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Whole genome sequencing for breast cancer risk testingReportExamining the impact of routine breast cancer risk testing using whole genome sequencing
Data sharing to support UK clinical genetics and genomics servicesReportOur recommendations for responsible and proportionate sharing of data for patient benefit
Pathogen genomics into practiceReportPioneering work on converting genomics into population wide, high quality, evidence based pathogen services. Full report, summary and policy briefings
Genetic screening programmes: an international review of assessment criteriaReportLiterature review to identify international criteria for appraising genetic screening programmes and to set out the relevant ethical, legal and social (ELS) issues.
Realising genomics in clinical practiceReportThe Realising Genomics report is intended to inform the ethical clinical implementation of these genomic technologies.
A guide to the investigation of intellectual disability and developmental delay in East AngliaReportRevision of the 2006 guidelines to include a diagnostic flowchart for clinicians supported by updated evidence and new parents' guides.
Enhanced Genetic Services ProjectReportPHG Foundation were commissioned to evaluate this pilot genetic services project in Birmingham
Stratified screening for cancerReportPHG Foundation's recommendations on implementing stratification in screening for three major cancers – breast, ovarian and prostate - following our work as part of the European Commission funded Collaborative Oncological Gene-Environment Study (COGS).
Managing incidental and pertinent findings from WGS in the 100,000 Genomes ProjectReportAn ethical framework for disclosing clinical and research findings to patients/research subjects.
Genomics of obesityReportThe genomics of obesity identifies a typical four-tier system of obesity services and care pathways in the NHS and proposes where and under what circumstances genetic testing for obesity could benefit patient care.