Interventions to support patients with sharing genetic test results with at-risk relatives: a synthesis without meta-analysis (SWiM)
LM Ballard, R Band, AM Lucassen - European Journal of Human …, 2023 - nature.com
Whilst the finding of heritable susceptibility to disease was once relatively rare,
mainstreaming of genetic testing has resulted in a steady increase. Patients are often …
mainstreaming of genetic testing has resulted in a steady increase. Patients are often …
Psychiatric implications of cancer genetic testing
AM Hirschberg, G Chan‐Smutko, WF Pirl - Cancer, 2015 - Wiley Online Library
As genetic testing for hereditary cancer syndromes has transitioned from research to clinical
settings, research regarding its accompanying psychosocial effects has grown. Men and …
settings, research regarding its accompanying psychosocial effects has grown. Men and …
[HTML][HTML] From genetic counseling to “genomic counseling”
KE Ormond - Molecular genetics & genomic medicine, 2013 - ncbi.nlm.nih.gov
Genetic counseling is “the process of helping people understand and adapt to the medical,
psychological, and familial implications of genetic contributions to disease.” Traditionally …
psychological, and familial implications of genetic contributions to disease.” Traditionally …
Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review
Evidence suggests that a significant proportion of individuals referred to cancer genetic
counselling (GC) do not attend, and thus may not be engaged in adequate cancer risk …
counselling (GC) do not attend, and thus may not be engaged in adequate cancer risk …
Patient reported outcomes and patient empowerment in clinical genetics services
M McAllister, A Dearing - Clinical genetics, 2015 - Wiley Online Library
Evaluation of clinical genetics services (CGS), including genetic counseling and genetic
testing, has been problematic. Patient mortality and morbidity are unlikely to be directly …
testing, has been problematic. Patient mortality and morbidity are unlikely to be directly …
Prevalence and correlates of receiving and sharing high-penetrance cancer genetic test results: findings from the Health Information National Trends Survey
JM Taber, CQ Chang, TK Lam, EM Gillanders… - Public Health …, 2015 - karger.com
Abstract Background/Aims: The aim of this study was to explore the prevalence and
correlates of receiving and sharing high-penetrance cancer genetic test results. Methods …
correlates of receiving and sharing high-penetrance cancer genetic test results. Methods …
Unsolicited information letters to increase awareness of Lynch syndrome and familial colorectal cancer: reactions and attitudes
HV Petersen, BL Frederiksen, CK Lautrup, LJ Lindberg… - Familial Cancer, 2019 - Springer
Dissemination of information on a genetically increased risk should according to guidelines
primarily be family-mediated. Incomplete and incorrect information spread has, however …
primarily be family-mediated. Incomplete and incorrect information spread has, however …
Predicting advanced neoplasia at colonoscopy in a diverse population with the National Cancer Institute colorectal cancer risk‐assessment tool
BACKGROUND Tailoring screening to colorectal cancer (CRC) risk could improve
screening effectiveness. Most CRCs arise from advanced neoplasia (AN) that dwells for …
screening effectiveness. Most CRCs arise from advanced neoplasia (AN) that dwells for …
Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome
DW Hadley, D Eliezer, Y Addissie, A Goergen… - Scientific reports, 2020 - nature.com
Cascade genetic testing provides a method to appropriately focus colonoscopy use in
families with Lynch syndrome (LS). However, research suggests that up to two-thirds at risk …
families with Lynch syndrome (LS). However, research suggests that up to two-thirds at risk …
[HTML][HTML] Experiences of living with Lynch syndrome: a reflexive thematic analysis
NZ Warner, C Gleeson, P Fahey, R Horgan… - European Journal of …, 2022 - Elsevier
Abstract Purpose Lynch Syndrome is one of the most common hereditary cancer syndromes,
arising from DNA mismatch repair. Lynch Syndrome carriers are at increased lifetime risk of …
arising from DNA mismatch repair. Lynch Syndrome carriers are at increased lifetime risk of …