Realizing the benefits of human genetics and genomics research for people everywhere.
Media Contact: Nalini Padmanabhan ASHG Communications Manager 301.634.7346 press@ashg.org For Immediate Release Thursday, October 20, 2016 11:15 a.m. U.S. Pacific Time Findings Reported at ASHG 2016 Annual Meeting BETHESDA, MD – Parents of children newly diagnosed with cancer value the results of whole exome sequencing for a variety of reasons beyond clinical actionability, according to... Read More
Media Contact: Nalini Padmanabhan ASHG Communications Manager 301.634.7346 press@ashg.org For Immediate Release Thursday, October 20, 2016 10:00 a.m. U.S. Pacific Time Findings Reported at ASHG 2016 Annual Meeting BETHESDA, MD – Relationships between the ancestors of modern humans and other archaic populations such as Neanderthals and Denisovans were likely more complex than previously thought, involving... Read More
Media Contact: Nalini Padmanabhan ASHG Communications Manager 301.634.7346 press@ashg.org For Immediate Release Wednesday, October 19, 2016 10:15 a.m. U.S. Pacific Time Findings Reported at ASHG 2016 Annual Meeting BETHESDA, MD – Infection with Zika virus disrupts fetal brain development by interfering with the proliferation of human neural progenitor cells (hNPCs), a type of cell that... Read More
Media Contact: Nalini Padmanabhan ASHG Communications Manager 301.634.7346 press@ashg.org For Immediate Release Wednesday, October 19, 2016 10:15 a.m. U.S. Pacific Time Findings Reported at ASHG 2016 Annual Meeting BETHESDA, MD – Adding non-invasive prenatal genetic screening (NIPS) for fetal chromosomal abnormalities to the current prenatal testing strategy in Quebec would be more cost-effective than current... Read More
Media Contact: Nalini Padmanabhan ASHG Communications Manager 301.634.7346 press@ashg.org For Immediate Release Wednesday, October 19, 2016 9:45 a.m. U.S. Pacific Time Findings Reported at ASHG 2016 Annual Meeting BETHESDA, MD – Early results from the BabySeq Project, a Boston-based study exploring the impact of whole-exome sequencing (WES) on newborn infants and their families, suggest some... Read More