1. Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variant

   • Timothy W. Grosel
   • Matthew Karl
   • Colleen M. Cebulla

   Short Communication 06 January 2021 Pages: 1 - 5

   

2. Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis

   • Paola Nix
   • Erin Mundt
   • Benjamin Roa

   Original Article Open access 20 January 2021 Pages: 7 - 19

   

3. The needs of Southeast Asian BRCA mutation carriers considering risk-reducing salpingo-oophorectomy: a qualitative study

   • Hamizah Sa’at
   • Yew-Kong Lee
   • Nur Aishah Mohd Taib

   Original Article 19 February 2021 Pages: 21 - 33

   

4. Knowledge and psychosocial impact of genetic counseling and multigene panel testing among individuals with ovarian cancer

   • Rachel A. Pozzar
   • Fangxin Hong
   • Meghan Underhill-Blazey

   Original Article 10 March 2021 Pages: 35 - 47

5. Progress Report: New insights into the prevention of CRC by colonoscopic surveillance in Lynch syndrome

   • Hans F. A. Vasen

   Review 19 January 2021 Pages: 49 - 56

6. Comparison of universal screening in major lynch-associated tumors: a systematic review of literature

   • George Kunnackal John
   • Vipin Das Villgran
   • Francis M. Giardiello

   Original Article 11 January 2021 Pages: 57 - 67

   

7. Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK

   • E. Cojocaru
   • S. Gennatas
   • T. P. McVeigh

   Original Article 06 February 2021 Pages: 69 - 74

   

8. Managing gastric cancer risk in lynch syndrome: controversies and recommendations

   • C. Richard Boland
   • Matthew B. Yurgelun
   • Patrick M. Boland

   Review Open access 21 February 2021 Pages: 75 - 78

9. Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients

   • Fadwa A. Elsayed
   • Carli M. J. Tops
   • Tom van Wezel

   Original Article Open access 08 March 2021 Pages: 79 - 83

   

10. Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome

    • Sue M. Huson
    • Timo Staab
    • Stefan Meyer

    Short Communication Open access 21 November 2020 Pages: 85 - 90

    

11. Correction to: Infantile fibrosarcoma with TPN3-NTRK3 fusion in a boy with Bloom Syndrome

    • Sue M. Huson
    • Timo Staab
    • Stefan Meyer

    Correction 06 January 2021 Pages: 91 - 91

12. Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromes

    • Jennifer L. Anderson
    • Robert Pilarski
    • Pamela Brock

    Original Article 07 January 2021 Pages: 93 - 100

    

13. Genetic predisposition to prostate cancer: an update

    • Holly Ni Raghallaigh
    • Rosalind Eeles

    Review Open access 24 January 2021 Pages: 101 - 114

    

14. Age of diagnosis in familial Barrett’s associated neoplasia

    • Benita K. Glamour
    • Omar Alaber
    • Andrew E. Blum

    Short Communication 11 March 2021 Pages: 115 - 120