Heike Olbrich
Muenster, NW, Germany
Last Updated: 09/26/2026
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Found 53 publications
Limitations of PICADAR as a diagnostic predictive tool for primary ciliary dyskinesia.
Journal: Frontiers in molecular biosciences
Published: August 24, 2025
mRNA therapy improves the composition and motility in CCDC40-deficient cilia in vitro and in vivo.
Journal: American journal of respiratory cell and molecular biology
Published: July 30, 2025
mRNA therapy improves the composition and motility in CCDC40-deficient cilia in vitro and in vivo.
Journal: American journal of respiratory cell and molecular biology
Published: July 30, 2025
Clinical, phenotype and genotype correlations in primary ciliary dyskinesia suspected children in Egypt.
Journal: Frontiers in molecular biosciences
Published: June 05, 2025
Pathogenic KIAA0586/TALPID3 variants are associated with defects in primary and motile cilia.
Journal: iScience
Published: June 19, 2024
Biallelic Variants in MNS1 Are Associated with Laterality Defects and Respiratory Involvement.
Journal: Cells
Published: April 30, 2024
Pathogenic variants in CFAP46, CFAP54, CFAP74 and CFAP221 cause primary ciliary dyskinesia with a defective C1d projection of the central apparatus.
Journal: The European respiratory journal
Published: April 25, 2024
Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.
Journal: American journal of respiratory and critical care medicine
Published: April 16, 2024
Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype-phenotype correlations.
Journal: The European respiratory journal
Published: October 17, 2023
A range of 30-62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearance.
Journal: The European respiratory journal
Published: August 25, 2023
Last Updated: 09/26/2026