Research Studies Archive

Corpus Callosum Dysgenesis is concomitant with reduced metacognitive efficiency and sensitivity across multiple cohorts and modalities

The corpus callosum is the largest commissure in the mammalian brain and has been implicated in supporting ...

Fetal midline anomalies: Diagnosis and counselling Part 1: Corpus callosum anomalies

Midline anomalies encompasses a heterogeneous group of conditions caused by an abnormal process of ventral ...

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

Agenesis of the corpus callosum in California 1983-2003: a population-based study

Abstract The objective of this study was to characterize the prevalence, demographic risk factors, and ...

Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations

Abstract Objective: We sought to categorize the structural brain anomalies associated with abnormalities of ...

Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies

Abstract Absence of the corpus callosum is often associated with cognitive deficits, autism, and epilepsy. ...

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

Abstract Brain malformations involving the corpus callosum are common in children with developmental ...

Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia

Abstract The corpus callosum is the principal cerebral commissure connecting the right and left hemispheres. ...

Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families

Abstract Objective: We sought to create a classification system for pediatric corpus callosal abnormalities ...

Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders

Abstract Objective: BCORL1, a transcriptional co-repressor, has a role in cortical migration, neuronal ...

Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities

Abstract The collapsin response mediator protein (CRMP) family proteins are intracellular mediators of ...

De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities

Abstract Introduction: Whole-exome sequencing (WES) has identified de novo variants in chromatin remodelling ...
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