Genetics
This practice focus brings together a body of studies on the delivery of genetic services and the social and ethical consequences of genetic knowledge. Current activity focuses on newborn screening, cancer genetics, genetic syndromes and genetics and psychiatry.
- The All Wales Psychosocial Evaluation of Newborn Screening for Duchenne Muscular Dystrophy (DMD) (Phase 1)
- The All Wales Psychosocial Evaluation of Newborn Screening for Duchenne Muscular Dystrophy (DMD) (Phase 2)
- The All Wales Psychosocial Evaluation of Newborn Screening for Duchenne Muscular Dystrophy (DMD). Final evaluation prior to service implementation (Phase 3)
- The All Wales Psychosocial Evaluation of Newborn Screening for Duchenne Muscular Dystrophy (DMD). Informed choice and equity in population screening (Phase 4)
- The All Wales Psychosocial evaluation of Newborn Screening for Duchenne Muscular Dystrophy (DMD)
- The meaning for mothers of a decision about antenatal screening for Down's syndrome
- Consent to newborn screening: a study of midwives and mothers
- Audit of families who have an abnormal newborn screening test result
- Antenatal Screening Decision Pathways for women at risk of Duchenne muscular dystrophy: A study of the perceived reproductive impact of newborn screening
- The All Wales Psychosocial Evaluation of Newborn Screening for Duchenne Muscular Dystrophy (DMD): A study of social distribution and screening uptake
- Psychosocial Implications of Newborn Screening for Cystic Fibrosis (CF)
- Women at intermediate risk for familial breast cancer: a study of long-term cancer worries, post-counselling pathways and resource implications for delivery of care (RETRACE)
- Midwife and mother in partnership: increasing parental choice about newborn screening
- Antenatal Screening Decision Pathways for women at risk of Duchenne muscular dystrophy: A study of the perceived reproductive impact of newborn screening
- Clinical, molecular and social aspects of genetic testing for Rett syndrome
- Banking on miracles: Cord blood stem cell collection and the implications for midwifery practice