardiomyopathy

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

scientific article published on 30 December 2019

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

scientific article published on 16 October 2018

Rare desmin variant causing penetrant life-threatening arrhythmic cardiomyopathy.

scientific article published on 28 April 2018

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

scientific article

Risk of sudden death and outcome in patients with hypertrophic cardiomyopathy with benign presentation and without risk factors

scientific article published on 12 February 2014

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

article

Social determinants of health in the setting of hypertrophic cardiomyopathy.

scientific article published on 5 March 2015

The emerging role of the cardiac genetic counselor

scientific article published on 20 July 2011

The role of large gene deletions and duplications in MYBPC3 and TNNT2 in patients with hypertrophic cardiomyopathy

scientific article published on 09 August 2009

Twelve-lead ambulatory electrocardiographic monitoring in Brugada syndrome: Potential diagnostic and prognostic implications

scientific article

Ventricular Tachycardia in a Patient With Dilated Cardiomyopathy Caused by a Novel Mutation of Lamin A/C Gene: Insights From Features on Electroanatomic Mapping, Catheter Ablation and Tissue Pathology

scientific article published on 05 October 2020

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

scientific article published on 27 April 2020

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