Elizabeth A. Cromwell

University of North Carolina at Chapel Hill — United States

Medicine · Health Sciences

33h-index58.1kcitations127works3.02yr avg

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Research Topics

Cystic Fibrosis Research Advances(33), Agricultural Innovations and Practices(14), Reproductive tract infections research(14), Parasitic Diseases Research and Treatment(12), Neonatal Respiratory Health Research(11)

Publications111 total

Process and validity of linking cystic fibrosis patient registry with national Medicaid databases

UNC Libraries·2025Open Access

Global prevalence of CFTR variants with respect to their responsiveness to elexacaftor-tezacaftor-ivacaftor

4 cited

Journal of Cystic Fibrosis·2025· 4 citedOpen Access

746 Hospitalizations during the first two years of life in infants and young children with cystic fibrosis

Journal of Cystic Fibrosis·2025

Evaluating Long-Term Effectiveness of Cystic Fibrosis Modulator Therapies after Rapid Adoption: A Dual-Approach Study

Annals of the American Thoracic Society·2025Open Access

Identifying cystic fibrosis programs in the United States with disproportionately disadvantaged patient populations: Methodology and implications for care

Journal of Cystic Fibrosis·2025

Exploring reduced pulmonary exacerbation rates in cystic fibrosis: a pandemic or modulator effect?

2 cited

ERJ Open Research·2025· 2 citedOpen Access

Effects of azithromycin in young adults with cystic fibrosis: a protocol for emulating a published randomised controlled trial using registry data

BMJ Open·2025Open Access

Real-world association between ivacaftor initiation and lung function variability: A registry study

2 cited

Journal of Cystic Fibrosis·2025· 2 cited

Validating the Data Completeness and Accuracy of the Canadian Cystic Fibrosis Registry

1 cited

Canadian Respiratory Journal·2025· 1 citedOpen Access

Process and validity of linking cystic fibrosis patient registry with national Medicaid databases

Journal of Cystic Fibrosis·2024

Aging with CF: Characteristics of people with CF aged 40 and older in the United States

4 cited

Journal of Cystic Fibrosis·2024· 4 cited

Factors associated with prescription of elexacaftor/tezacaftor/ivacaftor among people with cystic fibrosis aged 12 years or older with at least one F508del allele

4 cited

Journal of Cystic Fibrosis·2024· 4 cited

Linkage of the CF Foundation Patient Registry with the Scientific Registry of Transplant Recipients database

1 cited

Journal of Cystic Fibrosis·2024· 1 citedOpen Access

Impact of the expanded label for elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with no F508del variant in the USA

13 cited

European Respiratory Journal·2024· 13 citedOpen Access

430 Association between socioeconomic status and in-hospital healthcare use and cost for children with CF

Journal of Cystic Fibrosis·2024

Impact of day-to-day variation in FEV1 on measures of change: A conceptual description

5 cited

Journal of Cystic Fibrosis·2024· 5 citedOpen Access

Characteristics of individuals with cystic fibrosis in the United States ineligible for ivacaftor and elexacaftor/tezacaftor/ivacaftor

9 cited

Journal of Cystic Fibrosis·2024· 9 citedOpen Access

Treatment of small as well as large declines in lung function enhances recovery to baseline in people with CF

3 cited

Pediatric Pulmonology·2024· 3 citedOpen Access

Forced Expiratory Volume in 1 Second Variability Predicts Lung Transplant or Mortality in People with Cystic Fibrosis in the United States

2 cited

Annals of the American Thoracic Society·2024· 2 cited

Impact of Treating Small and Large Declines in Lung Function in Cystic Fibrosis

2024Open Access

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Frequent Co-authors

Paul M. Emerson(17), Jonathan D. King(15), Jeremiah Ngondi(13), David M. Pigott(8), Kebede Deribe(7), Simon I Hay(6), Tesfaye Teferi(6), Elex Hill(5), Teshome Gebre(5), Aryc W. Mosher(5), Jalal Arabloo(4), Till Bärnighausen(4), Krittika Bhattacharyya(4), Ali Bijani(4), Zahid A Butt(4), Daniel Díaz(4), Irena Ilić(4), Milena Ilić(4), Seyed Sina Naghibi Irvani(4), Chris A. Schmidt(4)