The road to precision psychiatry: translating genetics into disease mechanisms

MJ Gandal, V Leppa, H Won, NN Parikshak… - Nature …, 2016 - nature.com
Hundreds of genetic loci increasing risk for neuropsychiatric disorders have recently been
identified. This success, perhaps paradoxically, has posed challenges for therapeutic …

Progress in the genetics of autism spectrum disorder

M Woodbury‐Smith, SW Scherer - Developmental Medicine & …, 2018 - Wiley Online Library
A genetic basis for autism spectrum disorder (ASD) is now well established, and with the
availability of high‐throughput microarray and sequencing platforms, major advances have …

[HTML][HTML] Negative symptoms of schizophrenia: clinical characteristics, pathophysiological substrates, experimental models and prospects for improved treatment

MJ Millan, K Fone, T Steckler, WP Horan - European …, 2014 - Elsevier
Schizophrenia is a complex and multifactorial disorder generally diagnosed in young adults
at the time of the first psychotic episode of delusions and hallucinations. These positive …

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls

E Pettersson, P Lichtenstein, H Larsson… - Psychological …, 2019 - cambridge.org
BackgroundMost studies underline the contribution of heritable factors for psychiatric
disorders. However, heritability estimates depend on the population under study, diagnostic …

Toward recovery in schizophrenia: current concepts, findings, and future research directions

T Onitsuka, Y Hirano, T Nakazawa… - Psychiatry and …, 2022 - Wiley Online Library
Schizophrenia was initially defined as “dementia praecox” by E. Kraepelin, which implies
progressive deterioration. However, recent studies have revealed that early effective …

[HTML][HTML] Increased l1 retrotransposition in the neuronal genome in schizophrenia

M Bundo, M Toyoshima, Y Okada, W Akamatsu, J Ueda… - Neuron, 2014 - cell.com
Recent studies indicate that long interspersed nuclear element-1 (L1) are mobilized in the
genome of human neural progenitor cells and enhanced in Rett syndrome and ataxia …

Altered cortical ensembles in mouse models of schizophrenia

JP Hamm, DS Peterka, JA Gogos, R Yuste - Neuron, 2017 - cell.com
In schizophrenia, brain-wide alterations have been identified at the molecular and cellular
levels, yet how these phenomena affect cortical circuit activity remains unclear. We studied …

Behavioral neuroscience of autism

T Takumi, K Tamada, F Hatanaka, N Nakai… - … & Biobehavioral Reviews, 2020 - Elsevier
Autism spectrum disorder (ASD) is a neurodevelopmental disorder. Several genetic causes
of ASD have been identified and this has enabled researchers to construct mouse models …

Neurobiological perspective of 22q11. 2 deletion syndrome

JR Zinkstok, E Boot, AS Bassett, N Hiroi… - The Lancet …, 2019 - thelancet.com
Summary 22q11. 2 deletion syndrome is characterised by a well defined microdeletion that
is associated with a high risk of neuropsychiatric disorders, including intellectual disability …

[HTML][HTML] CNV biology in neurodevelopmental disorders

T Takumi, K Tamada - Current Opinion in Neurobiology, 2018 - Elsevier
Highlights•Pathogenic CNVs are shared among neurodevelopmental and neuropsychiatric
disorders.•Understanding epigenetic regulation provides important insights not only into …