[HTML][HTML] Schizophrenia shows a unique metabolomics signature in plasma

Y He, Z Yu, I Giegling, L Xie, AM Hartmann… - Translational …, 2012 - nature.com
Schizophrenia is a severe complex mental disorder affecting 0.5–1% of the world
population. To date, diagnosis of the disease is mainly based on personal and thus …

[HTML][HTML] Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

R Corominas, X Yang, GN Lin, S Kang, Y Shen… - Nature …, 2014 - nature.com
Increased risk for autism spectrum disorders (ASD) is attributed to hundreds of genetic loci.
The convergence of ASD variants have been investigated using various approaches …

Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex

I Guella, A Sequeira, B Rollins, L Morgan, F Torri… - Journal of psychiatric …, 2013 - Elsevier
MicroRNAs (miRNAs) are small non-coding RNAs that act as potent regulators of gene
expression. A recent GWAS reported the rs1625579 SNP, located downstream of miR-137 …

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16. 1, 2q22. 3 and 17q21. 32

Epicure Consortium, EMINet Consortium… - Human molecular …, 2012 - academic.oup.com
Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% and account for
20–30% of all epilepsies. Despite their high heritability of 80%, the genetic factors …

Using genetic, cognitive and multi-modal neuroimaging data to identify ultra-high-risk and first-episode psychosis at the individual level

W Pettersson-Yeo, S Benetti, AF Marquand… - Psychological …, 2013 - cambridge.org
BackgroundGroup-level results suggest that relative to healthy controls (HCs), ultra-high-risk
(UHR) and first-episode psychosis (FEP) subjects show alterations in neuroanatomy …

Disruption of TCF4 regulatory networks leads to abnormal cortical development and mental disabilities

H Li, Y Zhu, YM Morozov, X Chen, SC Page… - Molecular …, 2019 - nature.com
The TCF4 gene is the subject of numerous and varied investigations of it's role in the
genesis of neuropsychiatric disease. The gene has been identified as the cause of Pitt …

Genome‐wide association study of autism spectrum disorder in the East Asian populations

X Liu, T Shimada, T Otowa, YY Wu… - Autism …, 2016 - Wiley Online Library
Autism spectrum disorder is a heterogeneous neurodevelopmental disorder with strong
genetic basis. To identify common genetic variations conferring the risk of ASD, we …

What is the impact of genome-wide supported risk variants for schizophrenia and bipolar disorder on brain structure and function? A systematic review

R Gurung, DP Prata - Psychological medicine, 2015 - cambridge.org
The powerful genome-wide association studies (GWAS) revealed common mutations that
increase susceptibility for schizophrenia (SZ) and bipolar disorder (BD), but the vast majority …

Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia

A Doostparast Torshizi, C Armoskus, H Zhang… - Science …, 2019 - science.org
Applying tissue-specific deconvolution of transcriptional networks to identify their master
regulators (MRs) in neuropsychiatric disorders has been largely unexplored. Here, using …

Genome-wide association studies of schizophrenia: does bigger lead to better results?

SE Bergen, TL Petryshen - Current opinion in psychiatry, 2012 - journals.lww.com
Identifying the genetic underpinnings of complex diseases offers insight into the etiological
mechanisms leading to manifestation of the disease. New and more effective treatments for …