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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...
Behavioral Genetics and Its Designs01:23

Behavioral Genetics and Its Designs

Behavior genetics explores how genetic inheritance influences human behavior. It focuses on how genes, passed from parents to offspring, contribute to the development of behavioral traits and tendencies. This branch of genetics seeks to understand the complex interplay between inherited genetic factors and environmental influences in shaping our behaviors.
The primary methodologies used in behavior genetics include family studies, twin studies, and adoption studies, each providing unique...
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...
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.
Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Gene-Environment Interactions01:20

Gene-Environment Interactions

Gene expression is a dynamic process that is significantly influenced by environmental factors. This interaction underlies the complex nature of biological development and the phenotypic differences observed among individuals, even among those with identical genetic makeups. Factors such as radiation, temperature, behavior, nutrition, and stress play pivotal roles in determining how genes are expressed. The concept of the reaction range is central to understanding this interaction. It posits...

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Related Experiment Video

Updated: May 10, 2026

Investigating Drivers of Antireward in Addiction Behavior with Anatomically Specific Single-Cell Gene Expression Methods
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Candidate gene associations with withdrawn behavior.

David H Rubin1, Robert R Althoff, Erik A Ehli

  • 1Weill-Cornell Medical College, New York, NY, USA.

Journal of Child Psychology and Psychiatry, and Allied Disciplines
|July 2, 2013
PubMed
Summary
This summary is machine-generated.

Social withdrawal, a key trait in developmental psychopathology, is linked to serotonin receptor 2A (HTR2A) and alpha 2-adrenergic (ADRA2A) genes. These findings highlight the genetic underpinnings of withdrawn behavior in children.

Keywords:
Adult Self-ReportChild Behavior ChecklistWithdrawn behaviorbehavioral inhibitionsocial withdrawal

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An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
10:17

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

Published on: November 3, 2010

Area of Science:

  • Neuroscience
  • Genetics
  • Developmental Psychology

Background:

  • Social withdrawal is a significant indicator of various psychiatric conditions, including depression, autism, and anxiety.
  • This behavior is highly heritable, persistent, and often worsens without intervention.
  • Previous genetic studies have been limited by the use of categorical measures for this phenotype.

Purpose of the Study:

  • To investigate the genetic associations with a dimensional measure of social withdrawal.
  • To identify specific candidate genes linked to withdrawn behavior.

Main Methods:

  • Analysis of 20 single-nucleotide polymorphisms (SNPs) and 4 variable number of tandem repeat (VNTR) genes in 551 individuals from 187 families.
  • Utilized linear mixed modeling to assess the relationship between genotypes and the Child Behavior Checklist (CBCL) Withdrawn Behavior Subscale Score (WBS).
  • Controlled for gender and age using multiple linear regressions.

Main Results:

  • Significant associations were found between withdrawn behavior and polymorphisms in the serotonin receptor 2A (HTR2A) gene (rs6314) and the alpha 2-adrenergic (ADRA2A) gene (rs1800544).
  • The association with ADRA2A was more pronounced in younger children.
  • These findings were robust after correcting for gender and age.

Conclusions:

  • The serotonin receptor 2A (HTR2A) and alpha 2-adrenergic (ADRA2A) genes are significantly associated with social withdrawal.
  • This study supports the role of catecholaminergic genes in the heritability of withdrawn behavior.
  • Dimensional measurement approaches are crucial for uncovering genetic links to complex behaviors.