1. Components of genetic counsellor education: A systematic review of the peer-reviewed literature

   • C. Ingvoldstad
   • M. Seven
   • H. Skirton

   Review 09 October 2015 Pages: 107 - 118

   

2. Wide disparity of clinical genetics services and EU rare disease research funding across Europe

   • Sally Ann Lynch
   • Isabella Borg

   Original Article 04 November 2015 Pages: 119 - 126

   

3. Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica

   • Karlene Mason
   • Felicea Gibson
   • Graham R. Serjeant

   Original Article 02 December 2015 Pages: 127 - 132

   

4. Participant views on consent in cancer genetics research: preparing for the precision medicine era

   • Karen L. Edwards
   • Diane M. Korngiebel
   • Celeste M. Condit

   Original Article 22 January 2016 Pages: 133 - 143

5. Was it worth it? Patients’ perspectives on the perceived value of genomic-based individualized medicine

   • Colin ME Halverson
   • Kristin E Clift
   • Jennifer B McCormick

   Original Article 09 February 2016 Pages: 145 - 152

6. Consenting postpartum women for use of routinely collected biospecimens and/or future biospecimen collection

   • Claudia A. Kozinetz
   • Kathryn Royse
   • Chantal Caviness

   Original Article 11 February 2016 Pages: 153 - 158

7. “It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare

   • Alison D. Archibald
   • Chriselle L. Hickerton
   • Sylvia A. Metcalfe

   Original Article 03 February 2016 Pages: 159 - 171

8. Health research: working with Indigenous People in Peru

   • Carol Zavaleta
   • Kelika Konda
   • Eduardo Gotuzzo

   Letter to the Editor 03 February 2016 Pages: 173 - 174

9. Relevant ethical consideration in research with indigenous people in Peru

   • Gabriela Minaya

   Letter to the Editor 27 February 2016 Pages: 175 - 176