Toward more predictive genetic mouse models of Alzheimer’s disease

Por Onos, Kristen D., Sukoff Rizzo, Stacey J., Howell, Gareth R., Sasner, Michael
Publicado no Brain Res Bull (2015)

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy

Por Asinof, Samuel K., Sukoff Rizzo, Stacey J., Buckley, Alexandra R., Beyer, Barbara J., Letts, Verity A., Frankel, Wayne N., Boumil, Rebecca M.
Publicado no PLoS Genet (2015)

Negative Allosteric Modulation of the mGluR5 Receptor Reduces Repetitive Behaviors and Rescues Social Deficits in Mouse Models of Autism

Por Silverman, Jill L., Smith, Daniel G., Sukoff Rizzo, Stacey J., Karras, Michael N., Turner, Sarah M., Tolu, Seda S., Bryce, Dianne K., Smith, Deborah L., Fonseca, Kari, Ring, Robert H., Crawley, Jacqueline N.
Publicado no Sci Transl Med (2012)

Behavioral Characterization of A53T Mice Reveals Early and Late Stage Deficits Related to Parkinson’s Disease

Por Paumier, Katrina L., Sukoff Rizzo, Stacey J., Berger, Zdenek, Chen, Yi, Gonzales, Cathleen, Kaftan, Edward, Li, Li, Lotarski, Susan, Monaghan, Michael, Shen, Wei, Stolyar, Polina, Vasilyev, Dmytro, Zaleska, Margaret, D. Hirst, Warren, Dunlop, John
Publicado em 2013

Analysis of sleep traits in knockout mice from the large-scale KOMP2 population using a non-invasive, high-throughput piezoelectric system

Por Sethi, Mansi, Joshi, Shreyas S, Striz, Martin, Cole, Neil, Ryan, Jennifer, Lhamon, Michael E, Agarwal, Anuj, Sukoff Rizzo, Stacey J, Denegre, James M, Braun, Robert E, Fardo, David W, Donohue, Kevin D, Chesler, Elissa J, Svenson, Karen L, O'Hara, Bruce F
Publicado no BMC Bioinformatics (2015)

Phosphodiesterase 11A in brain is enriched in ventral hippocampus and deletion causes psychiatric disease-related phenotypes

Por Kelly, Michele P., Logue, Sheree F., Brennan, Julie, Day, Jonathon P., Lakkaraju, Subha, Jiang, Lixin, Zhong, Xiaotian, Tam, May, Sukoff Rizzo, Stacey J., Platt, Brian J., Dwyer, Jason M., Neal, Sarah, Pulito, Virginia L., Agostino, Michael J., Grauer, Steven M., Navarra, Rachel L., Kelley, Cody, Comery, Thomas A., Murrills, Richard J., Houslay, Miles D., Brandon, Nicholas J.
Publicado em 2010

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

Por Diggle, Christine P., Sukoff Rizzo, Stacey J., Popiolek, Michael, Hinttala, Reetta, Schülke, Jan-Philip, Kurian, Manju A., Carr, Ian M., Markham, Alexander F., Bonthron, David T., Watson, Christopher, Sharif, Saghira Malik, Reinhart, Veronica, James, Larry C., Vanase-Frawley, Michelle A., Charych, Erik, Allen, Melanie, Harms, John, Schmidt, Christopher J., Ng, Joanne, Pysden, Karen, Strick, Christine, Vieira, Päivi, Mankinen, Katariina, Kokkonen, Hannaleena, Kallioinen, Matti, Sormunen, Raija, Rinne, Juha O., Johansson, Jarkko, Alakurtti, Kati, Huilaja, Laura, Hurskainen, Tiina, Tasanen, Kaisa, Anttila, Eija, Marques, Tiago Reis, Howes, Oliver, Politis, Marius, Fahiminiya, Somayyeh, Nguyen, Khanh Q., Majewski, Jacek, Uusimaa, Johanna, Sheridan, Eamonn, Brandon, Nicholas J.
Publicado no Am J Hum Genet (2016)