Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results: a systematic review and meta-analysis Kelly F. J. StewartAnke WesseliusMaurice P. Zeegers Review Open access 29 June 2017 Pages: 1 - 18
Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results Robyn HylindMaureen SmithSharon Aufox Original Article 27 June 2017 Pages: 19 - 26
Exploring Asian Indian and Pakistani views about cancer and participation in cancer genetics research: toward the development of a community genetics intervention Amy E. LeaderSalini MohantyVeda N. Giri Original Article 28 June 2017 Pages: 27 - 35
Diagnosis of rare diseases under focus: impacts for Canadian patients Daphne Esquivel-SadaMinh Thu Nguyen Original Article Open access 21 July 2017 Pages: 37 - 50
Association of DD genotype of angiotensin-converting enzyme gene (I/D) polymorphism with hypertension among a North Indian population Garima RanaSuniti YadavK. N. Saraswathy Original Article 02 August 2017 Pages: 51 - 55
Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership Laura ForrestGillian MitchellMary-Anne Young Original Article 18 August 2017 Pages: 57 - 64
The clinical and genetic Spectrum of Maroteaux-Lamy syndrome (Mucopolysaccharidosis VI) in the Eastern Province of Saudi Arabia Nouriya Abbas Al-SannaaHind Yousif Al-AbdulwahedIssam Hassan Bouholaigah Original Article 15 September 2017 Pages: 65 - 70
Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening Anita GorrieAlison D. ArchibaldBelinda McClaren Original Article 02 October 2017 Pages: 71 - 80
Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families Belinda VicuñaHarold D. DelaneyAnita Y. Kinney Original Article 02 October 2017 Pages: 81 - 92
Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study Alice LopesAlexandra SousaPaula Freitas Original Article 19 October 2017 Pages: 93 - 99
The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages Arseni MarkoffNadja Bogdanova Correspondence 14 October 2017 Pages: 101 - 102