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Familial Cancer|May 24, 2017
Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genesElisabeth A Rosenthal, John Michael O Ranola, Brian H Shirts
Familial Cancer|September 23, 2016
Pancreas-sparing total duodenectomy for Spigelman stage IV duodenal polyposis associated with familial adenomatous polyposis: experience of 10 cases at a single institutionYuichiro Watanabe, Hideyuki Ishida, Hiroyuki Baba, et al.
Familial Cancer|June 9, 2018
Cholesterol profile in women with premature menopause after risk reducing salpingo-oophorectomyNatalia Teixeira, Marian J Mourits, Jan C Oosterwijk, et al.
Familial Cancer|May 31, 2018
The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practiceFred H Menko, Jacqueline A Ter Stege, Lizet E van der Kolk, et al.
Familial Cancer|June 26, 2019
Energy balance related lifestyle factors and risk of endometrial and colorectal cancer among individuals with lynch syndrome: a systematic reviewAdriana M Coletta, Susan K Peterson, Leticia A Gatus, et al.
Familial Cancer|September 30, 2018
Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinomaEvan J Walker, Julia Carnevale, Christina Pedley, et al.
Familial Cancer|May 23, 2019
Targeted next generation sequencing screening of Lynch syndrome in Tunisian populationRihab Ben Sghaier, Anne Maria Lucia Jansen, Ahlem Bdioui, et al.
Familial Cancer|January 20, 2021
Interpretation of BRCA2 Splicing Variants: A Case Series of Challenging Variant Interpretations and the Importance of Functional RNA AnalysisPaola Nix, Erin Mundt, Bradford Coffee, et al.
Familial Cancer|February 3, 2021
Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working GroupM C Frühwald, K Nemes, H Boztug, et al.
Familial Cancer|October 7, 2022
Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?Ryan Matthew Kahn, Muhammad Danyal Ahsan, Eloise Chapman-Davis, et al.
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