Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Equipped with faster, cheaper technologies for sequencing DNA and assessing variation in genomes on scales ranging from one to millions of bases, researchers are finding out how truly different we are from one another.
Community-Based Dialogue: Engaging Communities of Color in the United States' Genetics Policy Conversation.
V. L. Bonham, T. Citrin, S. M. Modell, T. H. Franklin, E. W. B. Bleicher, and L. M. Fleck (2009)
Journal of Health Politics Policy and Law
34, 325-359
|Abstract »|PDF »
Personalized medicine: A transformative approach is needed.
T. J. Hudson (2009)
Can. Med. Assoc. J.
180, 911-913
|Full Text »|PDF »
Introduction to the Special Issue on Society and Genetics.
Guang Guo (2008)
Sociological Methods Research
37, 159-163
|PDF »
Don't throw the baby out with the bathwater: Enabling a bottom-up approach in genome-wide association studies.
S. E. McGuire and A. L. McGuire (2008)
Genome Res.
18, 1683-1685
|Full Text »|PDF »
Race, genetics, and disease: questions of evidence, matters of consequence..
J. H. Fujimura, T. Duster, and R. Rajagopalan (2008)
Social Studies of Science
38, 643-656
|Abstract »|PDF »
Reply.
Y. Bosse, P. Mathieu, and P. Pibarot (2008)
J. Am. Coll. Cardiol.
52, 498-499
|Full Text »|PDF »
Hidden copy number variation in the HapMap population.
J. C. Marioni, M. White, S. Tavare, and A. G. Lynch (2008)
PNAS
105, 10067-10072
|Abstract »|Full Text »|PDF »
Dermatology in the Postgenomic Era: Harnessing Human Variation for Personalized Medicine.
