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Wayne Morgan, M.D.

Affiliations: 
University of Arizona, Tucson, AZ 
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"Wayne Morgan"

Parents

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Lynn Taussig fellowship/program director 1980-1982 University of Arizona

Children

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Robert Tepper fellowship/program director 1981-1983 University of Arizona
John L. Carroll fellowship/program director 1982-1983 University of Arizona
James E. Clayton fellowship/program director 1982-1984 University of Arizona
Nancy N. Dambro fellowship/program director 1983-1986 University of Arizona
David Geller fellowship/program director 1983-1986 University of Arizona
James Cunningham fellowship/program director 1984-1987 University of Arizona
Roni Grad fellowship/program director 1985-1988 University of Arizona
Jeff Smith fellowship/program director 1985-1988 University of Arizona
Paul H. Sammut fellowship/program director 1986-1988 University of Arizona
Diane Neddenriep fellowship/program director 1986-1989 University of Arizona
Jane Gwinn fellowship/program director 1988-1991 University of Arizona
Vinit Mahesh fellowship/program director 1988-1991 University of Arizona
Charles Judy fellowship/program director 1989-1992 University of Arizona
Susan L. Millard fellowship/program director 1989-1992 University of Arizona
John K. Pfaff fellowship/program director 1990-1993 University of Arizona
Mohy Gad El-Karim Morris fellowship/program director 1992-1994 University of Arizona
Autumn P. Clos fellowship/program director 1995-1998 University of Arizona
Maria Martinez fellowship/program director 1996-1999 University of Arizona
Fazilet Karakoc fellowship/program director 1998-2000 University of Arizona
Francesca Marotti fellowship/program director 2000-2001 University of Arizona
Edward W. Fong fellowship/program director 2001-2004 University of Arizona
Kimberly N. Otsuka fellowship/program director 2001-2007 University of Arizona
Esmeralda E. Morales fellowship/program director 2005-2008 University of Arizona
Dima Ezmigna fellowship/program director 2010-2013 University of Arizona
Ali Asseri fellowship/program director 2015-2018 University of Arizona
Nasim A. Khattab fellowship/program director 2016-2019 University of Arizona
BETA: Related publications

Publications

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Fitzpatrick AM, Bacharier LB, Jackson DJ, et al. (2020) Heterogeneity of mild-to-moderate persistent asthma in children: Confirmation by latent class analysis and association with one-year outcomes. The Journal of Allergy and Clinical Immunology. in Practice
Oates GR, Baker E, Rowe SM, et al. (2020) Tobacco smoke exposure and socioeconomic factors are independent predictors of pulmonary decline in pediatric cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
Ong T, Schechter M, Yang J, et al. (2017) Socioeconomic Status, Smoke Exposure, and Health Outcomes in Young Children With Cystic Fibrosis. Pediatrics
Sanders DB, Emerson J, Ren CL, et al. (2015) Early Childhood Risk Factors for Decreased FEV1 at Age Six to Seven Years in Young Children with Cystic Fibrosis. Annals of the American Thoracic Society. 12: 1170-6
Subbarao P, Milla C, Aurora P, et al. (2015) Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report. Annals of the American Thoracic Society. 12: 932-9
Cogen J, Emerson J, Sanders DB, et al. (2015) Risk factors for lung function decline in a large cohort of young cystic fibrosis patients. Pediatric Pulmonology. 50: 763-70
Daines C, VanDeVanter D, Khan U, et al. (2014) Serology as a diagnostic tool for predicting initialPseudomonas aeruginosa acquisition in children with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 13: 542-9
Mayer-Hamblett N, Rosenfeld M, Gibson RL, et al. (2014) Pseudomonas aeruginosa in vitro phenotypes distinguish cystic fibrosis infection stages and outcomes. American Journal of Respiratory and Critical Care Medicine. 190: 289-97
Rosenfeld M, Emerson J, McNamara S, et al. (2012) Risk factors for age at initial Pseudomonas acquisition in the cystic fibrosis epic observational cohort. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. 11: 446-53
Simon MR, Chinchilli VM, Phillips BR, et al. (2010) Forced expiratory flow between 25% and 75% of vital capacity and FEV1/forced vital capacity ratio in relation to clinical and physiological parameters in asthmatic children with normal FEV1 values. The Journal of Allergy and Clinical Immunology. 126: 527-34.e1-8
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