Rare Disease Genetics: Unlocking Insights for All
Автор: New York Genome Center
Загружено: 2018-04-08
Просмотров: 518
Описание:
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
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