Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome? Ryan Matthew KahnMuhammad Danyal AhsanMelissa K. Frey Original Article 08 October 2022 Pages: 127 - 133
A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland Terri Patricia McVeighKarl J. SweeneyAngela J. George Original Article 27 August 2022 Pages: 135 - 149
Identifying the BRCA1 c.-107A > T variant in Dutch patients with a tumor BRCA1 promoter hypermethylation Vincent M. T. de JongRoelof PruntelSabine C. linn Short Communication Open access 16 September 2022 Pages: 151 - 154
Determinants of adherence to recommendations on physical activity, red and processed meat intake, and body weight among lynch syndrome patients M HoedjesA VrielingE Kampman Original Article Open access 24 September 2022 Pages: 155 - 166
Characterization of sebaceous and non-sebaceous cutaneous manifestations in patients with lynch syndrome: a systematic review Shahram AzizHazel O’SullivanTerri P. McVeigh Review Open access 23 November 2022 Pages: 167 - 175
Laboratory variation in the grading of dysplasia of duodenal adenomas in familial adenomatous polyposis patients E. SoonsP. D. SiersemaF. Atsma Original Article Open access 19 November 2022 Pages: 177 - 186
CDH1 mutations recurrence and global clustering in genetically tested families with hereditary diffuse gastric cancer syndrome: results from a systematic study Giovanni CorsoValentina TagliaferriFrancesca Magnoni Short Communication 27 July 2022 Pages: 187 - 192
Analysis of uveal melanomas and paired constitutional DNA for exclusion of a BAP1-tumor predisposition syndrome Yasaman Arjmand AbbassiClaudia Le GuinDietmar R. Lohmann Original Article Open access 03 August 2022 Pages: 193 - 202
Disclosure of genetic risk to dating partners among young adults with von Hippel-Lindau disease Elysa BondBeverly YasharMonica Marvin Original Article 19 August 2022 Pages: 203 - 215
A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an SDHD pathogenic variant Madeline FoleyAnu SharmaSamantha Greenberg Original Article 12 October 2022 Pages: 217 - 224
Next-generation universal hereditary cancer screening: implementation of an automated hereditary cancer screening program for patients with advanced cancer undergoing tumor sequencing in a large HMO Trevor L. HoffmanHilary KershbergMonica Alvarado Original Article Open access 20 October 2022 Pages: 225 - 235
2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022 Abstract 23 January 2023 Pages: 237 - 282