Tag: Parkinson’s Research Community

Parkinson’s Research Challenges

Things aren’t always as they seem with Parkinson’s disease with one recent study showing as many as half those diagnosed with the disease don’t have it, according Dr. J. William Langston. At a recent visit to 23andMe, Langston, a pioneering Parkinson’s researcher as well as the founder and chief science ...

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Steady On

Like all good photographers Alan Babbitt sees what’s invisible to most of us. With a steady hand and a willingness to go almost anywhere for a good shot, Alan spent decades turning his lens on people and places to create images he thought would draw the viewer in and tell a story. “I’d call it street ...

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Let’s Talk About Parkinson’s

On Thursday and Friday, 23andMe will be participating in two online events hosted by the Michael J. Fox Foundation focused on Parkinson’s disease and some of the latest research into its genetic underpinning. On Thursday February 19th, at 12 pm EST, the Michael J. Fox Foundation will host a webinar titled ...

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23andMe In The News

Last week was a good one for research at 23andMe with two announcements that offer more examples of the power of our research model. First was the publication of a massive Parkinson’s disease study that our scientists worked on with a consortium of 50 other organizations that were lead by researchers at ...

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Debate Around Informing Research Participants

This post comes to us from our friends at the Michael J. Fox Foundation, which has worked with us through our Parkinson’s Research Community. There are many different points of view on whether to inform research participants. For 23andMe our approach has always been to give customers and research participants ...

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23andMe Looks Back One More Time

In honor of the Chinese New Year, we’re taking one last look at the genetic milestones of 2013. From a Supreme Court ruling on patenting genes, to Angelina Jolie’s bold revelations about her genetic risk for breast cancer, to the FDA ordering 23andMe to stop offering health results pending a regulatory ...

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Getting In the Race

A friend of Gwen Schroeder once told her: “Don’t cheer from the sidelines if you can run the race.” So when her father was diagnosed with Parkinson’s disease, Gwen laced up her shoes. A post-production manager who works in New York City for the TED Conferences, Gwen signed up to run a marathon to raise ...

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People Powered Research at 23andMe

There are a lot of reasons why Thelma Ackley signed up for 23andMe — she’s fascinated by her ancestry and she's curious about her health — but the main reason is her husband and her six grandchildren. A few years ago her husband Jim, a former engineer, developed Parkinson’s disease. The neurodegenerative ...

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23andMe Reaches Parkinson’s Research Goal

We’re excited to announce that the 23andMe Parkinson’s Research Community has exceeded its goal, enrolling more than 10,000 people with the disease and creating the largest cohort of genotyped people with Parkinson’s in the world. Reaching this milestone offers scientists an incredible opportunity to better ...

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23andMe Goes to Washington

As we near our goal of enrolling 10,000 patients in 23andMe’s Parkinson’s research community, we are ever more eager to share what we are doing. Last month our CEO, Anne Wojcicki, along with our Parkinson’s research manager Emily Drabant, went to Washington D.C with two friends of 23andMe — Maryum Ali, a ...

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