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 …

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 …

[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 …

Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review

AM Willis, SK Smith, B Meiser, ML Ballinger… - Clinical …, 2017 - Wiley Online Library
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 …

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 …

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 …

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 …

Predicting advanced neoplasia at colonoscopy in a diverse population with the National Cancer Institute colorectal cancer risk‐assessment tool

U Ladabaum, A Patel, A Mannalithara, V Sundaram… - Cancer, 2016 - Wiley Online Library
BACKGROUND Tailoring screening to colorectal cancer (CRC) risk could improve
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 …

[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 …