Barker, Karen
Institute of Cancer Research
3 papers on CoChatORCID 0000-0002-2357-3894
Most cited papers
- Verified
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
Reid, S., Schindler, D., Hanenberg, H., Barker, K., Hanks, S., Kalb, R., Neveling, K., Kelly, P., Seal, S., Freund, M., et al. (2007) · Nature Genetics
DNA Repair MechanismsBRCA gene mutations in cancer
Cited by 642
- Verified
Mutation of the RAD51C gene in a Fanconi anemia–like disorder
Vaz, F., Hanenberg, H., Schuster, B., Barker, K., Wiek, C., Erven, V., Neveling, K., Endt, D., Kesterton, I., Autore, F., et al. (2010) · Nature Genetics
DNA Repair MechanismsBlood disorders and treatments
Cited by 408
- Verified
Combined MYC and P53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease
Hill, R. M., Kuijper, S., Lindsey, J. C., Petrie, K., Schwalbe, E. C., Barker, K., Boult, J. K. R., Williamson, D., Ahmad, Z., Hallsworth, A., et al. (2015) · Cancer Cell
Glioma Diagnosis and TreatmentCancer-related Molecular Pathways
Cited by 210
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free