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Thursday, Nov 16th
10:15 AM - 11:45 AM
MST
Polygenic Risk Scores - Implementation and Clinical Utility
Location: 255EF, Second Level
Co-Moderator:
Honey Reddi, PhD
– Medical College of Wisconsin
Co-Moderator:
Meng-Chang Hsiao, PhD
– Vanderbilt University Medical Center
Advocacy
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Thursday, Nov 16th
10:15 AM - 10:45 AM
MST
Clinical Implementation of Polygenic Risk Scores
Location: 255EF, Second Level
Speaker:
Aya Abu-El-Haija, MD MPH
– Boston Children's Hospital
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Thursday, Nov 16th
10:45 AM - 11:15 AM
MST
Implementation of Polygenic Risk Scores - Laboratory Perspectives
Location: 255EF, Second Level
Speaker:
Matthew Lebo, PhD (he/him/his)
– Lab for Molecular Medicine, Mass General Brigham Personalized Medicine
Advocacy
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Thursday, Nov 16th
11:15 AM - 11:45 AM
MST
Status of the Use of Polygenic Scores for PGT
Location: 255EF, Second Level
Speaker:
Patrick Turley, PhD (he/him/his)
– University of Southern California
Advocacy
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Friday, Nov 17th
10:55 AM - 11:15 AM
MST
Novel Diagnostic DNA Methylation Episignatures Expand and Refine the Epigenetic Landscapes of Mendelian Disorders
Location: 255EF, Second Level
Speaker:
Bekim Sadikovic, PhD
– London Health Sciences Centre, Western University, London, ON, Canada.
Lab Management
Inherited Conditions
Molecular Methodologies & Technologies
CE: NOT CME/CMLE
Friday, Nov 17th
11:15 AM - 11:45 AM
MST
Panel Discussion
Location: 255EF, Second Level
Speaker:
Michael E. Talkowski, PhD (he/him/his)
– Center for Genomic Medicine of Massachusetts General Hospital, Harvard Medical School
Speaker:
Bekim Sadikovic, PhD
– London Health Sciences Centre, Western University, London, ON, Canada.
Speaker:
Danny Miller, MD, PhD (he/him/his)
– University of Washington
Lab Management
Inherited Conditions
Molecular Methodologies & Technologies
CE: NOT CME/CMLE
Friday, Nov 17th
1:15 PM - 1:45 PM
MST
Newborn Screening by Genomic Sequencing: Opportunities and Challenges
Location: 355BC, Third Level
Speaker:
Wendy Chung, MD, PhD (she/her/hers)
– Boston Children's Hospital/Harvard Medical School
Advocacy
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Friday, Nov 17th
1:45 PM - 2:15 PM
MST
Adding Genomic Sequencing and Genetic Risk Scores to the Early Check Newborn Screening Study
Location: 355BC, Third Level
Speaker:
Katerina S. Kucera, PhD
– RTI International
Advocacy
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Friday, Nov 17th
2:15 PM - 2:45 PM
MST
Exploring Whole Genome Sequencing for Newborn Screening: Lessons from the BabySeq Project
Location: 355BC, Third Level
Speaker:
Matthew Lebo, PhD (he/him/his)
– Lab for Molecular Medicine, Mass General Brigham Personalized Medicine
Advocacy
Inherited Conditions
Molecular Methodologies & Technologies
CE: 1.50
Saturday, Nov 18th
8:15 AM - 9:15 AM
MST
DNA Hypomethylation Restrains Malignant Progression
Location: Grand Ballroom, Lower Concourse
Speaker:
Sarah Johnstone, MD, PhD
– Dana-Farber Cancer Institute
Oncology
Inherited Conditions
CE: 1.0
Saturday, Nov 18th
1:15 PM - 1:45 PM
MST
AMP Working Group: Standardization of Pharmacogenomics Alleles
Location: 250, Upper Concourse
Speaker:
Karen Weck, MD (she/her/hers)
– University of North Carolina at Chapel Hill
Lab Management
Inherited Conditions
Molecular Methodologies & Technologies
CE: NOT CME/CMLE
Saturday, Nov 18th
1:45 PM - 2:15 PM
MST
Panel Discussion: AMP Working Group: Standardization of Pharmacogenomics Alleles
Location: 250, Upper Concourse
Panelist:
Karen Weck, MD (she/her/hers)
– University of North Carolina at Chapel Hill
Panelist:
Lisa V. Kalman, PhD
– Centers for Disease Control and Prevention
Panelist:
Stuart A. Scott, PhD
– Stanford University
Panelist:
Houda Hachad, PharmD. M Res. (she/her/hers)
– AccessDx Laboratory
Lab Management
Inherited Conditions
Molecular Methodologies & Technologies
CE: NOT CME/CMLE