January 11 Nancy Cox, PhD
Professor of Medicine
Mary Phillips Edmonds Gray Chair
Dan Roden, MD
Professor of Medicine, Pharmacology, and Biomedical Informatics
Sam L. Clark, MD, PhD Endowed Chair
Senior Vice President for Personalized Medicine
Where we are and where we are going in Genomic and Personalized Medicine
January 25 Jehannine C. Austin, PhD FCAHS CGC
Professor, UBC Departments of Psychiatry and Medical Genetics
Executive Director BC Mental Health and Substance Use Services Research Institute
Applying genomics and personalized medicine to psychiatric disorders: evidence based strategies to improve
outcomes for people with psychiatric disorders
February 1 Laura Raffield, PhD
Assistant Professor, University of North Carolina at Chapel Hill
Genomic Analysis of Inflammation in Diverse Cohort Studies
February 8 Tom Stricker, MD, PhD
Assistant Professor, Pathology, Microbiology, and Immunology
Medical Director, Clinical Genomics Lab
Associate Director, VANTAGE
Updates from the Clinical Genomics Lab
February 15 Kaitlin E. Samocha, PhD
Assistant Professor
Center for Genomic Medicine
Massachusetts General Hospital
Contribution of rare variants to developmental disorders
February 22 Sonya Reid, MD, MPH
Assistant Professor of Medicine
Racial Disparities in Germline and Somatic Testing
March 1 Adam Wright, PhD
Professor of Biomedical Informatics
Clinical Informatics and Personalized Medicine
March 8 Jay Shendure, MD, PhD
Investigator, Howard Hughes Medical Institute
Director, Allen Discovery Center for Lineage Tracing
Director, Brotman Baty Institute for Precision Medicine
Professor, Genome Sciences, University of Washington
New Methods in Genetics & Genomics
March 22 Noura S. Abul-Husn, MD, PhD
Associate Professor of Medicine and Genetics
Chief, Division of Genomic Medicine, Department of Medicine
Clinical Director, The Institute for Genomic Health
Icahn School of Medicine at Mount Sinai
Genomic Medicine in Diverse Populations: From Biobanks to Patients
March 29 Victoria N. Parikh, MD
Assistant Professor of Medicine
Stanford Center for Inherited Cardiovascular Disease
Stanford University School of Medicine
Interpreting and editing the genome for arrhythmogenic cardiomyopathies
April 5 Robert Carroll, PhD
Assistant Professor of Biomedical Informatics
Genomic analyses on ~90k WGS and ~165k arrays in the All of Us Researcher Workbench
April 12 Mya Roberson, PhD
Assistant Professor of Health Policy
Equity considerations for genetic and genomic testing in cancer patients
April 19 Kevin Ess, MD, PhD
Gerald M. Fenichel Chair in Neurology
Chief, Division of Pediatric Neurology
Vanderbilt Pediatric Rare Diseases Center
Stem Cell Modeling of Human Disease: What’s More Personal Than That?
April 26 Maggie Ng, PhD
Associate Professor of Genetic Medicine
Polygenic Risk Score of Type 2 Diabetes in Diverse Ancestries
Extended a week!
May 3 Jeffrey N. Weitzel, MD
Vice President of Medical Affairs, Hereditary Cancer, Natera
Professor, Latin American School of Oncology
Addressing global implementation of genomic cancer risk assessment - Lessons learned in Latin America