Genetic Syndromes in Newborns - December 2, 2015
Explore neonatal genetic syndromes with Dr. Samir Alabsi, focusing on identification, diagnosis, and management strategies for healthcare professionals working with newborns.
Genetics and Cancer - What It Means for You and Your Family
Explore inherited cancer risk, genetic testing, and common cancer syndromes with Stanford experts. Learn about current tests and future developments in cancer genetics.
Dr. Jane Chueh on Prenatal Screening and Diagnosis
Explore advancements in prenatal genetic screening and diagnosis, including noninvasive tests, ultrasounds, and blood tests, to make informed decisions during pregnancy.
Carrier Screening Recommendations for Pregnant and Family Planning Individuals
Learn about carrier screening recommendations, test options, and family history considerations for pregnancy and family planning.
I Have a Family Member with Dementia - Am I at Risk?
Explore genetic factors in dementia, understand testing options, and learn about the rarity of hereditary causes in this informative presentation by a genetic counselor.
NextGen Genomic Medicine - Making Variants of Unknown Significance Obsolete
Explore cutting-edge genomic medicine and its impact on understanding genetic variants. Learn how advanced techniques are revolutionizing the interpretation of previously unknown genetic variations in cardiovascular health.
MPG Primer - A Brief History of Non-Invasive Prenatal Testing
Explore the evolution of non-invasive prenatal testing in this comprehensive overview, covering key developments, technological advancements, and their impact on genetic screening.
Cardiomyopathy Genetics: Current and Evolving Applications
Uncover the genetic foundations of cardiomyopathies, exploring testing methods and their impact on our understanding of heart muscle diseases.
Autism Awareness and Inclusion - Raising a Child on the Spectrum
Powerful Arabic TEDx talk on autism, neurodiversity, and inclusive actions. Dr. Fatema Marhoon shares personal experiences as a parent and medical professional, advocating for social acceptance and awareness.
Prostate Cancer Genetic Risk Assessment - Webinar - Ambry Genetics
Comprehensive overview of genetic risk assessment in prostate cancer, covering polygenic risk scores, rare pathogenic mutations, and their clinical implications for personalized screening and treatment.
Overview of Cardiovascular Genetics - Getting to the Heart of the Matter
Comprehensive overview of cardiovascular genetics, covering inherited heart conditions, genetic testing, and counseling approaches for healthcare professionals in the field.
Cardiovascular Genetic Testing - Incorporating and Applying Results by Erin Miller and Amy Sturm
Explore cardiovascular genetic testing, result interpretation, and clinical applications through case studies, focusing on family history analysis and cascade testing implications.
Genetic Testing for Prostate Cancer - Advances and Considerations
Explore advances in genetic testing for prostate cancer, including risk prediction, precision therapies, and genetic counseling. Learn about implementation strategies and guidelines for germline testing in prostate cancer care.
Navigating Transitions Between Telehealth and In-Person Clinic - Ambry Genetics
Genetic counselors discuss transitioning between telehealth and in-person care during COVID-19, sharing experiences from various specialties and locations to address medical and social impacts on patients and providers.
Evaluating the Family After Sudden Death in the Young
Understand postmortem genetic testing and family evaluation after sudden cardiac death in young individuals. Learn about pathology, causes, and risk assessment for inherited cardiovascular diseases.
Leveraging Innovation to Improve the Identification of Patients with Hereditary Cancer
Explore innovative techniques in hereditary cancer detection, including RNA genetic testing and AI-powered risk assessment, to improve diagnostic yield and patient identification for genetic counseling.
Bioinformatics and Computational Terminology for the Clinic - Webinar - Ambry Genetics
Demystifying bioinformatics concepts in genetic testing reports, focusing on key terminology and underlying details for NGS panel and exome-sequencing tests to enhance clinicians' understanding and interpretation.
Diagnosis, Management, and Genetics of hATTR Amyloidosis - Webinar - Ambry Genetics
Comprehensive overview of hATTR amyloidosis, covering diagnosis, management, and genetic aspects. Experts discuss clinical presentations, genotype-phenotype correlations, and genetic counseling challenges for patients and families.
Exome Sequencing for Congenital Anomalies or Neurodevelopmental Disorders - Webinar - Ambry Genetics
Explore exome sequencing for congenital anomalies and neurodevelopmental disorders, comparing testing methods, discussing clinical implementation, and examining diagnostic yields for various patient populations.
New Directions in Access to Genetic Counseling Information for Precision Medicine - Webinar
Exploring digital tools for efficient dissemination of genetic counseling information in precision medicine, addressing challenges in access and timely updates for clinicians and patients.
Gene Specific Cancer Associations and Sensitivity of Genetic Testing Criteria
Explore gene-specific cancer risks, prevalence of pathogenic variants, and sensitivity of testing criteria for BRCA1/2 and Lynch syndrome based on a large multigene panel cohort study.