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3. BRCA-DIRECT digital pathway for diagnostic germline genetic testing within a UK breast oncology setting: a randomised, non-inferiority trial

8. Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosure

10. Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK)

13. GA4GH: International policies and standards for data sharing across genomic research and healthcare

17. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

20. Direct-to-consumer genetic testing

29. Why digital innovation may not reduce healthcare's environmental footprint.

33. Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

35. Ancestry, race and ethnicity: the role and relevance of language in clinical genetics practice.

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.

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

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