{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,5,17]],"date-time":"2024-05-17T17:36:03Z","timestamp":1715967363478},"reference-count":32,"publisher":"Elsevier BV","issue":"9","license":[{"start":{"date-parts":[[2011,6,1]],"date-time":"2011-06-01T00:00:00Z","timestamp":1306886400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2013,7,22]],"date-time":"2013-07-22T00:00:00Z","timestamp":1374451200000},"content-version":"vor","delay-in-days":782,"URL":"https:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["European Journal of Cancer"],"published-print":{"date-parts":[[2011,6]]},"DOI":"10.1016\/j.ejca.2010.12.024","type":"journal-article","created":{"date-parts":[[2011,1,26]],"date-time":"2011-01-26T09:17:34Z","timestamp":1296033454000},"page":"1407-1413","source":"Crossref","is-referenced-by-count":10,"title":["Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome"],"prefix":"10.1016","volume":"47","author":[{"given":"P.","family":"Manders","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Spruijt","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.M.","family":"Kets","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.W.","family":"Willems","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D.","family":"Bodmer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.M.","family":"Hebeda","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.D.","family":"Nagtegaal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.H.J.M.","family":"van Krieken","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.J.L.","family":"Ligtenberg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N.","family":"Hoogerbrugge","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"31","key":"10.1016\/j.ejca.2010.12.024_b0005","doi-asserted-by":"crossref","first-page":"4943","DOI":"10.3748\/wjg.v12.i31.4943","article-title":"Hereditary non-polyposis colorectal cancer: the rise and fall of a confusing term","volume":"12","author":"Jass","year":"2006","journal-title":"World J Gastroenterol"},{"issue":"10","key":"10.1016\/j.ejca.2010.12.024_b0010","doi-asserted-by":"crossref","first-page":"919","DOI":"10.1056\/NEJMra012242","article-title":"Hereditary colorectal cancer","volume":"348","author":"Lynch","year":"2003","journal-title":"N Engl J Med"},{"issue":"21","key":"10.1016\/j.ejca.2010.12.024_b0015","doi-asserted-by":"crossref","first-page":"1481","DOI":"10.1056\/NEJM199805213382101","article-title":"Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease","volume":"338","author":"Aaltonen","year":"1998","journal-title":"N Engl J Med"},{"issue":"26","key":"10.1016\/j.ejca.2010.12.024_b0020","doi-asserted-by":"crossref","first-page":"2751","DOI":"10.1056\/NEJMoa053493","article-title":"Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer","volume":"354","author":"Barnetson","year":"2006","journal-title":"N Engl J Med"},{"issue":"4","key":"10.1016\/j.ejca.2010.12.024_b0025","doi-asserted-by":"crossref","first-page":"780","DOI":"10.1086\/323658","article-title":"The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas","volume":"69","author":"Cunningham","year":"2001","journal-title":"Am J Hum Genet"},{"issue":"18","key":"10.1016\/j.ejca.2010.12.024_b0030","doi-asserted-by":"crossref","first-page":"1851","DOI":"10.1056\/NEJMoa043146","article-title":"Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)","volume":"352","author":"Hampel","year":"2005","journal-title":"N Engl J Med"},{"issue":"5","key":"10.1016\/j.ejca.2010.12.024_b0035","doi-asserted-by":"crossref","first-page":"829","DOI":"10.1016\/S0016-5085(00)70168-5","article-title":"Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer","volume":"118","author":"Jarvinen","year":"2000","journal-title":"Gastroenterology"},{"issue":"28","key":"10.1016\/j.ejca.2010.12.024_b0040","doi-asserted-by":"crossref","first-page":"4793","DOI":"10.1200\/JCO.2009.23.7784","article-title":"Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members","volume":"27","author":"Jarvinen","year":"2009","journal-title":"J Clin Oncol"},{"issue":"1","key":"10.1016\/j.ejca.2010.12.024_b0045","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1136\/gut.2004.039123","article-title":"Cost effectiveness of a new strategy to identify HNPCC patients","volume":"54","author":"Kievit","year":"2005","journal-title":"Gut"},{"issue":"9","key":"10.1016\/j.ejca.2010.12.024_b0050","doi-asserted-by":"crossref","first-page":"1632","DOI":"10.1002\/(SICI)1097-0142(19980501)82:9<1632::AID-CNCR6>3.0.CO;2-C","article-title":"A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers","volume":"82","author":"Vasen","year":"1998","journal-title":"Cancer"},{"issue":"10","key":"10.1016\/j.ejca.2010.12.024_b0055","doi-asserted-by":"crossref","first-page":"1605","DOI":"10.1038\/sj.bjc.6603754","article-title":"Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer","volume":"96","author":"Overbeek","year":"2007","journal-title":"Br J Cancer"},{"issue":"11","key":"10.1016\/j.ejca.2010.12.024_b0060","doi-asserted-by":"crossref","first-page":"1540","DOI":"10.1007\/BF02236735","article-title":"Family history of colorectal cancer: how often and how accurately is it recorded?","volume":"43","author":"Church","year":"2000","journal-title":"Dis Colon Rectum"},{"issue":"9","key":"10.1016\/j.ejca.2010.12.024_b0065","doi-asserted-by":"crossref","first-page":"813","DOI":"10.1016\/S1542-3565(04)00352-0","article-title":"Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients","volume":"2","author":"Grover","year":"2004","journal-title":"Clin Gastroenterol Hepatol"},{"issue":"9","key":"10.1016\/j.ejca.2010.12.024_b0070","doi-asserted-by":"crossref","first-page":"1228","DOI":"10.1046\/j.0007-1323.2001.01868.x","article-title":"Patient accuracy of reporting on hereditary non-polyposis colorectal cancer-related malignancy in family members","volume":"88","author":"Katballe","year":"2001","journal-title":"Br J Surg"},{"issue":"3","key":"10.1016\/j.ejca.2010.12.024_b0075","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1038\/sj.ejhg.5200441","article-title":"Accuracy of family history of cancer: clinical genetic implications","volume":"8","author":"Sijmons","year":"2000","journal-title":"Eur J Hum Genet"},{"issue":"23","key":"10.1016\/j.ejca.2010.12.024_b0080","doi-asserted-by":"crossref","first-page":"1758","DOI":"10.1093\/jnci\/89.23.1758","article-title":"A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines","volume":"89","author":"Rodriguez-Bigas","year":"1997","journal-title":"J Natl Cancer Inst"},{"issue":"4","key":"10.1016\/j.ejca.2010.12.024_b0085","doi-asserted-by":"crossref","first-page":"261","DOI":"10.1093\/jnci\/djh034","article-title":"Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability","volume":"96","author":"Umar","year":"2004","journal-title":"J Natl Cancer Inst"},{"issue":"32","key":"10.1016\/j.ejca.2010.12.024_b0090","first-page":"1792","article-title":"More hereditary intestinal cancer can be detected if patients with colorectal carcinoma that are selected by the pathologist are examined for microsatellite instability","volume":"149","author":"de Bruin","year":"2005","journal-title":"Ned Tijdschr Geneeskd"},{"issue":"6","key":"10.1016\/j.ejca.2010.12.024_b0095","doi-asserted-by":"crossref","first-page":"653","DOI":"10.1007\/s00428-010-0907-7","article-title":"Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial","volume":"456","author":"Overbeek","year":"2010","journal-title":"Virchows Arch"},{"issue":"1","key":"10.1016\/j.ejca.2010.12.024_b0100","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1038\/ng.283","article-title":"Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3\u2032 exons of TACSTD1","volume":"41","author":"Ligtenberg","year":"2009","journal-title":"Nat Genet"},{"issue":"6","key":"10.1016\/j.ejca.2010.12.024_b0105","doi-asserted-by":"crossref","first-page":"653","DOI":"10.1007\/s00428-010-0907-7","article-title":"Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial","volume":"456","author":"Overbeek","year":"2010","journal-title":"Virchows Arch"},{"issue":"5","key":"10.1016\/j.ejca.2010.12.024_b0110","doi-asserted-by":"crossref","first-page":"450","DOI":"10.1111\/j.1463-1318.2009.01898.x","article-title":"Family history? The forgotten question in high-risk colorectal cancer patients","volume":"11","author":"Foo","year":"2009","journal-title":"Colorectal Dis"},{"issue":"8","key":"10.1016\/j.ejca.2010.12.024_b0115","doi-asserted-by":"crossref","first-page":"1249","DOI":"10.1007\/s10350-008-9345-x","article-title":"Most patients with colorectal tumors at young age do not visit a cancer genetics clinic","volume":"51","author":"Overbeek","year":"2008","journal-title":"Dis Colon Rectum"},{"issue":"4","key":"10.1016\/j.ejca.2010.12.024_b0120","first-page":"124","article-title":"Inadequate referral for genetic evaluations of patients with colorectal carcinoma","volume":"153","author":"Staal-Rosier","year":"2009","journal-title":"Ned Tijdschr Geneeskd"},{"issue":"1","key":"10.1016\/j.ejca.2010.12.024_b0125","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1007\/s10689-006-9114-8","article-title":"Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data","volume":"6","author":"van Dijk","year":"2007","journal-title":"Fam Cancer"},{"issue":"11","key":"10.1016\/j.ejca.2010.12.024_b0130","doi-asserted-by":"crossref","first-page":"812","DOI":"10.1097\/GIM.0b013e3181b99b75","article-title":"Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer","volume":"11","author":"South","year":"2009","journal-title":"Genet Med"},{"issue":"4","key":"10.1016\/j.ejca.2010.12.024_b0135","first-page":"317","article-title":"Genetic testing offered directly after the diagnosis of colorectal cancer: a pilot study on the reactions of patients","volume":"20","author":"Landsbergen","year":"2009","journal-title":"Genet Couns"},{"issue":"4","key":"10.1016\/j.ejca.2010.12.024_b0140","doi-asserted-by":"crossref","first-page":"608","DOI":"10.1002\/ijc.1372","article-title":"Psychological consequences of predictive genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a prospective follow-up study","volume":"93","author":"Aktan-Collan","year":"2001","journal-title":"Int J Cancer"},{"issue":"2","key":"10.1016\/j.ejca.2010.12.024_b0145","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1016\/j.pec.2003.11.002","article-title":"Predictive testing for hereditary non-polyposis colorectal cancer: motivation, illness representations and short-term psychological impact","volume":"55","author":"Claes","year":"2004","journal-title":"Patient Educ Couns"},{"issue":"6","key":"10.1016\/j.ejca.2010.12.024_b0150","doi-asserted-by":"crossref","first-page":"502","DOI":"10.1111\/j.1399-0004.2004.00339.x","article-title":"Psychological impact of genetic testing for hereditary non-polyposis colorectal cancer","volume":"66","author":"Meiser","year":"2004","journal-title":"Clin Genet"},{"issue":"8","key":"10.1016\/j.ejca.2010.12.024_b0155","doi-asserted-by":"crossref","first-page":"519","DOI":"10.1136\/jmg.38.8.519","article-title":"Predictive genetic testing in children and adults: a study of emotional impact","volume":"38","author":"Michie","year":"2001","journal-title":"J Med Genet"},{"issue":"4","key":"10.1016\/j.ejca.2010.12.024_b0160","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1007\/s10689-005-0658-9","article-title":"Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures","volume":"4","author":"Wagner","year":"2005","journal-title":"Fam Cancer"}],"container-title":["European Journal of Cancer"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0959804910012293?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0959804910012293?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,6,8]],"date-time":"2019-06-08T04:02:52Z","timestamp":1559966572000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0959804910012293"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,6]]},"references-count":32,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2011,6]]}},"alternative-id":["S0959804910012293"],"URL":"https:\/\/doi.org\/10.1016\/j.ejca.2010.12.024","relation":{},"ISSN":["0959-8049"],"issn-type":[{"value":"0959-8049","type":"print"}],"subject":[],"published":{"date-parts":[[2011,6]]}}}