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Cells|September 26, 2025
ODAD4-Related Primary Ciliary Dyskinesia: Report of Five Cases and a Founder Variant in QuebecMarie-Hélène Bourassa, Guillaume Sillon, Shuizi Ding, et al.
Annals of the American Thoracic Society|September 13, 2013
Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesiaMargaret W Leigh, Milan J Hazucha, Kunal K Chawla, et al.
HGG Advances|June 1, 2022
Accounting for population structure in genetic studies of cystic fibrosisHanley Kingston, Adrienne M Stilp, William Gordon, et al.
Chronic Obstructive Pulmonary Diseases (Miami, Fla.)|October 27, 2020
Nutrition and Markers of Disease Severity in Patients With BronchiectasisKatherine A Despotes, Radmila Choate, Doreen Addrizzo-Harris, et al.
American Journal of Respiratory and Critical Care Medicine|July 22, 2006
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutationMaimoona A Zariwala, Margaret W Leigh, Franck Ceppa, et al.
Nature|February 27, 2009
Identification of IFRD1 as a modifier gene for cystic fibrosis lung diseaseYuanYuan Gu, Isaac T W Harley, Lindsay B Henderson, et al.
American Journal of Medical Genetics. Part A|October 4, 2024
Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary DyskinesiaM Makenzie Beaman, Weining Yin, Amanda J Smith, et al.
American Journal of Respiratory and Critical Care Medicine|November 26, 2019
Airway Mucus Hyperconcentration in Non-Cystic Fibrosis BronchiectasisKathryn A Ramsey, Alice C H Chen, Giorgia Radicioni, et al.
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