A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing Maria SiermannZoë ClaesenPascal Borry Review 14 January 2022 Pages: 1 - 11
Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification Alma Levin FridmanAviad RazShiri Shkedi-Rafid Original Article 05 October 2021 Pages: 13 - 18
When guidelines face reality — Lynch syndrome screening in the setting of public health system in a developing country Vanessa Nascimento KozakEnilze Maria de Souza Fonseca RibeiroJose Claudio Casali da Rocha Original Article 08 October 2021 Pages: 19 - 29
Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study Antoine RajkovicAllison L. CirinoKimberly Zayhowski Original Article 12 October 2021 Pages: 31 - 48
“Right diet for the right person”: a focus group study of nutritionist-dietitians’ perspectives on nutritional genomics and gene-based nutrition advice Jacus S. NacisMarilou R. GalangMarietta P. Rodriguez Original Article Open access 27 October 2021 Pages: 49 - 57
Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study Bettina MeiserMelissa MonnikRajneesh Kaur Original Article 02 November 2021 Pages: 59 - 73
Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants Michael P. DouglasGrace A. LinKathryn A. Phillips Original Article Open access 06 November 2021 Pages: 75 - 80
IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy Susan ChristianJulia TagoeRaechel Ferrier Original Article 11 November 2021 Pages: 81 - 89
Parents’ perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS) Courtney B. CookCaitlin SlompJehannine Austin Original Article 16 November 2021 Pages: 91 - 101
Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia Susi SusanahNur Melani SariYunia Sribudiani Original Article Open access 16 November 2021 Pages: 103 - 112
Comprehension of skin cancer genetic risk feedback in primary care patients Erva KhanKimberly A. KaphingstJennifer L. Hay Original Article 19 November 2021 Pages: 113 - 119
Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community Kristine Barlow-StewartKayley BardsleyLeslie Burnett Original Article Open access 30 November 2021 Pages: 121 - 131
A collaborative genetic carrier screening model for the British Ashkenazi Jewish community Monica ZiffJuliette Harris Program Reports 29 November 2021 Pages: 133 - 135
Development and pilot testing of an online decision aid for women considering risk-stratified breast screening Jocelyn LippeyLouise KeoghLaura Forrest Program Reports 21 January 2022 Pages: 137 - 141
Treatment decision-making in sickle cell disease patients A. BoothV. BonhamK. E. Ormond Short Communication 04 November 2021 Pages: 143 - 151
Correction to: Treatment decision‑making in sickle cell disease patients A. BoothV. BonhamK. E. Ormond Correction 23 December 2021 Pages: 153 - 154