Eye on DNA September Winner and October Contest
by Dr. Hsien-Hsien Lei
Posted October 1, 2007 in DNA and Disease, DNA in General
Congratulations to KathyF of What Do I Know? She’s the winner of the Eye on DNA September contest!
Kathy has a very personal connection with genetics. Her mother died of Huntington’s Disease earlier this year and while Kathy tested negative for the genetic mutation eight years ago, her aunt tested positive last week. Look out for an exclusive Eye on DNA interview with Kathy soon about her experience with Huntington’s Disease.
For the October Eye on DNA Contest, I’ll be giving away a copy of Dr. J Craig Venter’s book - A Life Decoded: My Genome: My Life. It’s set to be released on October 18, 2007 and you can win a copy by leaving a comment on any post at Eye on DNA. The winner will be randomly selected from eligible comments. Good luck!
Tags: genetics, genes, dna, contest, huntington’s disease

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Count me in!
Hi Lesha, Consider yourself counted!
I’m totally in this one! Add me to the contestants
Okie doke. The more comments you leave, the more chances you get!
well, after his recent fiasco regarding “superiority” claims, J. Watson is no longer any leading scientist to me… C. Venter has an interesting charisma, isn’t he? I’ve read text in amazon about his new book, and liked his notes regarding public science and medicine.
Therefore this book would be my digest and fit well near the Watson’s “Double helix” or “DNA” on my shelf:)
When Watson is wrong, Venter is right
Would love to read this book.
I have involved in the project of genetic diagnosis of hereditary colorectal cancer several years and I’d like to share a little bit opinion about the field. The usefulness of the diagnosis depends on the knowledge of the disease, genetics and genes study. For the field of hereditary colorectal cancer (FAP and HNPCC), there are some information available from research and service, it is very useful for the index patient and their family member to take the diagnosis to deal with the cancer. Also as we knew the penetrate of APC mutation to cause FAP phenotype is almost 100%, while penetrate of MLH1 and MSH2 mutation to cause HNPCC phenotype can increase the cancer at least five fold, genetic diagnosis of APC gene can give more precise and accurate prediction (though MLH1 and MSH2 genetic diagnosis still provide important information of the index patient and their family member).
Wilson, Thanks for the informative comment on colon cancer.
Francis Collins is indeed alive and well. I heard him speak and met with him several times at the ASHG conference in San Diego this week. He spoke more about ENCODE, GINA, the Human Microbiome Project, the current reality that your knowing your personal genome today is not the key to knowing everything about your health (it may be in the future as science advances), and Secretary Leavitt’s personalized medicine emphasis.
Dean Suhr
President
Dean, Good to hear Dr. Collins is still thinking about science and medicine! (He seems to have strayed off topic a bit in recent months.) I’ll be sure to check out the MLD Foundation.
[...] randomly selected winner of the October Eye on DNA Comment Contest is Dr. Ramunas Janavicius of Cancer Genetics! He wins a copy of J. Craig Venter’s new book - [...]