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Cascade testing for hereditary cancer: comprehensive multigene panels identify unexpected actionable findings in relatives.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2024, v. 116, n. 2, p. 334, doi. 10.1093/jnci/djad203
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- Publication type:
- Article
POLD1 DEDD Motif Mutation Confers Hypermutation in Endometrial Cancer and Durable Response to Pembrolizumab.
- Published in:
- Cancers, 2023, v. 15, n. 23, p. 5674, doi. 10.3390/cancers15235674
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- Publication type:
- Article
Moving the Needle Forward in Genomically-Guided Precision Radiation Treatment.
- Published in:
- Cancers, 2023, v. 15, n. 22, p. 5314, doi. 10.3390/cancers15225314
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- Publication type:
- Article
Turning the Page on Breast Cancer in Ohio: Lessons learned from implementing a multilevel intervention to reduce breast cancer mortality among Black women.
- Published in:
- Cancer (0008543X), 2023, v. 129, p. 3114, doi. 10.1002/cncr.34845
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- Publication type:
- Article
Turning the Page on Breast Cancer in Ohio: Lessons learned from implementing a multilevel intervention to reduce breast cancer mortality among Black women.
- Published in:
- Cancer (0008543X), 2023, v. 129, n. 19, p. 3114, doi. 10.1002/cncr.34845
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- Publication type:
- Article
Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31840-0
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- Publication type:
- Article
Author Correction: Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-38170-1
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- Publication type:
- Article
Integrating Early-Stage Drug Development with Clinical Networks; Challenges and Opportunities: The City of Hope Developing Experience.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 12, p. 4061, doi. 10.3390/jcm12124061
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- Publication type:
- Article
A mainstreaming oncogenomics model: improving the identification of Lynch syndrome.
- Published in:
- Frontiers in Oncology, 2023, p. 1, doi. 10.3389/fonc.2023.1140135
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- Publication type:
- Article
Application of Mendelian randomization to explore the causal role of the human gut microbiome in colorectal cancer.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31840-0
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- Publication type:
- Article
Rethinking Patient Engagement in Cancer Research.
- Published in:
- Patient, 2023, v. 16, n. 2, p. 89, doi. 10.1007/s40271-022-00604-9
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- Publication type:
- Article
Promoting patient engagement in cancer genomics research programs: An environmental scan.
- Published in:
- Frontiers in Genetics, 2023, v. 14, p. 1, doi. 10.3389/fgene.2023.1053613
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- Publication type:
- Article
MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome.
- Published in:
- Cancers, 2023, v. 15, n. 2, p. 391, doi. 10.3390/cancers15020391
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- Publication type:
- Article
Universal tumor screening for lynch syndrome on colorectal cancer biopsies impacts surgical treatment decisions.
- Published in:
- Familial Cancer, 2023, v. 22, n. 1, p. 71, doi. 10.1007/s10689-022-00302-3
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- Publication type:
- Article
Mainstreaming germline genetic testing for patients with pancreatic cancer increases uptake.
- Published in:
- Familial Cancer, 2023, v. 22, n. 1, p. 91, doi. 10.1007/s10689-022-00300-5
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- Publication type:
- Article
Multiple colorectal adenomas in Lynch syndrome.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 01, doi. 10.3389/fonc.2022.1038678
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- Publication type:
- Article
Mismatch Repair and Microsatellite Instability Testing for Immune Checkpoint Inhibitor Therapy: Guideline From the College of American Pathologists in Collaboration With the Association for Molecular Pathology and Fight Colorectal Cancer.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2022, v. 146, n. 10, p. 1194, doi. 10.5858/arpa.2021-0632-CP
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- Publication type:
- Article
Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 3, p. 568, doi. 10.1002/jgc4.1546
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- Publication type:
- Article
Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients.
- Published in:
- Cancers, 2022, v. 14, n. 10, p. 2426, doi. 10.3390/cancers14102426
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- Publication type:
- Article
Utilizing Public Health Frameworks and Partnerships to Ensure Equity in DNA-Based Population Screening.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.886755
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- Publication type:
- Article
Differences in somatic TP53 mutation type in breast tumors by race and receptor status.
- Published in:
- Breast Cancer Research & Treatment, 2022, v. 192, n. 3, p. 639, doi. 10.1007/s10549-022-06509-3
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- Publication type:
- Article
Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis.
- Published in:
- PLoS Medicine, 2022, v. 19, n. 2, p. 1, doi. 10.1371/journal.pmed.1003897
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- Publication type:
- Article
Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis.
- Published in:
- 2022
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- Publication type:
- journal article
Economic Evaluation of Universal Lynch Syndrome Screening Protocols among Newly Diagnosed Patients with Colorectal Cancer.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 12, p. 1284, doi. 10.3390/jpm11121284
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- Publication type:
- Article
Advanced adenomas may be a red flag for hereditary cancer syndromes.
- Published in:
- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00164-9
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- Publication type:
- Article
Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposis.
- Published in:
- Familial Cancer, 2020, v. 19, n. 3, p. 223, doi. 10.1007/s10689-020-00170-9
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- Publication type:
- Article
Tumor Budding Detection System in Whole Slide Pathology Images.
- Published in:
- Journal of Medical Systems, 2020, v. 44, n. 2, p. 1, doi. 10.1007/s10916-019-1515-y
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- Publication type:
- Article
What guidance does HIPAA offer to providers considering familial risk notification and cascade genetic testing?
- Published in:
- Journal of Law & the Biosciences, 2020, v. 7, n. 1, p. 1, doi. 10.1093/jlb/lsaa071
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- Publication type:
- Article
Universal screening for Lynch syndrome in a large consecutive cohort of Chinese colorectal cancer patients: High prevalence and unique molecular features.
- Published in:
- International Journal of Cancer, 2019, v. 144, n. 9, p. 2161, doi. 10.1002/ijc.32044
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- Publication type:
- Article
Modified capture-recapture estimates of the number of families with Lynch syndrome in Central Ohio.
- Published in:
- Familial Cancer, 2019, v. 18, n. 1, p. 67, doi. 10.1007/s10689-018-0096-0
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- Publication type:
- Article
Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.
- Published in:
- Familial Cancer, 2018, v. 17, n. 3, p. 431, doi. 10.1007/s10689-017-0048-0
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- Publication type:
- Article
Colorectal Carcinomas With Isolated Loss of PMS2 Staining by Immunohistochemistry.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2018, v. 142, n. 4, p. 523, doi. 10.5858/arpa.2017-0156-OA
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- Publication type:
- Article
Challenges and Opportunities for Cancer Predisposition Cascade Screening for Hereditary Breast and Ovarian Cancer and Lynch Syndrome in Switzerland: Findings from an International Workshop.
- Published in:
- 2018
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- Publication type:
- Proceeding
Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance.
- Published in:
- Journal of Genetic Counseling, 2017, v. 26, n. 4, p. 866, doi. 10.1007/s10897-017-0066-y
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- Publication type:
- Article
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
- Published in:
- Nature Communications, 2017, v. 8, n. 5, p. 14755, doi. 10.1038/ncomms14755
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- Publication type:
- Article
Understanding the contribution of family history to colorectal cancer risk and its clinical implications: A state-of-the-science review.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Discordant Mismatch Repair Protein Immunoreactivity in Lynch Syndrome-Associated Neoplasms: A Recommendation for Screening Synchronous/Metachronous Neoplasms.
- Published in:
- 2016
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- Publication type:
- journal article
Genetic counseling and cascade genetic testing in Lynch syndrome.
- Published in:
- Familial Cancer, 2016, v. 15, n. 3, p. 423, doi. 10.1007/s10689-016-9893-5
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- Publication type:
- Article
Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 253, doi. 10.1007/s10689-015-9856-2
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- Publication type:
- Article
Comparison of Prediction Models for Lynch Syndrome Among Individuals With Colorectal Cancer.
- Published in:
- 2016
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- Publication type:
- journal article
Allele-specific imbalance mapping at human orthologs of mouse susceptibility to colon cancer ( Scc) loci.
- Published in:
- International Journal of Cancer, 2015, v. 137, n. 10, p. 2323, doi. 10.1002/ijc.29599
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- Publication type:
- Article
Creation of a Network to Promote Universal Screening for Lynch Syndrome: The Lynch Syndrome Screening Network.
- Published in:
- Journal of Genetic Counseling, 2015, v. 24, n. 3, p. 421, doi. 10.1007/s10897-014-9770-z
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- Publication type:
- Article
A Modified Lynch Syndrome Screening Algorithm in Colon Cancer.
- Published in:
- American Journal of Clinical Pathology, 2015, v. 143, n. 3, p. 336, doi. 10.1309/AJCP4D7RXOBHLKGJ
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- Publication type:
- Article
ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes.
- Published in:
- American Journal of Gastroenterology (Springer Nature), 2015, v. 110, n. 2, p. 223, doi. 10.1038/ajg.2014.435
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- Publication type:
- Article
Biallelic MUTYH mutations can mimic Lynch syndrome.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 11, p. 1334, doi. 10.1038/ejhg.2014.15
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- Publication type:
- Article
Microsatellite Instability Detection by Next Generation Sequencing.
- Published in:
- Clinical Chemistry, 2014, v. 60, n. 9, p. 1192, doi. 10.1373/clinchem.2014.223677
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- Publication type:
- Article
BRAF V600E Mutation Analysis Simplifies the Testing Algorithm for Lynch Syndrome.
- Published in:
- American Journal of Clinical Pathology, 2013, v. 140, n. 2, p. 177, doi. 10.1309/AJCPB9FOVH1HGKFR
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- Publication type:
- Article
How do we approach the goal of identifying everybody with Lynch Syndrome?
- Published in:
- Familial Cancer, 2013, v. 12, n. 2, p. 313, doi. 10.1007/s10689-013-9611-5
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- Publication type:
- Article
Identification of Lynch Syndrome Among Patients With Colorectal Cancer.
- Published in:
- JAMA: Journal of the American Medical Association, 2012, v. 308, n. 15, p. 1555, doi. 10.1001/jama.2012.13088
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- Publication type:
- Article
Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patients.
- Published in:
- Human Mutation, 2012, v. 33, n. 8, p. 1294, doi. 10.1002/humu.22119
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- Publication type:
- Article