WORLD CANCER DAY: KNOW YOUR FAMILY HISTORY
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What's New
Last Updated: Feb 05, 2016- Tools for Bidirectional Cancer Registry Reporting to Identify Individuals at Risk for Hereditary Breast and Ovarian Cancer syndrome
Disease: Lynch syndrome; Type: Tools; State: Multiple States (From Implementation Database) - Tools for Bidirectional Cancer Registry Reporting to Identify Individuals at Risk for Lynch syndrome
Disease: Lynch syndrome; Type: Tools; State: Multiple States (From Implementation Database) - Personalizing chemotherapy dosing using pharmacological methods.
Patel Jai N et al. Cancer chemotherapy and pharmacology 2015 Nov 76(5) 879-96 (From Genomics & Health Impact Scan Database) - Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool.
Jongmans Marjolijn C J et al. European journal of medical genetics 2016 Jan (From Genomics & Health Impact Scan Database) - Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer.
Lin Po-Han, et al. Oncotarget 2016 1 (From HuGE Literature Finder) - CDC Family History Page
(From CDC Information Database) - CDC Blog Posts on Family History
(From CDC Information Database) - Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families.
Talseth-Palmer Bente A, et al. Cancer medicine 2016 1 (From HuGE Literature Finder) - Genetic polymorphisms by deletion in genes that encode for glutathione S-transferases are associated with nicotine dependence and tobacco use-related medical disorders.
de Melo Luiz Gustavo Piccoli, et al. Neuro endocrinology letters 2015 12 (6) 529-538 (From HuGE Literature Finder) - Family history of breast cancer and its association with disease severity and mortality.
Melvin Jennifer C et al. Cancer medicine 2016 Jan (From Genomics & Health Impact Scan Database) - A two-stage approach to genetic risk assessment in primary care.
Biswas Swati et al. Breast cancer research and treatment 2016 Jan (From Genomics & Health Impact Scan Database) - Perceptions of Cancer Risk, Cause, and Needs in Participants from Low Socioeconomic Background at Risk for Hereditary Cancer.
Underhill Meghan L et al. Behavioral medicine (Washington, D.C.) 2016 Jan 0 (From Genomics & Health Impact Scan Database) - Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
Thompson Ella R et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 Jan (From Genomics & Health Impact Scan Database) - Selecting Patients with Ovarian Cancer for Germline BRCA Mutation Testing: Findings from Guidelines and a Systematic Literature Review.
Eccles Diana M et al. Advances in therapy 2016 Jan (From Genomics & Health Impact Scan Database) - Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.
Bruno William, et al. Journal of the American Academy of Dermatology 2016 2 (2) 325-32 (From HuGE Literature Finder) - Pharmacogenomics of fluorouracil -based chemotherapy toxicity.
Matsusaka Satoshi et al. Expert opinion on drug metabolism & toxicology 2015 May (5) 811-21 (From Discoveries and Insights Database) - UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Sudlow Cathie et al. PLoS medicine 2015 Mar 12(3) e1001779 (From Genomics & Health Impact Scan Database) - Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Cancer Targets (MSK-IMPACT): A Hybridization Capture-Based Next-Generation Sequencing Clinical Assay for Solid Tumor Molecular Oncology.
Cheng Donavan T et al. The Journal of molecular diagnostics : JMD 2015 May 17(3) 251-64 (From Genomics & Health Impact Scan Database)
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