Participation of low-income women in genetic cancer risk assessment and BRCA 1/2 testing: the experience of a safety-net institution Ian K. KomenakaJesse N. NodoraMaria Elena Martinez Original Article 21 December 2015 Pages: 177 - 183
A cost analysis of a cancer genetic service model in the UK Ingrid SladeHelen Hansonfor the MCG programme Original Article Open access 27 February 2016 Pages: 185 - 194
Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana Kofi A. AnieMarsha J. TreadwellKwaku Ohene-Frempong Original Article 18 April 2016 Pages: 195 - 202
Swedish healthcare providers’ perceptions of preconception expanded carrier screening (ECS)—a qualitative study A. MatarU. KihlbomA. T. Höglund Original Article 25 May 2016 Pages: 203 - 214
Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England Sarah SalwayParveen AliOliver Quarrell Original Article Open access 16 June 2016 Pages: 215 - 228
Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information Vigdis StefansdottirOskar Th. JohannssonJon J. Jonsson Original Article 02 July 2016 Pages: 229 - 235
Why do pregnant women accept or decline prenatal diagnosis for Down syndrome? Ellen TernbyOve AxelssonCharlotta Ingvoldstad Original Article 20 July 2016 Pages: 237 - 242
Carrier screening for beta-thalassemia in the Maldives: perceptions of parents of affected children who did not take part in screening and its consequences Fazeela WaheedColleen FisherDavid Stanley Original Article 08 July 2016 Pages: 243 - 253
Successful implementation of Lynch syndrome screening in a safety net institution Trilokesh D. KidambiRobin LeeLukejohn Day Short Communication 02 July 2016 Pages: 255 - 260
