Eighth International Symposium on hereditary breast and ovarian cancer Abstracts 15 September 2021 Pages: 255 - 288
A recurrent pathogenic BRCA2 exon 5–11 duplication in the Christian Arab population in Israel Gili Reznick LeviGal LaromKarin Weiss Original Article 17 May 2021 Pages: 289 - 294
Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer Kyra BokkersRonald P. ZweemerMargreet G. E. M. Ausems Original Article Open access 07 October 2021 Pages: 295 - 304
Re-evaluating cancer risks associated with the CHEK2 p.Ser428Phe Ashkenazi Jewish founder pathogenic variant Yael LaitmanSarah M. NielsenEitan Friedman Short Communication 08 October 2021 Pages: 305 - 308
Identification of women at risk of hereditary breast–ovarian cancer among participants in a population-based breast cancer screening Luigina BonelliIvana ValleLiliana Varesco Original Article 20 October 2021 Pages: 309 - 318
A de novo pathogenic variant in the MSH6 gene in a 52 years-old woman Elise Pierre-NoëlFabrice AiraudCaroline Abadie Short Communication 14 September 2021 Pages: 319 - 324
Familial colorectal cancer and tooth agenesis caused by an AXIN2 variant: how do we detect families with rare cancer predisposition syndromes? Janni M. JensenAnne SkakkebækLone Sunde Original Article 12 October 2021 Pages: 325 - 332
Utility of interim blood tests for cancer screening in Li-Fraumeni syndrome Leatrisse ObaAna F. BestPayal P. Khincha Short Communication 02 June 2021 Pages: 333 - 336
A patient with very early onset FH-deficient renal cell carcinoma diagnosed at age seven Rieko TaniguchiHideki MuramatsuYoshiyuki Takahashi Short Communication 22 June 2021 Pages: 337 - 341
PTCH2 is not a strong candidate gene for gorlin syndrome predisposition Miriam J. SmithD. Gareth Evans Short Communication Open access 25 June 2021 Pages: 343 - 346
Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family Kevin M. BrownMai XuMaria Teresa Landi Original Article 03 July 2021 Pages: 347 - 355
Uterine leiomyomatosis in adolescents and young adults (AYAs) may represent a narrow phenotypic variant of FH tumour predisposition syndrome Tiffany FooVivek NamaTerri P. McVeigh Short Communication 14 September 2021 Pages: 357 - 362
Fibroadenoma in vulval ectopic breast tissue in a patient with PTEN Hamartoma Tumour Syndrome Hannah DawsonAlannah SmrkeTerri P. McVeigh Short Communication 15 September 2021 Pages: 363 - 368
Patient ethnicity and cascade genetic testing: a descriptive study of a publicly funded hereditary cancer program Eryn F. BraleyAngela C. BedardKasmintan A. Schrader Short Communication 07 July 2021 Pages: 369 - 374
Outcomes of retesting in patients with previously uninformative cancer genetics evaluations Shenin A. DettwylerErika S. KoeppeElena M. Stoffel Original Article 21 September 2021 Pages: 375 - 385
Correction to: Outcomes of retesting in patients with previously uninformative cancer genetics evaluations Shenin A. DettwylerErika S. KoeppeElena M. Stoffel Correction 28 October 2021 Pages: 387 - 388