Kelly Halliday
Publications by Year
Research Areas
Glioma Diagnosis and Treatment, Cancer Genomics and Diagnostics, MicroRNA in disease regulation, Genetics and Neurodevelopmental Disorders, Lung Cancer Treatments and Mutations
Most-Cited Works
- → Patterns of somatic mutation in human cancer genomes(2007)3,129 cited
- → Intragenic ERBB2 kinase mutations in tumours(2004)787 cited
- → Somatic Mutations of the Protein Kinase Gene Family in Human Lung Cancer(2005)466 cited
- → X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment(2008)444 cited
- → Mutation analysis of 24 known cancer genes in the NCI-60 cell line set(2006)440 cited
- → A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy(2006)432 cited
- → A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer(2005)333 cited
- → Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation(2007)290 cited
- → Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor(2007)224 cited
- → Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marfanoid Habitus(2007)174 cited