Components of genetic counsellor education: A systematic review of the peer-reviewed literature C. IngvoldstadM. SevenH. Skirton Review 09 October 2015 Pages: 107 - 118
Wide disparity of clinical genetics services and EU rare disease research funding across Europe Sally Ann LynchIsabella Borg Original Article 04 November 2015 Pages: 119 - 126
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica Karlene MasonFelicea GibsonGraham R. Serjeant Original Article 02 December 2015 Pages: 127 - 132
Participant views on consent in cancer genetics research: preparing for the precision medicine era Karen L. EdwardsDiane M. KorngiebelCeleste M. Condit Original Article 22 January 2016 Pages: 133 - 143
Was it worth it? Patients’ perspectives on the perceived value of genomic-based individualized medicine Colin ME HalversonKristin E CliftJennifer B McCormick Original Article 09 February 2016 Pages: 145 - 152
Consenting postpartum women for use of routinely collected biospecimens and/or future biospecimen collection Claudia A. KozinetzKathryn RoyseChantal Caviness Original Article 11 February 2016 Pages: 153 - 158
“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare Alison D. ArchibaldChriselle L. HickertonSylvia A. Metcalfe Original Article 03 February 2016 Pages: 159 - 171
Health research: working with Indigenous People in Peru Carol ZavaletaKelika KondaEduardo Gotuzzo Letter to the Editor 03 February 2016 Pages: 173 - 174
Relevant ethical consideration in research with indigenous people in Peru Gabriela Minaya Letter to the Editor 27 February 2016 Pages: 175 - 176