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One or more keywords matched the following items that are connected to Syngal, Sapna
Item TypeName
Academic Article Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients.
Academic Article Colorectal cancer risk perception on the basis of genetic test results in individuals at risk for Lynch syndrome.
Academic Article Intraductal papillary mucinous neoplasm of the pancreas with loss of mismatch repair in a patient with Lynch syndrome.
Academic Article Risk of pancreatic cancer in families with Lynch syndrome.
Academic Article Clinical presentation correlates with the type of mismatch repair gene involved in hereditary nonpolyposis colon cancer.
Academic Article Attitudes toward childbearing and prenatal testing in individuals undergoing genetic testing for Lynch syndrome.
Academic Article The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.
Academic Article Microsatellite instability and DNA mismatch repair protein deficiency in Lynch syndrome colorectal polyps.
Academic Article Phenotype comparison of MLH1 and MSH2 mutation carriers in a cohort of 1,914 individuals undergoing clinical genetic testing in the United States.
Academic Article Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome.
Academic Article Aberrant DNA methylation in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.
Academic Article Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer.
Academic Article Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome.
Academic Article Data reduction for prediction: a case study on robust coding of age and family history for the risk of having a genetic mutation.
Academic Article Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) cases.
Concept DNA Mismatch Repair
Academic Article Elevated risk of prostate cancer among men with Lynch syndrome.
Academic Article Screening for germline mismatch repair mutations following diagnosis of sebaceous neoplasm.
Academic Article Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
Academic Article PMS2 monoallelic mutation carriers: the known unknown.
Academic Article Association of Common Susceptibility Variants of Pancreatic Cancer in Higher-Risk Patients: A PACGENE Study.
Academic Article Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC).
Academic Article Universal Screening for Mismatch-Repair Deficiency in Endometrial Cancers to Identify Patients With Lynch Syndrome and Lynch-like Syndrome.
Grant INHERITED MSH6 MUTATIONS IN DIVERSE COLORECTAL CANCERS
Grant Development and validation of clinical prediction models for the use and interpretation of multigene hereditary cancer risk assessment
Academic Article Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Academic Article Biallelic Mismatch Repair Deficiency: Management and Prevention of a Devastating Manifestation of the Lynch Syndrome.
Academic Article Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.
Academic Article Poor performance of clinical prediction models: the harm of commonly applied methods.
Academic Article Commentary: PREMM5 threshold of 2.5% is recommended to improve identification of PMS2 carriers.
Academic Article Recent advances in Lynch syndrome.
Academic Article Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting.
Academic Article Clinical Factors Associated with Urinary Tract Cancer in Individuals with Lynch Syndrome.
Academic Article Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing.
Academic Article Familial Burden and Other Clinical Factors Associated With Various Types of Cancer in Individuals With Lynch Syndrome.
Academic Article A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study.
Search Criteria
  • DNA Mismatch Repair
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.