Tag: research

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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23andMe’s Third Publication Demonstrates Efficient Replication of Over 180 Genetic Associations

As we’ve mentioned here previously, science can be a slow process. Researchers spend a long time -- sometimes upward of five years -- gathering enough people with a particular disease to study, collecting samples and data from them, analyzing that data, and then publishing the results. Imagine if you had to ...

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My Father, Myelofibrosis, and Me

by Ashley Gould Vice President Corporate Development & Chief Legal Officer, 23andMe Linda Avey and Anne Wojcicki created 23andMe based on a number of visions. They described one of these to me in early 2007, capturing my imagination and playing a large role in my decision to become a member of the ...

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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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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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Ethnicity Matters in Research: A Case Study in Prostate Cancer

By Angela Liu and Shirley Wu Nearly one in six men in the United States develops prostate cancer. This sobering statistic has spurred tremendous advances in research over the years, such that prostate cancer is now one of the most treatable and survivable cancers. But there is still much we don’t know ...

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23andMe Hosting One-of-a-Kind Sarcoma Community Night

Are you a sarcoma patient or survivor? Do you treat sarcoma patients? Maybe you know or care for someone suffering from this rare form of cancer. If sarcoma has touched your life, we invite you to join us for 23andMe’s Sarcoma Community Night on Tuesday, June 28, to connect to, learn from, and share with ...

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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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