University of Utah Health scientists, Mark Yandell, PhD, and Martin Tristani-Firouzi, MD, used artificial intelligence to better predict the onset and outcomes of heart disease
In collaboration with ARUP and U of U’s Center for Genomic Medicine, Mark Yandell from the Utah Center for Genetic Discovery use rapid whole genome…
UCGD analysts are participating in gene discovery research for the Penelope clinic.
Ryan Layer, Ph.D., senior postdoctoral fellow in Aaron Quinlan’s lab at the Department of Human Genetics at U of U Health and the USTAR Center for…
Aaron Quinlan, PhD, Associate Professor of Human Genetics and Co-Director of the USTAR Center for Genetic Discovery, and his graduate student, Tom Sasani, develop a…
Dr. Mark Yandell and collaborators, Drs. Martin Tristani-Firouzi and H. Joseph Yost, take part in a large national “Bench-to-Bassinet” NIH consortium to study congenital heart…
Researchers at the U of U, in collaboration with Janssen Research and Development LLC, search genetic clues to better understand the relationship between suicidal behavior and psychiatric conditions.
Drs. Gabor Marth and Martin Tristani-Firouzi use a software tool, iobio, to assist doctors with providing clinical care based on information found within their patient’s DNA.
Mark Yandell, Ph.D., professor of human genetics and director of the USTAR Center for Genetic Discovery has created new tools, CAE and WARP, to uncover…
The Quinlan Laboratory is using the diminutive MinION genome sequencing device to study viral genome evolution.
Drs. Martin Tristani-Firouzi and Mark Yandell launch the Sudden Death in the Young project to discover the genetic causes of sudden cardiac death.
Dr. Robert Schlaberg was awarded a Global Grand Challenges award from the Bill and Melinda Gates Foundation to study fatal childhood infectious diseases in resource-limited settings.
Investigators Hilary Coon, Gabor Marth, and Aaron Quinlan have been awarded a SFARI grant from the Simon’s Foundation for Autism Research to study the genetic causes of Austism Spectrum Disorder.
This month, two publications appear in a special issue of the journal Nature celebrating 25 years since the launch of the Human Genome Project and marking the completion of The 1000 Genomes Project, launched in 2008.
The Genomic Revolution Blog explores ethics and consequences of genetic testing in children.
