Query author contributions in Reactome

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Details on Person Werner, Claudius

Class:Id	Person:9945657
_displayName	Werner, Claudius
_timestamp	2025-04-16 19:18:13
created	[InstanceEdit:9945652] Rothfels, Karen, 2025-04-16
firstname	Claudius
initial	C
surname	Werner
(author)	[LiteratureReference:9945663] MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia [LiteratureReference:9961934] Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia [LiteratureReference:9961942] Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis [LiteratureReference:9966692] CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module [LiteratureReference:9966698] CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module [LiteratureReference:9968797] CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms [LiteratureReference:9968814] DYX1C1 is required for axonemal dynein assembly and ciliary motility [LiteratureReference:9969018] ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6 [LiteratureReference:9969740] Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms [LiteratureReference:9969774] Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects
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No pathways have been reviewed or authored by Werner, Claudius (9945657)