New surveillance guidelines for Li-Fraumeni and hereditary TP53 related cancer syndrome: implications for germline TP53 testing in breast cancer D. Gareth EvansEmma R. Woodward Editorial 28 September 2020 Pages: 1 - 7
The CAPP II trial of aspirin in Lynch syndrome/HNPCC: is it time for everyone to be treated? Patrick M. Lynch Editorial Comment 09 January 2021 Pages: 9 - 11
Improving primary care identification of familial breast cancer risk using proactive invitation and decision support Nadeem QureshiBrittany DuttonJoe Kai Original Article Open access 11 June 2020 Pages: 13 - 21
Chemoprevention in familial adenomatous polyposis: past, present and future Phillip M. Kemp BohanGautam MankaneyCarol A. Burke Review 08 June 2020 Pages: 23 - 33
Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD) Toni T. SeppäläMev Dominguez-ValentinPål Møller Review Open access 08 June 2020 Pages: 35 - 39
Low accuracy of self-reported family history of melanoma in high-risk patients Nicholas D. FlintMichael D. BishopAaron M. Secrest Original Article 21 May 2020 Pages: 41 - 48
Small fraction of testicular cancer cases may be causatively related to CHEK2 inactivating germ-line mutations: evidence for somatic loss of the remaining CHEK2 allele in the tumor tissue Valeriya I. NiAlexandr O. IvantsovEvgeny N. Imyanitov Original Article 26 May 2020 Pages: 49 - 53
Two cases of somatic STK11 mosaicism in Danish patients with Peutz–Jeghers syndrome Anne Marie JelsigBirgitte BertelsenJohn Gásdal Karstensen Short Communication 06 June 2020 Pages: 55 - 59
Germline variants discovered in lymphoma patients undergoing tumor profiling: a case series Anthony J. ScottMolly C. TokazRyan A. Wilcox Original Article 06 June 2020 Pages: 61 - 65
Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019 M. SuerinkK. WimmerH. F. A. Vasen Review Open access 02 July 2020 Pages: 67 - 73
Complete response of hereditary leiomyomatosis and renal cell cancer (HLRCC)-associated renal cell carcinoma to nivolumab and ipilimumab combination immunotherapy by: a case report Yasuhiro IribeMitsuko FuruyaNoboru Nakaigawa Short Communication 15 July 2020 Pages: 75 - 80
Multiple primary cancers (renal papillary, lymphoma and teratoma) and hepatic cysts in association with a pathogenic germline mutation in the MET gene Julian Adlard Short Communication 20 July 2020 Pages: 81 - 83