Depressive psychopathology in first-episode schizophrenia spectrum disorders: a systematic review, meta-analysis and meta-regression

SE Herniman, K Allott, LJ Phillips, SJ Wood… - Psychological …, 2019 - cambridge.org
BackgroundDespite knowing for many decades that depressive psychopathology is
common in first-episode schizophrenia spectrum disorders (FES), there is limited knowledge …

Immediate-early genes modulation by antipsychotics: translational implications for a putative gateway to drug-induced long-term brain changes

A De Bartolomeis, EF Buonaguro, G Latte… - Frontiers in behavioral …, 2017 - frontiersin.org
An increasing amount of research aims at recognizing the molecular mechanisms involved
in long-lasting brain architectural changes induced by antipsychotic treatments. Although …

Trappc9 deficiency in mice impairs learning and memory by causing imbalance of dopamine D1 and D2 neurons

Y Ke, M Weng, G Chhetri, M Usman, Y Li, Q Yu… - Science …, 2020 - science.org
Genetic mutations in the gene encoding transport protein particle complex 9 (trappc9), a
subunit of TRAPP that acts as a guanine nucleotide exchange factor for rab proteins, cause …

Intracranial and subcortical volumes in adolescents with early‐onset psychosis: A multisite mega‐analysis from the ENIGMA consortium

TP Gurholt, V Lonning, S Nerland… - Human brain …, 2022 - Wiley Online Library
Early‐onset psychosis disorders are serious mental disorders arising before the age of 18
years. Here, we investigate the largest neuroimaging dataset, to date, of patients with early …

Subcortical brain volume abnormalities in individuals with an at-risk mental state

D Sasabayashi, Y Takayanagi, T Takahashi… - Schizophrenia …, 2020 - academic.oup.com
Previous structural magnetic resonance imaging studies of psychotic disorders have
demonstrated volumetric alterations in subcortical (ie, the basal ganglia, thalamus) and …

Distinct autism spectrum disorder phenotype and hand-flapping stereotypes: two siblings with novel homozygous mutation in TRAPPC9 gene and literature review

H Bolat, G Ünsel-Bolat, H Derin, A Şen… - Molecular …, 2022 - karger.com
Objective: Pathogenic mutations of the TRAPPC9 gene are the rare genetic causes of
autosomal recessive intellectual disability (ID). There are several features that are not fully …

Prenatal stress alters mouse offspring dorsal striatal development and placental function in sex-specific ways

SV Maurer, BWQ Hing, S Lussier… - Journal of Psychiatric …, 2025 - Elsevier
Prenatal stress is a risk factor for neurodevelopmental disorders (NDDs), including autism
spectrum disorder (ASD). However, how early stress modification of brain development …

Reduced density of oligodendrocytes and oligodendrocyte clusters in the caudate nucleus in major psychiatric illnesses

VM Vostrikov, NA Uranova - Schizophrenia Research, 2020 - Elsevier
Functional dysconnectivity in schizophrenia and affective disorders may be associated with
myelin and oligodendrocyte abnormalities. Altered network integration involving the caudate …

Simultaneous effects on parvalbumin-positive interneuron and dopaminergic system development in a transgenic rat model for sporadic schizophrenia

H Hamburg, SV Trossbach, V Bader, C Chwiesko… - Scientific reports, 2016 - nature.com
To date, unequivocal neuroanatomical features have been demonstrated neither for
sporadic nor for familial schizophrenia. Here, we investigated the neuroanatomical changes …

Diminishing striatal activation across adolescent development during reward anticipation in offspring of schizophrenia patients

M Vink, M de Leeuw, R Pouwels… - Schizophrenia …, 2016 - Elsevier
Schizophrenia is a severe psychiatric disorder associated with impaired fronto-striatal
functioning. Similar deficits are observed in unaffected siblings of patients, indicating that …