| Impact of maternal intrapartum antibiotics, method of birth and breastfeeding on gut microbiota during the first year of life: a prospective cohort study MB Azad, T Konya, RR Persaud, DS Guttman, RS Chari, CJ Field, ... BJOG: An International Journal of Obstetrics & Gynaecology 123 (6), 983-993, 2016 | 646 | 2016 |
| European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia JS Lucas, A Barbato, SA Collins, M Goutaki, L Behan, D Caudri, S Dell, ... European Respiratory Journal 49 (1), 2017 | 621 | 2017 |
| Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome MW Leigh, JE Pittman, JL Carson, TW Ferkol, SD Dell, SD Davis, ... Genetics in Medicine 11 (7), 473-487, 2009 | 561 | 2009 |
| Diffuse lung disease in young children: application of a novel classification scheme GH Deutsch, LR Young, RR Deterding, LL Fan, SD Dell, JA Bean, ... American journal of respiratory and critical care medicine 176 (11), 1120-1128, 2007 | 559 | 2007 |
| Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test AC Lionel, G Costain, N Monfared, S Walker, MS Reuter, SM Hosseini, ... Genetics in Medicine 20 (4), 435-443, 2018 | 516 | 2018 |
| Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia MP Kennedy, H Omran, MW Leigh, S Dell, L Morgan, PL Molina, ... Circulation 115 (22), 2814-2821, 2007 | 496 | 2007 |
| An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy G Kurland, RR Deterding, JS Hagood, LR Young, AS Brody, RG Castile, ... American journal of respiratory and critical care medicine 188 (3), 376-394, 2013 | 434 | 2013 |
| Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review AJ Shapiro, MA Zariwala, T Ferkol, SD Davis, SD Sagel, SD Dell, ... Pediatric pulmonology 51 (2), 115-132, 2016 | 383 | 2016 |
| Canadian Thoracic Society 2012 guideline update: diagnosis and management of asthma in preschoolers, children and adults MD Lougheed, C Lemiere, FM Ducharme, C Licskai, SD Dell, BH Rowe, ... Canadian respiratory journal 19, 127-164, 2012 | 368 | 2012 |
| Diagnosis of primary ciliary dyskinesia. An official American Thoracic Society clinical practice guideline AJ Shapiro, SD Davis, D Polineni, M Manion, M Rosenfeld, SD Dell, ... American journal of respiratory and critical care medicine 197 (12), e24-e39, 2018 | 337 | 2018 |
| COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis LB Watkin, B Jessen, W Wiszniewski, TJ Vece, M Jan, Y Sha, M Thamsen, ... Nature genetics 47 (6), 654-660, 2015 | 336 | 2015 |
| Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia MW Leigh, MJ Hazucha, KK Chawla, BR Baker, AJ Shapiro, DE Brown, ... Annals of the American Thoracic Society 10 (6), 574-581, 2013 | 283 | 2013 |
| Canadian Thoracic Society Asthma Management Continuum–2010 Consensus Summary for children six years of age and over, and adults MD Lougheed, C Lemière, SD Dell, FM Ducharme, JM FitzGerald, ... Canadian respiratory journal 17, 15-24, 2010 | 273 | 2010 |
| Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype SD Davis, TW Ferkol, M Rosenfeld, HS Lee, SD Dell, SD Sagel, C Milla, ... American journal of respiratory and critical care medicine 191 (3), 316-324, 2015 | 267 | 2015 |
| Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure MR Knowles, MW Leigh, JL Carson, SD Davis, SD Dell, TW Ferkol, ... Thorax 67 (5), 433-441, 2012 | 242 | 2012 |
| Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy AJ Shapiro, SD Davis, T Ferkol, SD Dell, M Rosenfeld, KN Olivier, ... Chest 146 (5), 1176-1186, 2014 | 234 | 2014 |
| Zebrafish ciliopathy screen plus human mutational analysis identifies C21orf59 and CCDC65 defects as causing primary ciliary dyskinesia C Austin-Tse, J Halbritter, MA Zariwala, RM Gilberti, HY Gee, N Hellman, ... The American Journal of Human Genetics 93 (4), 672-686, 2013 | 231 | 2013 |
| Diagnosis and management of asthma in preschoolers: a Canadian Thoracic Society and Canadian Paediatric Society position paper FM Ducharme, SD Dell, D Radhakrishnan, RM Grad, WTA Watson, ... Paediatrics & child health 20 (7), 353-361, 2015 | 230 | 2015 |
| Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype MR Knowles, LE Ostrowski, MW Leigh, PR Sears, SD Davis, WE Wolf, ... American journal of respiratory and critical care medicine 189 (6), 707-717, 2014 | 222 | 2014 |
| ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6 MA Zariwala, HY Gee, M Kurkowiak, DA Al-Mutairi, MW Leigh, TW Hurd, ... The American Journal of Human Genetics 93 (2), 336-345, 2013 | 211 | 2013 |
