Epileptic Encephalopathies: New Genes and New Pathways

Por Esmaeeli Nieh, Sahar, Sherr, Elliott H.
Publicado no Neurotherapeutics (2014)

A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyria

Por Bassuk, Alexander G., Sherr, Elliott H.
Publicado no J Neurogenet (2016)

Agenesis of the Corpus Callosum in California 1983−2003: A Population-Based Study

Por Glass, Hannah C., Shaw, Gary M., Ma, Chen, Sherr, Elliott H.
Publicado em 2008

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes

Por Edwards, Timothy J., Sherr, Elliott H., Barkovich, A. James, Richards, Linda J.
Publicado em 2014

Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability

Por Edwards, Timothy J., Sherr, Elliott H., Barkovich, A. James, Richards, Linda J.
Publicado no Brain (2016)

Individuals with agenesis of the corpus callosum show sensory processing differences as measured by the Sensory Profile

Por Demopoulos, Carly, Arroyo, Monica S., Dunn, Winnie, Strominger, Zoe, Sherr, Elliott H., Marco, Elysa
Publicado no Neuropsychology (2014)

Diffusion Tensor Imaging of Aicardi Syndrome

Por Wahl, Michael, Strominger, Zoe A., Wakahiro, Mari, Jeremy, Rita J., Mukherjee, Pratik, Sherr, Elliott H.
Publicado em 2010

Detection of identity by descent using next-generation whole genome sequencing data

Por Su, Shu-Yi, Kasberger, Jay, Baranzini, Sergio, Byerley, William, Liao, Wilson, Oksenberg, Jorge, Sherr, Elliott, Jorgenson, Eric
Publicado em 2012

Identification of a Monogenic Locus (jams1) Causing Juvenile Audiogenic Seizures in Mice

Por Misawa, Hidemi, Sherr, Elliott H., Lee, David J., Chetkovich, Dane M., Tan, Andrew, Schreiner, Christoph E., Bredt, David S.
Publicado no J Neurosci (2002)

Microstructural Correlations of White Matter Tracts in the Human Brain

Por Wahl, Michael, Li, Yi-Ou, Ng, Joshua, LaHue, Sara C., Cooper, Shelly R., Sherr, Elliott H., Mukherjee, Pratik
Publicado em 2010

Laterality of brain and ocular lesions in Aicardi Syndrome

Por Cabrera, Michelle T., Winn, Bryan J., Porco, Travis, Strominger, Zoe, Barkovich, A. James, Hoyt, Creig S., Wakahiro, Mari, Sherr, Elliott H.
Publicado em 2011

Targeted 'Next-Generation' sequencing in anophthalmia and microphthalmia patients confirms SOX2, OTX2 and FOXE3 mutations

Por Lopez Jimenez, Nelson, Flannick, Jason, Yahyavi, Mani, Li, Jiang, Bardakjian, Tanya, Tonkin, Leath, Schneider, Adele, Sherr, Elliott H, Slavotinek, Anne M
Publicado em 2011

Mapk/Erk activation in an animal model of social deficits shows a possible link to autism

Por Faridar, Alireza, Jones-Davis, Dorothy, Rider, Eric, Li, Jiang, Gobius, Ilan, Morcom, Laura, Richards, Linda J, Sen, Saunak, Sherr, Elliott H
Publicado no Mol Autism (2014)

Abnormal Speech Motor Control in Individuals with 16p11.2 Deletions

Por Demopoulos, Carly, Kothare, Hardik, Mizuiri, Danielle, Henderson-Sabes, Jennifer, Fregeau, Brieana, Tjernagel, Jennifer, Houde, John F., Sherr, Elliott H., Nagarajan, Srikantan S.
Publicado no Sci Rep (2018)

Processing Speed Delays Contribute to Executive Function Deficits in Individuals with Agenesis of the Corpus Callosum

Por Marco, Elysa J., Harrell, Kathryn M., Brown, Warren S., Hill, Susanna S., Jeremy, Rita J., Kramer, Joel H., Sherr, Elliott H., Paul, Lynn K.
Publicado em 2012

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

Por Marco, Elysa Jill, Aitken, Anne Brandes, Nair, Vishnu Prakas, da Gente, Gilberto, Gerdes, Molly Rae, Bologlu, Leyla, Thomas, Sean, Sherr, Elliott H.
Publicado no BMC Med Genomics (2018)

Deletion of Tmtc4 activates the unfolded protein response and causes postnatal hearing loss

Por Li, Jiang, Akil, Omar, Rouse, Stephanie L., McLaughlin, Conor W., Matthews, Ian R., Lustig, Lawrence R., Chan, Dylan K., Sherr, Elliott H.
Publicado no J Clin Invest (2018)

Cerebrospinal Fluid Vasopressin and Symptom Severity in Children with Autism

Por Oztan, Ozge, Garner, Joseph P., Partap, Sonia, Sherr, Elliott H., Hardan, Antonio Y., Farmer, Cristan, Thurm, Audrey, Swedo, Susan E., Parker, Karen J.
Publicado no Ann Neurol (2018)

The Structural Connectome of the Human Brain in Agenesis of the Corpus Callosum

Por Owen, Julia P., Li, Yi-Ou, Ziv, Etay, Strominger, Zoe, Gold, Jacquelyn, Bukhpun, Polina, Wakahiro, Mari, Friedman, Eric J., Sherr, Elliott H., Mukherjee, Pratik
Publicado em 2012

Children with Autism Show Reduced Somatosensory Response: An MEG Study

Por Marco, Elysa J., Khatibi, Kasra, Hill, Susanna S., Siegel, Bryna, Arroyo, Monica S., Dowling, Anne F., Neuhaus, John M., Sherr, Elliott H., Hinkley, Leighton N. B., Nagarajan, Srikantan S.
Publicado em 2012