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Frontiers in Oncology|November 8, 2024
Pre-malignant conditions diagnosed following a positive cancer signal from a multi-cancer early detection testOmair A Choudhry, Angana B Kharge, Seema P Rego, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Implementing family health history risk stratification in primary care: impact of guideline criteria on populations and resource demandLori A Orlando, R Ryanne Wu, Chris Beadles, et al.
BMC Cancer|October 6, 2011
Activating mutation in MET oncogene in familial colorectal cancerDeborah W Neklason, Michelle W Done, Nykole R Sargent, et al.
JAMA Otolaryngology-- Head & Neck Surgery|January 5, 2023
Thyroidectomy Outcomes in Patients Identified With RET Pathogenic Variants Through a Population Genomic Screening ProgramPriscilla F A Pichardo, Ryan N Hellums, Jing Hao, et al.
Familial Cancer|February 12, 2014
Providing patient education: impact on quantity and quality of family health history collectionChris A Beadles, R Ryanne Wu, Tiffany Himmel, et al.
Public Health Genomics|November 6, 2024
Development and Pilot Testing of Evidence-Based Interventions to Improve Adherence after Receiving a Genetic ResultAnna May Baker, Jessica Goehringer, Makenzie Woltz, et al.
Molecular Genetics & Genomic Medicine|August 4, 2019
Research participants' experiences with return of genetic research results and preferences for web-based alternativesJill B Gaieski, Linda Patrick-Miller, Brian L Egleston, et al.
JNCI Cancer Spectrum|June 11, 2025
Increased colorectal and endometrial cancer rates in a genomically ascertained lynch syndrome cohortMiranda Lg Hallquist, Juliann M Savatt, Kristy Diloreto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 4, 2015
Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testingAngela R Bradbury, Linda J Patrick-Miller, Brian L Egleston, et al.
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