Insights Gained From Zebrafish Models for the Ciliopathy Joubert Syndrome by Rusterholz, Tamara D. S., Hofmann, Claudia, Bachmann-Gagescu, Ruxandra

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Shared and unique consequences of Joubert Syndrome gene dysfunction on the zebrafish central nervous system by Noble, Alexandra R, Masek, Markus, Hofmann, Claudia, Cuoco, Arianna, Rusterholz, Tamara D S, Özkoc, Hayriye, Greter, Nadja R, Phelps, Ian G, Vladimirov, Nikita, Kollmorgen, Sepp, Stoeckli, Esther, Bachmann-Gagescu, Ruxandra

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Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome by Latour, Brooke L, Van De Weghe, Julie C, Rusterholz, Tamara Ds, Letteboer, Stef Jf, Gomez, Arianna, Shaheen, Ranad, Gesemann, Matthias, Karamzade, Arezou, Asadollahi, Mostafa, Barroso-Gil, Miguel, Chitre, Manali, Grout, Megan E, van Reeuwijk, Jeroen, van Beersum, Sylvia Ec, Miller, Caitlin V, Dempsey, Jennifer C, Morsy, Heba, Bamshad, Michael J, Nickerson, Deborah A, Neuhauss, Stephan Cf, Boldt, Karsten, Ueffing, Marius, Keramatipour, Mohammad, Sayer, John A, Alkuraya, Fowzan S, Bachmann-Gagescu, Ruxandra, Roepman, Ronald, Doherty, Dan

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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish by Van De Weghe, Julie C., Rusterholz, Tamara D.S., Latour, Brooke, Grout, Megan E., Aldinger, Kimberly A., Shaheen, Ranad, Dempsey, Jennifer C., Maddirevula, Sateesh, Cheng, Yong-Han H., Phelps, Ian G., Gesemann, Matthias, Goel, Himanshu, Birk, Ohad S., Alanzi, Talal, Rawashdeh, Rifaat, Khan, Arif O., Bamshad, Michael J., Nickerson, Deborah A., Neuhauss, Stephan C.F., Dobyns, William B., Alkuraya, Fowzan S., Roepman, Ronald, Bachmann-Gagescu, Ruxandra, Doherty, Dan

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