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Related Concept Videos

Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
Diagnostic and Statistical Manual of Mental Disorders (DSM)01:27

Diagnostic and Statistical Manual of Mental Disorders (DSM)

The Diagnostic and Statistical Manual of Mental Disorders (DSM) serves as the primary classification system for mental health disorders, providing standardized diagnostic criteria for clinicians and researchers. First published by the American Psychiatric Association (APA) in 1952, the DSM has undergone several revisions to reflect evolving psychiatric understanding. The fifth edition, DSM-5, released in 2013, introduced key updates that expanded diagnostic categories and modified diagnostic...
Sex Linked Disorders01:43

Sex Linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Biological Causes of Schizophrenia01:29

Biological Causes of Schizophrenia

Schizophrenia, a severe psychiatric disorder, arises from a complex interplay of biological factors, including genetic predisposition, structural brain abnormalities, neurotransmitter dysregulation, and developmental irregularities. These factors collectively contribute to the onset and progression of the disorder, which typically manifests in late adolescence or early adulthood.
Genetic Factors in Schizophrenia
The genetic basis of schizophrenia is strongly supported by family and twin studies.

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Related Experiment Video

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Mapping Alzheimer's Disease Variants to Their Target Genes Using Computational Analysis of Chromatin Configuration
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

1, S Hong Lee, Stephan Ripke

  • 1The University of Queensland, Queensland Brain Institute, Brisbane, Queensland, Australia.

Nature Genetics
|August 13, 2013
PubMed
Summary

Genetic factors are shared across psychiatric disorders, with significant overlap found between schizophrenia, bipolar disorder, and major depressive disorder. This finding suggests common biological pathways influencing these conditions.

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Area of Science:

  • Psychiatric Genetics
  • Genomics
  • Quantitative Trait Analysis

Background:

  • Psychiatric disorders exhibit moderate to high heritability.
  • The extent of shared genetic underpinnings across different psychiatric conditions remains largely undetermined.
  • Understanding shared genetic etiology is crucial for advancing psychiatric nosology and treatment.

Purpose of the Study:

  • To investigate the shared genetic etiology among major psychiatric disorders.
  • To quantify the genetic correlations between schizophrenia, bipolar disorder, major depressive disorder, autism spectrum disorders (ASD), and attention-deficit/hyperactivity disorder (ADHD).

Main Methods:

  • Utilized genome-wide genotype data from the Psychiatric Genomics Consortium (PGC).
  • Applied univariate and bivariate statistical methods to estimate genetic variation and covariation.
  • Calculated genetic correlations between pairs of disorders using common Single Nucleotide Polymorphisms (SNPs).

Main Results:

  • Single Nucleotide Polymorphisms (SNPs) explained 17-29% of the liability variance for the studied disorders.
  • High genetic correlation observed between schizophrenia and bipolar disorder (0.68).
  • Moderate genetic correlations found between schizophrenia and major depressive disorder (0.43), bipolar disorder and major depressive disorder (0.47), and ADHD and major depressive disorder (0.32).
  • Low genetic correlation noted between schizophrenia and ASD (0.16); other pairs showed non-significant correlations.

Conclusions:

  • Provides empirical evidence for shared genetic etiology across several psychiatric disorders.
  • Findings support the investigation of common pathophysiologies for related psychiatric conditions.
  • The results can inform future psychiatric nosological classifications and research directions.