German Cancer Research Center
Andrey Korshunov focuses on Medulloblastoma, Pathology, Cancer research, Genome and Cancer. His Medulloblastoma research is multidisciplinary, relying on both Beta-catenin, Wnt signaling pathway, Cell migration, Gene knockdown and Sonic hedgehog. His research investigates the connection between Cancer research and topics such as Comparative genomic hybridization that intersect with problems in Gene mapping and Fluorescence in situ hybridization.
While the research belongs to areas of Genome, Andrey Korshunov spends his time largely on the problem of Bioinformatics, intersecting his research to questions surrounding Candidate gene, Pathogenesis and Tissue microarray. His Cancer study combines topics from a wide range of disciplines, such as Pinealoma and Mutation rate. His study in the field of Germline mutation, Mutation frequency, Germline and Mutation is also linked to topics like Chromothripsis.
Andrey Korshunov spends much of his time researching Cancer research, Medulloblastoma, Pathology, Internal medicine and Oncology. His Cancer research study combines topics in areas such as Fusion gene, Cancer and Transplantation. His research in Medulloblastoma intersects with topics in Immunohistochemistry, SGK1, Computational biology and Bioinformatics.
His Computational biology research includes themes of Genetics, Cancer genome and Deep sequencing. His research integrates issues of Carcinogenesis and Genome in his study of Bioinformatics. His work carried out in the field of Pathology brings together such families of science as Sonic hedgehog and Radiation therapy.
Andrey Korshunov mainly focuses on Cancer research, Gene, Glioma, Glioblastoma and Internal medicine. His Cancer research study frequently draws connections to other fields, such as Germline mutation. His work in the fields of Gene, such as Genome, MYB, Methylation and Mutation, intersects with other areas such as ROS1.
Andrey Korshunov combines subjects such as Carcinogenesis, Medulloblastoma and Bioinformatics with his study of Genome. Andrey Korshunov interconnects Pathology and Neural stem cell in the investigation of issues within Glioma. As part of one scientific family, Andrey Korshunov deals mainly with the area of Genomics, narrowing it down to issues related to the Human genetics, and often Mutation rate, Mutation, Germline and Mutation frequency.
His main research concerns Human genetics, Genome, Gene, Genomics and Medulloblastoma. His work deals with themes such as Cancer, Germline, Mutation rate and Mutation, which intersect with Human genetics. His studies in Genome integrate themes in fields like Grading, Internal medicine, Oncology, Disease specific and Methylation profiling.
His study on Exome sequencing is often connected to ROS1 as part of broader study in Gene. The Genomics study combines topics in areas such as Carcinogenesis, Human genome and Bioinformatics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
International network of cancer genome projects
Thomas J. Hudson;Thomas J. Hudson;Warwick Anderson;Axel Aretz;Anna D. Barker.
DNA methylation-based classification of central nervous system tumours
David Capper;David Capper;David Capper;David T. W. Jones;Martin Sill;Volker Hovestadt.
Medulloblastoma Comprises Four Distinct Molecular Variants
Paul A. Northcott;Andrey Korshunov;Hendrik Witt;Thomas Hielscher.
Journal of Clinical Oncology (2011)
Analysis of the IDH1 codon 132 mutation in brain tumors
Jörg Balss;Jochen Meyer;Wolf Mueller;Andrey Korshunov;Andrey Korshunov.
Acta Neuropathologica (2008)
Dissecting the genomic complexity underlying medulloblastoma
David T. W. Jones;Natalie Jäger;Marcel Kool;Thomas Zichner.
Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups
Kristian W. Pajtler;Kristian W. Pajtler;Hendrik Witt;Martin Sill;David T.W. Jones.
Cancer Cell (2015)
Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations
Tobias Rausch;David T.W. Jones;Marc Zapatka;Adrian M. Stütz.
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma
David T W Jones;Barbara Hutter;Natalie Jäger;Andrey Korshunov;Andrey Korshunov.
Nature Genetics (2013)
The whole-genome landscape of medulloblastoma subtypes
Paul A. Northcott;Paul A. Northcott;Ivo Buchhalter;Ivo Buchhalter;A. Sorana Morrissy;Volker Hovestadt.
Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition
Marcel Kool;David T.W. Jones;Natalie Jäger;Paul A. Northcott.
Cancer Cell (2014)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: