Lista de obras -

A Case for Inclusion of Genetic Counselors in Cardiac Care

artículo científico publicado en 2015

A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management.

artículo científico publicado en 2013

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

Broad Genetic Testing in a Clinical Setting Uncovers a High Prevalence of Titin Loss-of-Function Variants in Very Early Onset Atrial Fibrillation

scientific article published on 22 October 2019

Cardiopulmonary responses and prognosis in hypertrophic cardiomyopathy: a potential role for comprehensive noninvasive hemodynamic assessment.

artículo científico publicado en 2015

Care in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test Interpretation

artículo científico publicado en 2017

Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification

artículo científico publicado en 2017

Clinical interpretation and implications of whole-genome sequencing

artículo científico publicado en 2014

Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience

artículo científico publicado en 2017

Delivering Clinical Grade Sequencing and Genetic Test Interpretation for Cardiovascular Medicine

artículo científico publicado en 2017

Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes

article

Evolving Decisions: Perspectives of Active and Athletic Individuals with Inherited Heart Disease Who Exercise Against Recommendations

scientific article published on 15 September 2018

Exercise restrictions trigger psychological difficulty in active and athletic adults with hypertrophic cardiomyopathy

artículo científico publicado en 2016

Furthering the link between the sarcomere and primary cardiomyopathies: restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy

artículo científico publicado en 2011

Genetics and cardiovascular disease: a policy statement from the American Heart Association.

artículo científico publicado en 2012

How insensitive … How a mutation in the SCN5A voltage sensor leads to clinical arrhythmia ⬇️

artículo científico publicado el 25 de julio de 2012

Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy

article

Interdisciplinary psychosocial care for families with inherited cardiovascular diseases

artículo científico publicado en 2016

Invasive prenatal testing decisions in pregnancy after infertility

artículo científico publicado en 2010

Mindfulness Among Genetic Counselors Is Associated with Increased Empathy and Work Engagement and Decreased Burnout and Compassion Fatigue

artículo científico publicado en 2018

Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation

artículo científico publicado en 2016

Pathological Overlap of Arrhythmogenic Right Ventricular Cardiomyopathy and Cardiac Sarcoidosis

artículo científico publicado en 2019

Phased whole-genome genetic risk in a family quartet using a major allele reference sequence

artículo científico publicado en 2011

QTc prolongation and family history of sudden death in a patient with desmin cardiomyopathy

artículo científico publicado en 2010

Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy

scientific article published on 01 March 2019

Response to A Different Vantage Point Commentary: Psychotherapeutic Genetic Counseling, Is it?

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Sports genetics moving forward: lessons learned from medical research

artículo científico publicado en 2016

Structural Abnormalities on Cardiac Magnetic Resonance Imaging in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

scientific article published on 01 June 2020

Taming the genome: towards better genetic test interpretation

artículo científico publicado en 2016

Theories for Psychotherapeutic Genetic Counseling: Fuzzy Trace Theory and Cognitive Behavior Theory.

artículo científico publicado en 2016

Use and interpretation of genetic tests in cardiovascular genetics

artículo científico publicado en 2010

Lista de obras de

A Case for Inclusion of Genetic Counselors in Cardiac Care

A clinical approach to inherited hypertrophy: the use of family history in diagnosis, risk assessment, and management.

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

Broad Genetic Testing in a Clinical Setting Uncovers a High Prevalence of Titin Loss-of-Function Variants in Very Early Onset Atrial Fibrillation

Cardiopulmonary responses and prognosis in hypertrophic cardiomyopathy: a potential role for comprehensive noninvasive hemodynamic assessment.

Care in Specialized Centers and Data Sharing Increase Agreement in Hypertrophic Cardiomyopathy Genetic Test Interpretation

Clinical Cardiovascular Genetic Counselors Take a Leading Role in Team-based Variant Classification

Clinical interpretation and implications of whole-genome sequencing

Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience

Delivering Clinical Grade Sequencing and Genetic Test Interpretation for Cardiovascular Medicine

Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes

Evolving Decisions: Perspectives of Active and Athletic Individuals with Inherited Heart Disease Who Exercise Against Recommendations

Exercise restrictions trigger psychological difficulty in active and athletic adults with hypertrophic cardiomyopathy

Furthering the link between the sarcomere and primary cardiomyopathies: restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy

Genetics and cardiovascular disease: a policy statement from the American Heart Association.

How insensitive … How a mutation in the SCN5A voltage sensor leads to clinical arrhythmia ⬇️

Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy

Interdisciplinary psychosocial care for families with inherited cardiovascular diseases

Invasive prenatal testing decisions in pregnancy after infertility

Mindfulness Among Genetic Counselors Is Associated with Increased Empathy and Work Engagement and Decreased Burnout and Compassion Fatigue

Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation

Pathological Overlap of Arrhythmogenic Right Ventricular Cardiomyopathy and Cardiac Sarcoidosis

Phased whole-genome genetic risk in a family quartet using a major allele reference sequence

QTc prolongation and family history of sudden death in a patient with desmin cardiomyopathy

Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy

Response to A Different Vantage Point Commentary: Psychotherapeutic Genetic Counseling, Is it?

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

Sports genetics moving forward: lessons learned from medical research

Structural Abnormalities on Cardiac Magnetic Resonance Imaging in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Taming the genome: towards better genetic test interpretation

Theories for Psychotherapeutic Genetic Counseling: Fuzzy Trace Theory and Cognitive Behavior Theory.

Use and interpretation of genetic tests in cardiovascular genetics