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Author Details
Full Name
Nicolas Stransky
Affiliation
ORCID
Career Start Year
2004
Papers
41
H Index
37
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35927254
Molecular characterization of colorectal cancer related peritoneal metastatic disease.
Nat Commun
2022
31068700
Next-generation characterization of the Cancer Cell Line Encyclopedia.
Nature
2019
31639029
Accuracy assessment of fusion transcript detection via read-mapping and de novo fusion transcript assembly-based methods.
Genome Biol
2019
31575541
First-in-Human Phase I Study of Fisogatinib (BLU-554) Validates Aberrant FGF19 Signaling as a Driver Event in Hepatocellular Carcinoma.
Cancer Discov
2019
30559381
Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Nature
2019
30765874
TYRO3 as a molecular target for growth inhibition and apoptosis induction in bladder cancer.
British Journal of Cancer
2019
28297679
Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles.
Cell Rep
2017
28658632
Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles.
Cell Rep
2017
26181029
Genomic Correlate of Exceptional Erlotinib Response in Head and Neck Squamous Cell Carcinoma.
JAMA Oncol
2015
25932675
Targeting cancer with kinase inhibitors.
Journal of Clinical Investigation
2015
25776529
First Selective Small Molecule Inhibitor of FGFR4 for the Treatment of Hepatocellular Carcinomas with an Activated FGFR4 Signaling Pathway.
Cancer Discovery
2015
24737027
A small molecule that binds and inhibits the ETV1 transcription factor oncoprotein.
Mol Cancer Ther
2014
25233892
Genomic analyses of gynaecologic carcinosarcomas reveal frequent mutations in chromatin remodelling genes.
Nat Commun
2014
25204415
The landscape of kinase fusions in cancer.
Nat Commun
2014
23269662
ATARiS: computational quantification of gene suppression phenotypes from multisample RNAi screens.
Genome Res
2013
23770567
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Nature
2013
23993102
An interactive resource to identify cancer genetic and lineage dependencies targeted by small molecules.
Cell
2013
22817889
A landscape of driver mutations in melanoma.
Cell
2012
22343534
Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing.
Proc Natl Acad Sci U S A
2012
22622578
Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature
2012
22460905
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
Nature
2012
22722202
Sequence analysis of mutations and translocations across breast cancer subtypes.
Nature
2012
22610119
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.
Nat Genet
2012
21746896
Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer.
Proc Natl Acad Sci U S A
2011
21173382
A novel epigenetic phenotype associated with the most aggressive pathway of bladder tumor progression.
Journal of the National Cancer Institute
2011
20956946
Milk fat globule--epidermal growth factor--factor VIII (MFGE8)/lactadherin promotes bladder tumor development.
Oncogene
2011
21892161
Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion.
Nat Genet
2011
21764851
Nuclear factor I/B is an oncogene in small cell lung cancer.
Genes Dev
2011
21760589
Functional genomics reveal that the serine synthesis pathway is essential in breast cancer.
Nature
2011
21666749
Inhibitor-sensitive FGFR1 amplification in human non-small cell lung cancer.
PLoS One
2011
21798893
The mutational landscape of head and neck squamous cell carcinoma.
Science
2011
20527025
Frequent genomic structural alterations at HPV insertion sites in cervical carcinoma.
J Pathol
2010
21107320
COT drives resistance to RAF inhibition through MAP kinase pathway reactivation.
Nature
2010
18757432
Characterization of the recurrent 8p11-12 amplicon identifies PPAPDC1B, a phosphatase protein, as a new therapeutic target in breast cancer.
Cancer Res
2008
17099711
Regional copy number-independent deregulation of transcription in cancer.
Nature Genetics
2006
16434445
Computation of recurrent minimal genomic alterations from array-CGH data.
Bioinformatics
2006
16820431
VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles.
Bioinformatics
2006
15735024
Visualizing chromosomes as transcriptome correlation maps: evidence of chromosomal domains containing co-expressed genes--a study of 130 invasive ductal breast carcinomas.
Cancer Res
2005
16007141
Identification of a proliferation gene cluster associated with HPV E6/E7 expression level and viral DNA load in invasive cervical carcinoma.
Oncogene
2005
15262785
Selecting biomedical data sources according to user preferences.
Bioinformatics
2004
15381628
Analysis of array CGH data: from signal ratio to gain and loss of DNA regions.
Bioinformatics
2004
1 - 41 of 41
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