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Author/Creator Oram, Richard A

1. A single nucleotide polymorphism genetic risk score to aid diagnosis of coeliac disease: a pilot study in clinical care. Issue 7 (13th August 2020)

Authors:
Sharp, Seth A.; Jones, Samuel E.; Kimmitt, Robert A.; Weedon, Michael N.; Halpin, Anne M.; Wood, Andrew R.; Beaumont, Robin N.; King, Seema; van Heel, David A.; Campbell, Patricia M.; Hagopian, William A.; Turner, Justine M.; Oram, Richard A
Journal:
Alimentary pharmacology & therapeutics
Issue:
Volume 52:Issue 7(2020)
Page Start:
1165
Record Type:
Journal Article
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6. The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype. Issue 3 (27th November 2013)

Authors:
Hamilton, Alexander J; Bingham, Coralie; McDonald, Timothy J; Cook, Paul R; Caswell, Richard C; Weedon, Michael N; Oram, Richard A; Shields, Beverley M; Shepherd, Maggie; Inward, Carol D; Hamilton-Shield, Julian P; Kohlhase, Jürgen; Ellard, Sian; Hattersley, Andrew T
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 3(2014)
Page Start:
165
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. Urine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational study. Issue 12 (18th December 2013)

Authors:
Oram, Richard A; Rawlingson, Andrew; Shields, Beverley M; Bingham, Coralie; Besser, Rachel E J; McDonald, Tim J; Knight, Bridget A; Hattersley, Andrew T
Journal:
BMJ open
Issue:
Volume 3:Issue 12(2013)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗