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Cited by 299

The DOI matches its Crossref record; 86 of the 86 references it cites were found in a registry or an index.

New Targetable Oncogenes in Non–Small-Cell Lung Cancer

Open access
Oxnard, Geoffrey R., Binder, Adam, Jänne, Pasi A.·2013·Journal of Clinical Oncology

Abstract

The identification of oncogenic driver mutations underlying sensitivity to epidermal growth factor receptor and anaplastic lymphoma kinase tyrosine kinase inhibitors has led to a surge of interest in identifying additional targetable oncogenes in non–small-cell lung cancer. A number of new potentially oncogenic gene alterations have been characterized in recent years, including BRAF mutations, HER2 insertions, PIK3CA mutations, FGFR1 amplifications, DDR2 mutations, ROS1 rearrangements, and RET rearrangements. In this review, we will discuss the techniques used to discover each of these candidate oncogenes, the prevalence of each in non–small-cell lung cancer, the preclinical data supporting their role in lung cancer, and data on small molecular inhibitors in development.

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Registry

Crossref · 10.1200/jco.2012.42.9829

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Metadata

Authors
Oxnard, G. R., Binder, A., & Jänne, P. A.
Venue
Journal of Clinical Oncology
Published
2013-03-10
Volume
31
Issue
8
Pages
1097-1104
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2127919472
Cited by
299
References
86
FWCI
39.46
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: New Targetable Oncogenes in Non–Small-Cell Lung Cancer. https://app.cochat.ai/papers/10.1200/jco.2012.42.9829
The paper
Oxnard, G. R., Binder, A., & Jänne, P. A. (2013). New Targetable Oncogenes in Non–Small-Cell Lung Cancer. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2012.42.9829

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.