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Author Details
Full Name
Huriye Seker-Cin
Affiliation
Institute of Pathology, Heidelberg University Hospital
ORCID
Career Start Year
2008
Papers
21
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37586177
Analysis of rare fusions in NSCLC: Genomic architecture and clinical implications.
Lung Cancer
2023
34331337
Assigning evidence to actionability: An introduction to variant interpretation in precision cancer medicine.
Genes Chromosomes Cancer
2022
35681698
Early Development of Ubiquitous Acanthocytosis and Extravascular Hemolysis in Lung Cancer Patients Receiving Alectinib.
Cancers (Basel)
2022
35871236
Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing.
Br J Cancer
2022
34487971
The immune microenvironment in EGFR- and ERBB2-mutated lung adenocarcinoma.
ESMO Open
2021
33667718
Targeting rare and non-canonical driver variants in NSCLC - An uncharted clinical field.
Lung Cancer
2021
33046443
Functional Precision Medicine Identifies New Therapeutic Candidates for Medulloblastoma.
Cancer Res
2020
30349086
A biobank of patient-derived pediatric brain tumor models.
Nat Med
2018
26977882
HDAC and PI3K Antagonists Cooperate to Inhibit Growth of MYC-Driven Medulloblastoma.
Cancer Cell
2016
26378811
Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.
Oncotarget
2015
24651015
Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition.
Cancer Cell
2014
25043047
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma.
Nature
2014
24553142
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy.
Nature
2014
23817572
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.
Nat Genet
2013
24183680
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas.
Cancer Cell
2013
22265402
Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.
Cell
2012
22832583
Dissecting the genomic complexity underlying medulloblastoma.
Nature
2012
21190184
Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytoma.
Int J Cancer
2011
21911727
FSTL5 is a marker of poor prognosis in non-WNT/non-SHH medulloblastoma.
J Clin Oncol
2011
21424530
Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.
Acta Neuropathol
2011
18663494
Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2).
Neurogenetics
2008
1 - 21 of 21
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