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Familial Cancer|June 25, 2026
The impact of international care networks on the clinical management of constitutional mismatch repair deficiency (CMMRD): a review of recent developmentsHans F A Vasen, Katharina Wimmer, Mariëtte van Kouwen, et al.
Familial Cancer|June 25, 2026
When screentime fails: initiative to improve completion of hereditary cancer genetic testing after telemedicine counselingIsabel R Murray, Muhammad Danyal Ahsan, Lauren Mitchell, et al.
Familial Cancer|August 4, 2026
Opportunities to improve detection of genetic predisposition for ovarian cancer applying the Tumor-First workflowVera M Witjes, Joanne A de Hullu, Angela van Remortele, et al.
Familial Cancer|July 22, 2026
Clinical and surveillance outcomes of the TP53 c.1000G > C (p.Gly334Arg) variantYehudit Peerless, Rinat Bernstein-Molho, Iris Kventsel, et al.
Familial Cancer|August 29, 2026
The identification of a PRKACA duplication at 19p13.12 in a female with PPNAD and thyroid carcinoma after a 20-year diagnostic journeyMarjoleine F Broekema, Florian Violon, Patricia Vaduva, et al.
Familial Cancer|August 29, 2026
The evolution of hereditary cancer genetic counselling: mainstreaming, service redesign and patient experience in Lynch syndromeKelly Kohut, Sarah Cable, Alekhya Ashokan, et al.
Familial Cancer|September 17, 2026
Risk of desmoid tumor based on APC pathogenic variant location and surgical history in familial adenomatous polyposis: a U.S. community cohort studyPrakash I Thomas, Holly E Carwana, Sheng-Fang Jiang, et al.
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