Julia Wallmeier
Muenster, NW, Germany
Last Updated: 09/26/2026
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Found 31 publications
HIPK4 is a novel gene associated with teratozoospermia and male infertility.
Journal: Human reproduction open
Published: February 20, 2026
Pathogenic KIAA0586/TALPID3 variants are associated with defects in primary and motile cilia.
Journal: iScience
Published: June 19, 2024
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.
Journal: Science (New York, N.Y.)
Published: April 25, 2024
miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary Disassembly.
Journal: International journal of molecular sciences
Published: June 23, 2022
The role of cilia for hydrocephalus formation.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: February 24, 2022
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure.
Journal: Annals of the American Thoracic Society
Published: February 24, 2022
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly.
Journal: American journal of human genetics
Published: January 15, 2021
Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system.
Journal: Molecular human reproduction
Published: April 28, 2020
CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module.
Journal: Nature communications
Published: November 03, 2019
Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of DNAH5 in Humans and Mice.
Journal: Circulation. Genomic and precision medicine
Published: October 23, 2019
Last Updated: 09/26/2026