A new manuscript from the IGNITE Pragmatic Trials Network has been published in JAMA Network Open, describing the primary results of the GUARDD-US study. GUARDD-US is a randomized controlled trial examining the impact of returning APOL1 genetic risk results to ...
Thursday, September 29, 2022 | 3 - 4:15 p.m. ET | Virtual Beginning September 2022, NHGRI will host a new seminar series based on its Genomic Innovator Award Program, which supports […]
Monday, October 3 | 9-10 a.m. ET | Virtual The IHCC is debuting a new panel series as part of the IHCC Educational Webinar Series. This Panel Discussion will focus […]
Wednesday, October 5 - Thursday, October 6 | Boston, MA & Virtual The inaugural International Conference on Newborn Sequencing, to be held October 5-6 in Boston, will explore how DNA […]
October 6-7, 2022 | 10 a.m.-5 p.m. | Virtual The National Human Genome Research Institute (NHGRI) and the University at Buffalo Center for Disability Studies will hold a two-day symposium […]
Thursday, October 6 | 11 am-12 pm ET This seminar will review our emerging knowledge of the role of host genomic factors in the susceptibility and outcomes of COVID-19 infection, […]
Thursday, October 6, 2022 | 2-3 p.m. ET | Virtual & In Person (Bethesda, MD) The Division of Intramural Research (DIR) sponsors a monthly series of talks by intramural and […]
Wednesday, October 12, 2022 | 10:30 am - 6 pm ET | Virtual A planning committee of the National Academies of Sciences, Engineering, and Medicine will organize and conduct a […]
October 25-29 | Los Angeles, CA ASHG 2022 will take place October 25-29 in Los Angeles. The meeting provides a forum for the presentation and discussion of cutting-edge science in […]
Monday, October 31 | 12-1 pm ET | Virtual Virtual seminar: Race, Society, and Genetics Speaker: Marwa Elnagheeb, MPH, Senior Coordinator, Clinical Genome Resource, UNC Chapel Hill Seminar abstract: Interactions […]
Explore the Exposome: The Next Frontier of Individualizing Medicine November 2-3, 2022 | Rochester, MN & Virtual When genomics alone cannot explain a disease, we enter the world of the […]
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