Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth von Homan, Claire C., Kumar, Raman, Nguyen, Lam Son, Haan, Eric, Raymond, F. Lucy, Abidi, Fatima, Raynaud, Martine, Schwartz, Charles E., Wood, Stephen A., Gecz, Jozef, Jolly, Lachlan A.

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Viperin is an important host restriction factor in control of Zika virus infection von Van der Hoek, Kylie H., Eyre, Nicholas S., Shue, Byron, Khantisitthiporn, Onruedee, Glab-Ampi, Kittirat, Carr, Jillian M., Gartner, Matthew J., Jolly, Lachlan A., Thomas, Paul Q., Adikusuma, Fatwa, Jankovic-Karasoulos, Tanja, Roberts, Claire T., Helbig, Karla J., Beard, Michael R.

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PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy von Homan, Claire C., Pederson, Stephen, To, Thu-Hien, Tan, Chuan, Piltz, Sandra, Corbett, Mark A., Wolvetang, Ernst, Thomas, Paul Q., Jolly, Lachlan A., Gecz, Jozef

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A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability von LINGLI HUANG, JOLLY, Lachlan A, HACKETT, Anna, FIELD, Michael, FROYEN, Guy, HAO HU, HAAS, Stefan A, ROPERS, Hans-Hilger, KALSCHEUER, Vera M, CORBETT, Mark A, GECZ, Jozef, WILLIS-OWEN, Saffron, GARDNER, Alison, KUMAR, Raman, DOUGLAS, Evelyn, SHOUBRIDGE, Cheryl, WIECZOREK, Dagmar, TZSCHACH, Andreas, COHEN, Monika

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THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability von Kumar, Raman, Corbett, Mark A., van Bon, Bregje W.M., Woenig, Joshua A., Weir, Lloyd, Douglas, Evelyn, Friend, Kathryn L., Gardner, Alison, Shaw, Marie, Jolly, Lachlan A., Tan, Chuan, Hunter, Matthew F., Hackett, Anna, Field, Michael, Palmer, Elizabeth E., Leffler, Melanie, Rogers, Carolyn, Boyle, Jackie, Bienek, Melanie, Jensen, Corinna, Van Buggenhout, Griet, Van Esch, Hilde, Hoffmann, Katrin, Raynaud, Martine, Zhao, Huiying, Reed, Robin, Hu, Hao, Haas, Stefan A., Haan, Eric, Kalscheuer, Vera M., Gecz, Jozef

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Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors von Premarathne, Susitha, Murtaza, Mariyam, Matigian, Nicholas, Jolly, Lachlan A., Wood, Stephen A.

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Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis von Stegeman, Shane, Jolly, Lachlan A, Premarathne, Susitha, Gecz, Jozef, Richards, Linda J, Mackay-Sim, Alan, Wood, Stephen A

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La FAM fatale: USP9X in development and disease von Murtaza, Mariyam, Jolly, Lachlan A., Gecz, Jozef, Wood, Stephen A.

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Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment von Bhattacharjee, Rudrarup, Jolly, Lachlan A., Corbett, Mark A., Wee, Ing Chee, Rao, Sushma R., Gardner, Alison E., Ritchie, Tarin, van Hugte, Eline J. H., Ciptasari, Ummi, Piltz, Sandra, Noll, Jacqueline E., Nazri, Nazzmer, van Eyk, Clare L., White, Melissa, Fornarino, Dani, Poulton, Cathryn, Baynam, Gareth, Collins-Praino, Lyndsey E., Snel, Marten F., Nadif Kasri, Nael, Hemsley, Kim M., Thomas, Paul Q., Kumar, Raman, Gecz, Jozef

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USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors von Bridges, Caitlin R., Tan, Men-Chee, Premarathne, Susitha, Nanayakkara, Devathri, Bellette, Bernadette, Zencak, Dusan, Domingo, Deepti, Gecz, Jozef, Murtaza, Mariyam, Jolly, Lachlan A., Wood, Stephen A.

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La FAM fatale: USP9X in development and disease von Murtaza, Mariyam, Jolly, Lachlan A., Gecz, Jozef, Wood, Stephen A.

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Vav Proteins in Development of the Brain: A Potential Relationship to the Pathogenesis of Congenital Zika Syndrome? von Norbury, Aidan J, Jolly, Lachlan A, Kris, Luke P, Carr, Jillian M

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The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental Disorders von Jolly, Lachlan A., Kumar, Raman, Penzes, Peter, Piper, Michael, Gecz, Jozef

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Endogenous protein interactomes resolved through immunoprecipitation-coupled quantitative proteomics in cell lines von Kumar, Raman, Kamath, Karthik S., Carroll, Luke, Hoffmann, Peter, Gecz, Jozef, Jolly, Lachlan A.

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Robust imaging and gene delivery to study human lymphoblastoid cell lines von Jolly, Lachlan A, Sun, Ying, Carroll, Renée, Homan, Claire C, Gecz, Jozef

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USP9X enhances the polarity and self-renewal of embryonic stem cell-derived neural progenitors von Jolly, Lachlan A, Taylor, Verdon, Wood, Stephen A

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The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth von Jolly, Lachlan A, Homan, Claire C, Jacob, Reuben, Barry, Simon, Gecz, Jozef

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Missense variant contribution to USP9X-female syndrome von Jolly, Lachlan A., Parnell, Euan, Gardner, Alison E., Corbett, Mark A., Pérez-Jurado, Luis A., Shaw, Marie, Lesca, Gaetan, Keegan, Catherine, Schneider, Michael C., Griffin, Emily, Maier, Felicitas, Kiss, Courtney, Guerin, Andrea, Crosby, Kathleen, Rosenbaum, Kenneth, Tanpaiboon, Pranoot, Whalen, Sandra, Keren, Boris, McCarrier, Julie, Basel, Donald, Sadedin, Simon, White, Susan M., Delatycki, Martin B., Kleefstra, Tjitske, Küry, Sébastien, Brusco, Alfredo, Sukarova-Angelovska, Elena, Trajkova, Slavica, Yoon, Sehoun, Wood, Stephen A., Piper, Michael, Penzes, Peter, Gecz, Jozef

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Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder von Kumar, Raman, Corbett, Mark A, Smith, Nicholas J C, Jolly, Lachlan A, Tan, Chuan, Keating, Damien J, Duffield, Michael D, Utsumi, Toshihiko, Moriya, Koko, Smith, Katherine R, Hoischen, Alexander, Abbott, Kim, Harbord, Michael G, Compton, Alison G, Woenig, Joshua A, Arts, Peer, Kwint, Michael, Wieskamp, Nienke, Gijsen, Sabine, Veltman, Joris A, Bahlo, Melanie, Gleeson, Joseph G, Haan, Eric, Gecz, Jozef

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Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells von Lehmann, Rebecca J., Jolly, Lachlan A., Johnson, Brett V., Lord, Megan S., Kim, Ha Na, Saville, Jennifer T., Fuller, Maria, Byers, Sharon, Derrick-Roberts, Ainslie L.K.

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