Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives. Hunter Jessica Ezzell et al. Familial cancer 2017 Feb

Public Health Genomics Knowledge Base (v1.2)



Last Posted: Feb 16, 2017

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• Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives.
  Hunter Jessica Ezzell et al. Familial cancer 2017 Feb
• Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
  Hansen Maren F et al. Clinical genetics 2017 Feb
• Understanding patterns of genetic risk evaluation (GRE) referral and uptake in patients (pts) with epithelial ovarian cancer (EOC).
  Morgan Robert et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2016 Mar 34(7_suppl) 254
• Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.
  Cruz-Correa Marcia et al. Hereditary cancer in clinical practice 2017 153
• Less Than Half of Recommended Adults Screened for Lynch Syndrome,
  Fox Chase Cancer Center, January 20, 2017
• Medical Oncologists' Experiences in Using Genomic Testing for Lung and Colorectal Cancer Care.
  Gray Stacy W et al. Journal of oncology practice 2017 Jan JOP2016016659
• The Use of Social Media to Recruit Participants With Rare Conditions: Lynch Syndrome as an Example.
  Burton-Chase Allison M et al. JMIR research protocols 2017 Jan 6(1) e12
• Less Than Half of Recommended Adults Screened for Lynch Syndrome
  Fox Chase Cancer Center, January 20, 2017
• Approaches to Blue Ribbon Panel Recommendations: The Case of Lynch Syndrome
  NCI workshop, February 22-23, 2017
• Establishing universal screening for Lynch syndrome in the community[PDF 9.03 MB]
  Heather Hampel, NCI precision medicine & population health webinar slide presentation, December 14, 2016
• Prevention and Early Detection for Hereditary Cancer Syndromes
  NCI website with resources, events and funding
• A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome.
  Adar Tomer et al. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2017 Jan
• Confirmation of ProMisE: A simple, genomics-based clinical classifier for endometrial cancer.
  Talhouk Aline et al. Cancer 2017 Jan
• How does genetic risk information for Lynch syndrome translate to risk management behaviours?
  Steel Emma et al. Hereditary cancer in clinical practice 2017 151
• Lynch Syndrome: Knowing Your Cancer Risk Could Save Your Life
  H Hampel, Every day health, December 2016
• Reflex test reminders in required cancer synoptic templates decrease order entry error: An analysis of mismatch repair immunohistochemical orders to screen for Lynch syndrome.
  Kilgore Mark R et al. Journal of pathology informatics 2016 748

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