Professor

Scott Bell

Email: 

Availability

Professor Scott Bell is:
Available for supervision

Fields of research

Clinical sciences Medical microbiology

Search Professor Scott Bell’s works on UQ eSpace

410 works between 1991 and 2025
All (410) Journal Article (295) Book Chapter (6) Conference Publication (109)

161 - 180 of 410 works

2015

Journal Article

A new phase of CFTR treatment for cystic fibrosis?

Bell, Scott C. (2015). A new phase of CFTR treatment for cystic fibrosis?. The Lancet Respiratory Medicine, 3 (9) 203, 662-663. doi: 10.1016/S2213-2600(15)00282-9

A new phase of CFTR treatment for cystic fibrosis?

2015

Journal Article

The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: a cross-sectional analysis

Kidd, Timothy J., Magalhaes, Ricardo J. Soares, Paynter, Stuart and Bell, Scott C. (2015). The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: a cross-sectional analysis. The Lancet Respiratory Medicine, 3 (8), 640-650. doi: 10.1016/S2213-2600(15)00228-3

The social network of cystic fibrosis centre care and shared Pseudomonas aeruginosa strain infection: a cross-sectional analysis

2015

Journal Article

Burkholderia stagnalis sp. nov. and Burkholderia territorii sp. nov., two novel Burkholderia cepacia complex species from environmental and human sources

De Smet, Birgit., Mayo, Mark., Peeters, Charlotte., Zlosnik, James E.A., Spilker, Theodore., Hird, Trevor J., Li Puma, John J., Kidd, Timothy J., Kaestli, Mirjam., Ginther, Jennifer L., Wagner, David M., Keim, Paul., Bell, Scott C., Jacobs, Jan A., Currie, Bart J. and Vandamme, Peter. (2015). Burkholderia stagnalis sp. nov. and Burkholderia territorii sp. nov., two novel Burkholderia cepacia complex species from environmental and human sources. International Journal of Systematic and Evolutionary Microbiology, 65 (7), 2265-2271. doi: 10.1099/ijs.0.000251

Burkholderia stagnalis sp. nov. and Burkholderia territorii sp. nov., two novel Burkholderia cepacia complex species from environmental and human sources

2015

Journal Article

Cystic fibrosis

Ratjen, Felix, Bell, Scott C., Rowe, Steven M., Goss, Christopher H., Quittner, Alexandra L. and Bush, Andrew (2015). Cystic fibrosis. Nature Reviews. Disease Primers, 1 (1) 15010 . doi: 10.1038/nrdp.2015.10

Cystic fibrosis

2015

Journal Article

Idiosyncratic reactions are the most common cause of abnormal liver function tests in patients with cystic fibrosis

Jong, T., Geake, J., Yerkovich, S. and Bell, S. C. (2015). Idiosyncratic reactions are the most common cause of abnormal liver function tests in patients with cystic fibrosis. Internal Medicine Journal, 45 (4), 395-401. doi: 10.1111/imj.12707

Idiosyncratic reactions are the most common cause of abnormal liver function tests in patients with cystic fibrosis

2015

Journal Article

Evaluation of phenotypic screening tests for carbapenemase production in Pseudomonas aeruginosa from patients with cystic fibrosis

Tai, Anna S., Sidjabat, Hanna E., Kidd, Timothy J., Whiley, David M., Paterson, David L. and Bell, Scott C. (2015). Evaluation of phenotypic screening tests for carbapenemase production in Pseudomonas aeruginosa from patients with cystic fibrosis. Journal of Microbiological Methods, 111, 105-107. doi: 10.1016/j.mimet.2015.02.006

Evaluation of phenotypic screening tests for carbapenemase production in Pseudomonas aeruginosa from patients with cystic fibrosis

2015

Journal Article

Whole-genome sequences of five Burkholderia pseudomallei isolates from australian cystic fibrosis patients

Viberg, Linda T., Price, Erin P., Kidd, Timothy J., Bell, Scott C., Currie, Bart J. and Sarovich, Derek S. (2015). Whole-genome sequences of five Burkholderia pseudomallei isolates from australian cystic fibrosis patients. Genome Announcements, 3 (2) e00254-15. doi: 10.1128/genomeA.00254-15

Whole-genome sequences of five Burkholderia pseudomallei isolates from australian cystic fibrosis patients

2015

Journal Article

Molecular surveillance for carbapenemase genes in carbapenem-resistant Pseudomonas aeruginosa in Australian patients with cystic fibrosis

Tai, Anna S., Kidd, Timothy J., Whiley, David M., Ramsay, Kay A., Buckley, Cameron, Bell, Scott C., The ACPinCF Investigator Group and David, Michael (2015). Molecular surveillance for carbapenemase genes in carbapenem-resistant Pseudomonas aeruginosa in Australian patients with cystic fibrosis. Pathology, 47 (2), 156-160. doi: 10.1097/PAT.0000000000000216

Molecular surveillance for carbapenemase genes in carbapenem-resistant Pseudomonas aeruginosa in Australian patients with cystic fibrosis

2015

Journal Article

Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand

Chang, Anne B., Bell, Scott C., Torzillo, Paul J., King, Paul T., Maguire, Graeme P., Byrnes, Catherine A., Holland, Anne E., O’Mara, Peter, Grimwood, Keith, Alison, Jenny, Cull, Chris, Currie, Bart, Gardner, Inge, Holmes, Peter, Hunter, Cameron, Kolbe, John, Maclennan, Carolyn, McDonald, Malcolm, Morris, Peter, Nicolson, Caroline, Petsky, Helen, Pillarisetti, Naveen, Reynolds, Emma, Serisier, David, Thein, Frank, van Asperen, Peter, Voss, Lesley and Wong, Conroy (2015). Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand. Medical Journal of Australia, 202 (1), 21-24. doi: 10.5694/mja14.00287

Chronic suppurative lung disease and bronchiectasis in children and adults in Australia and New Zealand

2015

Journal Article

Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years

Kidd, Timothy J., Ramsay, Kay A., Vidmar, Suzanna, Carlin, John B., Bell, Scott C., Wainwright, Claire E. and Grimwood, Keith (2015). Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years. Journal of Cystic Fibrosis, 14 (3), 361-369. doi: 10.1016/j.jcf.2014.12.007

Pseudomonas aeruginosa genotypes acquired by children with cystic fibrosis by age 5-years

2015

Journal Article

Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: A randomised trial

Dwyer, Tiffany J., Robbins, Lisel, Kelly, Patrick, Piper, Amanda J., Bell, Scott C. and Bye, Peter T.P. (2015). Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: A randomised trial. Journal of Physiotherapy, 61 (3), 142-147. doi: 10.1016/j.jphys.2015.05.019

Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: A randomised trial

2015

Journal Article

Future trends in cystic fibrosis demography in 34 European countries

Burgel, Pierre-Régis, Bellis, Gil, Olesen, Hanne V., Viviani, Laura, Zolin, Anna, Blasi, Francesco, Elborn, J. Stuart, Bell, Scott, Castellani, Carlo, Dembski, Birgit, Drevinek, Pavel, Heijerman, Harry, Innes, Alastair, Lindblad, Anders, Madge, Susan, De Rijcke, Karleen and Solé, Amparo (2015). Future trends in cystic fibrosis demography in 34 European countries. European Respiratory Journal, 46 (1), 133-141. doi: 10.1183/09031936.00196314

Future trends in cystic fibrosis demography in 34 European countries

2015

Journal Article

New pharmacological approaches for cystic fibrosis: Promises, progress, pitfalls

Bell, S.C., De Boeck, K. and Amaral, M.D. (2015). New pharmacological approaches for cystic fibrosis: Promises, progress, pitfalls. Pharmacology and Therapeutics, 145, 19-34. doi: 10.1016/j.pharmthera.2014.06.005

New pharmacological approaches for cystic fibrosis: Promises, progress, pitfalls

2015

Journal Article

A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients

Stuart Elborn, J., Geller, David E., Conrad, Douglas, Aaron, Shawn D., Smyth, Alan R., Fischer, Rainald, Kerem, Eitan, Bell, Scott C., Loutit, Jeffery S., Dudley, Michael N., Morgan, Elizabeth E., VanDevanter, Donald R. and Flume, Patrick A. (2015). A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients. Journal of Cystic Fibrosis, 14 (4), 507-514. doi: 10.1016/j.jcf.2014.12.013

A phase 3, open-label, randomized trial to evaluate the safety and efficacy of levofloxacin inhalation solution (APT-1026) versus tobramycin inhalation solution in stable cystic fibrosis patients

2014

Journal Article

JCF - 2014 and beyond

Bell, Scott C., Heijerman, Harry and Hartl, Dominik (2014). JCF - 2014 and beyond. Journal of Cystic Fibrosis, 13 (6), 610-611. doi: 10.1016/j.jcf.2014.09.009

JCF - 2014 and beyond

2014

Journal Article

Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis

Smith, Daniel J., Hill, Geoffrey R., Bell, Scott C. and Reid, David W. (2014). Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis. PLoS ONE, 9 (10) e109891, 1-8. doi: 10.1371/journal.pone.0109891

Reduced mucosal associated invariant T-cells are associated with increased disease severity and Pseudomonas aeruginosa infection in cystic fibrosis

2014

Journal Article

Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics

Smith, Daniel J., Badrick, Alison C., Zakrzewski, Martha, Krause, Lutz, Bell, Scott C., Anderson, Gregory J. and Reid, David W. (2014). Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics. European Respiratory Journal, 44 (4), 922-930. doi: 10.1183/09031936.00203013

Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics

2014

Journal Article

Antimicrobial treatment of non-cystic fibrosis bronchiectasis

Grimwood, K., Bell, S.C. and Chang, A.B. (2014). Antimicrobial treatment of non-cystic fibrosis bronchiectasis. Expert Review of Anti-Infective Therapy, 12 (10), 1277-1296. doi: 10.1586/14787210.2014.952282

Antimicrobial treatment of non-cystic fibrosis bronchiectasis

2014

Journal Article

Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis

Knibbs, Luke D., Johnson, Graham R., Kidd, Timothy J., Cheney, Joyce, Grimwood, Keith, Kattenbelt, Jacqueline A., O'Rourke, Peter K., Ramsay, Kay A., Sly, Peter D., Wainwright, Claire E., Wood, Michelle E., Morawska, Lidia and Bell, Scott C. (2014). Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis. Thorax, 69 (8), 740-745. doi: 10.1136/thoraxjnl-2014-205213

Viability of Pseudomonas aeruginosa in cough aerosols generated by persons with cystic fibrosis

2014

Journal Article

A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis

Syrmis, Melanie W., Kidd, Timothy J., Moser, Ralf J., Ramsay, Kay A., Gibson, Kristen M., Anuj, Snehal, Bell, Scott C., Wainwright, Claire E., Grimwood, Keith, Nissen, Michael, Sloots, Theo P. and Whiley, David M. (2014). A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis. BMC Infectious Diseases, 14 (1) 307, 307.1-307.8. doi: 10.1186/1471-2334-14-307

A comparison of two informative SNP-based strategies for typing Pseudomonas aeruginosa isolates from patients with cystic fibrosis

Current funding

  • 2025 - 2028
    Combating pathogens from biofilms in premise plumbing systems
    ARC Linkage Projects
    Open grant
  • 2023 - 2026
    Making Australia resilient to airborne infection transmission (ARC Linkage Project administered by Queensland University of Technology)
    Queensland University of Technology
    Open grant
  • 2019 - 2025
    Finding the Optimal Regimen for Mycobacterium Abscessus Treatment (FORMAT)
    Cystic Fibrosis Foundation USA
    Open grant
  • 2019 - 2025
    Queensland cystic fibrosis research program
    The Children's Hospital Foundation
    Open grant
  • 2018 - 2025
    Multi-drug resistant non-tuberculous mycobacteria infection research
    Research Donation Generic
    Open grant

Past funding

  • 2021 - 2023
    Prevention of SARS-CoV-2 transmission in aged care (PETRA formerly PreSTAC): Effective evidence-based measures for rapid translation - External led SAHMRI
    South Australian Health and Medical Research Institute Limited
    Open grant
  • 2020
    BD Bactec MGIT 320 System
    Prince Charles Hospital Foundation
    Open grant
  • 2020 - 2023
    The emerging problem of non-tuberculous mycobacteria infection: Understanding aetiology, geospatial epidemiology and developing interventions
    NHMRC Project Grant
    Open grant
  • 2019 - 2024
    Early life origins of cystic fibrosis lung disease
    Cystic Fibrosis Foundation USA
    Open grant
  • 2019
    Establishing UQ Centre for Clinical Research as the centre for Aerosol therapy in critical care by optimising particle size of aerosols for effective drug delivery.
    UQ Major Equipment and Infrastructure
    Open grant
  • 2018 - 2021
    Enhancing detection and management of Mycobacterium abscessus complex (MABSC) infection in children with cystic fibrosis
    The Children's Hospital Foundation
    Open grant
  • 2016 - 2019
    Macrophages: the forgotten cells in CF lung disease
    Cystic Fibrosis Foundation Therapeutics Inc
    Open grant
  • 2016 - 2020
    The acquired resistome of Pseudomonas aeruginosa strains in people with cystic fibrosis (Joint UQ/QIMR AID seed grant awarded to QIMRB)
    Queensland Institute of Medical Research
    Open grant
  • 2016 - 2019
    The emerging problem of non-tuberculous mycobacteria infection: understanding aetiology, geospatial epidemiology and developing interventions (NHMRC Project led by QIMR Berghofer)
    Queensland Institute of Medical Research
    Open grant
  • 2015 - 2017
    Abnormal lung iron homeostasis in cystic fibrosis (NHMRC Project Grant administered by QIMR)
    Queensland Institute of Medical Research
    Open grant
  • 2014 - 2016
    Intra-strain diversity of Pseudomonas aeruginosa in the lungs of patients with CF and their role in exacerbation
    Prince Charles Hospital Foundation
    Open grant
  • 2013 - 2014
    Purchase of -80C Freezer - XYCYST
    Prince Charles Hospital Foundation
    Open grant
  • 2012 - 2014
    Airborne Infection Transport in Hospitals
    Prince Charles Hospital Foundation
    Open grant
  • 2010 - 2016
    Inflammatory airways disease in children with a focus on cystic fibrosis
    Royal Children's Hospital Foundation
    Open grant
  • 2010 - 2011
    Longitudinal study of clonal Pseudomonas aeruginosa in cystic fibrosis
    Queensland Health
    Open grant
  • 2010 - 2011
    Development of a novel assay for the detection of clonal P.aeruginosa in persons with CF
    Australian Cystic Fibrosis Research Trust
    Open grant
  • 2010 - 2011
    Longitudinal study of clonal Pseudomonas aeruginosa in cystic fibrosis
    Royal Children's Hospital Foundation
    Open grant
  • 2009 - 2015
    A statewide, electronic, disease specific, clinical record/database for children and adults with cystic fibrosis (electronic medical record for cystic fibrosis)
    Royal Children's Hospital Foundation
    Open grant
  • 2007 - 2010
    Clinical impact of clonal Pseudomonas aeruginosa in cystic fibrosis
    NHMRC Project Grant
    Open grant
  • 2005 - 2010
    How Children and adults with cystic fibrosis get lung infections with Pseudomonas aeruginosa
    Royal Children's Hospital Foundation
    Open grant

Availability

Professor Scott Bell is:
Available for supervision

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Supervision history

Current supervision

Completed supervision

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