265 results on '"Lucassen, Anneke"'
Search Results
2. Development of a digital risk-prediction tool based on family health history for the general population: legal and ethical implications
3. BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trial
4. I Had Genetic Testing for Alzheimer’s Disease Without My Consent
5. I Had Genetic Testing for Alzheimer’s Disease Without My Consent
6. Glowing gels and pipettes aplenty: how do commercial stock image banks portray genetic tests?
7. Ethical considerations in prenatal genomic testing
8. Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosure
9. Population screening requires robust evidence—genomics is no exception
10. Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)
11. In the family: access to, and communication of, familial information in clinical practice
12. Re-imagining ‘the patient’: Linked lives and lessons from genomic medicine
13. GA4GH: International policies and standards for data sharing across genomic research and healthcare
14. Using biomarkers in acute medicine to prevent hearing loss : should this require specific consent?
15. Old consent and new developments : health professionals should ask and not presume
16. Couple-based expanded carrier screening provided by general practitioners to couples in the Dutch general population: psychological outcomes and reproductive intentions
17. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
18. Retrospective Cohort Study on the Limitations of Direct-to-Consumer Genetic Screening in Hereditary Breast and Ovarian Cancer
19. What is the meaning of a ‘genomic result’ in the context of pregnancy?
20. Direct-to-consumer genetic testing
21. Familial genetic risks : how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?
22. The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics
23. Is it acceptable to contact an anonymous egg donor to facilitate diagnostic genetic testing for the donor-conceived child?
24. Cognitive and affective outcomes of genetic counselling in the Netherlands at group and individual level: a personalized approach seems necessary
25. Exploring broad consent in the context of the 100,000 Genomes Project: a mixed methods study
26. Genome sequencing in healthcare: understanding the UK general public’s views and implications for clinical practice
27. GP-provided couple-based expanded preconception carrier screening in the Dutch general population: who accepts the test-offer and why?
28. Fostering trust in healthcare: Participants’ experiences, views, and concerns about the 100,000 genomes project
29. Why digital innovation may not reduce healthcare's environmental footprint.
30. Towards a national genomics medicine service : the challenges facing clinical-research hybrid practices and the case of the 100 000 genomes project
31. A validated PROM in genetic counselling: the psychometric properties of the Dutch version of the Genetic Counselling Outcome Scale
32. Feasibility of couple-based expanded carrier screening offered by general practitioners
33. Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
34. A 'joint venture' model of recontacting in clinical genomics: challenges for responsible implementation
35. Ancestry, race and ethnicity: the role and relevance of language in clinical genetics practice.
36. Limitations and Pitfalls of Using Family Letters to Communicate Genetic Risk: a Qualitative Study with Patients and Healthcare Professionals
37. Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom
38. Health-care professionals’ responsibility to patients’ relatives in genetic medicine: a systematic review and synthesis of empirical research
39. 'Is this knowledge mine and nobody else's? I don't feel that.' Patient views about consent confidentiality and information-sharing in genetic medicine
40. “A very big challenge”: a qualitative study to explore the early barriers and enablers to implementing a national genomic medicine service in England.
41. Prospective study design and data analysis in UK Biobank.
42. Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature
43. How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study
44. Predictive Genetic Testing of Children for Adult-Onset Conditions: Negotiating Requests with Parents
45. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
46. Challenges of whole genome sequencing in population newborn screening.
47. Advocating for a Context Specific Approach to Tackle Inequities.
48. Responsible implementation of expanded carrier screening
49. Genetic medicine and incidental findings: it is more complicated than deciding whether to disclose or not
50. Access to Biobanks: Responsibilities Within a Research Ecosystem.
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