1. Palmas K, Shanthikumar S, Robinson P. Assessment of Primary Ciliary Dyskinesia Predictive tools. ERJ accepted June 2020.

2. Kapur N, Nixon G, Robinson P, Massie RJ, Prentice B, Wilson A, Schilling S, Twiss J, Fitzgerald DA. Respiratory Management of Infants with Chronic Neonatal Lung Disease. A position statement from the Thoracic Society of Australia and New Zealand. Respirology Accepted May 2020.

3. Robinson P. Mucociliary clearance of the airway: More than hypersecretion of mucous. Ped Pulmonology 2019. 54 (10) 1495. DOI: 10.1002/ppul.24376

4. Breuer O, Schultz A, Turkovic L, de Klerk N, Keil AD, Brennan S, Harrison J, Robertson C, Robinson P, Sly PD, Ranganathan S, Stick SM, Caudri D. Changing prevalence of lower airway infections in young children with cystic fibrosis. Am J Respir Crit Care Med 2019;200:590–599.

5. Shoemark A, Rubbo B,  Haarman E, Hirst R, Hogg C, Jackson C,  Nielsen K, Papon J,  Robinson P, Walker W, Lucas J. The Controversies and Difficulties of Diagnosing Primary Ciliary Dyskinesia (PCD). American Journal of Respiratory and Critical Care Medicine. Published on line August 21 2019 https://doi.org/10.1164/rccm.201907-1334LE 

6. Altered airway ciliary orientation in patients with X-linked retinitis pigmentosa. McCray G, Griffin P, Martinello P, de Iongh R, Ruddle J, Robinson P. Thorax 2019;74:914–916. doi:10.1136/thoraxjnl-2018-212584

7. Andrew E, Connell T,  Robinson P , Curtis N, Massie  J,  Robertson C, Harrison J, Shanthikumar S,  Bryant P,  Starr M, Steer A, Ranganathan S, Gwee A.  Pulmonary Mycobacterium abscessus complex in children with cystic fibrosis: a practical management guideline. Journal of Paediatrics and Child Health published on line March 18 2019 doi:10.1111/jpc.14427

8. Tadd K, Morgan L, Rosenow T, Schultz A, Susanto C, Murray C. Robinson P. CF derived scoring systems do not fully describe the range of structural changes seen on CT scans in PCD. Ped Pulmonology accepted Dec 2018. DOI: 10.1002/ppul.24249

9. Lucas J, Gahleitner F; Amorim A, Boon M, Brown P, Constant, C, Cook S, Robinson P et al Pulmonary exacerbations in patients with primary ciliary dyskinesia: an expert consensus definition for use in clinical trials. ERJ  Open Research. 5(1), 2019 Feb

10. Robinson P. Never too old for an inherited condition. Internal Medicine 2018;48(10):1252-4.

11. KueK L, Griffin P, Martinello P, Graham AN, Kalitsis P, Robinson P, Mackay GA. Identification of an immortalised human airway epithelial cell line with dyskinetic cilia. American Journal of Respiratory Cell and Molecular Biology. 2018;59(3):375-382.

12. Robinson P, Morgan L. Bronchiectasis in PCD looks different to CF on CT scan. Multidisciplinary Respiratory Medicine 2018;13(1) 24-25.

13. Bolia R, Hardikaer W, Robinson P. ""No Sweat, No Genes": a diagnostic dilemma" J  Paediatr Child Health 2018;54(5);579-81

14. Vandeleur M, Walter L, Armstrong D, Robinson P, Nixon G,  Horne R. Quality of life and mood in children with Cystic Fibrosis; Associations with sleep quality. Jnl of CF 2018;17(6):811-820.

15.  JS, Alanin MC, Collins S, Harris A, Johanesen HK, Nielsen KG, Papo JF, Robinson P, Walker W. Clinical care of children with primary ciliary dyskinesia. Expert Review of Respiratory Medicine 2017; 11 (10): 779 - 790.

16. Lucas, J, Evans H, Haarman E, Hirst R, Hogg C, Jackson C, Nielsen K, Omran H, Papon J, Robinson P, Shoemark A, Walker W. Exploring the art of ciliary beating: the benefits of high-speed video analysis. Chest 2017;152(6):1348-49.

17. Vandeleur M, Walter L, Armstrong D, Robinson P, Nixon G, Horne R. What Keeps Children with Cystic Fibrosis awake at night? Jnl CF 2017;16(6): 719-726.

18. Robson E, Chetcuti P, Hirst R, Mitchison H, Moya E, Peckham D, Robinson P, Rutman A, O’Callaghan C. Update on primary ciliary dyskinesia Paediatrics and Child health. 2017; 27 (7): 337-342

19. Robinson P.  Situs inversus: When an incidental finding is not so incidental.  J  Paediatr Child Health.  2017;53 (7): 715-716.

20. Massie J, Robinson P J, and Cooper PJ. (2016). The story of cystic fibrosis 1965–2015. J Paediatr Child Health, 2016: 52: 991–994.

21. Vandeleur M WL, Armstrong D, Robinson P, Nixon G, Horne RSC. How well do children with cystic fibrosis sleep? An actigraphic and questionnaire based study. The Journal of Pediatrics. 2017; 182: 170-176. 

22. Weber H, Robinson P. Do children with cystic fibrosis receiving outreach care have poorer clinical outcomes than those treated at a specialist cystic fibrosis centre? Aust Jnl Rural Health 2017; 25(1): 34-41.

23. Bell, E, Griffin P, Martinello P, Robinson P. Primary Ciliary Dyskinesia in two English Cocker Spaniels. Aust Veterinary Jnl 2016;94(5) 149-153.

Publications as part of International study groups (Named as member of study group in publication)

24. Early markers of cystic fibrosis structural lung disease: follow-up of the ACFBAL cohort. Naomi E. Wijker, Suzanna Vidmar, Keith Grimwood, Peter D. Sly, Catherine A. Byrnes, John B. Carlin, Peter J. Cooper, Colin F. Robertson, R. John Massie, Mariette P.C. Kemner van de Corput, Joyce Cheney, Harm A.W.M. Tiddens, Claire E. Wainwright for the Australasian Cystic Fibrosis Bronchoalveolar Lavage (ACFBAL) and Follow-up of the ACFBAL (CF-FAB) study groups

25. Highlights from the nutrition guidelines for cystic fibrosis in Australia and New Zealand. Natalie van der Haaka N, , King S,  Crowderd T, Kenche A, Painterg C, Saxby N, the Nutrition Guidelines for Cystic Fibrosis in Australia and New Zealand Authorship Group and Interdisciplinary Steering Committee. Journal of Cystic Fibrosis, 2020, 19;1:16-25

26. Aspergillus and progression of lung disease in children with cystic fibrosis Harun S, Wainwright C, Grimwood K, Hennig S, on behalf of the Australasian Cystic Fibrosis Bronchoalveolar Lavage (ACFBAL) study group. Thorax  2019:74(2).

27. VX-445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles Keating D, Marigowda G, Burr L, Daines C, Mall M,  McKone E, Ramsey B, Rowe S,  Sass L, Tullis E, McKee C, Moskowitz S,  Robertson S, Savage J, Simard C,  Van Goor F,  Waltz D, Xuan F,  Young T, Taylor‑Cousar J, for the VX16-445-001 Study Group.  NEJM on line Oct 2018

28. The changing prevalence of lower airway infections in young children with cystic fibrosis. Reuer O, Schultz A et al and AREST CF Thorax on line Sept 2018

29. Interleukin-1 is associated with inflammation and structural lung disease in young children with cystic fibrosis. Montgomery ST, Dittrich AS, Garratt L, Turkovic L, Frey DL, Stick S, Mall M, Kicic A and AREST CF. Jnl of CF Published on line June 2018

30. Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial. Ratjen F, Hug C, Marigowda G, Tian S, Huang X,  Stanojevic S, on behalf of the  VX14-809-109 investigator group^.  The Lancet Respiratory Medicine, 2017 Vol. 5, No. 7, p557–567

31. Oxidative stress in early cystic fibrosis lung disease is exacerbated by airway glutathione deficiency. Dickerhof N, Pearson JF, Hoskin TS, Berry LJ, Turner R, Sly PD, Kettle AJ; AREST CF. Free Radic Biol Med. 2017 Dec;113:236-243. 

32. A randomised controlled trial of tiotropium in adolescents with severe symptomatic asthma. Hamelmann E, Bernstein JA, Vandewalker M, et al. Eur Respir J 2017; 49: 1601100

33. The association between Staphylococcus aureus and subsequent bronchiectasis in children with cystic fibrosis. Caudri D, Turkovic L, Ng J, de Klerk NH, Rosenow T, Hall GL, Ranganathan SC, Sly PD, Stick SM; AREST CF. Jnl of CF  Published on line Dec 2017

34. Quantitative assessment of airway dimensions in young children with cystic fibrosis lung disease using chest computed tomography. Kuo W, Soffers T, Andrinopoulou ER, Rosenow T, Ranganathan S, Turkovic L, Stick SM, Tiddens H; AREST CF. Pediatr Pulmonol. 2017 Nov;52(11):1414-1423. 

35. The AREST CF experience in biobanking - More than just tissues, tubes and time. Garratt LW, Kicic A, Robertson C, Ranganathan S, Sly PD, Stick SM; AREST CF. J Cyst Fibros. 2017 Sep;16(5):622-627. 

36. Family-centred care in cystic fibrosis: a pilot study in North Queensland, Australia. Smyth W, Abernethy G, Jessup M, Douglas T, Shields L; AREST‐CF. Nurs Open. 2017 May 11;4(3):168-173. 

37. Air trapping in early cystic fibrosis lung disease-Does CT tell the full story? Rosenow T, Ramsey K, Turkovic L, Murray CP, Mok LC, Hall GL, Stick SM; AREST CF. Pediatr Pulmonol. 2017 Sep; 52(9):1150-1156. 

38. The effect of 100% oxygen on tidal breathing parameters in preschool children. Foong RE, Harper AJ, Hall GL, Ramsey KA; AREST CF. Eur Respir J. 2017 Jun 1; 49(6). 1601959

39. Multiple-Breath Washout Outcomes Are Sensitive to Inflammation and Infection in Children with Cystic Fibrosis. Ramsey KA, Foong RE, Grdosic J, Harper A, Skoric B, Clem C, Davis M, Turkovic L, Stick SM, Davis SD, Ranganathan SC, Hall GL; AREST CF Ann Am Thorac Soc. 2017 Sep; 14(9):1436-1442. 

40. Lack of small colony variants of Staphylococcus aureus from lower respiratory tract specimens. Carzino R, Hart E, Sutton P, King L, Ranganathan S; AREST CF. Pediatr Pulmonol. 2017 May; 52(5):632-635

41. Effect of posture on lung ventilation distribution and associations with structure in children with cystic fibrosis. Ramsey KA, McGirr C, Stick SM, Hall GL, Simpson SJ; AREST CF. J Cyst Fibros. 2017 Nov; 16(6):713-718. 

42. Hypoxia and sterile inflammation in cystic fibrosis airways: mechanisms and potential therapies. Montgomery ST, Mall MA, Kicic A, Stick SM; AREST CF. Eur Respir J. 2017 Jan 4; 49(1). pii:  

43. Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?  Ranganathan SC, Hall GL, Sly PD, Stick SM, Douglas TA; AREST-CF. Am J Respir Crit Care Med. 2017 Jun 15; 195(12):1567-1575

44. Oxidized glutathione and uric acid as biomarkers of early cystic fibrosis lung disease. Dickerhof N, Turner R, Khalilova I, Fantino E, Sly PD, Kettle AJ; AREST CF. J Cyst Fibros. 2017 Mar; 16(2):214-221.

45. Family-centred care for families living with cystic fibrosis in a rural setting: A qualitative study. Jessup M, Smyth W, Abernethy G, Shields L, Douglas T; AREST-CF. J Clin Nurs. 2017 Oct 19. 

46. Serious Asthma Events with Fluticasone plus Salmeterol versus Fluticasone Alone David A. Stempel D, Raphiou I, Kral K, Yeakey A, Emmett A,  Prazma C, Buaron, K, Pascoe S, for the AUSTRI Investigators N Engl J Med 2016; 374:1822-1830.

47. A randomised controlled trail of tiotropium in adolescents with severe symptomatic asthma. Hamelmann E, Bernstein, JA, Vandewalker M, Moroni-Zentgraf P, verri D, Anna unsled A, engel M and Boner A.  European Resp Jnl 2017;49(1)

48. Safety of Adding Salmeterol to Fluticasone Propionate in Children with Asthma Stempel D, Szefler S, Pedersen S, Zeiger R,  Yeakey A, Lee L, Liu A, Mitchell H, Kral K, Raphiou I, Prillaman B, Buaron K, Yun Kirby S, Pascoe S, for the VESTRI Investigators. N Engl J Med 2016; 375:840-849.

49. Metabolomic biomarkers predictive of early structural lung disease in cystic fibrosis. Esther CR Jr, Turkovic L, Rosenow T, Muhlebach MS, Boucher RC, Ranganathan S, Stick SM; ARESTCF. Eur Respir J. 2016 Dec; 48(6):1612-1621.