Category: inside 23andMe

Talking about Sarcoma with George Demetri

On a recent visit to 23andMe George Demetri —a physician and scientist who is an unpaid advisor to our Sarcoma research initiative — sat down for a short interview after talking to our team. Demetri, who is also director of the Dana-Farber Center for Sarcoma and Bone Oncology, said he has a lot to be ...

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When DNA Discoveries Hit Close to Home

In August of last year, I wrote  with hope and excitement about the launch of the 23andMe MPN Research Initiative because my father, Harvey, suffers from myelofibrosis.  On March 5, 23andMe scientist Bethann Hromatka posted a SNPWatch report about the association between the JAK2 gene and MPNs. 23andMe ...

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Silver Linings in Rare Disease

Luck is not the word you typically associate with a cancer diagnosis or even a heightened risk of cancer, but some people can see a silver lining even in the darkest storms. Harvey Gould and John Lauerman certainly have. “Some believe that blessings come out of serious adversity,” said Harvey, who was ...

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Did You Know? It’s Not so Rare to Have a Rare Disease

Today, February 29, is Rare Disease Day — a concept first initiated by the European Rare Disease Organization (EURORDIS) and now recognized around the world. Join the Global Genes Project™ and help unite one million people for rare diseases. The Global Genes Project™ is a campaign that works to ...

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23andAli

At a Las Vegas gala celebrating Muhammad Ali’s 70th birthday, we premièred the video "Give Us Your Hand," featuring the boxing legend and his involvement with 23andMe’s Parkinson’s Disease Research Initiative. By Emily Drabant As the Research Manager for the 23andMe Parkinson’s Community, I spend my ...

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More at ICHG/ASHG: The Nuts and Bolts Behind Health and Ancestry

If you're just joining us, our scientists are busy this week presenting findings from our research at ICHG/ASHG 2011 in Montreal. But not all of our scientific contributions are in the realm of genetic associations. As some of our other conference posters have shown, we also spend a lot of time thinking about ...

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A Recipe for Disease Research: Give People Tools, Add Passion, and Shake

[Update: View a video recap of Sarcoma Community Night at http://www.23andme.com/sarcoma/] Three. That was the average number of patients enrolled in studies for sarcoma four years ago when Nathalie Criou, a sarcoma cancer survivor and founder of Beat Sarcoma, looked around for new information about her ...

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Sarcoma Community Update

Genetic research is a numbers game. The more people who contribute to the effort, the more powerful it gets. As our Sarcoma Community grows with survey responses and genetic data from participants, we learn more about sarcoma and people’s responses to treatment. We are over halfway to our goal of 1,000 ...

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23andMe Research Team Presents Findings at International Human Genetics Meeting

By Kim Barnholt and Amy Kiefer It’s an exciting week for 23andMe! A number of our research scientists have headed to Washington, D.C. to showcase some of our research discoveries at the annual meeting of the American Society of Human Genetics (ASHG). ASHG is the primary professional membership organization ...

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Update on 23andMe and the FDA

On June 10, 2010, 23andMe received a letter from the Food and Drug administration (FDA) expressing the agency's view that our Personal Genome Service™ may be subject to FDA regulation.  We have responded to this letter and are in the process of scheduling a meeting with the agency for further discussions.  ...

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