Inherited Cardiomyopathies - Genetic Heart Disease
Explore inherited cardiomyopathies, their genetic components, and management implications. Learn about diagnostic criteria, genetic testing, and clinical approaches for various heart conditions.
Familial Hypercholesterolemia - Genetic High Cholesterol - Webinar - Ambry Genetics
Explore genetic high cholesterol: symptoms, diagnosis, genetics, testing, and treatment. Learn about familial hypercholesterolemia and its impact on cardiovascular health.
DNA Mapping for Preventive Health - Insights from 23andMe
Explore DNA mapping's potential in preventive healthcare with 23andMe co-founder Anne Wojcicki, discussing genetic insights and research initiatives.
Increasing the Positive Yield of Hereditary Cancer Testing with DNA and RNA - Ambry Genetics
Explore how combining DNA and RNA genetic testing enhances detection of clinically-actionable variants and reduces inconclusive results in hereditary cancer testing, improving diagnostic yield.
Talking to Patients About Genetic Testing and Psychosocial Implications of That Discussion - Webinar
Explore psychosocial challenges in genetic testing decisions, communication strategies, and patient support. Learn to create personalized information plans and navigate emotional complexities across various hereditary conditions.
Will RNA Testing Be the Next Del-Dup for Clinical Genetics - Webinar - Ambry Genetics
Explore how RNA genetic testing enhances hereditary cancer diagnostics, increasing detection of actionable variants and reducing inconclusive results through concurrent DNA and RNA analysis.
Genetic Testing for Hereditary Neurological Disorders - Webinar - Ambry Genetics
Explore genetic testing for neurological disorders, covering diagnosis, treatment options, and ethical considerations for pediatric and adult cases.
Assessing Patients for Hereditary Cancer Risk - Genetics 101 - Ambry Genetics
Learn to identify patients at risk for hereditary cancer, understand genetic testing benefits, and explore tools for assessment. Gain insights into cancer genetics and patient considerations for informed decision-making.
Analyzing Historical Mutations in the Cystic Fibrosis Gene - Ambry Genetics
Genetic counselors analyze CFTR gene mutations, discussing reclassified variants and implications for genetic testing in cystic fibrosis and related disorders.
Are DNA Testing Kits Good? - Benefits and Concerns
Explore the science, accuracy, and ethical implications of at-home DNA testing kits with experts in genetic genealogy, evolutionary genetics, and scientific publishing.
Genomic Medicine XV: Population Screening - Welcome and Keynotes - Session 1
Explore the current state, barriers, and opportunities of population genomic screening in the U.S., discussing its impact on clinical practice, technologies, costs, and future research directions.
Genetics in Primary Care - September 25, 2013
Explore genetic testing, diagnosis, and management in primary care settings, focusing on developmental disorders and ethical considerations.
The Intricacies of Splicing and RNA Data in Germline Variant Classification
Explore RNA splicing's impact on protein function and disease, focusing on complexities in interpreting RNA data and its role in germline variant classification.
Quality in Genetic Testing Laboratories - Opening the Black Box
Explore quality measures for genetic testing accuracy and clinical utility, with case-based examples demonstrating their impact on next-generation sequencing panel testing.
Improvements in Clinical Interpretation of Copy Number Variants (CNVs)
Explore advancements in clinical interpretation of Copy Number Variants (CNVs), addressing challenges and showcasing how unified guidelines can enhance consistency and quality in genomic diagnostics.
Genetic Testing in Adult Neurology Patients
Explore the utility and diagnostic yield of genetic testing in adult neurology patients, reviewing recent research findings and implications for clinical practice.
Integrating Functional Studies into Variant Interpretation
Explore DNA and RNA functional data integration in ACMG classification, evaluating assay quality and weighting in variant interpretation, with insights from recent ClinGen SVI recommendations.
Genetic Testing Results on Clinical Management for Lipid Patients
Explore genetic testing's impact on lipid patient management, focusing on Familial Hypercholesterolemia and Familial Chylomicronemia Syndrome. Learn from case studies and expert insights.
Clinical Validity Assessment of Gene-Disease Associations for Variant Classification
Explore standardized assessment of gene-disease associations and its role in determining variant pathogenicity for clinical reporting, aiding in diagnosis and management of genetic conditions.
Inherited Arrhythmias - Understanding Channelopathies and Sudden Cardiac Events
Explore potentially fatal but preventable causes of sudden cardiac arrest, focusing on channelopathies like LQTS, CPVT, BrS, and SCA/D in this informative webinar on inherited arrhythmias.
Familial Thoracic Aortic Aneurysms and Dissections - Genetic Testing and Patient Care
Explore hereditary cardiovascular diseases, focusing on thoracic aortic aneurysms and dissections. Learn how genetic testing enhances patient care for conditions like Loeys-Dietz syndrome and vascular Ehlers-Danlos syndrome.