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Odd Terje Brustugun

Researcher at University of Oslo

Publications -  19
Citations -  2625

Odd Terje Brustugun is an academic researcher from University of Oslo. The author has contributed to research in topics: Lung cancer & Cancer. The author has an hindex of 10, co-authored 19 publications receiving 2256 citations. Previous affiliations of Odd Terje Brustugun include Vestre Viken Hospital Trust & Oslo University Hospital.

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Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer

Martin Peifer, +94 more
- 01 Oct 2012 - 
TL;DR: This study implicates histone modification as a major feature of SCLC, reveals potentially therapeutically tractable genomic alterations and provides a generalizable framework for the identification of biologically relevant genes in the context of high mutational background.
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Mutations in the DDR2 Kinase Gene Identify a Novel Therapeutic Target in Squamous Cell Lung Cancer

TL;DR: Findings suggest that gain-of-function mutations in DDR2 are important oncogenic events and are amenable to therapy with dasatinib, and provide a rationale for designing clinical trials with the FDA-approved drug d asatinib in patients with lung SCCs.
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A genomics-based classification of human lung tumors

Danila Seidel, +118 more
TL;DR: Support is provided for broad implementation of genome-based diagnosis of lung cancer by demonstrating the correlation between lung tumor subtype and its predominant mutations, and the benefit of genetic testing and targeted therapy in these patients.
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Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors

Julie George, +66 more
TL;DR: It is shown LCNECs represent a distinct transcriptional subgroup among lung cancers and comprise two molecular subgroups, type I (TP53 and STK11/KEAP1 alterations) and type II ( TP53 and RB1 inactivation).
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BRAF-mutations in non-small cell lung cancer

TL;DR: Clinopathological characteristics of nearly one thousand unselected NSCLC patients tested for the targetable V600E/K BRAF-mutation should be part of the subtyping of non-squamous NSCLc.