Author: 23andMe

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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Public Comments Due on Possible FDA Regulation of Direct to Consumer Genetic Testing

From its founding 23andMe has made clear its views that people should have a right to access their own genetic information. And in the debate over regulation of direct to consumer genetic testing, we’ve made our views clear to officials at the Federal Drug Administration (FDA). Have you? May 2nd ...

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Call to Participate in a New Study on Social Networking and Personal Genomics

Invitation to Participate in New Research Project -- Social Networking and Personal Genomics: Emerging Issues For Health Research Do you share your information with others? How has your personal genetic information influenced your lifestyle and the way you approach your health and medical decisions? Can ...

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23andMe Launches Health Report on Alzheimer’s Disease

Alzheimer’s disease is the most common form of dementia in older people and is projected to become a major health burden as the population of the United States ages. Currently more than five million Americans are thought to have the disease, but by the year 2050 that number is estimated to reach 15 million. ...

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DTC Genetic Tests and the Future of Regulation: Make Your Voices Heard

On March 8th, the FDA convened a two-day advisory panel meeting to discuss questions related to direct-to-consumer genetic tests. The questions focused on the benefits and risks of providing consumers with direct access to these tests, potential strategies for communication and education to mitigate any ...

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23andMe Presents at FDA Advisory Panel Meeting on Direct-to-Consumer Genetic Tests

Editor's note: This post has been altered from the original. The slides from the presentation have been removed. 23andMe, like many others, believes that individuals have a right to access their own genetic information and that personal genetics will pave the way for significant advances in healthcare. ...

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23andMe to Attend FDA Public Advisory Committee Meeting on Direct-to-Consumer Genetic Tests

Last summer, the Food and Drug Administration (FDA) indicated that it would be revising its regulatory guidelines pertaining to laboratory-developed tests (LDTs), and that direct-to-consumer genetic tests such as 23andMe's Personal Genome Service® would potentially fall under that category. 23andMe has ...

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