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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.
Irish Journal of Medical Science|October 19, 2022
Uptake of BRCA1/BRCA2 predictive genetic testing in an Irish population is low: a missed opportunityDavid E O'Reilly, Lucy Dooley, Geoffrey A Watson, et al.
Cancer Prevention Research (Philadelphia, Pa.)|February 14, 2020
A Multi-Institutional Cohort of Therapy-Associated Polyposis in Childhood and Young Adulthood Cancer SurvivorsLeah H Biller, Chinedu Ukaegbu, Tara G Dhingra, et al.
Cancer|January 17, 2018
Phase 1 trial evaluating cisplatin, gemcitabine, and veliparib in 2 patient cohorts: Germline BRCA mutation carriers and wild-type BRCA pancreatic ductal adenocarcinomaEileen M O'Reilly, Jonathan W Lee, Maeve A Lowery, et al.
BMC Medical Genomics|May 21, 2017
Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testingDonavan T Cheng, Meera Prasad, Yvonne Chekaluk, et al.
Human Molecular Genetics|March 22, 2021
Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genesRosalie Griffin Waller, Robert J Klein, Joseph Vijai, et al.
Cancer|August 12, 2009
Sequential adjuvant chemotherapy after surgical resection of high-risk urothelial carcinomaDavid J Gallagher, Matthew I Milowsky, Alexia Iasonos, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 11, 2002
Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancersKenneth Offit, Shlomit Gilad, Shoshana Paglin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2009
Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cellsStephen J Salipante, Matthew E Mealiffe, Jeremy Wechsler, et al.
American Journal of Medical Genetics. Part A|December 22, 2025
Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder VariantLauren G Banaszak, Elise Fiala, Ozge Ceyhan-Birsoy, et al.
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