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23andMe Parkinsonís Community Hits 10,000 Members; Enrollment Still Free of Charge to Parkinsonís Patients

Posted by  Holly Teichholtz, March 04, 2013

23andMe Parkinsonís Community Hits 10,000 Members; Enrollment Still Free of Charge to Parkinsonís Patients

Congratulations are in order for personal genetics company 23andMe and the volunteers who have helped it exceed its goal of enrolling 10,000 people in its Parkinsonís Research Community, now officially the largest cohort of genotyped people with Parkinsonís in the world.

ďHaving reached this important milestone, the next step for us is to focus on the data that we have collected,Ē said 23andMeís Parkinsonís Research Manager Emily Drabant, PhD.† ďThis is a tremendously rich dataset and we want to learn as much as we can from it.Ē

According to the 23andMe blog, the companyís research goals include helping answer such scientific questions as:

  • The relationship between environmental and genetic factors in the development of Parkinsonís.
  • How those with Parkinsonís react differently to treatment so that treatments may be better individually targeted.
  • Better understanding the disease and its progression through continuing engagement with community members.

Want to be part of the genetics revolution in Parkinsonís? 23andMe continues to welcome people to participate in its research. The Brin-Wojcicki Foundation, which had pledged to cover the costs for the first 10,000 people with Parkinsonís to enroll, is continuing to make it free for anyone with Parkinsonís to join 23andMe and be part of this research initiative.

(As always, more research participation opportunities, including the 23andMe PD Community and other genetics studies, can be found at Fox Trial Finder.)

23andMe was founded by longtime Michael J. Fox Foundation supporter Anne Wojcicki.

TAGS: 23andMe

 

 

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