Identification of a Genetic Susceptibility Locus for Idiopathic Pulmonary Fibrosis in the 16p Subtelomere Using Whole-Genome Sequencing
Author:
Affiliation:
1. Genentech, Inc., South San Francisco, California;
2. Hoffman-La Roche, Mississauga, Ontario, Canada;
3. University of California, San Francisco, California;
4. Vanderbilt University Medical Center, Nashville, Tennessee
Funder
NIH
Publisher
American Thoracic Society
Subject
Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine
Link
https://www.atsjournals.org/doi/pdf/10.1164/rccm.202206-1139LE
Reference15 articles.
1. Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics
2. Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis
3. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
4. Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study
5. An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
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