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Human Mutation|January 19, 2016
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential DiagnosisIsrael Amirav, Julia Wallmeier, Niki T Loges, et al.
American Journal of Respiratory Cell and Molecular Biology|September 24, 2019
SPEF2- and HYDIN-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia DiagnosticsSandra Cindrić, Gerard W Dougherty, Heike Olbrich, et al.
Nature Genetics|January 29, 2013
The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humansMaureen Wirschell, Heike Olbrich, Claudius Werner, et al.
American Journal of Human Genetics|September 22, 2015
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory ComplexHeike Olbrich, Carolin Cremers, Niki T Loges, et al.
Developmental Cell|December 20, 2017
Evolutionary Proteomics Uncovers Ancient Associations of Cilia with Signaling PathwaysMonika Abedin Sigg, Tabea Menchen, Chanjae Lee, et al.
The European Respiratory Journal|July 11, 2024
A range of 30-62% of functioning multiciliated airway cells is sufficient to maintain ciliary airway clearanceNiki T Loges, June Kehlet Marthin, Johanna Raidt, et al.
American Journal of Human Genetics|August 4, 2016
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dyskinesia with Left-Right Body Asymmetry RandomizationJulia Wallmeier, Hidetaka Shiratori, Gerard W Dougherty, et al.
American Journal of Human Genetics|May 5, 2018
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein ArmsInga M Höben, Rim Hjeij, Heike Olbrich, et al.
American Journal of Human Genetics|November 26, 2018
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating DefectsNiki T Loges, Dinu Antony, Ales Maver, et al.
Nature Genetics|April 22, 2014
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile ciliaJulia Wallmeier, Dalal A Al-Mutairi, Chun-Ting Chen, et al.
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