Peadar G. Noone - Concepedia

Author

Peadar G. Noone

University of North Carolina at Chapel Hill

Also Known As

Airik, Rannar, Daniels, M. Leigh Anne, De la Cruz, Gabriela, Dewar, Ann, Ebneter, Daria, Esserman, Denise A., Ghio, Andrew, Knowles, Michael, Lobo, Jason, Morgan, Lucy C.

Publications

8.4K

Citations

H-Index

Concepts

All Affiliations

University of North Carolina at Chapel Hill University of Colorado Denver National Jewish Health National Heart Lung and Blood Institute University of Pennsylvania

About

Peadar G. Noone is an author at University of North Carolina at Chapel Hill specializing in medicine, pathology, and pulmonary fibrosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	15	4K
2	Epidemiology	2	2	917
3	Health Sciences	1	1	576
4	Allergy	1	1	44
5	Gastroenterology	1	1	25

Peadar G. Noone

Publications

7.9K

Citations

H-Index

Page 1

	Year	Citations
Relation between Mutations of the Cystic Fibrosis Gene and Idiopathic Pancreatitis Jonathan Cohn, Kenneth J. Friedman, Peadar G. Noone, New England Journal of Medicine	1998	927
Primary Ciliary Dyskinesia Peadar G. Noone, Margaret W. Leigh, Aruna Sannuti, American Journal of Respiratory and Critical Care Medicine Recurrent Otitis MediaNeurological DisorderRespiratory DiseasesNasal Nitric OxidePathogenesis	2003	840
Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium Josephine M. Bryant, Dorothy Grogono, Daniela Rodriguez-Rincon, Science Medical MicrobiologyAntimicrobial Resistance GenePathogenic MicrobiologyMycobacterium AbscessusHealth Sciences	2016	576
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry Heike Olbrich, Karsten Häffner, Andreas Kispert, Nature Genetics Genome InstabilityMendelian DisorderGenetic DisorderGeneticsPathology	2002	550
US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis R. Andrés Floto, Kenneth N. Olivier, Lisa Saiman, Thorax Pulmonary TuberculosisEpidemiologyPreventive MedicineAdvanced Lung DiseaseTuberculosis Prevention	2015	459
US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary R. Andrés Floto, Kenneth N. Olivier, Lisa Saiman, Thorax Pulmonary TuberculosisEpidemiologyConsensus RecommendationsPulmonary PathologyAdvanced Lung Disease	2015	458
Congenital Heart Disease and Other Heterotaxic Defects in a Large Cohort of Patients With Primary Ciliary Dyskinesia Marcus P. Kennedy, Heymut Omran, Margaret W. Leigh, Circulation	2007	444
Chronic Mycobacterium abscessus infection and lung function decline in cystic fibrosis Charles R. Esther, Denise Esserman, Peter H. Gilligan, Journal of Cystic Fibrosis Microbial DiseasePathologyRespiratory InfectionInfectious Respiratory DiseasePulmonary Fibrosis	2010	400
<i>DNAH5</i> Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects Nada Hornef, Heike Olbrich, Judit Horváth, American Journal of Respiratory and Critical Care Medicine	2006	342
Cystic fibrosis gene mutations and pancreatitis risk: Relation to epithelial ion transport and trypsin inhibitor gene mutations Peadar G. Noone, Zhaoqing Zhou, Lawrence M. Silverman, Gastroenterology FibrosisEpithelial Ion TransportPancreatic CancerPathogenesisImmunology	2001	308

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