1. An integrative review of factors that influence reproductive decisions in women with sickle cell disease

   • Josephine Claire Rance
   • Heather Skirton

   Review 03 October 2018 Pages: 161 - 169

2. What do people think about genetics? A systematic review

   • Erin LePoire
   • Baishakhi Basu
   • Deborah J. Bowen

   Review 07 November 2018 Pages: 171 - 187

   

3. Experiences of patients seeking to participate in variant of uncertain significance reclassification research

   • Sukh Makhnoon
   • Lauren Thomas Garrett
   • Brian H. Shirts

   Original Article 19 July 2018 Pages: 189 - 196

4. High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information

   • Laura Elenor Forrest
   • Sarah Dilys Sawyer
   • Mary-Anne Young

   Original Article 10 August 2018 Pages: 197 - 206

   

5. Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM)

   • Janella Hudson
   • Amy C. Sturm
   • Susan T. Vadaparampil

   Original Article 18 August 2018 Pages: 207 - 217

   

6. Family health history and genetic services—the East Baltimore community stakeholder interview project

   • Kunal Sanghavi
   • Ivy Moses
   • Joann Bodurtha

   Original Paper 31 August 2018 Pages: 219 - 227

7. Barriers to the identification of familial hypercholesterolemia among primary care providers

   • John Zimmerman
   • Daniel Duprez
   • Heather A. Zierhut

   Original Article 11 September 2018 Pages: 229 - 236

8. Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility?

   • Kirsten F. L. Douma
   • Fonnet E. Bleeker
   • Ellen M. A. Smets

   Original Paper Open access 12 September 2018 Pages: 237 - 247

9. Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation

   • Kim C. A. Holtkamp
   • Lidewij Henneman
   • Phillis Lakeman

   Original Article Open access 18 September 2018 Pages: 249 - 257

10. Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome

    • Isabelle Henriksson
    • Karin Henriksson
    • Samuel Gebre-Medhin

    Original Article Open access 24 September 2018 Pages: 259 - 266

    

11. “A perfect society”— Swedish policymakers’ ethical and social views on preconception expanded carrier screening

    • Amal Matar
    • Mats G. Hansson
    • Anna T. Höglund

    Original Article Open access 26 September 2018 Pages: 267 - 280

    

12. Risk perception and screening behavior of Filipino women at risk for breast cancer: implications for cancer genetic counseling

    • John Benedict B. Lagarde
    • Mercy Y. Laurino
    • Elizabeth R. Ventura

    Original Article 27 September 2018 Pages: 281 - 289

13. “This could be me”: exploring the impact of genetic risk for Huntington’s disease young caregivers

    • Danielle S. Dondanville
    • Andrea K. Hanson-Kahn
    • Joanna H. Fanos

    Original Article 14 November 2018 Pages: 291 - 302

    

14. Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors’ and counselees’ views

    • Niki M. Medendorp
    • Marij A. Hillen
    • Ellen M. A. Smets

    Original Article Open access 14 November 2018 Pages: 303 - 312

15. Exploring the perceived self-efficacy of genetic counselors as teachers

    • Justin Gasparini
    • Tatiana Yuzyuk
    • Irene De Biase

    Program Reports 05 September 2018 Pages: 313 - 319

    

16. Correction to: Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results:a systematic review and meta-analysis

    • Kelly F. J. Stewart
    • Anke Wesselius
    • Maurice P. Zeegers

    Correction 02 January 2018 Pages: 321 - 321

17. Correction to: EUROCAT: an update on its functions and activities

    • F. D. Tucker
    • J. K. Morris
    • A. K. Rissmann

    Correction 25 October 2018 Pages: 323 - 323