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By participating in one of the world’s largest genetic studies, New Yorkers will help bring precision medicine to their communities, Columbia’s David Goldstein explains.
A new study finds that regulatory gene variants can affect the severity of a genetic disease among people with the same protein-coding mutation.
- June 1, 2016
Columbia oncologist and Pulitzer Prize-winning author Siddhartha Mukherjee talks about why he wrote his latest book, "The Gene: An Intimate History."
- April 25, 2016
For some types of autism, gastrointestinal problems may originate from the same genetic changes that lead to the behavioral and social characteristics of the condition.
- January 26, 2016
College of Physicians & Surgeons Dean Lee Goldman discusses his new book, which examines the role DNA plays in attempting to treat diabetes, obesity, and cardiovascular disease.
- January 12, 2016
Wayne Frankel, the newest member of the Institute for Genomic Medicine, says recent advances in gene discovery and editing are illuminating epilepsy.
- December 9, 2015
P&S researcher Wendy Chung and colleagues find genetic mutations that explain why many children with congenital heart disease also have neurodevelopmental disorders.
- October 2, 2015
Funding from the ALS Association and the Tow Foundation will be used by the New York Genome Center to determine the entire genetic sequence of people with ALS who donated their tissues after death.
- September 23, 2015
The Columbia Combined Cancer Panel has been granted full approval by the New York State Department of Health.
- June 1, 2015
A rare eye disorder marked by color blindness, light sensitivity, and other vision problems can result from a newly discovered gene mutation identified by an international research team, including scientists from Columbia University Medical Center (CUMC). The findings could lead to new, targeted treatments for this form of color blindness.
- April 20, 2015
A significant proportion of children with chronic kidney disease (CKD) have unsuspected chromosomal imbalances, including DNA anomalies that have been linked to neurocognitive disorders.