Tag: Anne Wojcicki


March 13, 2013

Getting to Know Your Genome

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You may not have thought about your genome lately, but one day you will and so will your doctor. In an opinion piece published in the Guardian, Anne Wojcicki, our CEO and co-founder, offered some thoughts about why knowing your own genetic information will become increasingly important for your [...]

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December 11, 2012

One Million Strong, A Note from 23andMe’s Anne Wojcicki

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Today we’re announcing some big news. I don’t want this moment to go by without a note of gratitude to our customers and those who have been advocates for 23andMe over the years. We have come a long way together.  Because of you we pioneered the use of personal genetics.  You are helping us establish [...]

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October 17, 2012

23andMe Goes to Washington

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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 [...]

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April 27, 2012

Michael J. Fox, Our Big-Time Hero

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Todd Sherer, CEO of the Michael J. Fox Foundation, with Michael J. Fox and Anne Wojcicki Michael J. Fox is a great actor, but his smiles and good humor during a visit to 23andMe headquarters in Mountain View this week were fully sincere. “I really mean what I say when I express optimism, positivity and [...]

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April 16, 2012

An Astronaut Tells His Secret

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On his first Space Shuttle mission, Rich Clifford whispered a little prayer. “Please Lord let something go wrong so that I can fix it,” he recalls with a smile. But on the launch pad, strapped into the Shuttle with its two massive solid rocket boosters primed for ignition, Rich had second [...]

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January 12, 2012

Before You Are Pregnant…

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My sister learned she was a carrier for a recessive disease, Bloom syndrome, late in one of her pregnancies. I remember the panicked call and the weeks of worry as she and her husband awaited his test results; if he was also a carrier, this meant their daughter had a one in four chance of being born with the [...]

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January 5, 2012

A Look Forward: A Letter from 23andMe’s Anne Wojcicki

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Each and every one of you -- our 23andMe customers -- is a pioneer who has helped define the field of personal genetics and has made 23andMe a unique and special place.  I want to thank all of you for being customers. We’ve been exploring DNA and taking a journey of self discovery together. And while [...]

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July 20, 2010

23andMe at FDA/CDRH Public Meeting on Oversight of Laboratory Developed Tests (LDTs)

The 23andMe Blog

The FDA/CDRH Public Meeting on Oversight of Laboratory Developed Tests (LDTs) took place yesterday and today (July 19 and 20) in Washington, DC. Webcasts of both days will be available from the FDA for the next year. 23andMe's President and Co-Founder Anne Wojcicki spoke about the promise and power of [...]

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March 18, 2010

NIH to Create Public Database of Genetic Tests

The 23andMe Blog

Today the National Institutes of Health (NIH) announced its plans to create a public database in which genetic test providers will voluntarily deposit information about their services that can then be searched by researchers, consumers, health care providers, and others. The aim of this Genetic Testing [...]

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July 7, 2009

Introducing a Do-It-Yourself Revolution in Disease Research

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There's a high likelihood that a disease of some sort affects you or one of your relatives — every family seems to have ripples in its gene pool that define and shape its health dynamics. Your family might have a propensity for rheumatoid arthritis or a particular type of cancer. Whatever it is, there [...]

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