Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Digital innovation for cancer risk assessment allows large-scale service redevelopment of regional cancer genetics service delivery.

Familial cancer - 1 Nov 2024

Youngs Alice, Forman Andrea, Elms Marisa, Kohut Kelly, Hlaing Min Theik, Short John, Hanson Helen, Snape Katie

Abstract excerpt

Family-history assessment can identify individuals above population-risk for cancer to enable targeted Screening, Prevention and Early Detection (SPED). The online patient-facing cancer Family History Questionnaire Service (cFHQS) is a digitalised, resource efficient tool for family history data capture to facilitate this. The capturing of digital data from cFHQS allows for data interrogation of patients referred...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Early Detection of Cancer

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Medical History Taking

Share to Neoplasms

Share to Referral and Consultation

Share to Risk Assessment

Share to Surveys and Questionnaires

Source

Open in PubMed Open full text

Identifiers

PMID: 38954285
DOI: 10.1007/s10689-024-00407-x
PMCID: PMC11512827

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Digital innovation for cancer risk assessment allows large-scale service redevelopment of regional cancer genetics service delivery.PMID 38954285Read ↗

Validation of a guidelines-based digital tool to assess the need for germline cancer genetic testingSemantic proximity Read ↗

Protocol for Health Risk Information Technology-Assisted Genetic Evaluation (HeRITAGE): a randomised controlled trial of digital genetic cancer risk assessment in a diverse underserved gynaecology clinic.Semantic proximity Read ↗

Implementation of a Health History Disease Risk Instrument in Clinics Serving Medically Marginalized Patients.Semantic proximity Read ↗

Helix: A Digital Tool to Address Provider Needs for Prostate Cancer Genetic Testing in Clinical PracticeSemantic proximity Read ↗

Co-design of patient information leaflets for germline predisposition to cancer: recommendations for clinical practice from the UK Cancer Genetics Group (UKCGG), Cancer Research UK (CRUK) funded CanGene-CanVar Programme and the Association of Genetic Nurse Counsellors (AGNC).Semantic proximity Read ↗

Streamlining Inherited Cancer Identification via an EMR-Integrated Risk Assessment Platform: A Nonrandomized Clinical Trial.Semantic proximity Read ↗

Validation of a Digital Identification Tool for Individuals at Risk for Hereditary Cancer SyndromesSemantic proximity Read ↗

Clinically relevant lessons from Family HealthLink: a cancer and coronary heart disease familial risk assessment tool.Semantic proximity Read ↗

Comparison of a Cancer Family History Collection and Risk Assessment Tool - ItRunsInMyFamily - with Risk Assessment by Health-Care Professionals.Semantic proximity Read ↗

BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trialSemantic proximity Read ↗

High-risk family colorectal cancer screening service in Ireland: Critical review of clinical outcomes.Semantic proximity Read ↗

Integration and usability of a digital cancer risk stratification tool to optimize identification of patients at risk for hereditary cancers: A pilot study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.