Staff Profile
Publications
- Duncan CJA, Dinnigan E, Theobald R, Grainger A, Skelton AJ, Hussain R, Willet JDP, Swan DJ, Coxhead J, Thomas MF, Thomas J, Zamvar V, Slatter MA, Cant AJ, Engelhardt KR, Hambleton S. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20). Annals of the Rheumatic Diseases 2018, 77(5), 783-786.
- Engelhardt KR, Xu Y, Grainger A, Germani Batacchi MGC, Swan DJ, Willet JDP, Abd Hamid IJ, Agyeman P, Barge D, Bibi S, Jenkins L, Flood TJ, Abinun M, Slatter MA, Gennery AR, Cant AJ, Santibanez Koref M, Gilmour K, Hambleton S. Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing. Journal of Clinical Immunology 2017, 37(1), 42-50.
- Engelhardt KR, Xu YB, Grainger A, Batacchi MGCG, Swan DJ, Willet JDP, Abd Hamid IJ, Agyeman P, Barge D, Bibi S, Jenkins L, Flood T, Abinun M, Slatter M, Gennery AR, Cant AJ, Koref MS, Hambleton S. Identification Of Heterozygous Single- And Multi-exon Deletions In IL7R By Whole Exome Sequencing. In: UKPIN 2015 Meeting. 2015, Belfast, Northern Ireland: Wiley-Blackwell Publishing Ltd.
- Hambleton S, McDonald DO, Morgan NV, Griffin H, Singh-Dang T, Grainger A, Reynard L, Gennery AR, Slatter M, Flood TJ, McKiernan P, Barge D, Abinun M, Hackett S, Loughlin J, Lakey J, Cant AJ, Santibanez-Koref M. Autosomal recessive combines immunodeficiency due to loss of function mutation in Tripeptidyl Peptidase II. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
- Madhra M, Mavin E, Grainger A, Barge D, Wang XN, Walter J, Matthew D, Notarangelo LD, Gennery A. Regulatory T cell subsets, T cell receptor repertoire, and autoantibodies in RAG1-deficient Omenn syndrome. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
- Griffin H, McDonald DO, Singh-Dang T, Dickinson R, Grainger A, Reynard L, Hussain R, Cant AJ, Gennery AR, Abinun M, Flood TJ, Collin MP, Loughlin J, Morgan NV, Santibanez-Koref M, Hambleton S. Whole exome sequencing as a diagnostic tool in primary immunodeficiency. In: 15th Biennial Meeting European Society for Immunodeficiency (ESID). 2012, Florence, Italy: Springer.
- McDonald D, Morgan N, Griffin H, Dang TS, Grainger A, Reynard L, Loughlin J, Santibanez-Koref M, Hambleton S. Whole-exome deep sequencing identifies a novel causative mutation in primary immunodeficiency. In: Immunology: Annual Congress of the British Society for Immunology. 2011, Liverpool, UK: Wiley-Blackwell Publishing Ltd.
- Spratt J, Worthy S, Grainger A, Bourke S. Right apical opacification on a chest radiograph and chest pain. Chest 2003, 124(3), 1143-1144.
- Coady D, Grainger A, Ajdukiewicz K. Persistent back pain after a fall. JCR: Journal of Clinical Rheumatology 2002, 8(1), 55-56.
- Grainger AJ, Zammit-Maempel I. Antrochoanal polyps in children. European Radiology 2001, 11(2), 347-347.
- Campbell RSD, Grainger AJ. Current concepts in imaging of tendinopathy. Clinical Radiology 2001, 56(4), 253-267.
- Grainger AJ. Imaging of the subcoracoid bursa - Bursa. American Journal of Roentgenology 2001, 176(3), 812-813.
- Shakhapur S, Grainger AJ. MR arthrography. Current Orthopaedics 2001, 15(5), 376-387.
- Hide IG, Grainger AJ, Wallace IW, Hui A, Campbell RSD. A radiological technique for the assessment of wear in prosthetic knee replacements. Skeletal Radiology 2000, 29(10), 583-586.
- Grainger AJ, Elliott JM, Campbell RSD, Tirman PFJ, Steinbach LS, Genant HK. Direct MR arthrography: A review of current use. Clinical Radiology 2000, 55(3), 163-176.
- Grainger AJ, Zammit-Maempel I. CT of unusual nasal masses. British Journal of Radiology 1999, 72(855), 313-316.