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Researchers from the University of Michigan School of Public Health and the Jackson Laboratory for Genomic Medicine will lead an interdisciplinary, multi-institution study of the ethical, legal and social implications of workplace genomic testing in the United States.
Sickle cell disease affects about 100,000 Americans, most of them African-Americans. There are few treatments for it, and experts say not enough is being done to prevent complications.
Collecting DNA samples for human genetic studies can be an expensive, lengthy process that has often made it difficult to include diverse populations. Now, University of Michigan researchers believe they have found a way to harness the power of social media to recruit a large, diverse participant pool.
An international consortium of scientists has analyzed protein-coding genes from nearly 46,000 people, linking rare DNA alterations to type 2 diabetes. The study, one of the largest known of its type, includes data from people of European, African American, Hispanic/Latino, East Asian, and South Asian ancestries.
Scott Roberts, professor of Health Behavior and Health Education at the University of Michigan School of Public Health, has been appointed co-chair of the Michigan Dementia Coalition (MDC). The MDC is a statewide group of >120 individuals from approximately 65 organizations that works to identify opportunities to improve quality of life for Michigan residents with dementia and their families.
Five years in, the US$360 million Accelerating Medicines Partnership is yielding tools to speed up drug discovery for rheumatoid arthritis, lupus, diabetes, Alzheimer disease and Parkinson disease.