Karen Barker
Institute of Cancer Research(GB)
Publications by Year
Research Areas
Neuroblastoma Research and Treatments, Cancer, Hypoxia, and Metabolism, Cancer therapeutics and mechanisms, Neuroendocrine Tumor Research Advances, Lung Cancer Research Studies
Most-Cited Works
- → Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer(2002)1,602 cited
- → Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer(2006)641 cited
- → Mutations in PTF1A cause pancreatic and cerebellar agenesis(2004)457 cited
- → Mutation of the RAD51C gene in a Fanconi anemia–like disorder(2010)403 cited
- → The ALKF1174L Mutation Potentiates the Oncogenic Activity of MYCN in Neuroblastoma(2012)322 cited
- → Combined MYC and P53 Defects Emerge at Medulloblastoma Relapse and Define Rapidly Progressive, Therapeutically Targetable Disease(2014)207 cited
- → Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor(2008)197 cited
- → p53 mutation with frequent novel codons but not a mutator phenotype in BRCA1- and BRCA2-associated breast tumours(1998)178 cited
- → BRK tyrosine kinase expression in a high proportion of human breast carcinomas(1997)163 cited
- → Localization of a Gene (MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43(2001)160 cited