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Journal of Psychosomatic Research|July 4, 2021
The impact of the coronavirus (COVID-19) pandemic on individuals with gastrointestinal disorders: A protocol of an international collaborative studyNuno Ferreira, Antonina Mikocka-Walus, Miranda A L van Tilburg, et al.
American Journal of Human Genetics|January 23, 2019
Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary ClearanceXimena M Bustamante-Marin, Wei-Ning Yin, Patrick R Sears, et al.
Annals of the American Thoracic Society|November 28, 2022
Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and GenotypeBreAnna Kinghorn, Margaret Rosenfeld, Erin Sullivan, et al.
American Journal of Human Genetics|February 3, 2015
Gene expression in transformed lymphocytes reveals variation in endomembrane and HLA pathways modifying cystic fibrosis pulmonary phenotypesWanda K O'Neal, Paul Gallins, Rhonda G Pace, et al.
Pediatric Pulmonology|April 5, 2011
A novel lung disease phenotype adjusted for mortality attrition for cystic fibrosis genetic modifier studiesChelsea Taylor, Clayton W Commander, Joseph M Collaco, et al.
The Journal of Pediatrics|February 8, 2025
Overlapping Clinical Phenotypes in Patients with Primary Ciliary Dyskinesia or Activated Phosphoinositide 3-Kinase Delta SyndromeAdam J Shapiro, Eveline Y Wu, Deborah J Morris-Rosendahl, et al.
Hepatology (Baltimore, Md.)|March 27, 2024
Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesisJaclyn R Stonebraker, Rhonda G Pace, Paul J Gallins, et al.
Neurogastroenterology and Motility|May 11, 2026
A Clinical Practice Update for the Management of Patients With Disorders of Gut-Brain Interaction and Altered Food Intake BehaviorAyesha Shah, Nicholas J Talley, Simon R Knowles, et al.
Plos Genetics|February 27, 2019
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier lociJiafen Gong, Fan Wang, Bowei Xiao, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|April 12, 2019
The Clinical Features of Bronchiectasis Associated with Alpha-1 Antitrypsin Deficiency, Common Variable Immunodeficiency and Primary Ciliary Dyskinesia--Results from the U.S. Bronchiectasis Research RegistryEdward Eden, Radmila Choate, Alan Barker, et al.
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