About: Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

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scientific article published on 31 August 2009

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2009 (uk) im Oktober 2009 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 31 August 2009 (en) artículu científicu espublizáu n'agostu de 2009 (ast)
publication date	wds:Q57567514-F7F4362B-EF85-40F4-8A4B-76CE4DC156AA
publication date	2009-08-31 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57567514-5816F040-7EFA-47B5-A518-043FA50D2B46
language of work or name	English
author name string	wds:Q57567514-118B584A-4371-4C72-A19C-5E148A1694F0 wds:Q57567514-F5AB6595-E72B-44B2-911C-6D17036546D6
author name string	Heikki J Järvinen Katja Aktán-Collán
rdfs:label	Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members (en) Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members (nl)
skos:prefLabel	Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members (en) Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members (nl)
name	Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members (en) Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members (nl)
author	wds:Q57567514-4D6553E2-B56E-4B6D-81F3-185CEA483AA1 wds:Q57567514-DCC169C4-F521-41E3-A6D4-320F22B1F041 wds:Q57567514-EBDF40A9-D741-4F6A-BEB2-43014A5FF8B9 wds:Q57567514-EF082A43-84DA-4BB8-98D7-7032D16E3746
author	Jukka-Pekka Mecklin Lauri Aaltonen Päivi Peltomäki Laura Renkonen-Sinisalo
title	wds:Q57567514-6592EBB2-E27F-45CC-A4A1-C26007F9627C
title	Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members (en)
page(s)	wds:Q57567514-8474E107-5124-48BB-ACFA-2BDAFD1F18C3
page(s)	4793-4797
instance of	wds:Q57567514-FB10EBA7-1E11-4678-A59C-0D6975C4DDF7
instance of	scholarly article
main subject	wds:Q57567514-D12AE77E-AF30-482F-ACBF-CF23398313B1
main subject	Lynch syndrome
PubMed ID	wds:Q57567514-5B183FA2-6544-41F6-B972-26C50372AA54
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19720893
PubMed ID	19720893
published in	wds:Q57567514-2DEC7436-25A4-44D4-B406-A25F5B2AAB05
published in	Journal of Clinical Oncology
issue	wds:Q57567514-90A60563-41CD-4C41-B7BF-D6FCA1E43840
volume	wds:Q57567514-B3AB8901-C486-43C3-8481-59094BE367F8
issue	28
volume	27
DOI	wds:Q57567514-A5E1A964-161F-42CA-8716-8798E6D9356D
DOI	http://dx.doi.org/10.1200/JCO.2009.23.7784
DOI	10.1200/JCO.2009.23.7784
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57567514
is cites work of	ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer. The population impact of familial cancer, a major cause of cancer Recurrent and founder mutations in the PMS2 gene. Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine A high degree of LINE-1 hypomethylation is a unique feature of early-onset colorectal cancer Extending comprehensive cancer center expertise in clinical cancer genetics and genomics to diverse communities: the power of partnership A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease. Family perspectives in lynch syndrome becoming a family at risk, patterns of communication and influence on relations. Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing. The dual nature of mismatch repair as antimutator and mutator: for better or for worse Comparing universal Lynch syndrome tumor-screening programs to evaluate associations between implementation strategies and patient follow-through Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis Current Lynch syndrome tumor screening practices: a survey of genetic counselors. The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome Anticipation in lynch syndrome: where we are where we go A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation The search for unaffected individuals with Lynch syndrome: do the ends justify the means? A review of mismatch repair gene transcripts: issues for interpretation of mRNA splicing assays Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory. Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome Gynecologic cancer screening and communication with health care providers in women with Lynch syndrome How do we approach the goal of identifying everybody with Lynch syndrome? Prevalence of Lynch syndrome and Lynch-like syndrome among patients with colorectal cancer in a Japanese hospital-based population Lynch syndrome: clinical, pathological, and genetic insights Early-onset colorectal cancer: a sporadic or inherited disease? A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants. Preferences for genetic testing for colorectal cancer within a population-based screening program: a discrete choice experiment Advanced colorectal adenomas in patients under 45 years of age are mostly sporadic Genetic counseling and cascade genetic testing in Lynch syndrome. 100 years Lynch syndrome: what have we learned about psychosocial issues? Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review Endometrial and ovarian cancer in women with Lynch syndrome: update in screening and prevention Cost sharing and hereditary cancer risk: predictors of willingness-to-pay for genetic testing Creation of a network to promote universal screening for Lynch syndrome: the LynchSyndrome Screening Network Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database Causes of death of mutation carriers in Finnish Lynch syndrome families MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer. Fourfold increased detection of Lynch syndrome by raising age limit for tumour genetic testing from 50 to 70 years is cost-effective. Cost-effectiveness of routine screening for Lynch syndrome in colorectal cancer patients up to 70 years of age. Prospective study of combined colon and endometrial cancer screening in women with lynch syndrome: a patient-centered approach Combined colonoscopy and endometrial biopsy cancer screening results in women with Lynch syndrome Commentary on 'Colonoscopy screening compliance and outcomes in patients with Lynch syndrome'. Testing women with endometrial cancer to detect Lynch syndrome Gastrointestinal Malignancy: Genetic Implications to Clinical Applications. A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients

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