Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome

Author:

Blackmon Karen12,Thesen Thomas123,Green Sophie1,Ben-Avi Emma12,Wang Xiuyuan13,Fuchs Benjamin1,Kuzniecky Ruben1,Devinsky Orrin1

Affiliation:

1. Department of Neurology, Epilepsy Division, New York University School of Medicine, New York, NY, USA

2. Department of Physiology, Neuroscience, and Behavioral Sciences, St. George’s University School of Medicine, Grenada, West Indies

3. Department of Radiology, New York University School of Medicine, New York, NY, USA

Funder

Simons Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

Reference44 articles.

1. Cortical feature analysis and machine learning improves detection of “MRI-negative” focal cortical dysplasia;Ahmed;Epilepsy Behav,2015

2. Hierarchical conditional random fields for outlier detection: an application to detecting epileptogenic cortical malformations;Ahmed;J Mach Learn Res,2014

3. Abnormal auditory and language pathways in children with 16p11.2 deletion;Berman;Neuroimage Clin,2015

4. Focal cortical dysplasias in autism spectrum disorders;Casanova;Acta Neuropathol Commun,2013

5. Perisylvian language networks of the human brain;Catani;Ann Neurol,2005

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