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2020

Journal Article

A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis

Cosgriff, Rebecca, Ahern, Susannah, Bell, Scott C., Brownlee, Keith, Burgel, Pierre-Régis, Byrnes, Cass, Corvol, Harriet, Cheng, Stephanie Y., Elbert, Alexander, Faro, Albert, Goss, Christopher H., Gulmans, Vincent, Marshall, Bruce C., McKone, Edward, Middleton, Peter G., Ruseckaite, Rasa, Stephenson, Anne L. and Carr, Siobhán B (2020). A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis. Journal of Cystic Fibrosis, 19 (3), 355-358. doi: 10.1016/j.jcf.2020.04.012

A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis

2020

Journal Article

Seven P's of publication practices

Bell, Scott C., Flume, Patrick A. and Castellani, Carlo (2020). Seven P's of publication practices. Journal of Cystic Fibrosis, 19 (3), 333-335. doi: 10.1016/j.jcf.2020.02.007

Seven P's of publication practices

2020

Journal Article

Pathogen to commensal? Longitudinal within-host population dynamics, evolution, and adaptation during a chronic >16-year Burkholderia pseudomallei infection

Pearson, Talima, Sahl, Jason W., Hepp, Crystal M., Handady, Karthik, Hornstra, Heidie, Vazquez, Adam J., Settles, Erik, Mayo, Mark, Kaestli, Mirjam, Williamson, Charles H. D., Price, Erin P., Sarovich, Derek S., Cook, James M., Wolken, Spenser R., Bowen, Richard A., Tuanyok, Apichai, Foster, Jeffrey T., Drees, Kevin P., Kidd, Timothy J., Bell, Scott C., Currie, Bart J. and Keim, Paul (2020). Pathogen to commensal? Longitudinal within-host population dynamics, evolution, and adaptation during a chronic >16-year Burkholderia pseudomallei infection. PLoS Pathogens, 16 (3) e1008298, e1008298. doi: 10.1371/journal.ppat.1008298

Pathogen to commensal? Longitudinal within-host population dynamics, evolution, and adaptation during a chronic >16-year Burkholderia pseudomallei infection

2020

Journal Article

Finding the relevance of antimicrobial stewardship for cystic fibrosis

Cogen, Jonathan D., Kahl, Barbara C., Maples, Holly, McColley, Susanna A., Roberts, Jason A., Winthrop, Kevin L., Morris, Andrew M., Holmes, Alison, Flume, Patrick A., VanDevanter, Donald R., Waters, Valerie, Muhlebach, Marianne S., Elborn, J. Stuart, Saiman, Lisa and Bell, Scott C. (2020). Finding the relevance of antimicrobial stewardship for cystic fibrosis. Journal of Cystic Fibrosis, 19 (4), 511-520. doi: 10.1016/j.jcf.2020.02.012

Finding the relevance of antimicrobial stewardship for cystic fibrosis

2020

Journal Article

Centralised versus outreach models of cystic fibrosis care should be tailored to the needs of the individual patient

Geake, James, Ballard, Emma, O'Rourke, Peter, Wainwright, Claire E., Reid, David W. and Bell, Scott C. (2020). Centralised versus outreach models of cystic fibrosis care should be tailored to the needs of the individual patient. Internal Medicine Journal, 50 (2), 232-235. doi: 10.1111/imj.14724

Centralised versus outreach models of cystic fibrosis care should be tailored to the needs of the individual patient

2020

Journal Article

Current infection control practices used in Australian and New Zealand cystic fibrosis centers

Stockwell, Rebecca Elizabeth, Wood, Michelle ELizabeth, Ballard, Emma, Moore, Vanessa, Wainwright, Claire Elizabeth and Bell, Scott Cameron (2020). Current infection control practices used in Australian and New Zealand cystic fibrosis centers. BMC Pulmonary Medicine, 20 (1) 16, 16. doi: 10.1186/s12890-020-1052-y

Current infection control practices used in Australian and New Zealand cystic fibrosis centers

2020

Journal Article

The rise of non-tuberculosis mycobacterial lung disease

Ratnatunga, Champa N., Lutzky, Viviana P., Kupz, Andreas, Doolan, Denise L., Reid, David W., Field, Matthew, Bell, Scott C., Thomson, Rachel M. and Miles, John J. (2020). The rise of non-tuberculosis mycobacterial lung disease. Frontiers in Immunology, 11 303, 303. doi: 10.3389/fimmu.2020.00303

The rise of non-tuberculosis mycobacterial lung disease

2020

Journal Article

Building global development strategies for cf therapeutics during a transitional cftr modulator era

Mayer-Hamblett, N., van Koningsbruggen-Rietschel, S., Nichols, D. P., VanDevanter, D. R., Davies, J. C., Lee, T., Durmowicz, A. G., Ratjen, F., Konstan, M. W., Pearson, K., Bell, S. C., Clancy, J. P., Taylor-Cousar, J. L., De Boeck, K., Donaldson, S. H., Downey, D. G., Flume, P. A., Drevinek, P., Goss, C. H., Fajac, I., Magaret, A. S., Quon, B. S., Singleton, S. M., VanDalfsen, J. M. and Retsch-Bogart, G. Z. (2020). Building global development strategies for cf therapeutics during a transitional cftr modulator era. Journal of Cystic Fibrosis, 19 (5), 677-687. doi: 10.1016/j.jcf.2020.05.011

Building global development strategies for cf therapeutics during a transitional cftr modulator era

2019

Journal Article

Genomic and phenotypic comparison of environmental and patient-derived isolates of Pseudomonas aeruginosa suggest that antimicrobial resistance is rare within the environment

Ramsay, Kay A., Wardell, Samuel J. T., Patrick, Wayne M., Brockway, Ben, Reid, David W., Winstanley, Craig, Bell, Scott C. and Lamont, Iain L. (2019). Genomic and phenotypic comparison of environmental and patient-derived isolates of Pseudomonas aeruginosa suggest that antimicrobial resistance is rare within the environment. Journal of Medical Microbiology, 68 (11), 1591-1595. doi: 10.1099/jmm.0.001085

Genomic and phenotypic comparison of environmental and patient-derived isolates of Pseudomonas aeruginosa suggest that antimicrobial resistance is rare within the environment

2019

Journal Article

Disruption in research publishing – the open access revolution

Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2019). Disruption in research publishing – the open access revolution. Journal of Cystic Fibrosis, 18 (6), 747-749. doi: 10.1016/j.jcf.2019.10.024

Disruption in research publishing – the open access revolution

2019

Journal Article

Quantitative real-time PCR assay for the rapid identification of the intrinsically multidrug-resistant bacterial pathogen Stenotrophomonas maltophilia

Fraser, Tamieka A., Bell, Mikaela G., Harris, Patrick N. A., Bell, Scott C., Bergh, Haakon, Thuy-Khanh Nguyen,, Kidd, Timothy J., Nimmo, Graeme R., Sarovich, Derek S. and Price, Erin P. (2019). Quantitative real-time PCR assay for the rapid identification of the intrinsically multidrug-resistant bacterial pathogen Stenotrophomonas maltophilia. Microbial Genomics, 5 (10) 000307. doi: 10.1099/mgen.0.000307

Quantitative real-time PCR assay for the rapid identification of the intrinsically multidrug-resistant bacterial pathogen Stenotrophomonas maltophilia

2019

Journal Article

Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review

Stockwell, Rebecca E., Ballard, Emma L., O’Rourke, Peter, Knibbs, Luke D., Morawska, Lidia and Bell, Scott C. (2019). Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review. Journal of Hospital Infection, 103 (2), 175-184. doi: 10.1016/j.jhin.2019.06.016

Indoor hospital air and the impact of ventilation on bioaerosols: a systematic review

2019

Journal Article

Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trial

Milross, Maree A., Piper, Amanda J., Dwyer, Tiffany J., Wong, Keith, Bell, Scott C., Bye, Peter T. P., Robbins, Lisel, Dobbin, Catherine, Moriarty, Carmel, Willson, G., Norman, M., Regnis, Jeff, Sullivan, Colin, Grunstein, Ron and Douglas, James (2019). Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trial. Respirology, 24 (12) resp.13604, 1191-1197. doi: 10.1111/resp.13604

Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trial

2019

Journal Article

A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopy

Matson, A. G., Bunting, J. P., Kaul, A., Smith, D. J., Stonestreet, J., Herd, K., Hodgson, R. S. and Bell, S. C. (2019). A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopy. BMC Gastroenterology, 19 (1) 89. doi: 10.1186/s12876-019-0979-z

A non-randomised single centre cohort study, comparing standard and modified bowel preparations, in adults with cystic fibrosis requiring colonoscopy

2019

Journal Article

Multi-centre ethics and research governance review can impede non-interventional clinical research

Duplancic, Christine, Crough, Tania, Bell, Scott C., Australian NTM in CF Study Group and Thomson, Rachel (2019). Multi-centre ethics and research governance review can impede non-interventional clinical research. Internal Medicine Journal, 49 (6), 722-728. doi: 10.1111/imj.14158

Multi-centre ethics and research governance review can impede non-interventional clinical research

2019

Journal Article

Mutations in ACTL6B cause neurodevelopmental deficits and epilepsy and lead to loss of dendrites in human neurons

Bell, Scott, Rousseau, Justine, Peng, Huashan, Aouabed, Zahia, Priam, Pierre, Theroux, Jean-Francois, Jefri, Malvin, Tanti, Arnaud, Wu, Hanrong, Kolobova, Ilaria, Silviera, Heika, Manzano-Vargas, Karla, Ehresmann, Sophie, Hamdan, Fadi F., Hettige, Nuwan, Zhang, Xin, Antonyan, Lilit, Nassif, Christina, Ghaloul-Gonzalez, Lina, Sebastian, Jessica, Vockley, Jerry, Begtrup, Amber G., Wentzensen, Ingrid M., Crunk, Amy, Nicholls, Robert D., Herman, Kristin C., Deignan, Joshua L., Al-Hertani, Walla, Efthymiou, Stephanie ... Campeau, Philippe M. (2019). Mutations in ACTL6B cause neurodevelopmental deficits and epilepsy and lead to loss of dendrites in human neurons. American Journal of Human Genetics, 104 (5), 815-834. doi: 10.1016/j.ajhg.2019.03.022

Mutations in ACTL6B cause neurodevelopmental deficits and epilepsy and lead to loss of dendrites in human neurons

2019

Journal Article

Abolition of Pseudomonas aeruginosa AUST-01 from an Australian CF center: Do other strains remain?

Kidd, Timothy J, Grimwood, Keith and Bell, Scott C (2019). Abolition of Pseudomonas aeruginosa AUST-01 from an Australian CF center: Do other strains remain?. Pediatric Pulmonology, 54 (5), 515-516. doi: 10.1002/ppul.24258

Abolition of Pseudomonas aeruginosa AUST-01 from an Australian CF center: Do other strains remain?

2019

Journal Article

Transmission of bacteria in bronchiectasis and chronic obstructive pulmonary disease: Low burden of cough aerosols

Stockwell, Rebecca E., Chin, Melanie, Johnson, Graham R., Wood, Michelle E., Sherrard, Laura J., Ballard, Emma, O'Rourke, Peter, Ramsay, Kay A., Kidd, Timothy J., Jabbour, Nassib, Thomson, Rachel M., Knibbs, Luke D., Morawska, Lidia and Bell, Scott C. (2019). Transmission of bacteria in bronchiectasis and chronic obstructive pulmonary disease: Low burden of cough aerosols. Respirology, 24 (10) resp.13544, 980-987. doi: 10.1111/resp.13544

Transmission of bacteria in bronchiectasis and chronic obstructive pulmonary disease: Low burden of cough aerosols

2019

Journal Article

Differentiation of Human Induced Pluripotent Stem Cells (iPSCs) into an effective model of forebrain neural progenitor cells and mature neurons

Bell, Scott, Hettige, Nuwan C., Silveira, Heika, Peng, Huashan, Wu, Hanrong, Jefri, Malvin, Antonyan, Lilit, Zhang, Ying, Zhang, Xin and Ernst, Carl (2019). Differentiation of Human Induced Pluripotent Stem Cells (iPSCs) into an effective model of forebrain neural progenitor cells and mature neurons. Bio-Protocol, 9 (5) e3188, 1-18. doi: 10.21769/BioProtoc.3188

Differentiation of Human Induced Pluripotent Stem Cells (iPSCs) into an effective model of forebrain neural progenitor cells and mature neurons

2019

Journal Article

Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosis

Smith, Daniel J., Klein, Kerenaftali, Hartel, Gunter, Wainwright, Claire E., Bell, Scott C., Anderson, Gregory J. and Reid, David W. (2019). Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosis. Gene, 683, 12-17. doi: 10.1016/j.gene.2018.10.002

Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosis