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BMC Medical Genomics|May 24, 2019
Transcriptional consequences of impaired immune cell responses induced by cystic fibrosis plasma characterized via dual RNA sequencingJustin E Ideozu, Vittobai Rangaraj, Hiam Abdala-Valencia, et al.
Pediatric Pulmonology|August 11, 2015
Changing incidence of cystic fibrosis in Wisconsin, USAKatelyn Parker-McGill, Melodee Nugent, Rachel Bersie, et al.
Journal of Medical Case Reports|April 28, 2010
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case reportHara Levy, Carolynn L Cannon, Daniel Asher, et al.
American Journal of Respiratory Cell and Molecular Biology|March 9, 2019
Cystic Fibrosis Plasma Blunts the Immune Response to Bacterial InfectionXi Zhang, Amy Pan, Shuang Jia, et al.
The Journal of Pediatrics|January 29, 2017
Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive DiagnosisClement L Ren, Drucy S Borowitz, Tanja Gonska, et al.
The European Respiratory Journal|January 8, 2022
C FTR variants are associated with chronic bronchitis in smokersAabida Saferali, Dandi Qiao, Wonji Kim, et al.
Pediatric Pulmonology|January 25, 2007
Inflammatory markers of lung disease in adult patients with cystic fibrosisHara Levy, Leslie A Kalish, Ian Huntington, et al.
Pediatric Pulmonology|March 26, 2008
Predictors of mucoid Pseudomonas colonization in cystic fibrosis patientsHara Levy, Leslie A Kalish, Carolyn L Cannon, et al.
The American Journal of Clinical Nutrition|March 25, 2011
Growth and pulmonary outcomes during the first 2 y of life of breastfed and formula-fed infants diagnosed with cystic fibrosis through the Wisconsin Routine Newborn Screening ProgramSarah A Jadin, Grace S Wu, Zhumin Zhang, et al.
Genome Medicine|March 22, 2024
Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequencesJustin E Ideozu, Mengzhen Liu, Bridget M Riley-Gillis, et al.
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