1. Risk stratification, genomic data and the law

   • Alison Hall
   • Thomas Finnegan
   • Hilary Burton

   Review 22 February 2018 Pages: 195 - 199

2. Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives

   • Martin P. Nilsson
   • Monica Emmertz
   • Niklas Loman

   Original Article Open access 30 October 2017 Pages: 201 - 208

3. From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals

   • Bianca M. Augusto
   • Paige Lake
   • Susan T. Vadaparampil

   Original Article 09 November 2017 Pages: 209 - 215

4. Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk

   • K. M. Broady
   • K. E. Ormond
   • Cinnamon S. Bloss

   Original Article 13 November 2017 Pages: 217 - 225

5. The effect of parental age on NF1 patients in Turkey

   • P. Sharafi
   • B. Anlar
   • S. Ayter

   Original Article 15 November 2017 Pages: 227 - 232

6. A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings

   • Huma Q. Rana
   • Sarah R. Cochrane
   • Christopher S. Lathan

   Original Article 18 November 2017 Pages: 233 - 241

   

7. Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services

   • A. Dearing
   • N. Taverner

   Original Article 20 November 2017 Pages: 243 - 256

8. The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study

   • Thomas M. Roston
   • Laura Dewar
   • Andrew D. Krahn

   Original Article 23 November 2017 Pages: 257 - 262

   

9. Cancer genetic counseling communication with low-income Chinese immigrants

   • Janice Ka Yan Cheng
   • Claudia Guerra
   • Galen Joseph

   Original Article 01 December 2017 Pages: 263 - 276

   

10. Thalassemia: a prevalent disease yet unknown term among college students in Saudi Arabia

    • Duaa Ibrahim Olwi
    • Leena Adnan Merdad
    • Eman Kamal Ramadan

    Original Article 14 December 2017 Pages: 277 - 282

11. Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach

    • Lauren Puryear
    • Natalie Downs
    • Latha Palaniappan

    Original Article 27 December 2017 Pages: 283 - 291

    

12. Experience of Asian males communicating cardiac genetic risk within the family

    • Sylvia Kam
    • Yasmin Bylstra
    • Roger Foo

    Original Article 08 January 2018 Pages: 293 - 303

13. “I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings

    • M. Vornanen
    • K. Aktan-Collan
    • A. Haukkala

    Original Article 16 January 2018 Pages: 305 - 314

14. Reproductive decision making: interviews with mothers of children with undiagnosed developmental delay

    • Emily Pond
    • Rebecca Dimond

    Original Article 01 February 2018 Pages: 315 - 325

    

15. An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis

    • Staci Martin
    • Kari L. Struemph
    • Pamela Wolters

    Original Article 02 March 2018 Pages: 327 - 334