Publications
Journal Articles
Kasherman, Maria A., Premarathne, Susitha, Burne, Thomas H. J., Wood, Stephen A. and Piper, Michael (2020). The ubiquitin system: a regulatory hub for intellectual disability and autism spectrum disorder. Molecular Neurobiology, 57 (5), 2179-2193. doi: 10.1007/s12035-020-01881-x
Johnson, Brett V., Kumar, Raman, Oishi, Sabrina, Alexander, Suzy, Kasherman, Maria, Vega, Michelle Sanchez, Ivancevic, Atma, Gardner, Alison, Domingo, Deepti, Corbett, Mark, Parnell, Euan, Yoon, Sehyoun, Oh, Tracey, Lines, Matthew, Lefroy, Henrietta, Kini, Usha, Van Allen, Margot, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Bézieau, Stéphane, Pasquier, Laurent, Raynaud, Martine, Afenjar, Alexandra, Billette de Villemeur, Thierry, Keren, Boris, Désir, Julie, Van Maldergem, Lionel, Marangoni, Martina ... Jolly, Lachlan A. (2020). Partial loss of USP9X function leads to a male neurodevelopmental and behavioural disorder converging on TGFβ signalling. Biological Psychiatry, 87 (2), 100-112. doi: 10.1016/j.biopsych.2019.05.028
Oishi, Sabrina, Zalucki, Oressia, Sanchez Vega, Michelle, Harkins, Danyon, Harvey, Tracey J., Kasherman, Maria, Davila, Raul A., Hale, Lauren, White, Melissa, Piltz, Sandra, Thomas, Paul, Burne, Thomas H.J., Harris, Lachlan and Piper, Michael (2020). Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1. Genes, Brain and Behavior, 19 (4) e12637, e12637. doi: 10.1111/gbb.12637
Oishi, Sabrina, Harkins, Danyon, Kurniawan, Nyoman D., Kasherman, Maria, Harris, Lachlan, Zalucki, Oressia, Gronostajski, Richard M., Burne, Thomas H.J. and Piper, Michael (2018). Heterozygosity for Nuclear Factor One X in mice models features of Malan syndrome. EBioMedicine, 39, 388-400. doi: 10.1016/j.ebiom.2018.11.044