1. A short history of the first 3 years of the Community Genetics Network and its newsletter

   • Leo P. ten Kate
   • Annie Plourde

   Case Report Open access 04 June 2011 Pages: 111 - 115

   

2. Access to genetic testing and genetic counseling in vulnerable populations: the d/Deaf and hard of hearing population

   • Sandra Cooke-Hubley
   • Victor Maddalena

   Review 01 May 2011 Pages: 117 - 125

3. Newborn screening education on the internet: a content analysis of North American newborn screening program websites

   • Makda H. Araia
   • Beth K. Potter

   Original Article 15 April 2011 Pages: 127 - 134

   

4. Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

   • Yeyang Su
   • Heidi C. Howard
   • Pascal Borry

   Original Article 28 May 2011 Pages: 135 - 146

5. Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem

   • Pradeep K. Patra
   • Virander S. Chauhan
   • Graham R. Serjeant

   Original Article 15 June 2011 Pages: 147 - 151

6. Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study

   • Samantha A. Streicher
   • Saskia C. Sanderson
   • Lynne D. Richardson

   Original Article 07 June 2011 Pages: 153 - 163

7. Young smokers’ views of genetic susceptibility testing for lung cancer risk: minding unintended consequences

   • Sharron L. Docherty
   • Colleen M. McBride
   • Isaac M. Lipkus

   Original Article 30 June 2011 Pages: 165 - 172

8. Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives

   • Naila Firdous
   • Stephen Gibbons
   • Bernadette Modell

   Original Article 17 June 2011 Pages: 173 - 189