Julie C. Van De Weghe
University of Washington(US)
Publications by Year
Research Areas
Genetic and Kidney Cyst Diseases, Hedgehog Signaling Pathway Studies, Protist diversity and phylogeny, Fetal and Pediatric Neurological Disorders, Epigenetics and DNA Methylation
Most-Cited Works
- → Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome(2017)176 cited
- → Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish(2017)88 cited
- → Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome(2020)83 cited
- → The Joubert–Meckel–Nephronophthisis Spectrum of Ciliopathies(2022)59 cited
- → Diffusion rather than intraflagellar transport likely provides most of the tubulin required for axonemal assembly in Chlamydomonas(2020)53 cited
- → Protein transport in growing and steady‐state cilia(2017)52 cited
- → Systematic analysis of cilia characteristics and Hedgehog signaling in five immortal cell lines(2022)16 cited
- → TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes(2020)14 cited
- → Diffusion rather than IFT provides most of the tubulin required for axonemal assembly(2018)9 cited
- → Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome(2017)8 cited