Professor

Scott Bell

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Availability

Professor Scott Bell is:
Available for supervision

Fields of research

Clinical sciences Medical microbiology

Search Professor Scott Bell’s works on UQ eSpace

411 works between 1991 and 2025
All (411) Journal Article (292) Book Chapter (6) Conference Publication (109) Other Outputs (4)

101 - 120 of 411 works

2018

Journal Article

Defining antimicrobial resistance in cystic fibrosis

Kidd, Timothy J., Canton, Rafael, Ekkelenkamp, Miquel, Johansen, Helle Krogh, Gilligan, Peter, LiPuma, John J., Bell, Scott C., Elborn, J. Stuart, Flume, Patrick A., VanDevanter, Donald R. and Waters, Valerie J. (2018). Defining antimicrobial resistance in cystic fibrosis. Journal of Cystic Fibrosis, 17 (6), 696-704. doi: 10.1016/j.jcf.2018.08.014

Defining antimicrobial resistance in cystic fibrosis

2018

Journal Article

Antimicrobial resistance in cystic fibrosis: Does it matter?

Flume, Patrick A., Waters, Valerie J., Bell, Scott C., Van Devanter, Donald R. and Stuart Elborn, J. (2018). Antimicrobial resistance in cystic fibrosis: Does it matter?. Journal of Cystic Fibrosis, 17 (6), 687-689. doi: 10.1016/j.jcf.2018.08.015

Antimicrobial resistance in cystic fibrosis: Does it matter?

2018

Journal Article

Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment

Nagy, Béla, Bene, Zsolt, Fejes, Zsolt, Heltshe, Sonya L, Reid, David, Ronan, Nicola J, McCarthy, Yvonne, Smith, Daniel, Nagy, Attila, Joseloff, Elizabeth, Balla, György, Kappelmayer, János, Macek, Milan, Bell, Scott C, Plant, Barry J, Amaral, Margarida D and Balogh, István (2018). Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment. Journal of Cystic Fibrosis, 18 (2), 271-277. doi: 10.1016/j.jcf.2018.08.013

Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment

2018

Journal Article

Work environment risks for health care workers with cystic fibrosis

Bell, Scott C., Armstrong, David, Harrington, Glenys, Jardine, Luke, Divakaran, Rebekah, Loff, Bebe, Middleton, Peter G., McDonald, Tim, Rowland, Karen, Wishart, Michael, Wood, Michelle E. and Stuart, Rhonda L. (2018). Work environment risks for health care workers with cystic fibrosis. Respirology, 23 (12), 1190-1197. doi: 10.1111/resp.13404

Work environment risks for health care workers with cystic fibrosis

2018

Conference Publication

PREVALENCE OF SHARED <i>MYCOBACTERIUM ABSCESSUS</i> COMPLEX IN THE QUEENSLAND CYSTIC FIBROSIS POPULATION

Stockwell, R. E., Leong, L., Wheeler, N., Bryant, J., Wood, M. E., Sherrard, L., Thomson, R., Rogers, G., Wainwright, C., Parkhill, J., Floto, R. A. and Bell, S. C. (2018). PREVALENCE OF SHARED MYCOBACTERIUM ABSCESSUS COMPLEX IN THE QUEENSLAND CYSTIC FIBROSIS POPULATION. HOBOKEN: WILEY.

PREVALENCE OF SHARED <i>MYCOBACTERIUM ABSCESSUS</i> COMPLEX IN THE QUEENSLAND CYSTIC FIBROSIS POPULATION

2018

Journal Article

Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre

Wee, Bryan A., Tai, Anna S., Sherrard, Laura J., Ben Zakour, Nouri L., Hanks, Kirt R., Kidd, Timothy J., Ramsay, Kay A., Lamont, Iain, Whiley, David M., Bell, Scott C. and Beatson, Scott A. (2018). Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre. BMC Genomics, 19 (1) 644, 644. doi: 10.1186/s12864-018-5018-x

Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre

2018

Journal Article

Face Masks Reduce the Release of Pseudomonas aeruginosa Cough Aerosols when Worn for Clinically-Relevant Time Periods

Stockwell, Rebecca E., Wood, Michelle E., He, Congrong, Sherrard, Laura J., Ballard, Emma L., Kidd, Timothy J., Johnson, Graham R., Knibbs, Luke D., Morawska, Lidia, Bell, Scott C., CF Cough Aerosol Group and Duplancic, Christine (2018). Face Masks Reduce the Release of Pseudomonas aeruginosa Cough Aerosols when Worn for Clinically-Relevant Time Periods. American Journal of Respiratory and Critical Care Medicine, 198 (10) rccm.201805-0823LE, 1339-1342. doi: 10.1164/rccm.201805-0823LE

Face Masks Reduce the Release of Pseudomonas aeruginosa Cough Aerosols when Worn for Clinically-Relevant Time Periods

2018

Journal Article

Transcriptomic analysis of longitudinal Burkholderia pseudomallei infecting the cystic fibrosis lung

Price, Erin P., Viberg, Linda T., Kidd, Timothy J., Bell, Scott C., Currie, Bart J. and Sarovich, Derek S. (2018). Transcriptomic analysis of longitudinal Burkholderia pseudomallei infecting the cystic fibrosis lung. Microbial Genomics, 4 (8) 000194. doi: 10.1099/mgen.0.000194

Transcriptomic analysis of longitudinal Burkholderia pseudomallei infecting the cystic fibrosis lung

2018

Journal Article

Anomalies in T cell function are associated with individuals at risk of Mycobacterium abscessus complex infection

Lutzky, Viviana P., Ratnatunga, Champa N., Smith, Daniel J., Kupz, Andreas, Doolan, Denise L., Reid, David W., Thomson, Rachel M., Bell, Scott C. and Miles, John J. (2018). Anomalies in T cell function are associated with individuals at risk of Mycobacterium abscessus complex infection. Frontiers in Immunology, 9 (June) 1319, 1319. doi: 10.3389/fimmu.2018.01319

Anomalies in T cell function are associated with individuals at risk of Mycobacterium abscessus complex infection

2018

Journal Article

Optimism, opportunities, outcomes: the Australian Cystic Fibrosis Data Registry

Ahern, Susannah, Sims, Geoff, Earnest, Arul and Bell, Scott C. (2018). Optimism, opportunities, outcomes: the Australian Cystic Fibrosis Data Registry. Internal Medicine Journal, 48 (6), 721-723. doi: 10.1111/imj.13807

Optimism, opportunities, outcomes: the Australian Cystic Fibrosis Data Registry

2018

Journal Article

Biomarkers: their role in CFTR modulator therapies from early development to the clinic

Bell, Scott C. and Wood, Michelle E. (2018). Biomarkers: their role in CFTR modulator therapies from early development to the clinic. American Journal of Respiratory and Critical Care Medicine, 197 (11), 1375-1376. doi: 10.1164/rccm.201801-0177ED

Biomarkers: their role in CFTR modulator therapies from early development to the clinic

2018

Journal Article

Inhaled corticosteroids for bronchiectasis (review)

Kapur, Nitin, Petsky, Helen L., Bell, Scott, Kolbe, John and Chang, Anne B. (2018). Inhaled corticosteroids for bronchiectasis (review). Cochrane Database of Systematic Reviews, 2018 (5) CD000996. doi: 10.1002/14651858.CD000996.pub3

Inhaled corticosteroids for bronchiectasis (review)

2018

Journal Article

Bronchiectasis: yet another systemic disease?

Geake, James and Bell, Scott C. (2018). Bronchiectasis: yet another systemic disease?. Respirology, 23 (9), 797-798. doi: 10.1111/resp.13322

Bronchiectasis: yet another systemic disease?

2018

Journal Article

Cystic fibrosis pathogens survive for extended periods within cough-generated droplet nuclei

Wood, Michelle E., Stockwell, Rebecca E., Johnson, Graham R., Ramsay, Kay A., Sherrard, Laura J., Kidd, Timothy J., Cheney, Joyce, Ballard, Emma L., O'Rourke, Peter, Jabbour, Nassib, Wainwright, Claire E., Knibbs, Luke D., Sly, Peter D., Morawska, Lidia and Bell, Scott C. (2018). Cystic fibrosis pathogens survive for extended periods within cough-generated droplet nuclei. Thorax, 74 (1), thoraxjnl-2018. doi: 10.1136/thoraxjnl-2018-211567

Cystic fibrosis pathogens survive for extended periods within cough-generated droplet nuclei

2018

Journal Article

The experience of men and women with cystic fibrosis who have become a parent: a qualitative study

Jessup, Melanie, Li, Anne, Fulbrook, Paul and Bell, Scott (2018). The experience of men and women with cystic fibrosis who have become a parent: a qualitative study. Journal of Clinical Nursing, 27 (7-8), 1702-1712. doi: 10.1111/jocn.14229

The experience of men and women with cystic fibrosis who have become a parent: a qualitative study

2018

Other Outputs

Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre

Wee, Bryan A., Tai, Anna S., Sherrard, Laura J., Zakour, Nouri L. Ben, Hanks, Kirt R., Kidd, Timothy J., Ramsay, Kay A., Lamont, Iain, Whiley, David M., Bell, Scott C. and Beatson, Scott A. (2018). Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre. doi: 10.1101/261586

Whole genome sequencing reveals the emergence of a Pseudomonas aeruginosa shared strain sub-lineage among patients treated within a single cystic fibrosis centre

2018

Journal Article

ECFS best practice guidelines: the 2018 revision

Castellani, Carlo, Duff, Alistair J. A., Bell, Scott C., Heijerman, Harry G. M., Munck, Anne, Ratjen, Felix, Sermet-Gaudelus, Isabelle, Southern, Kevin W., Barben, Jurg, Flume, Patrick A., Hodková, Pavla, Kashirskaya, Nataliya, Kirszenbaum, Maya N., Madge, Sue, Oxley, Helen, Plant, Barry, Schwarzenberg, Sarah Jane, Smyth, Alan R., Taccetti, Giovanni, Wagner, Thomas O. F., Wolfe, Susan P. and Drevinek, Pavel (2018). ECFS best practice guidelines: the 2018 revision. Journal of Cystic Fibrosis, 17 (2), 153-178. doi: 10.1016/j.jcf.2018.02.006

ECFS best practice guidelines: the 2018 revision

2018

Journal Article

Face masks and cough etiquette reduce the cough aerosol concentration of Pseudomonas aeruginosa in people with cystic fibrosis

Wood, Michelle E., Stockwell, Rebecca E., Johnson, Graham R., Ramsay, Kay A., Sherrard, Laura J., Jabbour, Nassib, Ballard, Emma, O'Rourke, Peter, Kidd, Timothy J., Wainwright, Claire E., Knibbs, Luke D., Sly, Peter D., Morawska, Lidia and Bell, Scott C. (2018). Face masks and cough etiquette reduce the cough aerosol concentration of Pseudomonas aeruginosa in people with cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 197 (3), 338-355. doi: 10.1164/rccm.201707-1457OC

Face masks and cough etiquette reduce the cough aerosol concentration of Pseudomonas aeruginosa in people with cystic fibrosis

2018

Conference Publication

Infection control in Australian and New Zealand cystic fibrosis centres

Stockwell, R., Wood, M., Moore, V and Bell, S. (2018). Infection control in Australian and New Zealand cystic fibrosis centres. ANZSRS/TSANZ Annual Scientific Meeting, Adelaide, Australia, 23-27 March 2018. Richmond, VIC, Australia: Wiley-Blackwell.

Infection control in Australian and New Zealand cystic fibrosis centres

2018

Journal Article

How many days are enough?: capturing routine human mobility

Stanley, Kevin, Yoo, Eun-Hye, Paul, Tuhin and Bell, Scott (2018). How many days are enough?: capturing routine human mobility. International Journal of Geographical Information Science, 32 (7), 1485-1504. doi: 10.1080/13658816.2018.1434888

How many days are enough?: capturing routine human mobility

Current funding

  • 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

  • Doctor Philosophy

    Risk and mitigation of cough aerosols for people with cystic fibrosis.

    Principal Advisor

    Other advisors: Professor Rachel Thomson

  • Doctor Philosophy

    Risk and mitigation of cough aerosols for people with cystic fibrosis.

    Principal Advisor

    Other advisors: Professor Rachel Thomson

  • Doctor Philosophy

    Pharmacokinetics of anti-mycobacterial drugs in patients with cystic fibrosis

    Associate Advisor

    Other advisors: Professor Rachel Thomson, Professor Jason Roberts

Completed supervision

Enquiries

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