Dr Meryl Lusher
Telephone: +44 (0) 191 246 4387 Fax: +44 (0) 191 246 4301 Address: Northern Institute for Cancer Research
Ryan SL, Schwalbe EC, Cole M, Lu Y, Lusher ME, Megahed H, O'Toole K, Nicholson SL, Bognar L, Garami M, Hauser P, Korshunov A, Pfister SM, Williamson D, Taylor RE, Ellison DW, Bailey S, Clifford SC. MYC family amplification and clinical risk-factors interact to predict an extremely poor prognosis in childhood medulloblastoma .
Acta Neuropathologica 2012, 123 (4), 501-513.
Schwalbe EC, Lindsey JC, Straughton D, Hogg TL, Cole M, Megahed H, Ryan SL, Lusher ME, Taylor MD, Gilbertson RJ, Ellison DW, Bailey S, Clifford SC. Rapid Diagnosis of Medulloblastoma Molecular Subgroups .
Clinical Cancer Research 2011, 17 (7), 1883-1894.
Levesley J, Lusher ME, Lindsey JC, Clifford SC, Grundy R, Coyle B. RASSF1A and the BH3-only mimetic ABT-737 promote apoptosis in pediatric medulloblastoma cell lines .
Neuro-Oncology 2011, 13 (12), 1265-1276.
Lindsey JC, Hill RM, Megahed H, Lusher ME, Schwalbe EC, Cole M, Hogg TL, Gilbertson RJ, Ellison DW, Bailey S, Clifford SC. TP53 Mutations in Favorable-Risk Wnt/Wingless-Subtype Medulloblastomas .
Journal of Clinical Oncology 2011, 29 (12), E344-E346.
Krishnan KJ, Lusher M, Lindey J, Birch-Machin MA. Direct generation of the mitochondrial DNA common deletion in cultured skin cells by repetitive ultraviolet irradiation .
In: British Journal of Dermatology: Annual meeting of the British Society for Investigative Dermatology . 2003, Southampton, UK: Wiley-Blackwell Publishing Ltd.
Tonkin E, Smith M, Eichhorn P, Hagan DM, Herrell S, Lusher M, Ireland M, Burn J, Strachan T. A novel gene is disrupted by a Cornelia de Lange-associated translocation breakpoint at 3q26.3 .
In: American Journal of Human Genetics . 2001, Cell Press.
McDermott CJ, White K, Lindsey JC, Lusher ME, Bushby KMD, Shaw PJ. Genotype-phenotype correlation in hereditary spastic paraparesis .
In: Journal of Neurology, Neurosurgery and Psychiatry . 2001, BMJ Group.
