Published pathways
DPYD
Familial hypercholesterolaemia
Generation Study
Inherited cardiovascular conditions
Lynch syndrome
Sickle cell disease
Pathways in development
Below you will see a table of established CPI projects so that, if you are inspired to initiate a pathway project, you can see which ones are already under way. If you have any questions about a particular CPI project, you can contact the lead author via the links below.
| Clinical Pathway Initiative project | Author (click to contact via email) |
| Aminoglycoside toxicity in neonates (point-of-care testing) | Lianne Gompertz |
| Childhood epilepsy | Lianne Gompertz |
| CYP2C19 Pharmacogenomic testing | Dharmisha Chauhan |
| Cystic fibrosis carrier testing | Pooja Dasani |
| Cystic renal | Vicky Carr |
| Familial breast cancer risk (primary care) | Donna Gillen |
| Glioma | Philandra Costello |
| Genetic causes of dementia | Nick Bass |
| Haematology-oncology | Olga Tsoulaki |
| Hirschsprung disease | Jo Kennedy / Sarah Smithson / Sam Boland |
| Hypotonic infant | Melody Redman |
| Inherited retinal dystrophy | Sian Sperring |
| Intellectual disability | Nicole Eady |
| Learning disability | Gill Moss |
| Neurology (adult with a neurological condition) | Heidy Brandon |
| Non-invasive prenatal testing | Joanne Hargrave / Karen Creed |
| R14 Acutely unwell children with a likely monogenic disorder in the NICU setting | Danni Bogue |
| R142 Glucokinase-related fasting hyperglycaemia | Joanne Hargrave |
| R21 Prenatal exome sequencing | Lauren Capacchione |
| R441 Unexplained death in infancy and sudden unexplained death in childhood | Joanne Mumford |
| Sickle cell carrier status | Rossby Awadzi |
| WGS nurse-led neurology | Helen Bethell / Alistair McNeill |
