1. A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing

   • Maria Siermann
   • Zoë Claesen
   • Pascal Borry

   Review 14 January 2022 Pages: 1 - 11

   

2. Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification

   • Alma Levin Fridman
   • Aviad Raz
   • Shiri Shkedi-Rafid

   Original Article 05 October 2021 Pages: 13 - 18

3. When guidelines face reality — Lynch syndrome screening in the setting of public health system in a developing country

   • Vanessa Nascimento Kozak
   • Enilze Maria de Souza Fonseca Ribeiro
   • Jose Claudio Casali da Rocha

   Original Article 08 October 2021 Pages: 19 - 29

   

4. Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study

   • Antoine Rajkovic
   • Allison L. Cirino
   • Kimberly Zayhowski

   Original Article 12 October 2021 Pages: 31 - 48

5. “Right diet for the right person”: a focus group study of nutritionist-dietitians’ perspectives on nutritional genomics and gene-based nutrition advice

   • Jacus S. Nacis
   • Marilou R. Galang
   • Marietta P. Rodriguez

   Original Article Open access 27 October 2021 Pages: 49 - 57

6. Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study

   • Bettina Meiser
   • Melissa Monnik
   • Rajneesh Kaur

   Original Article 02 November 2021 Pages: 59 - 73

   

7. Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants

   • Michael P. Douglas
   • Grace A. Lin
   • Kathryn A. Phillips

   Original Article Open access 06 November 2021 Pages: 75 - 80

8. IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy

   • Susan Christian
   • Julia Tagoe
   • Raechel Ferrier

   Original Article 11 November 2021 Pages: 81 - 89

   

9. Parents’ perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS)

   • Courtney B. Cook
   • Caitlin Slomp
   • Jehannine Austin

   Original Article 16 November 2021 Pages: 91 - 101

   

10. Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia

    • Susi Susanah
    • Nur Melani Sari
    • Yunia Sribudiani

    Original Article Open access 16 November 2021 Pages: 103 - 112

    

11. Comprehension of skin cancer genetic risk feedback in primary care patients

    • Erva Khan
    • Kimberly A. Kaphingst
    • Jennifer L. Hay

    Original Article 19 November 2021 Pages: 113 - 119

12. Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community

    • Kristine Barlow-Stewart
    • Kayley Bardsley
    • Leslie Burnett

    Original Article Open access 30 November 2021 Pages: 121 - 131

    

13. A collaborative genetic carrier screening model for the British Ashkenazi Jewish community

    • Monica Ziff
    • Juliette Harris

    Program Reports 29 November 2021 Pages: 133 - 135

14. Development and pilot testing of an online decision aid for women considering risk-stratified breast screening

    • Jocelyn Lippey
    • Louise Keogh
    • Laura Forrest

    Program Reports 21 January 2022 Pages: 137 - 141

    

15. Treatment decision-making in sickle cell disease patients

    • A. Booth
    • V. Bonham
    • K. E. Ormond

    Short Communication 04 November 2021 Pages: 143 - 151

    

16. Correction to: Treatment decision‑making in sickle cell disease patients

    • A. Booth
    • V. Bonham
    • K. E. Ormond

    Correction 23 December 2021 Pages: 153 - 154