Debbie Hicks
Newcastle University(GB)
Publications by Year
Research Areas
Glioma Diagnosis and Treatment, Muscle Physiology and Disorders, Cancer Genomics and Diagnostics, Epigenetics and DNA Methylation, Cell Adhesion Molecules Research
Most-Cited Works
- → Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study(2017)507 cited
- → Second-generation molecular subgrouping of medulloblastoma: an international meta-analysis of Group 3 and Group 4 subtypes(2019)304 cited
- → Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity(2020)227 cited
- → A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy(2010)224 cited
- → Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice(2013)137 cited
- → Congenital myasthenic syndromes due to mutations inALG2andALG14(2013)134 cited
- → A comparative analysis of collagen VI production in muscle, skin and fibroblasts from 14 Ullrich congenital muscular dystrophy patients with dominant and recessive COL6A mutations(2006)118 cited
- → Collagen Type VI Myopathies(2013)116 cited
- → Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial(2018)115 cited
- → Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy(2013)109 cited