Prediction of germline mutations and cancer risk in the Lynch syndrome - Wikidata - awgldk - TriplyDB

Prediction of germline mutations and cancer risk in the Lynch syndrome

Prediction of germline mutations and cancer risk in the Lynch syndrome

http://www.wikidata.org/entity/Q36882484

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Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications Inherited colorectal cancer syndromes Cost-Effectiveness Analysis of Different Genetic Testing Strategies for Lynch Syndrome in Taiwan American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers Development and validation of a colon cancer risk assessment tool for patients undergoing colonoscopy.Risks of Lynch syndrome cancers for MSH6 mutation carriers.The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery Genetic testing strategies in newly diagnosed endometrial cancer patients aimed at reducing morbidity or mortality from lynch syndrome in the index case or her relatives Incorporating medical interventions into carrier probability estimation for genetic counseling.Reclassification of predictions for uncovering subgroup specific improvement Genetic testing for hereditary colorectal cancer.Predictive model for high-frequency microsatellite instability in colorectal cancer patients over 50 years of age.Hereditary pancreatic cancer: related syndromes and clinical perspective.Evaluation of clinical criteria for the identification of Lynch syndrome among unselected patients with endometrial cancer.Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries Estimating CDKN2A carrier probability and personalizing cancer risk assessments in hereditary melanoma using MelaPRO.Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinoma Clinicopathological and genetic features of Chinese hereditary nonpolyposis colorectal cancer (HNPCC).Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repair.Hereditary cancer risk assessment: essential tools for a better approach.An internal performance assessment of CancerGene Connect: an electronic tool to streamline, measure and improve the genetic counseling process.Cost-effectiveness and diagnostic effectiveness analyses of multiple algorithms for the diagnosis of Lynch syndrome.Microsatellite instability in colorectal cancer-the stable evidence.Identification of patients at risk for hereditary colorectal cancer Familial colorectal cancer, beyond Lynch syndrome Providing access to risk prediction tools via the HL7 XML-formatted risk web service.Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.Prevalence and predictors of appropriate colorectal cancer surveillance in Lynch syndrome.Cancer risk assessment for the primary care physician.A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory.Comparative effectiveness of screening strategies for Lynch syndrome.Identification of cancer patients with Lynch syndrome: clinically significant discordances and problems in tissue-based mismatch repair testing.Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.Do hereditary syndrome-related gynecologic cancers have any specific features?Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance Identification of Lynch syndrome: how should we proceed in the 21st century?

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Prediction of germline mutations and cancer risk in the Lynch syndrome

http://www.wikidata.org/entity/Q36882484

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2006年の論文

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2006年论文

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2006年论文

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2006年论文

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Prediction of germline mutations and cancer risk in the Lynch syndrome

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Prediction of germline mutations and cancer risk in the Lynch syndrome

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Prediction of germline mutations and cancer risk in the Lynch syndrome

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JAMA.296.12.1479

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Journal of the American Medical Association

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Prediction of germline mutations and cancer risk in the Lynch syndrome

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Colon Cancer Family Registry

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David Euhus

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Francis M Giardiello

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Giovanni Parmigiani

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Graham Casey

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Jeremy Jass

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Johanna Lee

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Kathy Romans

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Khedoudja Nafa

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Nathan Ellis

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P2860

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

Mutation of a mutL homolog in hereditary colon cancer

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer.

BayesMendel: an R environment for Mendelian risk prediction

Genetic susceptibility to non-polyposis colorectal cancer.

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

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1479-1487

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296

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Kenneth W Kinzler

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2006-09-01T00:00:00Z

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6791985

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