All Stories

  1. ‘Your DNA, Your Say’: global survey gathering attitudes toward genomics: design, delivery and methods
  2. Australians’ views on personal genomic testing: focus group findings from the Genioz study
  3. Genetic counselling in the era of genomic medicine
  4. The Global Landscape of Nursing and Genomics
  5. Society and personal genome data
  6. Genetic counseling globally: Where are we now?
  7. APPLaUD: access for patients and participants to individual level uninterpreted genomic data
  8. Genetics in the 21st Century: Implications for patients, consumers and citizens
  9. Genetics in the 21st Century: Implications for patients, consumers and citizens
  10. Stakeholders in psychiatry and their attitudes toward receiving pertinent and incident findings in genomic research
  11. Human Germline Genome Editing
  12. Direct-to-consumer genetic testing: where and how does genetic counseling fit?
  13. Socialising the genome
  14. The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors
  15. Returning genome sequences to research participants: Policy and practice
  16. Prevalence and architecture of de novo mutations in developmental disorders
  17. Your DNA, Your Say
  18. Potential research participants support the return of raw sequence data
  19. Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research
  20. No expectation to share incidental findings in genomic research
  21. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
  22. Large-scale discovery of novel genetic causes of developmental disorders
  23. Genetic counselors and Genomic Counseling in the United Kingdom
  24. Ethical, Legal, and Social Issues in Clinical Genomics
  25. Online questionnaire development: Using film to engage participants and then gather attitudes towards the sharing of genomic data
  26. Finding people who will tell you their thoughts on genomics—recruitment strategies for social sciences research
  27. Position statement on opportunistic genomic screening from the Association of Genetic Nurses and Counsellors (UK and Ireland)
  28. Policy challenges of clinical genome sequencing
  29. Jennifer Wiggins and Anna Middleton (eds): Getting the Message Across: Communication with Diverse Populations in Clinical Genetics
  30. Empirical research on the ethics of genomic research
  31. Deaf Community and Genetics
  32. Communication about DTC Testing: Commentary on a ‘Family Experience of Personal Genomics’
  33. Communicating in a healthcare setting with people who have hearing loss
  34. Preferences for communication in clinic from deaf people: a cross-sectional study
  35. Whose Deaf Genes Are They Anyway?: The Deaf Community’s Challenge to Legislation on Embryo Selection
  36. Views, Knowledge, and Beliefs about Genetics and Genetic Counseling among Deaf People
  37. Cancers in BRCA1 and BRCA2 Carriers and in Women at High Risk for Breast Cancer: MR Imaging and Mammographic Features 1
  38. Clause 14(4)(9) of embryo bill should be amended or deleted
  39. Attitudes of deaf people and their families towards issues surrounding genetics
  40. Providing a Transcultural Genetic Counseling Service in the UK
  41. Report from the UK and Eire Association of Genetic Nurses and Counsellors (AGNC) Supervision Working Group on Genetic Counselling Supervision
  42. Reflections on the Experience of Counseling Supervision by a Team of Genetic Counselors from the UK
  43. Editorial on Supervision
  44. Deaf Community and Genetics
  45. Tailoring genetic information and services to clients’ culture, knowledge and language level
  46. Prenatal Diagnosis for Inherited Deafness-What is the Potential Demand?
  47. Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings
  48. Attitudes of Deaf Adults toward Genetic Testing for Hereditary Deafness
  49. Culture, Kinship and Genes: Towards Cross-Cultural Genetics
  50. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene