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Local synchronization of cilia and tissue-scale cilia alignment are sufficient for global metachronal waves2021 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genetic and Kidney Cyst Diseases Open access
Christa Ringers, Stephan Bialonski, A. S. Solov’ev, Jan N. Hansen, Mert Ege, Benjamin M. Friedrich, +1 more
2citations -
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability2025 The American Journal of Human Genetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Ariane Kröll‐Hermi, Corinne Stoetzel, Christelle Etard, Levon Halabelian, Élise Schaefer, Sophie Scheidecker, +80 more
1citations -
A Homozygous CPSF1 Variant Causes Congenital Cataract, Intellectual Disability and Hyperphagia2026 Clinical Genetics article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases
Ozge Aksel Kilicarslan, Andrea Gangfuß, Andreas Hentschel, Heike Kölbel, David Muhmann, Ana Töpf, +10 more
1citations -
LacR and TrxB are key virulence factors involved in pneumococcal meningitis as identified by a genome-wide association study2026 Communications Biology article Immunology and Microbiology Bacterial Infections and Vaccines Open access
Rutger Koning, Kin Ki Jim, Philip H. C. Kremer, Hsueh-Chien Raymond Cheng, Valery Jaspers, Bart Ferwerda, +9 more
0citations -
DRAM1 promotes antibacterial autophagy and lysosomal delivery of Mycobacterium marinum in macrophages2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Medicine Autophagy in Disease and Therapy Open access
Adrianna Banducci-Karp, Jiajun Xie, Sem A.G. Engels, Christos Sarantaris, Mónica Varela, Annemarie H. Meijer, +1 more
0citations