Amanda J. Walne
Queen Mary University of London(GB)Genomics England(GB)
Publications by Year
Research Areas
Telomeres, Telomerase, and Senescence, DNA Repair Mechanisms, Acute Myeloid Leukemia Research, Advanced biosensing and bioanalysis techniques, Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Most-Cited Works
- → Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC(2004)460 cited
- → Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation(2005)336 cited
- → Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita(2008)327 cited
- → TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes(2008)313 cited
- → Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10(2007)309 cited
- → Inflammatory Skin and Bowel Disease Linked toADAM17Deletion(2011)306 cited