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Molecular Phenotypes Distinguish Patients with Relatively Stable from Progressive Idiopathic Pulmonary Fibrosis (IPF)

Overview of attention for article published in PLOS ONE, April 2009
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Title
Molecular Phenotypes Distinguish Patients with Relatively Stable from Progressive Idiopathic Pulmonary Fibrosis (IPF)
Published in
PLOS ONE, April 2009
DOI 10.1371/journal.pone.0005134
Pubmed ID
Authors

Kathy Boon, Nathaniel W. Bailey, Jun Yang, Mark P. Steel, Steve Groshong, Dolly Kervitsky, Kevin K. Brown, Marvin I. Schwarz, David A. Schwartz

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive, chronic interstitial lung disease that is unresponsive to current therapy and often leads to death. However, the rate of disease progression differs among patients. We hypothesized that comparing the gene expression profiles between patients with stable disease and those in which the disease progressed rapidly will lead to biomarker discovery and contribute to the understanding of disease pathogenesis.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 102 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 2%
United Kingdom 1 <1%
Germany 1 <1%
Argentina 1 <1%
Unknown 97 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 17 17%
Other 14 14%
Researcher 14 14%
Student > Bachelor 12 12%
Student > Master 10 10%
Other 17 17%
Unknown 18 18%
Readers by discipline Count As %
Medicine and Dentistry 39 38%
Agricultural and Biological Sciences 18 18%
Biochemistry, Genetics and Molecular Biology 11 11%
Nursing and Health Professions 2 2%
Pharmacology, Toxicology and Pharmaceutical Science 2 2%
Other 9 9%
Unknown 21 21%