Category: announcements

23andMe’s MPN Initiative Welcomes Dr. Ruben Mesa as Scientific Advisor

In just three months, 23andMe’s Myeloproliferative Neoplasms (MPN) Research Initiative has grown to more than 330 active participants. Our Scientific Advisory Board has grown as well with another prestigious scientist, Dr. Ruben Mesa, joining Dr. Jason Gotlib and Dr. James Zehnder from the Stanford University ...

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A Prescription for Personalizing Medicine

While a lot of the discussion about personalized medicine is focused on the future, Felix Frueh of Medco Health Solutions believes the most promising possibilities for individualized care could be implemented right now. Knowing a person’s underlying genetics with currently available tests could make ...

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23andMe Scientists Head to Montreal for ICHG/ASHG, Eh

The joint 12th International Congress of Human Genetics and 61st Annual Meeting of the American Society of Human Genetics held this week in Montreal is expected to draw more than 7,000 attendees over five days. Joining the throng will be about a dozen scientists from 23andMe. We’ll be there presenting a ...

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Join 23andMe at ICHG/ASHG 2011 for Drinks and a Chance to Win an Exome!

What: 23andMe Mixer and Exome Giveaway* Date: Wednesday, October 12th Time: 8:30-10:00pm Where: Les 3 Brasseurs, St-Paul, 105 St-Paul St. E., Montreal, Quebec The world’s top scientists and researchers in human genetics will gather in Montreal next week to chase down plates of “poutine” with pints of La ...

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FDA to Hold Public Town Hall Discussion in San Francisco

In March earlier this year, 23andMe presented its views on possible federal regulation of the direct-to-consumer (DTC) genetic testing industry at an Advisory Committee meeting convened by the FDA. We reiterated our belief that individuals have a right to access their own genetic information without physician ...

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Roots into the Future: A New 23andMe Research Initiative For African Americans

http://www.youtube.com/watch?v=kTYFNwxl3Pw A recent article in Wired Magazine highlighted how the genome revolution has been skipping most people in the world: 96% of participants in recent genomic studies trace most of their ancestry to Europe. Why? Statistical analysis is simpler in groups tracing ...

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23andMe Publishes Parkinson’s Paper Identifying Two Novel Genetic Associations

On the eve of the anniversary of our first publication, 23andMe is excited to announce the publication of our second research paper, "Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson’s disease", posted online today in PLoS Genetics. This study ...

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23andMe Research Findings: From You, Back to You

It’s been nearly a year since we published our first scientific paper. Titled “Web-based, Participant-Driven Studies Yield Novel Genetic Associations for Common Traits,” the paper demonstrated that 23andWe, our revolutionary new research model, works. Since then we’ve been making exciting progress, ...

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23andMe 2011 State of the Database Address

Database Snapshot: 100,611 users genotyped 76% have agreed to participate in research 59% take surveys 57% are male 47% are sharing with other users 12% have multiple ancestry 45 is the average age 100,409 posts in our community forums 60,000 pairs of relatives among users (4th ...

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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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