Rare Disease Genetics: Unlocking Insights for All скачать в хорошем качестве

Rare Disease Genetics: Unlocking Insights for All

On February 28, 2018 (Rare Disease Day 2018), the New York Genome Center hosted a scientist panel that Join us for a discussion with our scientist panel to learn more about new advances in understanding the genetics behind pediatric rare diseases, how next-generation sequencing is uncovering the genetic variants responsible for rare disease risks, and how the genomic study of rare diseases has furthered the understanding of all diseases. The panel included: MODERATOR Max Gomez, PhD Medical Correspondant CBS News Co-Author Cells Are the New Cure: The Cutting-Edge Medical Breakthroughs That Are Transforming Our Health SPEAKERS Tuuli Lappalainen, PhD Core Faculty Member New York Genome Center Assistant Professor Department of Systems Biology Columbia University Jean-Laurent Casanova, MD, PhD Professor St. Giles Laboratory of Human Genetics of Infectious Diseases The Rockefeller University Investigator Howard Hughes Medical Institute Bruce D. Gelb, MD Gogel Family Chair and Director Mindich Child Health and Development Institute Professor of Pediatrics and Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai