Multiple sclerosis (MS) is a heterogenous autoimmune disease in which autoreactive
lymphocytes attack the myelin sheath of the central nervous system. B lymphocytes in the …

Tuberous sclerosis complex (TSC) is an autosomal dominant monogenetic disorder that is
characterized by the formation of benign tumors in several organs as well as brain …

Individuals with coronavirus disease 2019 (COVID-19) frequently develop neurological
symptoms, but the biological underpinnings of these phenomena are unknown. Through single-…

Neuronal migration is a fundamental component of brain development whose failure is
associated with various neurological and psychiatric disorders. Reelin is essential for the …

Postmitotic cortical neurons that fail to initiate migration can remain near their site of origin
and form persistent periventricular nodular heterotopia (PH). In human telencephalon, this …

… Bartley et al. … Drs Bartley and Wilson had full access to all of the data in the study and take
responsibility for the integrity of the data and the accuracy of the data analysis. Drs Bartley and …

Cerebellar granule neuron (CGN) survival depends on activity of the myocyte enhancer factor-2
(MEF2) transcription factors. Neuronal MEF2 activity is regulated by depolarization via a …

Periventricular heterotopia (PVH) is a congenital malformation of human cerebral cortex
frequently associated with Filamin-A (FLN-A) mutations but the pathogenetic mechanisms …

… This article has been retracted at the request of corresponding author Christopher Bartley,
with agreement from all authors and with approval from Biological Psychiatry Editor John H. …

Abnormal dendritic complexity is a shared feature of many neurodevelopmental disorders
associated with neurological defects. Here, we found that the actin-crosslinking protein filamin …