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Julie Craft Van De Weghe

TitleProf,Asst
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentCell Biology
AddressBRC 264
975 NE 10th St
Oklahoma City OK 73104
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    R00HD100554     (VAN DE WEGHE, JULIE CRAFT)Sep 15, 2022 - Aug 31, 2025
    NIH
    Integrating functional proteomics, genome engineering, and live-cell microscopy to the study of ciliopathies
    Role: Principal Investigator
    K99HD100554     (VAN DE WEGHE, JULIE CRAFT)May 1, 2020 - Jul 31, 2022
    NIH
    Integrating functional proteomics, genome engineering, and live-cell microscopy to the study of ciliopathies
    Role: Principal Investigator
    F32HD095599     (VAN DE WEGHE, JULIE CRAFT)Aug 16, 2018 - Aug 15, 2021
    NIH
    Determining the Molecular Mechanisms of Joubert Syndrome Using Patient Derived Cell Lines
    Role: Principal Investigator

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    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. G?mez AE, Christman AK, Van De Weghe JC, Finn M, Doherty D. Systematic analysis of cilia characteristics and Hedgehog signaling in five immortal cell lines. PLoS One. 2022; 17(12):e0266433. PMID: 36580465; PMCID: PMC9799305.
      Citations: 2     Fields:    Translation:HumansAnimalsCells
    2. Van De Weghe JC, Gomez A, Doherty D. The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies. Annu Rev Genomics Hum Genet. 2022 08 31; 23:301-329. PMID: 35655331; PMCID: PMC9437135.
      Citations: 8     Fields:    Translation:HumansCells
    3. Van De Weghe JC, Giordano JL, Mathijssen IB, Mojarrad M, Lugtenberg D, Miller CV, Dempsey JC, Mohajeri MSA, van Leeuwen E, Pajkrt E, Klaver CCW, Houlden H, Eslahi A, Waters AM, University of Washington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Aggarwal VS, de Vries BBA, Maroofian R, Doherty D. TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes. HGG Adv. 2021 Jan 14; 2(1). PMID: 33791682; PMCID: PMC8009330.
      Citations: 8     Fields:    
    4. Latour BL, Van De Weghe JC, Rusterholz TD, Letteboer SJ, Gomez A, Shaheen R, Gesemann M, Karamzade A, Asadollahi M, Barroso-Gil M, Chitre M, Grout ME, van Reeuwijk J, van Beersum SE, Miller CV, Dempsey JC, Morsy H, University of Washington Center for Mendelian Genomics, Bamshad MJ, Genomics England Research Consortium, Nickerson DA, Neuhauss SC, Boldt K, Ueffing M, Keramatipour M, Sayer JA, Alkuraya FS, Bachmann-Gagescu R, Roepman R, Doherty D. Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome. J Clin Invest. 2020 08 03; 130(8):4423-4439. PMID: 32453716; PMCID: PMC7410078.
      Citations: 28     Fields:    Translation:HumansAnimalsCells
    5. Shi X, Garcia G, Van De Weghe JC, McGorty R, Pazour GJ, Doherty D, Huang B, Reiter JF. Erratum: Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome. Nat Cell Biol. 2017 10 31; 19(11):1379. PMID: 29087383.
      Citations: 6     Fields:    
    6. Shi X, Garcia G, Van De Weghe JC, McGorty R, Pazour GJ, Doherty D, Huang B, Reiter JF. Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome. Nat Cell Biol. 2017 Oct; 19(10):1178-1188. PMID: 28846093; PMCID: PMC5695680.
      Citations: 77     Fields:    Translation:HumansAnimalsCells
    7. Van De Weghe JC, Rusterholz TDS, Latour B, Grout ME, Aldinger KA, Shaheen R, Dempsey JC, Maddirevula S, Cheng YH, Phelps IG, Gesemann M, Goel H, Birk OS, Alanzi T, Rawashdeh R, Khan AO, University of Washington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Neuhauss SCF, Dobyns WB, Alkuraya FS, Roepman R, Bachmann-Gagescu R, Doherty D. Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish. Am J Hum Genet. 2017 Jul 06; 101(1):23-36. PMID: 28625504; PMCID: PMC5501774.
      Citations: 41     Fields:    Translation:HumansAnimalsCells
    8. Lechtreck KF, Van De Weghe JC, Harris JA, Liu P. Protein transport in growing and steady-state cilia. Traffic. 2017 05; 18(5):277-286. PMID: 28248449; PMCID: PMC5389924.
      Citations: 17     Fields:    Translation:HumansAnimalsCells
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