An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
About this item
Full title
Author / Creator
Petrovski, Slavé , Todd, Jamie L , Durheim, Michael T , Wang, Quanli , Chien, Jason W , Kelly, Fran L , Frankel, Courtney , Mebane, Caroline M , Ren, Zhong , Bridgers, Joshua , Urban, Thomas J , Malone, Colin D , Finlen Copeland, Ashley , Brinkley, Christie , Allen, Andrew S , O'Riordan, Thomas , McHutchison, John G , Palmer, Scott M and Goldstein, David B
Publisher
United States: American Thoracic Society
Journal title
Language
English
Formats
Publication information
Publisher
United States: American Thoracic Society
Subjects
More information
Scope and Contents
Contents
Idiopathic pulmonary fibrosis (IPF) is an increasingly recognized, often fatal lung disease of unknown etiology.
The aim of this study was to use whole-exome sequencing to improve understanding of the genetic architecture of pulmonary fibrosis.
We performed a case-control exome-wide collapsing analysis including 262 unrelated individuals with...
Alternative Titles
Full title
An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
Authors, Artists and Contributors
Author / Creator
Todd, Jamie L
Durheim, Michael T
Wang, Quanli
Chien, Jason W
Kelly, Fran L
Frankel, Courtney
Mebane, Caroline M
Ren, Zhong
Bridgers, Joshua
Urban, Thomas J
Malone, Colin D
Finlen Copeland, Ashley
Brinkley, Christie
Allen, Andrew S
O'Riordan, Thomas
McHutchison, John G
Palmer, Scott M
Goldstein, David B
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5519963
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5519963
Other Identifiers
ISSN
1073-449X
E-ISSN
1535-4970
DOI
10.1164/rccm.201610-2088OC
