An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis

Author:

Petrovski Slavé12ORCID,Todd Jamie L.34,Durheim Michael T.34ORCID,Wang Quanli1,Chien Jason W.5ORCID,Kelly Fran L.3,Frankel Courtney3,Mebane Caroline M.1,Ren Zhong1,Bridgers Joshua1,Urban Thomas J.6,Malone Colin D.1,Finlen Copeland Ashley3,Brinkley Christie3,Allen Andrew S.7ORCID,O’Riordan Thomas5,McHutchison John G.5,Palmer Scott M.34,Goldstein David B.1

Affiliation:

1. Institute for Genomic Medicine, Columbia University Medical Center, New York, New York

2. Department of Medicine, Austin Health and Royal Melbourne Hospital, The University of Melbourne, Melbourne, Victoria, Australia

3. Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Duke University Medical Center, Durham, North Carolina

4. Duke Clinical Research Institute, Durham, North Carolina

5. Gilead Sciences, Foster City, California

6. Division of Pharmacotherapy and Experimental Therapeutics, Center for Pharmacogenomics and Individualized Therapy, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina; and

7. Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

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