Session Title
|
Session Type
|
CME
|
P.A.C.E.®
|
NSGC
|
Genetic Counselors Forum (NSGC Credits only)
|
Genetic Counselor Forum
|
|
|
1.25
|
Featured Platform Presentations
|
Platform
|
1
|
1
|
1
|
Platform Presentations - Biochemical/Metabolic Genetics
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Cancer Genetics and Therapeutics
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Clinical Genetics and Therapeutics
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Genetic Counseling
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Laboratory Genetics and Genomics
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Legal and Ethical Issues; Education
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Prenatal Genetics
|
Platform
|
1.5
|
1.5
|
1.5
|
Platform Presentations - Public Health, Health Services and Implementation
|
Platform
|
1.5
|
1.5
|
1.5
|
2022 Cardinal Signs
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Addressing the Challenges of Variant Reinterpretation
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Adult & Cancer Diagnostic Challenges
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Artificial Intelligence in Genomics: Potential and Peril - A SELI-Sponsored Session
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Balancing Evidence and Expertise: Clinical Practice Resource Development for PALB2, CHEK2, ATM and Beyond
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Down Syndrome Regression Disorder: Phenotype and Diagnostic Evaluation
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Exploring the Role of Medical Genetics and Genomics in Advancing Newborn Screening Research
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Health Disparities and Inherited Cancer Syndromes
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Hot Topics in Reproductive Genetics
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Human Ring Chromosome Disorders: An international Collaboration Towards Better Diagnosis, Interpretations, and Clinical Management
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Laboratory Diagnostic Challenges (Constitutional and Neoplastic Cases in Molecular, Cytogenomic, and Biochemical Genetics Specialties)
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Prenatal Diagnostic Challenges
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Reimagining Pediatric Genetic Service Delivery - Telemedicine Models in the Post COVID-19 Era
|
Concurrent
|
1.5
|
1.5
|
1.5
|
Rethinking Schwannoma Predisposition Syndromes - Neurofibromatosis Type 2 and Schwannomatosis
|
Concurrent
|
1.5
|
1.5
|
1.5
|
The Role of the HNRNP Gene Family in Neurodevelopmental Disorders
|
Concurrent
|
1.5
|
1.5
|
1.5
|
When is 'Non-Syndromic' Really Metabolic: Metabolic Causes of Intellectual Disability, Autism and Epilepsy
|
Concurrent
|
1.5
|
1.5
|
1.5
|
2022 Presidential Plenary Session - From Exceptional to Routine: Transformation of Genomic Medicine in the 21st Century
|
Plenary
|
1.5
|
1.5
|
1.5
|
Developing Recommendations for the Application of Direct-to-Consumer Genetic Testing in Clinical Care
|
Plenary
|
1.5
|
1.5
|
1.5
|
R. Rodney Howell Symposium | Population Genomic Health: Expanding the Reach of Genomic Medicine to Diverse Populations
|
Plenary
|
1.5
|
1.5
|
1.5
|
What are the Important Issues in the Arena of Public Policy and Legislation for Medical Genetics?
|
Plenary
|
1.5
|
1.5
|
1.5
|
An Action Plan for Inclusion, Diversity, Equity and Anti-Racism in Publishing: Putting IDEAs into Practice at Genetics in Medicine
|
Workshop
|
1.5
|
1.5
|
1.5
|
The ACMG Evidence-Based Guideline Program: Our Roadmap from Evidence to Recommendations and the impact on Patient Care
|
Workshop
|
1.5
|
1.5
|
1.5
|
Total Credits
|
|
46
|
46
|
47.25
|