Genetics

  • Read more: Open Access to Health Research: Highlights from the NIH Public Access Policy panel

    Open Access to Health Research: Highlights from the NIH Public Access Policy panel

    By Adriana Benedict As of 2008, the NIH Public Access Policy requires “that all investigators funded by the NIH submit or have submitted for them to the National Library of Medicine’s PubMed Central an electronic version of their final, peer-reviewed manuscripts upon acceptance for publication, to be made publicly available no later than 12 months…

  • Read more: Twitter Round-Up (11/4-11/10)

    Twitter Round-Up (11/4-11/10)

    By Casey Thomson [Ed. Note. 11/12/12: Just to be clear, retweeting should not be read as an endorsement of or agreement with the content of the original tweet.] With Election Day now come and gone, our bloggers were tweeting this week about the results, in addition to the greater happenings in health law and ethics….

  • Read more: Using Tissue Samples to Make Genetic Offspring after Death

    Using Tissue Samples to Make Genetic Offspring after Death

    By Yu-Chi Lyra Kuo Last month, John Gurdon and Shinya Yamanaka were jointly awarded the 2012 Nobel Prize for Medicine for their research on induced pluripotent stem cells (iPSCs).  iPSCs are capturing the public imagination as embryonic stem cells did fifteen years ago, but without the controversy surrounding the destruction of embryos: iPSCs can be…

  • Read more: Twitter Round-Up: What Our Bloggers Are Tweeting About (10/28-11/3)

    Twitter Round-Up: What Our Bloggers Are Tweeting About (10/28-11/3)

    By Casey Thomson   [Ed. Note: Several of our bloggers are active on Twitter.  In a new feature, we’ll be posting some highlights of their tweets each week so you can stay in the know – or think about following them directly!]   Dan Vorhaus (@genomicslawyer) linked to Bloomberg’s article on the current underutilization of…

  • Read more: PCSBI: Privacy and Progress in Whole Genome Sequencing

    PCSBI: Privacy and Progress in Whole Genome Sequencing

    Yesterday, President Obama’s Commission for the Study of Bioethical Issues released its fifth report: Privacy and Progress in Whole Genome Sequencing.  I haven’t had a chance to digest it yet, but for now, just wanted to call it to everyone’s attention.  The gist seems to be privacy, privacy, privacy. Here are the major recommendations, straight from…

  • Read more: TOMORROW: Glenn Cohen on Action Speaks! Diamond v. Chakrabarty

    TOMORROW: Glenn Cohen on Action Speaks! Diamond v. Chakrabarty

    Tomorrow, Wednesday, October 3 at 5:30 pm, Bill of Health co-editor I. Glenn Cohen will participate in a live national broadcast on Actionspeaksradio.org regarding Diamond v. Chakrabarty, the 1980 case that first established the right to patent life. For information on how to listen or attend the recording live in Providence, RI, click here. And for some background from Glenn…

  • Read more: “The New Normal” and Reproductive Technology and the Law

    “The New Normal” and Reproductive Technology and the Law

    Inspired in part by attending the “Baby Markets Roundtable” (an annual gathering of reproductive technology and the law scholars) this week at Indiana Bloomington, I wanted to share a few thoughts on the new NBC television show The New Normal. The series is a sitcom that follows the lives of a gay male couple (David and…

  • Read more: To Tell or Not to Tell: Should Researchers Contact Anonymous Donors to Help Them?

    To Tell or Not to Tell: Should Researchers Contact Anonymous Donors to Help Them?

    By Cansu Canca A recent New York Times article drew attention to an issue with increasing importance as technology develops. Gene samples collected under conditions of anonymity reveal more and more information that may be of crucial importance for the subjects or their relatives. Researchers feel a moral obligation to disclose these important findings, which…