|
| 37296526 | International genetic counseling: What do genetic counselors actually do? | J Genet Couns | 2024 |
| 36316491 | The genetic counsellor role in the United Kingdom : Position on behalf of the Association of Genetic Nurses and Counsellors (AGNC), Endorsed by the Genetic Counsellor Registration Board (GCRB) and Academy for Healthcare Science (AHCS). | Eur J Hum Genet | 2023 |
| 37928209 | Public engagement with genomics. | Wellcome Open Res | 2023 |
| 37869565 | The legacy of language: What we say, and what people hear, when we talk about genomics. | HGG Adv | 2023 |
| 37339292 | What Difference Can Public Engagement in Genome Editing Make, and for Whom? | Am J Bioeth | 2023 |
| 35972296 | Ethical Challenges Associated with Pathogen and Host Genetics in Infectious Disease. | New Bioeth | 2023 |
| 34930661 | Correspondence on "Ensuring best practice in genomics education and evaluation: Reporting item standards for education and its evaluation in genomics (RISE2 Genomics)" by Nisselle et al. | Genet Med | 2022 |
| 35773560 | Correction to: Coâ¿¿designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom. | J Community Genet | 2022 |
| 35523996 | Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom. | J Community Genet | 2022 |
| 35711926 | Developing a National Newborn Genomes Program: An Approach Driven by Ethics, Engagement and Co-design. | Front Genet | 2022 |
| 35158310 | Towards equitable and trustworthy genomics research. | EBioMedicine | 2022 |
| 35125311 | Return of genomic results does not motivate intent to participate in research for all: Perspectives across 22 countries. | Genet Med | 2022 |
| 34906473 | Decision-making, attitudes, and understanding among patients and relatives invited to undergo genome sequencing in the 100,000 Genomes Project: A multisite survey study. | Genet Med | 2022 |
| 35264738 | Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study. | Eur J Hum Genet | 2022 |
| 33223530 | Opportunistic genomic screening. Recommendations of the European Society of Human Genetics. | Eur J Hum Genet | 2021 |
| 35592835 | Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthcare implementation. | Wellcome Open Res | 2021 |
| 33678496 | Animation or leaflet: Does it make a difference when educating young people about genome sequencing? | Patient Educ Couns | 2021 |
| 33580589 | Second World Congress on Genetic Counseling: An introduction to the special issue. | J Genet Couns | 2021 |
| 34758253 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. | N Engl J Med | 2021 |
| 34748551 | Return of individual research results from genomic research: A systematic review of stakeholder perspectives. | PLoS One | 2021 |
| 34034801 | Demonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countries. | Genome Med | 2021 |
| 33433037 | The family transition experience when living with childhood neuromuscular disease: A grounded theory study. | J Adv Nurs | 2021 |
| 31595045 | ESHG PPPC Comments on postmortem use of genetic data for research purposes. | Eur J Hum Genet | 2020 |
| 32001839 | Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study. | Eur J Hum Genet | 2020 |
| 31896776 | Development and mixed-methods evaluation of an online animation for young people about genome sequencing. | Eur J Hum Genet | 2020 |
| 32946764 | Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data? | Am J Hum Genet | 2020 |
| 32835846 | Young people's understanding, attitudes and involvement in decision-making about genome sequencing for rare diseases: A qualitative study with participants in the UK 100, 000 Genomes Project. | Eur J Med Genet | 2020 |
| 32592453 | A Maturity Matrix for Nurse Leaders to Facilitate and Benchmark Progress in Genomic Healthcare Policy, Infrastructure, Education, and Delivery. | J Nurs Scholarsh | 2020 |
| 32523053 | Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland. | Eur J Hum Genet | 2020 |
| 32301236 | A Roadmap for Global Acceleration of Genomics Integration Across Nursing. | J Nurs Scholarsh | 2020 |
| 30622331 | Duplication of 10q24 locus: broadening the clinical and radiological spectrum. | Eur J Hum Genet | 2019 |
| 31784025 | Should doctors have a legal duty to warn relatives of their genetic risks? | Lancet | 2019 |
| 32055707 | Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting results. | Wellcome Open Res | 2019 |
| 31685495 | Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project. | BMJ Open | 2019 |
| 31323115 | Development of a measure of genome sequencing knowledge for young people: The kids-KOGS. | Clin Genet | 2019 |
| 31235869 | European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death. | Eur J Hum Genet | 2019 |
| 31004824 | World congress on genetic counselling. | Eur J Med Genet | 2019 |
| 30991113 | Point of View: An evolution from genetic counselling to genomic counselling. | Eur J Med Genet | 2019 |
| 30270361 | Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study. | Genet Med | 2019 |
| 30550831 | Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge. | Eur J Med Genet | 2019 |
| 30573802 | Communication about genetic testing with breast and ovarian cancer patients: a scoping review. | Eur J Hum Genet | 2019 |
| 28833975 | Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists. | J Appl Res Intellect Disabil | 2018 |
| 29617718 | Genetic counselling in the era of genomic medicine. | Br Med Bull | 2018 |
| 29691228 | The 100â¿¿000 Genomes Project: bringing whole genome sequencing to the NHS. | BMJ | 2018 |
| 29603867 | Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications. | Am J Med Genet B Neuropsychiatr Genet | 2018 |
| 27722995 | Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups. | J Genet Couns | 2017 |
| 28327572 | The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors. | Eur J Hum Genet | 2017 |
| 27450665 | Living a normal life in an extraordinary way: A systematic review investigating experiences of families of young people's transition into adulthood when affected by a genetic and chronic childhood condition. | Int J Nurs Stud | 2016 |
| 26443265 | Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery. | Eur J Hum Genet | 2016 |
| 27650969 | Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders. | Eur J Hum Genet | 2016 |