Altered structural connectivity networks in a mouse model of complete and partial dysgenesis of the corpus callosum

by Timothy J. Edwards, Laura R. Fenlon, Ryan J. Dean, Jens Bunt, Elliott H. Sherr, Linda J. Richards
Published 2020-08-01

Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

by Elysa Jill Marco, Anne Brandes Aitken, Vishnu Prakas Nair, Gilberto da Gente, Molly Rae Gerdes, Leyla Bologlu, Sean Thomas, Elliott H. Sherr
Published 2018-05-01

Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum

by Ilan Gobius, Laura Morcom, Rodrigo Suárez, Jens Bunt, Polina Bukshpun, William Reardon, William B. Dobyns, John L.R. Rubenstein, A. James Barkovich, Elliott H. Sherr, Linda J. Richards
Published 2016-10-01

Abnormal auditory and language pathways in children with 16p11.2 deletion

by Jeffrey I. Berman, Darina Chudnovskaya, Lisa Blaskey, Emily Kuschner, Pratik Mukherjee, Randall Buckner, Srikantan Nagarajan, Wendy K. Chung, John E. Spiro, Elliott H. Sherr, Timothy P.L. Roberts
Published 2015-01-01

Quantitative trait loci for interhemispheric commissure development and social behaviors in the BTBR T⁺ tf/J mouse model of autism.

by Dorothy M Jones-Davis, Mu Yang, Eric Rider, Nathan C Osbun, Gilberto J da Gente, Jiang Li, Adam M Katz, Michael D Weber, Saunak Sen, Jacqueline Crawley, Elliott H Sherr
Published 2013-01-01

Early Predictors of Impaired Social Functioning in Male Rhesus Macaques (Macaca mulatta).

by Valentina Sclafani, Laura A Del Rosso, Shannon K Seil, Laura A Calonder, Jesus E Madrid, Kyle J Bone, Elliott H Sherr, Joseph P Garner, John P Capitanio, Karen J Parker
Published 2016-01-01

Autism-associated biomarkers: test–retest reliability and relationship to quantitative social trait variation in rhesus monkeys

by Ozge Oztan, Catherine F. Talbot, Emanuela Argilli, Alyssa C. Maness, Sierra M. Simmons, Noreen Mohsin, Laura A. Del Rosso, Joseph P. Garner, Elliott H. Sherr, John P. Capitanio, Karen J. Parker
Published 2021-07-01

White Matter Changes of Neurite Density and Fiber Orientation Dispersion during Human Brain Maturation.

by Yi Shin Chang, Julia P Owen, Nicholas J Pojman, Tony Thieu, Polina Bukshpun, Mari L J Wakahiro, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, Elliott H Sherr, Pratik Mukherjee
Published 2015-01-01

DRAXIN regulates interhemispheric fissure remodelling to influence the extent of corpus callosum formation

by Laura Morcom, Timothy J Edwards, Eric Rider, Dorothy Jones-Davis, Jonathan WC Lim, Kok-Siong Chen, Ryan J Dean, Jens Bunt, Yunan Ye, Ilan Gobius, Rodrigo Suárez, Simone Mandelstam, Elliott H Sherr, Linda J Richards
Published 2021-05-01

The role of corpus callosum development in functional connectivity and cognitive processing.

by Leighton B N Hinkley, Elysa J Marco, Anne M Findlay, Susanne Honma, Rita J Jeremy, Zoe Strominger, Polina Bukshpun, Mari Wakahiro, Warren S Brown, Lynn K Paul, A James Barkovich, Pratik Mukherjee, Srikantan S Nagarajan, Elliott H Sherr
Published 2012-01-01

Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.

by Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun, Mari Wakahiro, Susan L Christian, Jean-Baptiste Rivière, Christopher T Sullivan, Jyotsna Sudi, Michael J Herriges, Alexander R Paciorkowski, A James Barkovich, Joseph T Glessner, Kathleen J Millen, Hakon Hakonarson, William B Dobyns, Elliott H Sherr
Published 2013-01-01

DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation

by Laura Morcom, Ilan Gobius, Ashley PL Marsh, Rodrigo Suárez, Jonathan WC Lim, Caitlin Bridges, Yunan Ye, Laura R Fenlon, Yvrick Zagar, Amelia M Douglass, Amber-Lee S Donahoo, Thomas Fothergill, Samreen Shaikh, Peter Kozulin, Timothy J Edwards, Helen M Cooper, IRC5 Consortium, Elliott H Sherr, Alain Chédotal, Richard J Leventer, Paul J Lockhart, Linda J Richards
Published 2021-04-01

NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.

by Weining Lu, Fabiola Quintero-Rivera, Yanli Fan, Fowzan S Alkuraya, Diana J Donovan, Qiongchao Xi, Annick Turbe-Doan, Qing-Gang Li, Craig G Campbell, Alan L Shanske, Elliott H Sherr, Ayesha Ahmad, Roxana Peters, Benedict Rilliet, Paloma Parvex, Alexander G Bassuk, David J Harris, Heather Ferguson, Chantal Kelly, Christopher A Walsh, Richard M Gronostajski, Koenraad Devriendt, Anne Higgins, Azra H Ligon, Bradley J Quade, Cynthia C Morton, James F Gusella, Richard L Maas
Published 2007-05-01