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Familial Cancer|January 23, 2018
Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the sameA J Huq, M Walsh, B Rajagopalan, et al.
Familial Cancer|May 21, 2022
Founder vs. non-founder BRCA1/2 pathogenic alleles: the analysis of Belarusian breast and ovarian cancer patients and review of other studies on ethnically homogenous populationsG A Yanus, E L Savonevich, A P Sokolenko, et al.
Familial Cancer|June 2, 2021
Utility of interim blood tests for cancer screening in Li-Fraumeni syndromeLeatrisse Oba, Ana F Best, Phuong L Mai, et al.
Familial Cancer|June 25, 2021
PTCH2 is not a strong candidate gene for gorlin syndrome predispositionMiriam J Smith, D Gareth Evans
Familial Cancer|March 21, 2020
Patient-reported burden of intensified surveillance and surgery in high-risk individuals under pancreatic cancer surveillanceKasper A Overbeek, Djuna L Cahen, Anne Kamps, et al.
Familial Cancer|March 23, 2020
De novo SDHB gene mutation in a family with extra-adrenal paragangliomaCaitlin B Mauer, Brian Reys, Jonathan Wickiser
Familial Cancer|March 16, 2020
Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposisBrandie Heald, Heather Hampel, James Church, et al.
Familial Cancer|December 4, 2019
Renal cell carcinoma in young FH mutation carriers: case series and review of the literatureJ A Hol, M C J Jongmans, A S Littooij, et al.
Familial Cancer|September 29, 2020
FRAMe: Familial Risk Assessment of Melanoma-a risk prediction tool to guide CDKN2A germline mutation testing in Australian familial melanomaElizabeth A Holland, Serigne Lo, Blake Kelly, et al.
Familial Cancer|August 27, 2022
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 IrelandTerri Patricia McVeigh, Karl J Sweeney, Donal J Brennan, et al.
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