Tom Vulliamy
Queen Mary University of London(GB)
Publications by Year
Research Areas
Telomeres, Telomerase, and Senescence, Neonatal Health and Biochemistry, Acute Myeloid Leukemia Research, DNA Repair Mechanisms, Blood disorders and treatments
Most-Cited Works
- → X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions(1998)954 cited
- → The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita(2001)950 cited
- → The Human Phenotype Ontology in 2017(2016)796 cited
- → Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC(2004)459 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)326 cited
- → Glucose-6-phosphate dehydrogenase deficiency