About: Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome

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About: Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome Goto Sponge NotDistinct Permalink

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scientific article published on 24 September 2018

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2018 (uk) article scientifique publié en 2018 (fr) im September 2018 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en setiembre de 2018 (ast) scientific article published on 24 September 2018 (en)
publication date	wds:Q57151653-5DF7E083-D50A-4615-A23A-1F3B5667FBCE
publication date	2018-09-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57151653-A3948266-4F68-4AB9-80F2-99D7D82DA2C2
language of work or name	English
cites work	wds:Q57151653-037FB98C-8B2E-4405-8E23-DEF2650C70BA wds:Q57151653-0390207E-6989-47F2-AAE5-75FB688555C7 wds:Q57151653-14213564-9ECB-4972-8251-251EED234AA9 wds:Q57151653-143A673C-26F4-4F6E-AB1C-1DC314631B70 wds:Q57151653-1F67D426-6B01-4954-96EC-D18A1D268F3C wds:Q57151653-2600219A-26E7-4866-8DAF-C0D5C724AC31 wds:Q57151653-2E37DC3C-C621-431C-B00A-858F47AE1930 wds:Q57151653-3380C67C-ED0C-4E71-9FD8-E93769016B41 wds:Q57151653-33C18215-3023-4692-A2F8-C709EEB36CEB wds:Q57151653-4BFDC125-514E-4D7B-8336-0794F7D79FCB wds:Q57151653-614FECD9-BDAB-4857-BC98-DB0642B7DEA0 wds:Q57151653-6553E343-3C7F-4BB1-AFFE-AA2C9C15A237 wds:Q57151653-66894F53-A95A-4BC9-92F6-934E01902815 wds:Q57151653-6ADED871-28E6-4C5E-A132-637ACB64C471 wds:Q57151653-77A1F2EB-B7D3-4F76-AAF8-B6A4028EB2F7 wds:Q57151653-81981B86-D862-4B06-BF10-0FE7E03B6D6C wds:Q57151653-8DB0589A-ECCB-427F-A7DA-7769CD2A8733 wds:Q57151653-9647460C-4770-44C5-9B39-9478672915EB wds:Q57151653-A387858B-7C91-4AE5-86A1-3319241CADE5 wds:Q57151653-B421EF92-DF09-4CD3-9386-E3A95FB420A7 wds:Q57151653-B69EC784-364B-4884-BA92-0EFC7942FFF6 wds:Q57151653-BB87AC4B-0F81-4007-BAC0-960D080EA57D wds:Q57151653-BE3928BD-72B3-485D-8DE1-5B862DBE625C wds:Q57151653-BFF5674C-61E7-461B-B4AD-53477AF09442 wds:Q57151653-C137E127-45D5-4B9B-B967-18E1A3EBE914 wds:Q57151653-C8831B68-6924-4012-9268-D24B32FF3387 wds:Q57151653-DB854EC1-2B78-4775-ABCA-0BA57F97487A wds:Q57151653-F3F2F5F5-6990-4A78-91DA-D0CADFABD249 wds:Q57151653-F759C616-40C8-4810-8A64-065D315D544A
cites work	Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database 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 The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas Clues to the pathogenesis of familial colorectal cancer The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations Milestones of Lynch syndrome: 1895-2015. Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium Recent discoveries in the genetics of familial colorectal cancer and polyposis Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification. Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) Diagnostics Risks of Lynch syndrome cancers for MSH6 mutation carriers Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer. Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas. The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes Microsatellite instability is rare in rectal carcinomas and signifies hereditary cancer Germline Genetic Features of Young Individuals with Colorectal Cancer Population-Based Lynch Syndrome Screening by Microsatellite Instability in Patients ≤50: Prevalence, Testing Determinants, and Result Availability Prior to Colon Surgery A model-based assessment of the cost-utility of strategies to identify Lynch syndrome in early-onset colorectal cancer patients Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database DNA Mismatch Repair Deficiency in Rectal Cancer: Benchmarking Its Impact on Prognosis, Neoadjuvant Response Prediction, and Clinical Cancer Genetics. BRAF-Mutated Colorectal Cancer: What Is the Optimal Strategy for Treatment? Genetics and Genetic Testing in Hereditary Colorectal Cancer The association of tumor microsatellite instability phenotype with family history of colorectal cancer Correlation of polyp number and family history of colon cancer with germline MYH mutations Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing
author name string	wds:Q57151653-81FB050C-2CB8-4319-951C-CBD494BE2E9F wds:Q57151653-F73C2702-64EC-4B3B-BE35-0AD54E4809D2
author name string	Karin Henriksson Isabelle Henriksson
rdfs:label	Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (en) Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (nl)
skos:prefLabel	Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (en) Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (nl)
name	Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (en) Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (nl)
author	wds:Q57151653-2C2DE3F2-D7BC-4AC5-AB03-E92B4FB56702 wds:Q57151653-5D09005C-DB3B-4DFF-98FF-2866812BCBDC
author	Hans Ehrencrona Samuel Gebre-Medhin
title	wds:Q57151653-B393562F-E437-4574-BE8A-F387A20D7B62
title	Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome (en)
page(s)	wds:Q57151653-147B1813-315D-4A98-8321-92E88C2B5D4D
page(s)	259-266
instance of	wds:Q57151653-079933C8-8536-4A03-B9D0-AECB8EF6F1BF
instance of	scholarly article
main subject	wds:Q57151653-0683767F-736F-427B-BB85-20C64012F148 wds:Q57151653-64841F26-49E7-4DFD-AF96-5B37230CA394 wds:Q57151653-6E1DC3E4-CCCC-4EC4-97B2-F0C43B9F56EA
main subject	Lynch syndrome Sweden colorectal cancer
PubMed ID	wds:Q57151653-396ADE49-A92F-489D-9FD9-437EEEC640D8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30251116
PubMed ID	30251116
published in	wds:Q57151653-70FAB75E-3E15-4E51-B394-EE450FA1CBB7
published in	Journal of Community Genetics

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