Dr Maria Kasherman
Casual Senior Research Technician
School of Biomedical Sciences
Publications
Journal Articles
Kojic, Marija, Gawda, Tomasz, Gaik, Monika, Begg, Alexander, Salerno-Kochan, Anna, Kurniawan, Nyoman D., Jones, Alun, Drożdżyk, Katarzyna, Kościelniak, Anna, Chramiec-Głąbik, Andrzej, Hediyeh-Zadeh, Soroor, Kasherman, Maria, Shim, Woo Jun, Sinniah, Enakshi, Genovesi, Laura A., Abrahamsen, Rannvá K., Fenger, Christina D., Madsen, Camilla G., Cohen, Julie S., Fatemi, Ali, Stark, Zornitza, Lunke, Sebastian, Lee, Joy, Hansen, Jonas K., Boxill, Martin F., Keren, Boris, Marey, Isabelle, Saenz, Margarita S., Brown, Kathleen ... Wainwright, Brandon J. (2021). Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype. Nature Communications, 12 (1) 2678, 2678. doi: 10.1038/s41467-021-22888-5
Kasherman, Maria A., Currey, Laura, Kurniawan, Nyoman D., Zalucki, Oressia, Vega, Michelle Sanchez, Jolly, Lachlan A., Burne, Thomas H. J., Wood, Stephen A. and Piper, Michael (2020). Abnormal behavior and cortical connectivity deficits in mice lacking Usp9x. Cerebral Cortex, 31 (3), 1763-1775. doi: 10.1093/cercor/bhaa324
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
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, 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