A new single gene deletion on 2q34:ERBB4is associated with intellectual disability

Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders

(2011) Fady M. Mikhail et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Conserved Interneuron-Specific ErbB4 Expression in Frontal Cortex of Rodents, Monkeys, and Humans: Implications for Schizophrenia

(2011) Jörg Neddens et al.   BIOLOGICAL PSYCHIATRY

Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons

(2011) Guo-He Tan et al.   NATURE NEUROSCIENCE

Biological Validation of Increased Schizophrenia Risk With NRG1, ERBB4, and AKT1 Epistasis via Functional Neuroimaging in Healthy Controls

(2010) Kristin K. Nicodemus et al.   ARCHIVES OF GENERAL PSYCHIATRY

Neuregulin 1–erbB4 pathway in schizophrenia: From genes to an interactome

(2010) Anamika Banerjee et al.   BRAIN RESEARCH BULLETIN

Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4

(2008) Liesbeth Backx et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE