schizophrenia - NextBio

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Search Term: schizophrenia (disease)

Overview

class of psychoses with disturbance mainly of cognition (content and form of thought, perception, sense of self versus external world, volition) and psychomotor function, rather than affect.

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Data Correlations | 7 studies

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Genes

Score

HTR2A

100

CTSC

100

CHI3L1

100

DISC1

100

RGS4

100

PPP3R1

100

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Biogroups

Score

B Lymphocyte Cell Surface Molecules

100

Antigen Processing and Presentation

Collagen triple helix repeat

Cell Adhesion Molecules (CAMs)

S100/CaBP-9k-type, calcium binding

Immunoglobulin subtype 2

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Individual Studies
Gene expression of postmortem prefrontal cortex of bipolar disorder or schizophrenia patients Homo sapiens \| RNA Expression We performed large-scale DNA microarray analysis of postmortem brains of patients with BD or SZ, and examined expression patterns of mitochondria-related genes. Authors: Iwamoto Kazuya, Bundo Miki, Kato Tadafumi Organization: RIKEN Brain Science Institute Lab for Mo…	OMIM - Psychotic disorder Homo sapiens \| Mutations/Phenotypic This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories. Source: NextBio Library/Mutation and Phenotypic data

Individual Studies

Gene expression of postmortem prefrontal cortex of bipolar disorder or schizophrenia patients

Homo sapiens | RNA Expression

We performed large-scale DNA microarray analysis of postmortem brains of patients with BD or SZ, and examined expression patterns of mitochondria-related genes.

Authors: Iwamoto Kazuya, Bundo Miki, Kato Tadafumi

Organization: RIKEN Brain Science Institute Lab for Mo…

OMIM - Psychotic disorder

Homo sapiens | Mutations/Phenotypic

This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

Source: NextBio Library/Mutation and Phenotypic data