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Public Health Genomics and Precision Health Knowledge Base (v8.2)
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Last data update: Feb 08, 2023
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Cultural adaptations to a telephone genetic counseling protocol and booklet for Latina breast cancer survivors at risk for hereditary breast and ovarian cancer.
Sara Gómez-Trillos et al. Translational behavioral medicine 2023
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MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome.
Knapp Stephen T et al. Cancers 2023 15(2)
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The Risk-Reducing Effect of Aspirin in Lynch Syndrome Carriers: Development and Evaluation of an Educational Leaflet.
Kaur Rajneesh et al. Advanced genetics (Hoboken, N.J.) 2023 3(2) 2100046
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Breast Cancer Awareness Month 2022 Digital Media Toolkit
CDC, October 5, 2022
CGV: Cancer Genome Viewer, a web service for integrative cancer genome and pharmacogenomic data analysis.
Choi Ji-Hye et al. Bioinformatics (Oxford, England) 2022
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PO2RDF: representation of real-world data for precision oncology using resource description framework.
Zhao Yiqing et al. BMC medical genomics 2022 15(1) 167
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Semi-supervised approach to event time annotation using longitudinal electronic health records.
Liang Liang et al. Lifetime data analysis 2022
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An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance.
Iversen Edwin S et al. NPJ genomic medicine 2022 7(1) 35
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Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery.
Shickh Salma et al. BMJ open 2022 12(4) e060899
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CHAIMELEON Project: Creation of a Pan-European Repository of Health Imaging Data for the Development of AI-Powered Cancer Management Tools.
Bonmatí Luis Martí et al. Frontiers in oncology 2022 12742701
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A Scalable Quality Assurance Process for Curating Oncology Electronic Health Records: The Project GENIE Biopharma Collaborative Approach.
Lavery Jessica A et al. JCO clinical cancer informatics 2022 6e2100105
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Genome Nexus: A Comprehensive Resource for the Annotation and Interpretation of Genomic Variants in Cancer.
de Bruijn Ino et al. JCO clinical cancer informatics 2022 6e2100144
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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.
Holter Spring et al. Journal of genetic counseling 2022
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cbpManager: a web application to streamline the integration of clinical and genomic data in cBioPortal to support the Molecular Tumor Board.
Ustjanzew Arsenij et al. BMC medical informatics and decision making 2021 21(1) 358
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Metrics for Evaluating Polygenic Risk Scores.
Baker Stuart G et al. JNCI cancer spectrum 2021 5(1) pkaa106
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De novo individualized disease modules reveal the synthetic penetrance of genes and inform personalized treatment regimens.
Weiskittel Taylor et al. Genome research 2021
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Digital twins for predictive oncology will be a paradigm shift for precision cancer care
TH Boussard et al, Nature Medicine, November 2, 2021
[HerediCaRe: Documentation and IT Solution of a Specialized Registry for Hereditary Breast and Ovarian Cancer].
Engel Christoph et al. Gesundheitswesen (Bundesverband der Arzte des Offentlichen Gesundheitsdienstes (Germany)) 2021 83(S 01) S12-S17
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A risk prediction tool for individuals with a family history of breast, ovarian, or pancreatic cancer: BRCAPANCPRO.
Blackford Amanda L et al. British journal of cancer 2021
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Cancer DEIso: An integrative analysis platform for investigating differentially expressed gene-level and isoform-level human cancer markers.
Yang Tzu-Hsien et al. Computational and structural biotechnology journal 2021 195149-5159
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MetaCancer: A deep learning-based pan-cancer metastasis prediction model developed using multi-omics data.
Albaradei Somayah et al. Computational and structural biotechnology journal 2021 194404-4411
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Multi-syndrome, multi-gene risk modeling for individuals with a family history of cancer with the novel R package PanelPRO.
Lee Gavin et al. eLife 2021 10
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MFHP Cancer
CDC, July 2021
Demetra Application: An integrated genotype analysis web server for clinical genomics in endometriosis.
Papageorgiou Louis et al. International journal of molecular medicine 2021 47(6)
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Training Institute for Dissemination and Implementation Research in Cancer (TIDIRC) OpenAccess
National Cancer Institute, Division of Cancer Control & Population Sciences
Practical instructions for testing and targeted therapy in adult patients with solid tumours with NTRK gene fusion in common clinical practice.
Büchler Tomáš et al. Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti 2020 33(6) 414-419
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OncoTree: A Cancer Classification System for Precision Oncology.
Kundra Ritika et al. JCO clinical cancer informatics 2021 5221-230
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The NCI Genomic Data Commons.
Heath Allison P et al. Nature genetics 2021
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Cancer Risk Reduction Through Education of Adolescents: Development of a Tailored Cancer Risk-Reduction Educational Tool.
Zeinomar Nur et al. Journal of cancer education : the official journal of the American Association for Cancer Education 2021 Feb
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Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes-Practice resource of the National Society of Genetic Counselors.
Berliner Janice L et al. Journal of genetic counseling 2021 Jan
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Page last reviewed:
Feb 1, 2023
Page last updated:
Feb 08, 2023
Content source:
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