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Journal of the American College of Surgeons|December 24, 2011
Systematic immunohistochemistry screening for Lynch syndrome in early age-of-onset colorectal cancer patients undergoing surgical resectionEmily Steinhagen, Jinru Shia, Arnold J Markowitz, et al.Cancer Prevention Research (Philadelphia, Pa.)|July 25, 2019
Outcome of Pancreatic Cancer Surveillance Among High-Risk Individuals Tested for Germline Mutations in BRCA1 and BRCA2Amethyst Saldia, Sara H Olson, Pamela Nunes, et al.BMC Genetics|October 6, 2007
The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-control association studiesLutécia H Mateus Pereira, Marbin A Pineda, William H Rowe, et al.Journal of the American College of Surgeons|February 22, 2003
A636P is associated with early-onset colon cancer in Ashkenazi JewsJosé G Guillem, Beth S Rapaport, Tomas Kirchhoff, et al.Oncotarget|February 13, 2016
Association and prognostic significance of BRCA1/2-mutation status with neoantigen load, number of tumor-infiltrating lymphocytes and expression of PD-1/PD-L1 in high grade serous ovarian cancerKyle C Strickland, Brooke E Howitt, Sachet A Shukla, et al.Breast Cancer Research and Treatment|March 7, 2012
Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effortSerena Masciari, Deborah A Dillon, Michelle Rath, et al.Gynecologic Oncology|October 14, 2025
SMARCA4 pathogenic variants: Gynecological cancer histories from a laboratory tested cohortBrittany A Borden, Adela Rodriguez-Hernandez, Magan Trottier, et al.Gynecologic Oncology|September 4, 2012
Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndromeMatthew B Yurgelun, Rowena Mercado, Margery Rosenblatt, et al.JCO Clinical Cancer Informatics|March 16, 2026
Interpretable Active Learning for Pedigree Data Deduplication in Cancer GeneticsMaria S Rosito, Aleck E Cervantes, Christine Hong, et al.Carcinogenesis|June 16, 2006
Increased frequency of disease-causing MYH mutations in colon cancer familiesPaolo Peterlongo, Nandita Mitra, Ana Sanchez de Abajo, et al.Pageof 68