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Anil Potti

Researcher at Duke University

Publications -  93
Citations -  7777

Anil Potti is an academic researcher from Duke University. The author has contributed to research in topics: Cancer & Lung cancer. The author has an hindex of 36, co-authored 93 publications receiving 7451 citations.

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Oncogenic pathway signatures in human cancers as a guide to targeted therapies.

TL;DR: It is shown that gene expression signatures can be identified that reflect the activation status of several oncogenic pathways and linked with sensitivity to therapeutics that target components of the pathway provides an opportunity to make use of these oncogens pathway signatures to guide the use of targeted therapeutics.
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Young Age at Diagnosis Correlates With Worse Prognosis and Defines a Subset of Breast Cancers With Shared Patterns of Gene Expression

TL;DR: This large-scale genomic analysis illustrates that breast cancer arising in young women is a unique biologic entity driven by unifying oncogenic signaling pathways, is characterized by less hormone sensitivity and higher HER-2/EGFR expression, and warrants further study to offer this poor-prognosis group of women better preventative and therapeutic options.
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A genomic strategy to refine prognosis in early-stage non-small-cell lung cancer.

TL;DR: The lung metagene model provides a potential mechanism to refine the estimation of a patient's risk of disease recurrence and, in principle, to alter decisions regarding the use of adjuvant chemotherapy in early-stage NSCLC.
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Genomic signatures to guide the use of chemotherapeutics.

TL;DR: Using in vitro drug sensitivity data coupled with Affymetrix microarray data, gene expression signatures that predict sensitivity to individual chemotherapeutic drugs are developed that can accurately predict clinical response in individuals treated with these drugs.
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A pathway-based classification of human breast cancer

TL;DR: A classification scheme for human breast cancer making use of patterns of pathway activity to build on previous subtype characterizations using intrinsic gene expression signatures, to provide a functional interpretation of the gene expression data that can be linked to therapeutic options.