2020 Citizen generated data and health: predictive prevention of disease Personalising breast cancer prevention – bridging the gap between research and policy The GDPR and genomic data Black box medicine and transparency Artificial intelligence for genomic medicine 2019 Our healthy future Person centred healthcare My healthy future: Overdiagnosis Privacy and autonomy Health technologies and social impacts My healthy future: policy context The technologies of a healthy future Algorithms as medical devices Regulating algorithms in healthcare: the GDPR and IVDR in practice Polygenic scores, risk and cardiovascular disease Personalising prevention for breast cancer Dementia risk prediction 2018 The personalised medicine technology landscape Genomics in mainstream clinical pathways Identification and genomic data 2017 Personalised prevention in breast cancer – the policy landscape Developing effective ctDNA testing services for lung cancer Linking and sharing routine health data for research Variant classification and interpretation - workshop report Whole exome sequencing in clinical genetics - a health economic evaluation Personalised healthcare:bringing the future into focus Delivering improved access to genetic testing in epithelial ovarian cancer 2016 Whole genome sequencing for breast cancer risk testing 2015 Data sharing to support UK clinical genetics and genomics services Pathogen Genomics Into Practice Genetic screening programmes: an international review of assessment criteria 2014 Realising Genomics in Clinical Practice A guide to the investigation of intellectual disability and developmental delay in East Anglia Enhanced Genetic Services Project Stratified Screening for Cancer 2013 Realising Genomics in Clinical Practice (interim report) Managing incidental and pertinent findings from WGS in the 100,000 Genomes Project Genomics of obesity 2012 Beyond the horizon: Connecting science and health Genomics in Medicine 2011 Epidemiology, risk and causation Next steps in the sequence Quality standards in risk prediction Genetics and mainstream medicine: service development and integration 2010 Public health in an era of genome-based and personalised medicine Expanded newborn screening Independent response to House of Lords Science and Technology Committee Genomic Medicine report Predicting the risk of coronary heart disease with conventional, genetic and novel molecular biomarkers 2009 Tay Sachs Disease carrier screening in the Ashkenazi Jewish population Heart to Heart: inherited cardiovascular conditions services Cell-free fetal nucleic acids for non-invasive prenatal diagnosis 2008 Evidence and evaluation: Building public trust in genetic tests for common diseases Genetic ophthalmology in focus The evaluation of diagnostic laboratory tests and complex biomarkers 2007 The evaluation of clinical validity and clinical utility of genetic tests Family history as a risk factor for common, complex disease Moving Beyond ACCE: An Expanded Framework for Genetic Test Evaluation 2006 Assessment of the Human Tissue Act Evaluation of array-CGH for chromosomal abnormalities in clinical practice Learning disability: the interface with genetics Biomarkers in familial colorectal cancer screening Ethical legal and social issues in stem cell research and therapy - 2nd edition 2005 Metabolic pathways: networks of care 2004 Evaluation of genetic tests: service development Cancer therapeutics in the 'omics' era: moving towards practical application in the NHS 2003 Addressing Genetics, Delivering Health - genetics education for health professionals Intellectual property rights and genetics Pharmacogenetics - My Very Own Medicine 2001 Genetics and health economics workshops 2000 Genetics and health - Nuffield Trust Genetics Scenario Project report