The PREMM 1,2,6 Model Predicts Risk of MLH1, MSH2, and MSH6 Germline Mutations Based on Cancer History (original) (raw)
Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer
Sean Young
International journal of cancer. Journal international du cancer, 2010
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A comparison of models used to predict MLH1, MSH2 and MSH6 mutation carriers
Gary Chong
Annals of Oncology, 2009
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Prediction of Germline Mutations and Cancer Risk In the Lynch Syndrome
Wenyi Wang
Jama, 2006
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Nathan Gluck
Genetics in Medicine
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Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic
Peter Risby
Journal of Clinical Oncology, 2004
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Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?
A. Boussioutas
European Journal of Cancer, 2013
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Criteria and prediction models for mismatch repair gene mutations: a review
Aung Myo Win
Journal of Medical Genetics, 2013
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MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families
Jan Kleibeuker
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2001
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Identification of predictive factors for the occurrence of predisposing MLH1 and MSH2 germline mutations among Sardinian patients with colorectal carcinoma
Grazia Palomba, Maria Colombino
European Journal of Cancer, 2005
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Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily theMSH2 gene
paulo fidalgo, Hélder Raposo
Cancer, 2004
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Association between family history and mismatch repair in colorectal cancer
Sandra Bell
2005
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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
Magnus von Knebel Doeberitz
Journal of Clinical Oncology, 2012
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Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario
Kevin Boyd
Hereditary cancer in clinical practice, 2009
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Multivariate analysis as a method for evaluating the pathogenicity of novel genetic MLH1 variants in patients with colorectal cancer and microsatellite instability
Angela Cavallo
International Journal of Molecular Medicine, 2015
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Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer
Harry Hollema
Gut, 2006
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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance
Yvonne Hendriks
Gastroenterology, 2004
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Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1
Richard Kolodner
Journal of Medical Genetics, 2000
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Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families
Mirjana Magic
BMC Cancer, 2010
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Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers
Michael Walsh
JNCI Journal of the National Cancer Institute, 2010
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Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study
Aung Myo Win
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2012
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Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than Hereditary Non Polyposis Colorectal Cancer cohorts
Lisa Devlin
The Ulster Medical Journal, 2008
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Prevalence of germline mutations of MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain
Iciar Carbonero
International journal of cancer. Journal international du cancer, 2002
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Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes
Gary Velan
Human Mutation, 2011
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Cancer risk in hereditary nonpolyposis colorectal cancer due to mutations: impact on counseling and surveillance
Franz Quehenberger
Gastroenterology, 2004
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Validation of Prediction Models for Mismatch Repair Gene Mutations in Koreans
Sungho Won
Cancer research and treatment : official journal of Korean Cancer Association, 2015
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