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MRC Centre for Neuropsychiatric Genetics & Genomics latest publications
Genetic risk for attention-deficit/hyperactivity disorder contributes to neurodevelopmental traits in the general population.
Epilepsy prevalence and socioeconomic deprivation in England.
A comprehensive neuropsychological description of cognition in drug-refractory juvenile myoclonic epilepsy.
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Am J Psychiatry,
The hidden genetics of epilepsy-a clinically important new paradigm.
Nat Rev Neurol,
A novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes.
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
Hum Mol Genet,
The penetrance of copy number variations for schizophrenia and developmental delay.
Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.
De novo mutations in schizophrenia implicate synaptic networks.