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Margaret W. Leigh, M.D. - Publications

Affiliations: 
University of North Carolina, Chapel Hill, Chapel Hill, NC 
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77 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Crowley S, Azevedo I, Boon M, Bush A, Eber E, Haarman E, Karadag B, Kötz K, Leigh M, Moreno-Galdó A, Mussaffi H, Nielsen KG, Omran H, Papon JF, Pohunek P, et al. Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesia. Erj Open Research. 6. PMID 32964005 DOI: 10.1183/23120541.00377-2020  0.302
2020 Kinghorn B, McNamara S, Genatossio A, Sullivan E, Siegel M, Bauer I, Clem C, Johnson RC, Davis M, Griffiths A, Wheeler W, Johnson K, Davis SD, Leigh MW, Rosenfeld M, et al. Comparison of Multiple Breath Washout and Spirometry in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis and Healthy Controls. Annals of the American Thoracic Society. PMID 32603187 DOI: 10.1513/Annalsats.201905-375Oc  0.355
2020 Pappa AK, Sullivan KM, Lopez EM, Adams KN, Zanation AM, Ebert CS, Thorp BD, Senior BA, Leigh MW, Knowles MR, Kimple AJ. Sinus Development and Pneumatization in a Primary Ciliary Dyskinesia Cohort. American Journal of Rhinology & Allergy. 1945892420933175. PMID 32551925 DOI: 10.1177/1945892420933175  0.404
2020 Shoemark A, Boon M, Brochhausen C, Bukowy-Bieryllo Z, Margherita De Santi M, Goggin P, Griffin P, Hegele RG, Hirst RA, Leigh MW, Lupton A, MacKenney K, Omran H, Pache JC, Pinto A, et al. International consensus guideline for reporting transmission electron microscopy results in the diagnosis of Primary Ciliary Dyskinesia (BEAT PCD TEM Criteria). The European Respiratory Journal. PMID 32060067 DOI: 10.1183/13993003.00725-2019  0.311
2019 Shapiro AJ, Dell SD, Gaston B, O'Connor M, Marozkina N, Manion M, Hazucha MJ, Leigh MW. Nasal Nitric Oxide Measurement in Primary Ciliary Dyskinesia: A Technical Paper on Standardized Testing Protocols. Annals of the American Thoracic Society. PMID 31770003 DOI: 10.1513/Annalsats.201904-347Ot  0.307
2019 Bustamante-Marin XM, Shapiro A, Sears PR, Charng WL, Conrad DF, Leigh MW, Knowles MR, Ostrowski LE, Zariwala MA. Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesia. Journal of Human Genetics. PMID 31636325 DOI: 10.1038/S10038-019-0686-1  0.369
2019 Wallmeier J, Frank D, Shoemark A, Nöthe-Menchen T, Cindric S, Olbrich H, Loges NT, Aprea I, Dougherty GW, Pennekamp P, Kaiser T, Mitchison HM, Hogg C, Carr SB, Zariwala MA, ... ... Leigh MW, et al. De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry. American Journal of Human Genetics. PMID 31630787 DOI: 10.1016/J.Ajhg.2019.09.022  0.318
2019 Vece TJ, Sagel SD, Zariwala MA, Sullivan KM, Burns KA, Dutcher SK, Yusupov R, Leigh MW, Knowles MR. Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia. Pediatric Pulmonology. PMID 31549486 DOI: 10.1002/Ppul.24528  0.343
2019 Morimoto K, Hijikata M, Zariwala MA, Nykamp K, Inaba A, Guo TC, Yamada H, Truty R, Sasaki Y, Ohta K, Kudoh S, Leigh MW, Knowles MR, Keicho N. Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patients. Molecular Genetics & Genomic Medicine. e838. PMID 31270959 DOI: 10.1002/Mgg3.838  0.356
2019 Shoemark A, Boon M, Brochhausen C, Bukowy-Bieryllo Z, Santi MMD, Goggin P, Griffin P, Hegele RG, Hirst RA, Leigh M, Lupton A, Mackenney K, Omran H, Pache J, Pinto A, et al. International consensus guideline for reporting transmission electron microscopy results in the diagnosis of Primary Ciliary Dyskinesia European Respiratory Journal. 54. DOI: 10.1183/13993003.Congress-2019.Pa1040  0.3
2018 Sanders CD, Leigh MW, Chao KC, Weck KE, King I, Wolf WE, Campbell DJ, Knowles MR, Zariwala MA, Shapiro AJ. The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort. Pediatric Pulmonology. PMID 30238669 DOI: 10.1002/Ppul.24159  0.32
2018 Davis SD, Rosenfeld M, Lee HS, Ferkol TW, Sagel SD, Dell SD, Milla C, Pittman JE, Shapiro AJ, Sullivan KM, Nykamp KR, Krischer JP, Zariwala MA, Knowles MR, Leigh MW, et al. Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype. American Journal of Respiratory and Critical Care Medicine. PMID 30067075 DOI: 10.1164/Rccm.201803-0548Oc  0.351
2017 Goutaki M, Halbeisen FS, Spycher BD, Maurer E, Belle F, Amirav I, Behan L, Boon M, Carr S, Casaulta C, Clement A, Crowley S, Dell S, Ferkol T, Haarman EG, ... ... Leigh MW, et al. Growth and nutritional status, and their association with lung function: a study from the international Primary Ciliary Dyskinesia Cohort. The European Respiratory Journal. 50. PMID 29269581 DOI: 10.1183/13993003.01659-2017  0.32
2017 Shapiro AJ, Leigh MW. Value of transmission electron microscopy for primary ciliary dyskinesia diagnosis in the era of molecular medicine: Genetic defects with normal and non-diagnostic ciliary ultrastructure. Ultrastructural Pathology. 1-13. PMID 28915070 DOI: 10.1080/01913123.2017.1362088  0.39
2017 Pittman JE, Noah H, Calloway HE, Davis SD, Leigh MW, Drumm M, Sagel SD, Accurso FJ, Knowles MR, Sontag MK. Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection. Plos One. 12: e0177215. PMID 28505188 DOI: 10.1371/Journal.Pone.0177215  0.316
2017 Shapiro AJ, Josephson M, Rosenfeld M, Yilmaz O, Davis SD, Polineni D, Guadagno E, Leigh MW, Lavergne V. Accuracy of Nasal Nitric Oxide Measurement as a Diagnostic Test for Primary Ciliary Dyskinesia: A Systematic Review and Meta-Analysis. Annals of the American Thoracic Society. PMID 28481653 DOI: 10.1513/Annalsats.201701-062Sr  0.357
2017 Goutaki M, Maurer E, Halbeisen FS, Amirav I, Barbato A, Behan L, Boon M, Casaulta C, Clement A, Crowley S, Haarman E, Hogg C, Karadag B, Koerner-Rettberg C, Leigh MW, et al. The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results. The European Respiratory Journal. 49. PMID 28052956 DOI: 10.1183/13993003.01181-2016  0.342
2016 Lucas JS, Barbato A, Collins SA, Goutaki M, Behan L, Caudri D, Dell S, Eber E, Escudier E, Hirst RA, Hogg C, Jorissen M, Latzin P, Legendre M, Leigh MW, et al. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia. The European Respiratory Journal. PMID 27836958 DOI: 10.1183/13993003.01090-2016  0.326
2016 Lewis WR, Malarkey EB, Tritschler D, Bower R, Pasek RC, Porath JD, Birket SE, Saunier S, Antignac C, Knowles MR, Leigh MW, Zariwala MA, Challa AK, Kesterson RA, Rowe SM, et al. Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease. Plos Genetics. 12: e1006220. PMID 27472056 DOI: 10.1371/Journal.Pgen.1006220  0.376
2016 Dell SD, Leigh MW, Lucas JS, Ferkol TW, Knowles MR, Alpern A, Behan L, Morris AM, Hogg C, DunnGalvin A, Quittner AL. Primary Ciliary Dyskinesia: First Health-related Quality of Life Measures for Pediatric Patients. Annals of the American Thoracic Society. PMID 27464304 DOI: 10.1513/Annalsats.201603-198Oc  0.309
2016 Leigh MW, Ferkol TW, Davis SD, Lee HS, Rosenfeld M, Dell SD, Sagel SD, Milla C, Olivier KN, Sullivan KM, Zariwala MA, Pittman J, Shapiro AJ, Carson JL, Krischer J, et al. Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents. Annals of the American Thoracic Society. PMID 27070726 DOI: 10.1513/Annalsats.201511-748Oc  0.362
2015 Werner C, Lablans M, Ataian M, Raidt J, Wallmeier J, Große-Onnebrink J, Kuehni CE, Haarman EG, Leigh MW, Quittner AL, Lucas JS, Hogg C, Witt M, Priftis KN, Yiallouros P, et al. An international registry for primary ciliary dyskinesia. The European Respiratory Journal. PMID 26659107 DOI: 10.1183/13993003.00776-2015  0.352
2015 Shapiro AJ, Zariwala MA, Ferkol T, Davis SD, Sagel SD, Dell SD, Rosenfeld M, Olivier KN, Milla C, Daniel SJ, Kimple AJ, Manion M, Knowles MR, Leigh MW. Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review. Pediatric Pulmonology. PMID 26418604 DOI: 10.1002/Ppul.23304  0.369
2015 Davis SD, Ferkol TW, Rosenfeld M, Lee HS, Dell SD, Sagel SD, Milla C, Zariwala MA, Pittman JE, Shapiro AJ, Carson JL, Krischer JP, Hazucha MJ, Cooper ML, Knowles MR, ... Leigh MW, et al. Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype. American Journal of Respiratory and Critical Care Medicine. 191: 316-24. PMID 25493340 DOI: 10.1164/Rccm.201409-1672Oc  0.319
2015 Shapiro AJ, Tolleson-Rinehart S, Zariwala MA, Knowles MR, Leigh MW. The prevalence of clinical features associated with primary ciliary dyskinesia in a heterotaxy population: results of a web-based survey. Cardiology in the Young. 25: 752-9. PMID 24905662 DOI: 10.1017/S1047951114000912  0.356
2014 Lin J, Yin W, Smith MC, Song K, Leigh MW, Zariwala MA, Knowles MR, Ostrowski LE, Nicastro D. Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesia. Nature Communications. 5: 5727. PMID 25473808 DOI: 10.1038/Ncomms6727  0.329
2014 Lucas JS, Leigh MW. Diagnosis of primary ciliary dyskinesia: searching for a gold standard. The European Respiratory Journal. 44: 1418-22. PMID 25435529 DOI: 10.1183/09031936.00175614  0.376
2014 Antoon JW, Hernandez ML, Roehrs PA, Noah TL, Leigh MW, Byerley JS. Endogenous lipoid pneumonia preceding diagnosis of pulmonary alveolar proteinosis. The Clinical Respiratory Journal. PMID 25103284 DOI: 10.1111/Crj.12197  0.332
2014 Shapiro AJ, Weck KE, Chao KC, Rosenfeld M, Nygren AO, Knowles MR, Leigh MW, Zariwala MA. Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5p. The Journal of Pediatrics. 165: 858-61. PMID 25066065 DOI: 10.1016/J.Jpeds.2014.06.048  0.346
2014 Henderson AG, Ehre C, Button B, Abdullah LH, Cai LH, Leigh MW, DeMaria GC, Matsui H, Donaldson SH, Davis CW, Sheehan JK, Boucher RC, Kesimer M. Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure. The Journal of Clinical Investigation. 124: 3047-60. PMID 24892808 DOI: 10.1172/Jci73469  0.317
2014 Knowles MR, Ostrowski LE, Leigh MW, Sears PR, Davis SD, Wolf WE, Hazucha MJ, Carson JL, Olivier KN, Sagel SD, Rosenfeld M, Ferkol TW, Dell SD, Milla CE, Randell SH, et al. Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype. American Journal of Respiratory and Critical Care Medicine. 189: 707-17. PMID 24568568 DOI: 10.1164/Rccm.201311-2047Oc  0.37
2013 Austin-Tse C, Halbritter J, Zariwala MA, Gilberti RM, Gee HY, Hellman N, Pathak N, Liu Y, Panizzi JR, Patel-King RS, Tritschler D, Bower R, O'Toole E, Porath JD, Hurd TW, ... ... Leigh MW, et al. Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia. American Journal of Human Genetics. 93: 672-86. PMID 24094744 DOI: 10.1016/J.Ajhg.2013.08.015  0.367
2013 Knowles MR, Ostrowski LE, Loges NT, Hurd T, Leigh MW, Huang L, Wolf WE, Carson JL, Hazucha MJ, Yin W, Davis SD, Dell SD, Ferkol TW, Sagel SD, Olivier KN, et al. Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms. American Journal of Human Genetics. 93: 711-20. PMID 24055112 DOI: 10.1016/J.Ajhg.2013.07.025  0.379
2013 Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, et al. ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. American Journal of Human Genetics. 93: 336-45. PMID 23891469 DOI: 10.1016/J.Ajhg.2013.06.007  0.34
2013 Tarkar A, Loges NT, Slagle CE, Francis R, Dougherty GW, Tamayo JV, Shook B, Cantino M, Schwartz D, Jahnke C, Olbrich H, Werner C, Raidt J, Pennekamp P, Abouhamed M, ... ... Leigh MW, et al. DYX1C1 is required for axonemal dynein assembly and ciliary motility. Nature Genetics. 45: 995-1003. PMID 23872636 DOI: 10.1038/Ng.2707  0.341
2013 Hjeij R, Lindstrand A, Francis R, Zariwala MA, Liu X, Li Y, Damerla R, Dougherty GW, Abouhamed M, Olbrich H, Loges NT, Pennekamp P, Davis EE, Carvalho CM, Pehlivan D, ... ... Leigh MW, et al. ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. American Journal of Human Genetics. 93: 357-67. PMID 23849778 DOI: 10.1016/J.Ajhg.2013.06.009  0.355
2013 Daniels ML, Leigh MW, Davis SD, Armstrong MC, Carson JL, Hazucha M, Dell SD, Eriksson M, Collins FS, Knowles MR, Zariwala MA. Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia. Human Mutation. 34: 1352-6. PMID 23798057 DOI: 10.1002/Humu.22371  0.396
2013 Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW. Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease. American Journal of Respiratory and Critical Care Medicine. 188: 913-22. PMID 23796196 DOI: 10.1164/Rccm.201301-0059Ci  0.439
2013 Ferkol TW, Puffenberger EG, Lie H, Helms C, Strauss KA, Bowcock A, Carson JL, Hazucha M, Morton DH, Patel AC, Leigh MW, Knowles MR, Zariwala MA. Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities. The Journal of Pediatrics. 163: 383-7. PMID 23477994 DOI: 10.1016/J.Jpeds.2013.01.061  0.316
2013 Knowles MR, Leigh MW, Ostrowski LE, Huang L, Carson JL, Hazucha MJ, Yin W, Berg JS, Davis SD, Dell SD, Ferkol TW, Rosenfeld M, Sagel SD, Milla CE, Olivier KN, et al. Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia. American Journal of Human Genetics. 92: 99-106. PMID 23261302 DOI: 10.1016/J.Ajhg.2012.11.003  0.359
2013 Antony D, Becker-Heck A, Zariwala MA, Schmidts M, Onoufriadis A, Forouhan M, Wilson R, Taylor-Cox T, Dewar A, Jackson C, Goggin P, Loges NT, Olbrich H, Jaspers M, Jorissen M, ... Leigh MW, et al. Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms. Human Mutation. 34: 462-72. PMID 23255504 DOI: 10.1002/Humu.22261  0.353
2013 Peterson-Carmichael SL, Harris WT, Goel R, Noah TL, Johnson R, Leigh MW, Davis SD. Erratum: Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis Pediatric Pulmonology. 48: 631-631. DOI: 10.1002/Ppul.22821  0.3
2012 Horani A, Druley TE, Zariwala MA, Patel AC, Levinson BT, Van Arendonk LG, Thornton KC, Giacalone JC, Albee AJ, Wilson KS, Turner EH, Nickerson DA, Shendure J, Bayly PV, Leigh MW, et al. Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia. American Journal of Human Genetics. 91: 685-93. PMID 23040496 DOI: 10.1016/J.Ajhg.2012.08.022  0.375
2012 Nakhleh N, Francis R, Giese RA, Tian X, Li Y, Zariwala MA, Yagi H, Khalifa O, Kureshi S, Chatterjee B, Sabol SL, Swisher M, Connelly PS, Daniels MP, Srinivasan A, ... ... Leigh M, et al. High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy. Circulation. 125: 2232-42. PMID 22499950 DOI: 10.1161/Circulationaha.111.079780  0.322
2012 Knowles MR, Leigh MW, Carson JL, Davis SD, Dell SD, Ferkol TW, Olivier KN, Sagel SD, Rosenfeld M, Burns KA, Minnix SL, Armstrong MC, Lori A, Hazucha MJ, Loges NT, et al. Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure. Thorax. 67: 433-41. PMID 22184204 DOI: 10.1136/Thoraxjnl-2011-200301  0.391
2012 Ferkol TW, Leigh MW. Ciliopathies: the central role of cilia in a spectrum of pediatric disorders. The Journal of Pediatrics. 160: 366-71. PMID 22177992 DOI: 10.1016/J.Jpeds.2011.11.024  0.346
2011 Olin JT, Burns K, Carson JL, Metjian H, Atkinson JJ, Davis SD, Dell SD, Ferkol TW, Milla CE, Olivier KN, Rosenfeld M, Baker B, Leigh MW, Knowles MR, Sagel SD, et al. Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experience. Pediatric Pulmonology. 46: 483-8. PMID 21284095 DOI: 10.1002/Ppul.21402  0.331
2011 Berg JS, Evans JP, Leigh MW, Omran H, Bizon C, Mane K, Knowles MR, Weck KE, Zariwala MA. Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 218-29. PMID 21270641 DOI: 10.1097/Gim.0B013E318203Cff2  0.353
2011 Pittman JE, Calloway EH, Kiser M, Yeatts J, Davis SD, Drumm ML, Schechter MS, Leigh MW, Emond M, Van Rie A, Knowles MR. Age of Pseudomonas aeruginosa acquisition and subsequent severity of cystic fibrosis lung disease. Pediatric Pulmonology. 46: 497-504. PMID 21194167 DOI: 10.1002/Ppul.21397  0.341
2010 Lie H, Zariwala MA, Helms C, Bowcock AM, Carson JL, Brown DE, Hazucha MJ, Forsen J, Molter D, Knowles MR, Leigh MW, Ferkol TW. Primary ciliary dyskinesia in Amish communities. The Journal of Pediatrics. 156: 1023-5. PMID 20350728 DOI: 10.1016/J.Jpeds.2010.01.054  0.334
2010 Noah TL, Ivins SS, Abode KA, Stewart PW, Michelson PH, Harris WT, Henry MM, Leigh MW. Inhaled versus systemic antibiotics and airway inflammation in children with cystic fibrosis and Pseudomonas. Pediatric Pulmonology. 45: 281-90. PMID 20146365 DOI: 10.1002/Ppul.21176  0.313
2009 Loges NT, Olbrich H, Becker-Heck A, Häffner K, Heer A, Reinhard C, Schmidts M, Kispert A, Zariwala MA, Leigh MW, Knowles MR, Zentgraf H, Seithe H, Nürnberg G, Nürnberg P, et al. Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. American Journal of Human Genetics. 85: 883-9. PMID 19944400 DOI: 10.1016/J.Ajhg.2009.10.018  0.345
2009 Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 473-87. PMID 19606528 DOI: 10.1097/Gim.0B013E3181A53562  0.432
2009 Peterson-Carmichael SL, Harris WT, Goel R, Noah TL, Johnson R, Leigh MW, Davis SD. Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis. Pediatric Pulmonology. 44: 503-11. PMID 19382221 DOI: 10.1002/Ppul.21044  0.323
2009 Leigh MW, Zariwala MA, Knowles MR. Primary ciliary dyskinesia: improving the diagnostic approach. Current Opinion in Pediatrics. 21: 320-5. PMID 19300264 DOI: 10.1097/Mop.0B013E328329Cddb  0.373
2008 Brown DE, Pittman JE, Leigh MW, Fordham L, Davis SD. Early lung disease in young children with primary ciliary dyskinesia. Pediatric Pulmonology. 43: 514-6. PMID 18383332 DOI: 10.1002/Ppul.20792  0.347
2007 Kennedy MP, Omran H, Leigh MW, Dell S, Morgan L, Molina PL, Robinson BV, Minnix SL, Olbrich H, Severin T, Ahrens P, Lange L, Morillas HN, Noone PG, Zariwala MA, et al. Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia. Circulation. 115: 2814-21. PMID 17515466 DOI: 10.1161/Circulationaha.106.649038  0.372
2007 Kennedy MP, Noone PG, Leigh MW, Zariwala MA, Minnix SL, Knowles MR, Molina PL. High-resolution CT of patients with primary ciliary dyskinesia. Ajr. American Journal of Roentgenology. 188: 1232-8. PMID 17449765 DOI: 10.2214/Ajr.06.0965  0.301
2007 Davis SD, Fordham LA, Brody AS, Noah TL, Retsch-Bogart GZ, Qaqish BF, Yankaskas BC, Johnson RC, Leigh MW. Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis. American Journal of Respiratory and Critical Care Medicine. 175: 943-50. PMID 17303797 DOI: 10.1164/Rccm.200603-343Oc  0.342
2006 Zariwala MA, Leigh MW, Ceppa F, Kennedy MP, Noone PG, Carson JL, Hazucha MJ, Lori A, Horvath J, Olbrich H, Loges NT, Bridoux AM, Pennarun G, Duriez B, Escudier E, et al. Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation. American Journal of Respiratory and Critical Care Medicine. 174: 858-66. PMID 16858015 DOI: 10.1164/Rccm.200603-370Oc  0.381
2006 Saito J, Harris WT, Gelfond J, Noah TL, Leigh MW, Johnson R, Davis SD. Physiologic, bronchoscopic, and bronchoalveolar lavage fluid findings in young children with recurrent wheeze and cough. Pediatric Pulmonology. 41: 709-19. PMID 16779841 DOI: 10.1002/Ppul.20387  0.31
2006 Muhlebach MS, Miller MB, Moore C, Wedd JP, Drake AF, Leigh MW. Are lower airway or throat cultures predictive of sinus bacteriology in cystic fibrosis? Pediatric Pulmonology. 41: 445-51. PMID 16547960 DOI: 10.1002/Ppul.20396  0.314
2006 Ferkol T, Leigh M. Primary Ciliary Dyskinesia and Newborn Respiratory Distress Seminars in Perinatology. 30: 335-340. DOI: 10.1053/J.Semperi.2005.11.001  0.404
2005 Esther CR, Henry MM, Molina PL, Leigh MW. Nontuberculous mycobacterial infection in young children with cystic fibrosis. Pediatric Pulmonology. 40: 39-44. PMID 15858802 DOI: 10.1002/Ppul.20222  0.351
2004 Leigh MW. Diagnosis of CF despite normal or borderline sweat chloride. Paediatric Respiratory Reviews. 5: S357-9. PMID 14980295 DOI: 10.1016/S1526-0542(04)90062-0  0.386
2004 Noone PG, Leigh MW, Sannuti A, Minnix SL, Carson JL, Hazucha M, Zariwala MA, Knowles MR. Primary ciliary dyskinesia: diagnostic and phenotypic features. American Journal of Respiratory and Critical Care Medicine. 169: 459-67. PMID 14656747 DOI: 10.1164/Rccm.200303-365Oc  0.353
2004 Zariwala M, O'Neal WK, Noone PG, Leigh MW, Knowles MR, Ostrowski LE. Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesia. American Journal of Respiratory Cell and Molecular Biology. 30: 428-34. PMID 14630615 DOI: 10.1165/Rcmb.2003-0338Rc  0.346
2003 Leigh MW. Primary ciliary dyskinesia. Seminars in Respiratory and Critical Care Medicine. 24: 653-62. PMID 16088581 DOI: 10.1016/J.Ccm.2016.04.008  0.392
2003 Noah TL, Murphy PC, Alink JJ, Leigh MW, Hull WM, Stahlman MT, Whitsett JA. Bronchoalveolar lavage fluid surfactant protein-A and surfactant protein-D are inversely related to inflammation in early cystic fibrosis. American Journal of Respiratory and Critical Care Medicine. 168: 685-91. PMID 12829455 DOI: 10.1164/Rccm.200301-005Oc  0.311
2001 Zariwala M, Noone PG, Sannuti A, Minnix S, Zhou Z, Leigh MW, Hazucha M, Carson JL, Knowles MR. Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia. American Journal of Respiratory Cell and Molecular Biology. 25: 577-83. PMID 11713099 DOI: 10.1165/Ajrcmb.25.5.4619  0.367
1999 Muhlebach MS, Stewart PW, Leigh MW, Noah TL. Quantitation of inflammatory responses to bacteria in young cystic fibrosis and control patients. American Journal of Respiratory and Critical Care Medicine. 160: 186-91. PMID 10390398 DOI: 10.1164/Ajrccm.160.1.9808096  0.343
1998 Friedman KJ, Leigh MW, Czarnecki P, Feldman GL. Cystic fibrosis transmembrane-conductance regulator mutations among African Americans. American Journal of Human Genetics. 62: 195-6. PMID 9443874 DOI: 10.1086/301681  0.366
1996 Reitnauer PJ, Black HR, Leigh MW, Aylsworth AS. A THREE GENERATION FAMILY WITH FEATURES OF LACRIMO-AURICULO-DENTO-DIGITAL SYNDROME (LADD) AND SEVERE CHRONIC LUNG DISEASE † 485 Pediatric Research. 39: 83-83. DOI: 10.1203/00006450-199604001-00505  0.302
1995 Leigh MW, Kylander JE, Yankaskas JR, Boucher RC. Cell proliferation in bronchial epithelium and submucosal glands of cystic fibrosis patients. American Journal of Respiratory Cell and Molecular Biology. 12: 605-12. PMID 7766425 DOI: 10.1165/Ajrcmb.12.6.7766425  0.338
1995 Knowles MR, Hohneker KW, Zhou Z, Olsen JC, Noah TL, Hu PC, Leigh MW, Engelhardt JF, Edwards LJ, Jones KR. A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis. The New England Journal of Medicine. 333: 823-31. PMID 7544439 DOI: 10.1056/Nejm199509283331302  0.329
1987 Wood RE, Leigh MW. What is a "pulmonary exacerbation" in cystic fibrosis? The Journal of Pediatrics. 111: 841-2. PMID 3681548 DOI: 10.1016/S0022-3476(87)80198-1  0.302
1985 Leigh MW, Henshaw NG, Wood RE. Diagnosis of Pneumocystis carinii pneumonia in pediatric patients using bronchoscopic bronchoalveolar lavage. Pediatric Infectious Disease. 4: 408-10. PMID 3875082 DOI: 10.1097/00006454-198507000-00017  0.309
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