UM John P. Hussman Institute for Human Genomics hosts DNA Day 2012 at Miami Science Museum
DNA Day event date: April 29th 11am-3pm
DNA Day event date: April 29th 11am-3pm
Liyong Wang, Ph.D.
Research Assistant Professor
Tuesday, April 17, 2012 at 4pm – Seminar Title:
“Life After Association?”
April 2, 2012 – Research led by Margaret A. Pericak-Vance, Ph.D., John R. Gilbert, Ph.D., and Dale Hedges, Ph.D., of the John P. Hussman Institute for Human Genomics at the University of Miami Miller School of Medicine again supports the importance of structural variation in autism spectrum disorder (ASD). This unique study using high-resolution arrays to detect changes in DNA structure as small as one thousand base pairs further strengthens the case that rare structural variants at multiple genes contribute to autism spectrum disorders…
Tuesday, April 3, 2012 at 4:00pm Human Genetics and Genomics Seminar Series
“We are very excited about the direction of genetic research in MS,” said Pericak-Vance in a release. “Our current research has the potential to identify new therapeutic targets.”
Paul A. Sieving, M.D., Ph.D., director of the National Eye Institute, National Institutes of Health, spoke Tuesday, March 6, 2012, in the Lois Pope 7th Floor Auditorium. The event was jointly sponsored by the John P. Hussman Institute for Human Genomics and Bascom Palmer Eye Institute, both of the University of Miami Miller School of Medicine.
February 21, 2012 – Powered by the University of Miami Miller School of Medicine’s groundbreaking research…
Tuesday, February 21, 2012 – Speaker: Mohammad Ali Faghihi, M.D., Ph.D., Research Assistant Professor, Department of Psychiatry and Behavioral Sciences
February 7, 2012 – A team of researchers led by Claes Wahlestedt, M.D., Ph.D., the Miller School’s associate dean for therapeutic innovation, has pinpointed a “master” regulatory molecule in the brain that is altered in people with schizophrenia. The finding could facilitate the development of better drugs for the debilitating psychiatric disorder that affects an estimated one percent of the world’s population.
January 13, 2012 – UM researchers have identified a genetic variant linked to a rare form of paraplegia in a paper titled, “Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 2” published online January 10, 2012 in the Journal of Clinical Investigation.