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Claire E. Wainwright

Claire E. Wainwright

D-Index & Metrics

Biology and Biochemistry

D-Index
53
Citations
14470
World Ranking
15966
National Ranking
446

Overview

Claire E. Wainwright is affiliated with the University of Queensland in Australia and has a research focus primarily within the field of Medicine, with significant contributions to Pulmonary and Respiratory Medicine.

The scientist's work has extensively covered various subfields including Epidemiology, Emergency Medical Services, Infectious Diseases, and Molecular Biology. Their research topics span several areas such as Cystic Fibrosis Research Advances, Neonatal Respiratory Health Research, Tracheal and Airway Disorders, Mycobacterium Research and Diagnosis, Pediatric Health and Respiratory Diseases, Respiratory Viral Infections Research, and Tuberculosis Research and Epidemiology.

Frequent publication venues for their work include:

  • Journal of Cystic Fibrosis
  • American Journal of Respiratory and Critical Care Medicine
  • The Lancet Respiratory Medicine
  • SSRN Electronic Journal
  • Scientific Reports

Their recent papers include:

  • A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele, 2021, American Journal of Respiratory and Critical Care Medicine
  • Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for F508del and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study, 2022, American Journal of Respiratory and Critical Care Medicine
  • Ivacaftor in Infants Aged 4 to <12 Months with Cystic Fibrosis and a Gating Mutation. Results of a Two-Part Phase 3 Clinical Trial, 2020, American Journal of Respiratory and Critical Care Medicine
  • Nebulised hypertonic saline solution for acute bronchiolitis in infants, 2023, Cochrane Database of Systematic Reviews
  • A phase 3, double-blind, parallel-group study to evaluate the efficacy and safety of tezacaftor in combination with ivacaftor in participants 6 through 11 years of age with cystic fibrosis homozygous for F508del or heterozygous for the F508del-CFTR mutation and a residual function mutation, 2020, Journal of Cystic Fibrosis

Collaborators frequently working alongside Claire E. Wainwright include:

  • Scott C. Bell
  • Peter D. Sly
  • Jane C. Davies
  • Keith Grimwood
  • Neil Ahluwalia

Best Publications

  • A CFTR potentiator in patients with cystic fibrosis and the G551D mutation

    Bonnie W. Ramsey;Jane Davies;N. Gerard McElvaney;Elizabeth Tullis

  • Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium.

    Josephine M Bryant;Josephine M Bryant;Dorothy M Grogono;Dorothy M Grogono;Daniela Rodriguez-Rincon;Isobel Everall

  • Efficacy and Safety of Ivacaftor in Patients Aged 6 to 11 Years with Cystic Fibrosis with a G551D Mutation

    Jane C. Davies;Jane C. Davies;Claire E. Wainwright;Gerard J. Canny;Mark A. Chilvers

  • Determination of the Minimal Clinically Important Difference Scores for the Cystic Fibrosis Questionnaire-Revised Respiratory Symptom Scale in Two Populations of Patients With Cystic Fibrosis and Chronic Pseudomonas aeruginosa Airway Infection

    Alexandra L. Quittner;Avani C. Modi;Claire Wainwright;Kelly Otto

  • A multicenter, randomized, double-blind, controlled trial of nebulized epinephrine in infants with acute bronchiolitis.

    Claire Wainwright;Luis Altamirano;Marise Cheney;Joyce Cheney

  • Genetic modifiers of liver disease in cystic fibrosis.

    Jaclyn R. Bartlett;Kenneth J. Friedman;Simon C. Ling;Rhonda G. Pace

  • Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study

    Margaret Rosenfeld;Claire E Wainwright;Mark Higgins;Linda T Wang

  • Long-term safety and efficacy of ivacaftor in patients with cystic fibrosis who have the Gly551Asp-CFTR mutation: a phase 3, open-label extension study (PERSIST)

    Edward F McKone;Drucy Borowitz;Pavel Drevinek;Matthias Griese;Matthias Griese

  • Drivers of seedling establishment success in dryland restoration efforts.

    Nancy Shackelford;Nancy Shackelford;Gustavo B. Paterno;Gustavo B. Paterno;Daniel E. Winkler;Todd E. Erickson

  • Effect of bronchoalveolar lavage-directed therapy on Pseudomonas aeruginosa infection and structural lung injury in children with cystic fibrosis: A randomized trial

    Claire E. Wainwright;Suzanna Vidmar;David S. Armstrong;Catherine A. Byrnes

  • A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele.

    Edith T. Zemanick;Jennifer L. Taylor-Cousar;Jane Davies;Ronald L. Gibson

  • Seasonal priority effects: implications for invasion and restoration in a semi-arid system.

    Claire E. Wainwright;Elizabeth M. Wolkovich;Elsa E. Cleland

  • Rapid genotyping of Pseudomonas aeruginosa isolates harboured by adult and paediatric patients with cystic fibrosis using repetitive-element-based PCR assays.

    Melanie W Syrmis;Mark R O'Carroll;Theo P Sloots;Chris Coulter

  • Comparison of DNA extraction methods for microbial community profiling with an application to pediatric bronchoalveolar lavage samples.

    Dana Willner;Joshua Daly;David Whiley;David Whiley;Keith Grimwood;Keith Grimwood

  • Cough-generated aerosols of Pseudomonas aeruginosa and other Gram-negative bacteria from patients with cystic fibrosis

    Claire E Wainwright;Peter O'Rourke;Snehal Anuj

  • Acute viral bronchiolitis in children- a very common condition with few therapeutic options

    Claire Wainwright

  • Clonal strains of Pseudomonas aeruginosa in paediatric and adult cystic fibrosis units

    M.R. O'Carroll;M.W. Syrmis;C.E. Wainwright;R.M. Greer

  • Early airway infection, inflammation, and lung function in cystic fibrosis

    G M Nixon;D S Armstrong;R Carzino;J B Carlin

  • Phenotypic Characterization of Clonal and Nonclonal Pseudomonas aeruginosa Strains Isolated from Lungs of Adults with Cystic Fibrosis

    Pholawat Tingpej;Lucas Smith;Barbara Rose;Hua Zhu

  • Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium

    J. M. Bryant;D. M. Grogono;D. Rodriguez-Rincon;I. Everall

Frequent Co-Authors

Scott C. Bell
Scott C. Bell University of Queensland
Keith Grimwood
Keith Grimwood Griffith University
Peter D. Sly
Peter D. Sly University of Queensland
Michael D. Nissen
Michael D. Nissen University of Queensland
John B. Carlin
John B. Carlin University of Melbourne
Theo P. Sloots
Theo P. Sloots University of Queensland
Colin F. Robertson
Colin F. Robertson Royal Children's Hospital
Luke D. Knibbs
Luke D. Knibbs University of Sydney
David M. Whiley
David M. Whiley University of Queensland
Lidia Morawska
Lidia Morawska Queensland University of Technology

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