Query author contributions in Reactome

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Details on Person Leigh, Margaret W

Class:Id	Person:9960882
_displayName	Leigh, Margaret W
_timestamp	2025-07-17 16:09:29
created	[InstanceEdit:9960901] Rothfels, Karen, 2025-07-17
firstname	Margaret W
initial	MW
surname	Leigh
(author)	[LiteratureReference:9960886] De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry [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:9969682] Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia [LiteratureReference:9969740] Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms [LiteratureReference:9975946] Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects [LiteratureReference:9976684] The role of SPAG1 in the assembly of axonemal dyneins in human airway epithelia [LiteratureReference:9980604] Motile ciliopathies [LiteratureReference:9981280] Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia [LiteratureReference:9983828] Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesia
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No pathways have been reviewed or authored by Leigh, Margaret W (9960882)