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Familial Cancer|September 5, 2025
Comparative insight: hereditary colorectal cancer registries in Iran, Singapore, and South AfricaLadan Goshayeshi, Ernest Wencong Eu, Raj Ramesar, et al.
Familial Cancer|June 9, 2020
Prospective observational data informs understanding and future management of Lynch syndrome: insights from the Prospective Lynch Syndrome Database (PLSD)Toni T Seppälä, Mev Dominguez-Valentin, Julian R Sampson, et al.
Familial Cancer|March 6, 2023
Hereditary acute myeloid leukemia associated with C-terminal CEBPA germline variantsAmye M Harrigan, Amy M Trottier
Familial Cancer|November 10, 2016
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the NetherlandsCharlotte J Dommering, Lidewij Henneman, Annemarie H van der Hout, et al.
Familial Cancer|November 20, 2016
All in the family? Analyzing the impact of family history in addition to genotype on medullary thyroid carcinoma aggressiveness in MEN2A patientsKristin L Long, Carol Etzel, Thereasa Rich, et al.
Familial Cancer|December 19, 2016
ATM mutations for surgeonsSara A Mansfield, Robert Pilarski, Doreen M Agnese
Familial Cancer|May 8, 2014
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patternsIolanda Borelli, Guido C Casalis Cavalchini, Serena Del Peschio, et al.
Familial Cancer|April 3, 2017
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteriaMaribel González-Acosta, Jesús Del Valle, Matilde Navarro, et al.
Familial Cancer|September 29, 2016
Exploring clinicians' attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancerYanni Chen, Michelle Peate, Rajneesh Kaur, et al.
Familial Cancer|March 20, 2017
Inherited DNA repair gene mutations detected by tumor next generation sequencing in urinary tract cancersSumati Gupta, Samantha Greenberg, Jade Grimmett, et al.
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