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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Last data update: Jan 30, 2023. (Total: 52323 Documents since 2012)
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MyLynch: A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome.
Knapp Stephen T et al. Cancers 2023 15(2)
Relative Risk of Bladder and Kidney Cancer in Lynch Syndrome: Systematic Review and Meta-Analysis.
Nassour Anthony-Joe et al. Cancers 2023 15(2)
Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study.
Adam Felicia et al. BMC medical genomics 2023 16(1) 7
Large Cancer Pedigree Involving Multiple Cancer Genes including Likely Digenic MSH2 and MSH6 Lynch Syndrome (LS) and an Instance of Recombinational Rescue from LS.
Vogelaar Ingrid P et al. Cancers 2023 15(1)
The Risk-Reducing Effect of Aspirin in Lynch Syndrome Carriers: Development and Evaluation of an Educational Leaflet.
Kaur Rajneesh et al. Advanced genetics (Hoboken, N.J.) 2023 3(2) 2100046
Application of machine learning in the prediction of deficient mismatch repair in patients with colorectal cancer based on routine preoperative characterization.
Xu Dong et al. Frontiers in oncology 2023 121049305
Mismatch Repair and Microsatellite Instability Testing for Immune Checkpoint Inhibitor Therapy: ASCO Endorsement of College of American Pathologists Guideline.
Vikas Praveen et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2023 JCO2202462
Rates and outcomes of testing for lynch syndrome in a national colorectal cancer screening programme.
Cudmore Jane et al. Cancer epidemiology 2023 82102314
Cost-Effectiveness of Risk-Reducing Surgery for Breast and Ovarian Cancer Prevention: A Systematic Review.
Wei Xia et al. Cancers 2022 14(24)
Implementation of microsatellite instability testing for the assessment of solid tumors in clinical practice.
Nakayama Izuma et al. Cancer medicine 2022
Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996-2020: development of a national resource of patient-level genomics laboratory records.
Loong Lucy et al. Journal of medical genetics 2022
Cancer prevention in cancer predisposition syndromes: A protocol for testing the feasibility of building a hereditary cancer research registry and nurse navigator follow up model.
Etchegary Holly et al. PloS one 2022 17(12) e0279317
The neglected role of preimplantation genetic testing for Lynch syndrome.
Dallagiovanna Chiara et al. Reproductive biomedicine online 2022
Person-based co-design of a decision aid template for people with a genetic predisposition to cancer.
Morton Kate et al. Frontiers in digital health 2022 41039701
Development and initial testing of a multi-stakeholder intervention for Lynch syndrome cascade screening: an intervention mapping approach.
Passero Lauren et al. BMC health services research 2022 22(1) 1411
Lessons learnt from the implementation of a colorectal cancer screening programme for lynch syndrome in a tertiary public hospital.
Dueñas Nuria et al. Cancer epidemiology 2022 82102291
Screening of Lynch syndrome in endometrial cancer in Iranian population with mismatch repair protein by immunohistochemistry.
Noei Teymoordash Somayyeh et al. Caspian journal of internal medicine 2022 13(4) 772-779
Prevalence and Genotype-Phenotype Correlation of Lynch Syndrome in a Selected High-Risk Cohort from Qatar's Population.
Sidenna Mariem et al. Genes 2022 13(11)
Genitourinary manifestations of Lynch syndrome in the urological practice.
Lonati Chiara et al. Asian journal of urology 2022 9(4) 443-450
Oncology Informatics for Lynch Syndrome Research and Care: A Literature Review.
Dehghani Soufi Mahsa et al. JCO clinical cancer informatics 2022 6e2200087
A comparative cost analysis of two screening strategies for colorectal cancer in Lynch Syndrome in a South African tertiary hospital.
Johnson Yasmina et al. Cancer causes & control : CCC 2022
From the patient to the population: Use of genomics for population screening.
Mighton Chloe et al. Frontiers in genetics 2022 13893832
Inherited Cancer Susceptibility Gene Sequence Variations Among Patients With Appendix Cancer.
Holowatyj Andreana N et al. JAMA oncology 2022
Pediatric manifestations of Lynch Syndrome: A single center experience.
MacArthur Taleen A et al. Journal of pediatric surgery case reports 2022 86
Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort.
Sarki Mahesh et al. Journal of personalized medicine 2022 12(10)
Population genomic screening: Ethical considerations to guide age at implementation.
Spencer Scott J et al. Frontiers in genetics 2022 13899648
Risk of cancer in individuals with Lynch-like syndrome and their families: a systematic review.
Nugroho Pandu P et al. Journal of cancer research and clinical oncology 2022
Proband-mediated interventions to increase disclosure of genetic risk in families with a BRCA or Lynch syndrome condition: a systematic review.
Young Alison Luk et al. European journal of human genetics : EJHG 2022
Comparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal Cancer
C Moretz et al, JAMA Network Open, October 24, 2022
Relatives from Hereditary Breast and Ovarian Cancer and Lynch Syndrome Families Forgoing Genetic Testing: Findings from the Swiss CASCADE Cohort
M Sarki et al, J Per Med, October 19, 2022
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