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Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Age-dependent Genetic Risk in Pulmonary Fibrosis Patients and RelativesDavid Zhang, Chad A Newton, Imre Noth, et al.
Chest|March 26, 2022
The Role of Genetic Testing in Pulmonary Fibrosis: A Perspective From the Pulmonary Fibrosis Foundation Genetic Testing Work GroupChad A Newton, Justin M Oldham, Carolyn Applegate, et al.
The Lancet. Respiratory Medicine|June 27, 2017
The MUC5B promoter polymorphism and telomere length in patients with chronic hypersensitivity pneumonitis: an observational cohort-control studyBrett Ley, Chad A Newton, Isabel Arnould, et al.
The European Respiratory Journal|January 13, 2019
Telomere length and genetic variant associations with interstitial lung disease progression and survivalChad A Newton, Justin M Oldham, Brett Ley, et al.
American Journal of Respiratory and Critical Care Medicine|August 9, 2022
Validation of Proposed Criteria for Progressive Pulmonary FibrosisJanelle Vu Pugashetti, Ayodeji Adegunsoye, Zhe Wu, et al.
The European Respiratory Journal|August 17, 2023
Telomere length and immunosuppression in non-idiopathic pulmonary fibrosis interstitial lung diseaseDavid Zhang, Ayodeji Adegunsoye, Justin M Oldham, et al.
The Lancet. Respiratory Medicine|January 22, 2022
Proteomic biomarkers of progressive fibrosing interstitial lung disease: a multicentre cohort analysisWillis S Bowman, Chad A Newton, Angela L Linderholm, et al.
The European Respiratory Journal|July 18, 2020
Myositis-specific antibodies identify a distinct interstitial pneumonia with autoimmune features phenotypeJulia Graham, Iazsmin Bauer Ventura, Chad A Newton, et al.
The European Respiratory Journal|November 5, 2021
Lung function trajectory in progressive fibrosing interstitial lung diseaseJustin M Oldham, Cathryn T Lee, Zhe Wu, et al.
JAMA Network Open|March 10, 2023
Evaluation of Pulmonary Fibrosis Outcomes by Race and Ethnicity in US AdultsAyodeji Adegunsoye, Elizabeth Freiheit, Emily N White, et al.
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