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Related Concept Videos

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,...
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Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
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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...
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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
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The human genome is over 99.9% identical between individuals, yet genetic differences exist at millions of bases. The human genome contains approximately 3 million variant positions per individual, many of which are heterozygous, contributing to genetic diversity and individual traits. Genetic variations include single-nucleotide polymorphisms (SNPs), insertions, deletions, and copy number variations (CNVs).SNPs, the most common variation, involve single-base changes in DNA. These can be...

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Single nucleotide polymorphisms and suicidal behaviour.

Peter Pregelj1

  • 1University of Ljubljana, Department of Psychiatry, Ljubljana, Slovenia. peter.pregelj@psih-klinika.si

Psychiatria Danubina
|September 5, 2012
PubMed
Summary
This summary is machine-generated.

Genetic factors, including single nucleotide polymorphisms (SNPs), influence suicidal behavior, particularly those affecting the serotonergic system and stress response pathways. Further research into genes like brain-derived neurotrophic factor is crucial.

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Area of Science:

  • Genetics
  • Neuroscience
  • Psychiatry

Background:

  • Suicide causes significant global mortality, with attempts far outnumbering completions.
  • Suicidal behavior stems from a complex interplay of environmental stressors and genetic predispositions.
  • The serotonergic system and neuronal stress response pathways are implicated in suicidal behavior.

Purpose of the Study:

  • To explore the genetic underpinnings of suicidal behavior.
  • To identify specific genes and polymorphisms associated with increased suicide risk.
  • To highlight areas for future genetic research in suicide prevention.

Main Methods:

  • Review of existing genetic studies on suicidal behavior.
  • Analysis of single nucleotide polymorphisms (SNPs) in genes related to neurotransmission.
  • Focus on polymorphisms in the serotonergic system, including serotonin transporter and tryptophan hydroxylase (TPH).

Main Results:

  • Abnormalities in the serotonergic system are frequently observed in individuals with a history of suicide.
  • Specific polymorphisms in genes regulating the serotonergic system and stress response are associated with suicidal behavior.
  • Previous studies have largely focused on monoaminergic neurotransmission genes.

Conclusions:

  • Genetic factors, particularly those influencing the serotonergic system, play a significant role in suicidal behavior.
  • Genes involved in neuronal stress response mechanisms are critical areas for further investigation.
  • Exploring genes such as brain-derived neurotrophic factor (BDNF) may offer new insights into suicide risk and prevention.