Human Kidney Cell Reprogramming: Applications for Disease Modeling and Personalized Medicine

Por O’Neill, Adam C., Ricardo, Sharon D.
Publicado em 2013

Mob2 Insufficiency Disrupts Neuronal Migration in the Developing Cortex

Por O’Neill, Adam C., Kyrousi, Christina, Einsiedler, Melanie, Burtscher, Ingo, Drukker, Micha, Markie, David M., Kirk, Edwin P., Götz, Magdalena, Robertson, Stephen P., Cappello, Silvia
Publicado no Front Cell Neurosci (2018)

Nucleus size and DNA accessibility are linked to the regulation of paraspeckle formation in cellular differentiation

Por Grosch, Markus, Ittermann, Sebastian, Rusha, Ejona, Greisle, Tobias, Ori, Chaido, Truong, Dong-Jiunn Jeffery, O’Neill, Adam C., Pertek, Anna, Westmeyer, Gil Gregor, Drukker, Micha
Publicado no BMC Biol (2020)

ECE2 regulates neurogenesis and neuronal migration during human cortical development

Por Buchsbaum, Isabel Y, Kielkowski, Pavel, Giorgio, Grazia, O'Neill, Adam C, Di Giaimo, Rossella, Kyrousi, Christina, Khattak, Shahryar, Sieber, Stephan A, Robertson, Stephen P, Cappello, Silvia
Publicado no EMBO Rep (2020)

Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

Por Bunn, Kieran J., Daniel, Phil, Rösken, Heleen S., O’Neill, Adam C., Cameron-Christie, Sophia R., Morgan, Tim, Brunner, Han G., Lai, Angeline, Kunst, Henricus P.M., Markie, David M., Robertson, Stephen P.
Publicado no Am J Hum Genet (2015)

De novo and inherited private variants in MAP1B in periventricular nodular heterotopia

Por Heinzen, Erin L., O'Neill, Adam C., Zhu, Xiaolin, Allen, Andrew S., Bahlo, Melanie, Chelly, Jamel, Chen, Ming Hui, Dobyns, William B., Freytag, Saskia, Guerrini, Renzo, Leventer, Richard J., Poduri, Annapurna, Robertson, Stephen P., Walsh, Christopher A., Zhang, Mengqi
Publicado no PLoS Genet (2018)