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Author/Creator McAnulty, Ciaron

1. Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemia. Issue 1 (2nd January 2023)

Authors:
Gallon, Richard; Phelps, Rachel; Betts, Leigh; Hayes, Christine; Masic, Dino; Irving, Julie A. E.; McAnulty, Ciaron; Saha, Vaskar; Vora, Ajay; Wimmer, Katharina; Motwani, Jayashree; Macartney, Christine; Burn, John; Jackson, Michael S.; Moorman, Anthony V.; Santibanez-Koref, Mauro
Journal:
Leukemia & lymphoma
Issue:
Volume 64:Issue 1(2023)
Page Start:
217
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Improving the identification of patients with a genetic diagnosis of familial hypercholesterolaemia in primary care: A strategy to achieve the NHS long term plan. (May 2021)

Authors:
Ingoe, Lorna; Potter, Aimee; Musson, Susan; Neely, Dermot; Pilkington, Guy; Allen, A. Joy; Reay, Danielle; Luvai, Ahai; McAnulty, Ciaron; Camm, Nick; Berry, Ian; Nichols, Jody; Forbes, Gareth; Newton, Julia; Carey, Peter E.
Journal:
Atherosclerosis
Issue:
Volume 325(2021)
Page Start:
38
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Sequencing‐based microsatellite instability testing using as few as six markers for high‐throughput clinical diagnostics. Issue 1 (15th September 2019)

Authors:
Gallon, Richard; Sheth, Harsh; Hayes, Christine; Redford, Lisa; Alhilal, Ghanim; O'Brien, Ottilia; Spiewak, Helena; Waltham, Amanda; McAnulty, Ciaron; Izuogu, Osagie G.; Arends, Mark J.; Oniscu, Anca; Alonso, Angel M.; Laguna, Sira M.; Borthwick, Gillian M.; Santibanez‐Koref, Mauro; Jackson, Mich...
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
332
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗