Tag: NIH

23andMe Launches Its First NIH Funded Study

  By Amy Kiefer and Kim Barnholt 23andMe is excited to announce the launch of our first National Institutes of Health (NIH) funded research project. In the fall of 2010, 23andMe received a NIH Small Business Innovative Research Grant (SBIR) to validate our web-based approach to pharmacogenomics ...

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NIH to Create Public Database of Genetic Tests

Today the National Institutes of Health (NIH) announced its plans to create a public database in which genetic test providers will voluntarily deposit information about their services that can then be searched by researchers, consumers, health care providers, and others. The aim of this Genetic Testing ...

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23andMe Parkinson’s Research Initiative Progress Update

By Nick Eriksson, 23andMe Principal Scientist, and Lizzie Dorfman, Parkinson's Research Project Manager Less than a year ago we announced the launch of the 23andMe Parkinson’s Research Initiative. Since then, we have built one of the world's most useful resources for studying the genetics of Parkinson's ...

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The Story of Henrietta Lacks: A Lesson in Biology and Ethics

Editor's note: We posted this a couple of years ago, but in light on the historic agreement between the family of Henrietta Lacks and National Institutes of Health, we thought it worthy of re-posting. Also read Carl Zimmer's great piece in the New York Times. The post has been slightly changed from the ...

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