Northcott, Paul A.
St. Jude Children's Research Hospital
29 papers on CoChatORCID 0000-0002-1220-5252
Most cited papers
- Verified
TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma
Remke, M., Ramaswamy, V., Peacock, J., Shih, D. J. H., Koelsche, C., Northcott, P. A., Hill, N., Cavalli, F. M. G., Kool, M., Wang, X., et al. (2013) · Acta Neuropathologica
Glioma Diagnosis and TreatmentCancer Genomics and Diagnostics
Cited by 164
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Hypermutation of the Inactive X Chromosome Is a Frequent Event in Cancer
Jäger, N., Schlesner, M., Jones, D. T. W., Raffel, S., Mallm, J.-P., Junge, K. M., Weichenhan, D., Bauer, T., Ishaque, N., Kool, M., et al. (2013) · Cell
Cancer Genomics and DiagnosticsChromatin Remodeling and Cancer
Cited by 90
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PCDH10 is a candidate tumour suppressor gene in medulloblastoma
Bertrand, K. C., Mack, S. C., Northcott, P. A., Garzia, L., Dubuc, A., Pfister, S. M., Rutka, J. T., Weiss, W. A., & Taylor, M. D. (2011) · Child's Nervous System
Glioma Diagnosis and TreatmentEpigenetics and DNA Methylation
Cited by 55
- Verified
Converging mechanism of UM171 and KBTBD4 neomorphic cancer mutations
Xie, X., Zhang, O., Yeo, M. J. R., Lee, C., Tao, R., Harry, S. A., Payne, N. C., Nam, E., Paul, L., Li, Y., et al. (2025) · Nature
Protein Degradation and InhibitorsUbiquitin and proteasome pathways
Cited by 50
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The Medulloblastoma Meta-Analysis Portal Enables Integrative Exploration of Clinical and Genomic Data from Patients
Gangwani, K., Lu, C., Dhanda, S. K., Sioson, E., Zaldívar Peraza, A., Matt, G. Y., Paul, R., Wang, J., Reilly, C., Acić, A., et al. (2025) · Cancer Research
Glioma Diagnosis and TreatmentCancer Genomics and Diagnostics
Cited by 1
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