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Genetics of Colorectal Cancer.
- Published in:
- Oncology (08909091), 2006, v. 20, n. 3, p. 269
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- Article
The Taylor/Mutch Article Reviewed.
- Published in:
- Oncology (08909091), 2006, v. 20, n. 1, p. 96
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- Publication type:
- Article
Screening for germline mismatch repair mutations following diagnosis of sebaceous neoplasm.
- Published in:
- 2014
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- Publication type:
- journal article
Screening for Germline Mismatch Repair Mutations Following Diagnosis of Sebaceous Neoplasm.
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- JAMA Dermatology, 2014, v. 150, n. 12, p. 1315, doi. 10.1001/jamadermatol.2014.1217
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- Publication type:
- Article
Experiences of patients and family members with follow-up care, information needs and provider support after identification of Lynch Syndrome.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00273-1
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- Publication type:
- Article
Uptake of genetic counseling and multi‐gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing.
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- Journal of Genetic Counseling, 2022, v. 31, n. 2, p. 470, doi. 10.1002/jgc4.1513
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- Article
Genetic Test Reporting and Counseling for Melanoma Risk in Minors May Improve Sun Protection Without Inducing Distress.
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- Journal of Genetic Counseling, 2018, v. 27, n. 4, p. 955, doi. 10.1007/s10897-017-0185-5
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- Publication type:
- Article
Pancreatic cancer as a sentinel for hereditary cancer predisposition.
- Published in:
- 2018
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- Publication type:
- journal article
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 12, p. 1, doi. 10.1002/mgg3.1532
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- Publication type:
- Article
Predictors of Women's Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members.
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- Public Health Genomics, 2023, v. 26, n. 1, p. 24, doi. 10.1159/000528522
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- Publication type:
- Article
Congenital abnormalities and hepatoblastoma: A report from the Children's Oncology Group (COG) and the Utah Population Database (UPDB).
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2250, doi. 10.1002/ajmg.a.36638
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- Article
Motivation-based intervention to promote colonoscopy screening: An integration of a fear management model and motivational interviewing.
- Published in:
- 2011
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- Publication type:
- Journal Article
Interactive Beliefs about Genes and Behavior Predict Improved Sun Protection Following Melanoma Genetic Counseling.
- Published in:
- 2022
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- Publication type:
- journal article
Priority of Risk (But Not Perceived Magnitude of Risk) Predicts Improved Sun-Protection Behavior Following Genetic Counseling for Familial Melanoma.
- Published in:
- 2021
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- Publication type:
- journal article
Increasing Skin Cancer Prevention in Young Adults: the Cumulative Impact of Personalized UV Photography and MC1R Genetic Testing.
- Published in:
- Journal of Cancer Education, 2023, v. 38, n. 3, p. 1059, doi. 10.1007/s13187-022-02232-1
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- Publication type:
- Article
Development of an Educational Program Integrating Concepts of Genetic Risk and Preventive Strategies for Children with a Family History of Melanoma.
- Published in:
- 2018
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- Publication type:
- journal article
Population-based relative risks for specific family history constellations of breast cancer.
- Published in:
- 2019
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- Publication type:
- journal article
Melanoma risk assessment based on relatives' age at diagnosis.
- Published in:
- 2018
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- Publication type:
- journal article
A pilot study of a telehealth family-focused melanoma preventive intervention for children with a family history of melanoma.
- Published in:
- 2020
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- Publication type:
- journal article
Effectiveness of the extended parallel process model in promoting colorectal cancer screening.
- Published in:
- 2015
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- Publication type:
- journal article
Genetic testing for hereditary melanoma and pancreatic cancer: a longitudinal study of psychological outcome.
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- Psycho-Oncology, 2013, v. 22, n. 2, p. 276, doi. 10.1002/pon.2080
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- Publication type:
- Article
Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing Approach.
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- JMIR Medical Informatics, 2022, v. 10, n. 8, p. 1, doi. 10.2196/37842
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- Publication type:
- Article
Association of Disparities in Family History and Family Cancer History in the Electronic Health Record With Sex, Race, Hispanic or Latino Ethnicity, and Language Preference in 2 Large US Health Care Systems.
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- JAMA Network Open, 2022, v. 5, n. 10, p. e2234574, doi. 10.1001/jamanetworkopen.2022.34574
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- Article
Different familial adenomatous polyposis phenotypes resulting from deletions of the entire APC exon 15.
- Published in:
- Human Genetics, 2002, v. 111, n. 1, p. 88, doi. 10.1007/s00439-002-0758-7
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- Publication type:
- Article
'I had a bigger cancer risk than I thought...': The experience of receiving personalized risk information as part of a skin cancer prevention intervention in the college setting.
- Published in:
- Health Expectations, 2022, v. 25, n. 6, p. 2937, doi. 10.1111/hex.13601
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- Publication type:
- Article
CHEK2 Founder Variants and Thyroid Cancer Risk.
- Published in:
- Thyroid, 2024, v. 34, n. 4, p. 477, doi. 10.1089/thy.2023.0529
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- Publication type:
- Article
Determinants of Breast Cancer Screening Adherence During the COVID-19 Pandemic in a Cohort at Increased Inherited Cancer Risk in the United States.
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- Cancer Control: Journal of the Moffitt Cancer Center, 2024, p. 1, doi. 10.1177/10732748241272727
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- Publication type:
- Article
Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomized controlled trial.
- Published in:
- 2021
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- Publication type:
- journal article
Breast cancer screening of pregnant and breastfeeding women with BRCA mutations.
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- Breast Cancer Research & Treatment, 2017, v. 162, n. 2, p. 225, doi. 10.1007/s10549-017-4122-y
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- Publication type:
- Article
GARDE: a standards-based clinical decision support platform for identifying population health management cohorts.
- Published in:
- 2022
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- Publication type:
- journal article
Radiation therapy and secondary malignancy in Li‐Fraumeni syndrome: A hereditary cancer registry study.
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- Cancer Medicine, 2020, v. 9, n. 21, p. 7954, doi. 10.1002/cam4.3427
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- Publication type:
- Article
Population prevalence of individuals meeting criteria for hereditary breast and ovarian cancer testing.
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- Cancer Medicine, 2019, v. 8, n. 15, p. 6789, doi. 10.1002/cam4.2534
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- Publication type:
- Article
Patient Interactions With an Automated Conversational Agent Delivering Pretest Genetics Education: Descriptive Study.
- Published in:
- 2021
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- Publication type:
- journal article
Difference of Opinion: Spousal Influence on Cancer Risk-reducing Behavior.
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- American Journal of Health Behavior, 2019, v. 43, n. 3, p. 582, doi. 10.5993/AJHB.43.3.12
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- Article
Pediatric Predispositional Genetic Risk Communication: Potential Utility for Prevention and Control of Melanoma Risk as an Exemplar.
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- Journal of Genetic Counseling, 2017, v. 26, n. 5, p. 887, doi. 10.1007/s10897-017-0105-8
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- Publication type:
- Article
Factors Associated with Interest in Gene-Panel Testing and Risk Communication Preferences in Women from BRCA1/2 Negative Families.
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- Journal of Genetic Counseling, 2017, v. 26, n. 3, p. 480, doi. 10.1007/s10897-016-0001-7
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- Publication type:
- Article
Perceived Risk Following Melanoma Genetic Testing: A 2-Year Prospective Study Distinguishing Subjective Estimates from Recall.
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- Journal of Genetic Counseling, 2014, v. 23, n. 3, p. 421, doi. 10.1007/s10897-013-9676-1
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- Article
Biallelic inactivation of the APC gene is associated with hepatocellular carcinoma in familial adenomatous polyposis coli.
- Published in:
- 2001
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- Publication type:
- journal article
Patient and provider attitudes toward genomic testing for prostate cancer susceptibility: a mixed method study.
- Published in:
- 2013
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- Publication type:
- journal article
Impact of melanoma genetic test reporting on perceived control over melanoma prevention.
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- Journal of Behavioral Medicine, 2015, v. 38, n. 5, p. 754, doi. 10.1007/s10865-015-9631-8
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- Publication type:
- Article
Genetic test reporting enhances understanding of risk information and acceptance of prevention recommendations compared to family history-based counseling alone.
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- Journal of Behavioral Medicine, 2015, v. 38, n. 5, p. 740, doi. 10.1007/s10865-015-9648-z
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- Publication type:
- Article
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 6, p. 943, doi. 10.1111/cge.13757
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- Article
The contribution of the rs55705857 G allele to familial cancer risk as estimated in the Utah population database.
- Published in:
- 2019
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- Publication type:
- journal article
Breast Cancer Risk Reduction Decisions of the BRCA-Positive Patient: An Observational Study at a Single Institution.
- Published in:
- Journal of Women's Health (15409996), 2017, v. 26, n. 6, p. 702, doi. 10.1089/jwh.2016.5931
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- Publication type:
- Article
Uptake of Cancer Genetic Services for Chatbot vs Standard-of-Care Delivery Models: The BRIDGE Randomized Clinical Trial.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 9, p. e2432143, doi. 10.1001/jamanetworkopen.2024.32143
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- Article
Characterization of Malignant Head and Neck Paragangliomas at a Single Institution Across Multiple Decades.
- Published in:
- 2019
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- Publication type:
- journal article
Can We Identify the High-Risk Patients to Be Screened? A Genetic Approach.
- Published in:
- Digestion, 2007, v. 76, n. 1, p. 7, doi. 10.1159/000108389
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- Publication type:
- Article
Familial risk of childhood cancer and tumors in the li-fraumeni spectrum in the utah population database: Implications for genetic evaluation in pediatric practice.
- Published in:
- International Journal of Cancer, 2013, v. 133, n. 10, p. 2444, doi. 10.1002/ijc.28266
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- Publication type:
- Article
Cost-effectiveness of early cancer surveillance for patients with Li-Fraumeni syndrome.
- Published in:
- 2019
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- Publication type:
- journal article
A need to tailor surveillance based on family history: describing a highly penetrant familial paraganglioma kindred with an SDHD pathogenic variant.
- Published in:
- Familial Cancer, 2023, v. 22, n. 2, p. 217, doi. 10.1007/s10689-022-00318-9
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- Publication type:
- Article