Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variant Timothy W. GroselMatthew KarlColleen M. Cebulla Short Communication 06 January 2021 Pages: 1 - 5
Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA Analysis Paola NixErin MundtBenjamin Roa Original Article Open access 20 January 2021 Pages: 7 - 19
The needs of Southeast Asian BRCA mutation carriers considering risk-reducing salpingo-oophorectomy: a qualitative study Hamizah Sa’atYew-Kong LeeNur Aishah Mohd Taib Original Article 19 February 2021 Pages: 21 - 33
Knowledge and psychosocial impact of genetic counseling and multigene panel testing among individuals with ovarian cancer Rachel A. PozzarFangxin HongMeghan Underhill-Blazey Original Article 10 March 2021 Pages: 35 - 47
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
Comparison of universal screening in major lynch-associated tumors: a systematic review of literature George Kunnackal JohnVipin Das VillgranFrancis M. Giardiello Original Article 11 January 2021 Pages: 57 - 67
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. CojocaruS. GennatasT. P. McVeigh Original Article 06 February 2021 Pages: 69 - 74
Managing gastric cancer risk in lynch syndrome: controversies and recommendations C. Richard BolandMatthew B. YurgelunPatrick M. Boland Review Open access 21 February 2021 Pages: 75 - 78
Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients Fadwa A. ElsayedCarli M. J. TopsTom van Wezel Original Article Open access 08 March 2021 Pages: 79 - 83
Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome Sue M. HusonTimo StaabStefan Meyer Short Communication Open access 21 November 2020 Pages: 85 - 90
Correction to: Infantile fibrosarcoma with TPN3-NTRK3 fusion in a boy with Bloom Syndrome Sue M. HusonTimo StaabStefan Meyer Correction 06 January 2021 Pages: 91 - 91
Genetic evaluation of patients and families with concern for hereditary endocrine tumor syndromes Jennifer L. AndersonRobert PilarskiPamela Brock Original Article 07 January 2021 Pages: 93 - 100
Genetic predisposition to prostate cancer: an update Holly Ni RaghallaighRosalind Eeles Review Open access 24 January 2021 Pages: 101 - 114
Age of diagnosis in familial Barrett’s associated neoplasia Benita K. GlamourOmar AlaberAndrew E. Blum Short Communication 11 March 2021 Pages: 115 - 120