Realizing the benefits of human genetics and genomics research for people everywhere.
Nascent Transcript Writer: Sumantra Chatterjee, PhD Large scale exome and whole genome sequencing have led to cataloging vast arrays of disease-associated genes and variants for various multifactorial disorders, yet the underlying biology for most of these has been difficult to unravel, leading to diagnostic uncertainty. This has been partly due to our incomplete knowledge of... Read More
Published: Friday, October 18, 2019, 5:35 p.m. U.S. Eastern Time Media Contact: Nalini Padmanabhan, 301.634.7346, press@ashg.org Findings Reported at ASHG 2019 Annual Meeting HOUSTON, Texas – Scientists are finding new ways to improve the use of the CRISPR enzyme Cas9 and reduce the chances of off-target mutations in laboratory mice, according to new results from... Read More
Researchers and genetic counselors can collaborate through grant funding. At a panel session at ASHG 2019, NSGC and ASHG experts shared advice on how. Read More
Published: Thursday, October 17, 2019, 5:00 p.m. U.S. Central Time Media Contact: Ann Klinck, 301.634.7342, press@ashg.org Findings Reported at ASHG 2019 Annual Meeting HOUSTON, Texas – Health reports from direct-to-consumer (DTC) genetic tests that use a limited variant screening approach often yield clinical false-negative results, which pose the risk of informing health care decisions based... Read More
Published: Thursday, October 17, 2019, 12:00 p.m. U.S. Central Time Media Contact: Ann Klinck, 301.634.7342, press@ashg.org Findings Reported at ASHG 2019 Annual Meeting HOUSTON, Texas – Researchers have found that carriers of the most common genetic variant that causes cystic fibrosis experience some symptoms similar to those of people with cystic fibrosis. These findings were... Read More