1. In memoriam Prof. Dr. Leo P. ten Kate

   • Martina C. Cornel
   • Lidewij Henneman

   Obituary 16 November 2020 Pages: 1 - 3

   

2. Genetic epidemiology of hemoglobinopathies among Iraqi Kurds

   • Nasir Al-Allawi
   • Sarah Al Allawi
   • Sana D. Jalal

   Review Article 22 November 2020 Pages: 5 - 14

   

3. Patients’ decision to contribute to a biobank in the light of the patient-recruiter relationship—a qualitative study of broad consent in a hospital setting

   • Francesca Bosisio
   • Gaia Barazzetti
   • Brenda Spencer

   Original Article Open access 10 August 2020 Pages: 15 - 25

4. Public engagement with genomic medicine: a summary of town hall discussions

   • Holly Etchegary
   • Mercy Winsor
   • Charlene Simmonds

   Original Article 31 August 2020 Pages: 27 - 35

5. Impacts of personal DNA ancestry testing

   • Caryn Kseniya Rubanovich
   • Riley Taitingfong
   • Cinnamon S. Bloss

   Original Article 13 August 2020 Pages: 37 - 52

   

6. Hmong participants’ reactions to return of individual and community pharmacogenetic research results: “A positive light for our community”

   • K. Holzer
   • K. A. Culhane-Pera
   • H. A. Zierhut

   Original Article 06 August 2020 Pages: 53 - 65

   

7. Knowing, relationships and trust—citizens’ perceptions of whole genome sequencing for the Genetics Clinic of the Future

   • Simone Schumann
   • Brigitte Gschmeidler
   • Giuseppe Pellegrini

   Original Article 30 September 2020 Pages: 67 - 80

8. Birth defect mortality in India 1990–2017: estimates from the Global Burden of Disease data

   • Dhammasagar Ujagare
   • Anita Kar

   Original Article 15 October 2020 Pages: 81 - 90

   

9. Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals

   • Jeanine van der Giessen
   • Mirjam P. Fransen
   • Margreet G. E. M. Ausems

   Original Article Open access 15 December 2020 Pages: 91 - 99

10. Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making

    • Kelly Reumkens
    • Marly H. E. Tummers
    • Liesbeth A. D. M. van Osch

    Original Article Open access 02 September 2020 Pages: 101 - 110

    

11. Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England

    • Siang Ing Lee
    • Helen Curtis
    • Nadeem Qureshi

    Original Article Open access 28 October 2020 Pages: 111 - 120

    

12. Dying to see you? Deaths on a clinical genetics waiting list in the Republic of Ireland; what are the consequences?

    • Lisa Bradley
    • Sally Ann Lynch

    Original Article 29 October 2020 Pages: 121 - 127

    

13. Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening tool

    • Smita K. Rao
    • Kimberly A. Thomas
    • Georgia L. Wiesner

    Original Article 03 January 2021 Pages: 129 - 136

    

14. Sickle cell trait newborn screen results: disclosure and management

    • Margaret Lilley
    • Stephanie Hoang
    • Susan Christian

    Original Article 26 October 2020 Pages: 137 - 142

15. Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania

    • Daima Bukini
    • Columba Mbekenga
    • Michael Parker

    Original Article 12 August 2020 Pages: 143 - 154

    

16. Feasibility of establishing a network of community health workers to support care of people with sickle cell disease in Kumasi, Ghana

    • Julie M. Buser
    • Ashura Bakari
    • Cheryl A. Moyer

    Original Article 05 January 2021 Pages: 155 - 161

17. Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate’s primary healthcare centers in 2018

    • Manar Al Sanaa Ali Al Zeedi
    • Zahir Ghassan Al Abri

    Original Article 21 November 2020 Pages: 163 - 169

18. Attitudes among South African university staff and students towards disclosing secondary genetic findings

    • Georgina Spies
    • Jolynne Mokaya
    • For the SHARED ROOTS Group

    Original Article 20 November 2020 Pages: 171 - 184

    

19. The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay

    • Megan E. Benoy
    • J. Igor Iruretagoyena
    • Elizabeth M. Petty

    Original Article 06 January 2021 Pages: 185 - 197

    

20. Electronic informed consent information for residual newborn specimen research: findings from focus groups with diverse populations

    • Caren J. Frost
    • Erin P. Johnson
    • Erin Rothwell

    Original Article 22 January 2021 Pages: 199 - 203