Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Probability Laws01:49

Probability Laws

Overview
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...
Principles of Pharmacogenetics: Types of Genetic Variants01:27

Principles of Pharmacogenetics: Types of Genetic Variants

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...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

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...
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...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Approaches to assessing genetic risks from exposure to chemicals.

Environmental health perspectives·1993
Same author

Assessment of antimutagenicity and anticarcinogenicity.

Mutation research·1992
Same author

The effect of multi-locus deletions in heterozygotes; a model study using Drosophila.

Mutation research·1990
Same author

The International Association of Environmental Mutagen Societies (IAEMS).

Mutation research·1990
Same author

International symposium on strategies for the control of mutagenic and carcinogenic risk: current status and perspectives, Friday, May 5, 1989, Bologna.

Teratogenesis, carcinogenesis, and mutagenesis·1990
Same author

The nature of X-ray and chemically induced mutations in Drosophila in relation with DNA repair.

Annali dell'Istituto superiore di sanita·1989

Related Experiment Video

Updated: Jul 23, 2026

In Vivo Modeling of the Morbid Human Genome using Danio rerio
12:31

In Vivo Modeling of the Morbid Human Genome using Danio rerio

Published on: August 24, 2013

Models and assumptions underlying genetic risk assessment.

F H Sobels1

  • 1Department of Radiation Genetics and Chemical Mutagenesis, State University of Leiden, The Netherlands.

Mutation Research
|May 1, 1989
PubMed
Summary

Estimating radiation

Area of Science:

  • Radiation biology
  • Genetics
  • Risk assessment

Background:

  • Review of methods for estimating genetic risks from radiation exposure.
  • Discussion of the doubling-dose method and its reliance on mouse data.
  • Consideration of recent findings on multifactorial diseases and spontaneous mutations.

Purpose of the Study:

  • To review and critically evaluate methods for estimating radiation-induced genetic risks.
  • To discuss the assumptions and limitations of current genetic risk assessment models.
  • To explore new approaches and data for more precise risk estimation.

Main Methods:

  • Review of the doubling-dose method, direct method, and parallelogram approach.
  • Analysis of data from mouse, monkey, and human studies.

More Related Videos

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
09:37

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

Published on: August 15, 2019

Related Experiment Videos

Last Updated: Jul 23, 2026

In Vivo Modeling of the Morbid Human Genome using Danio rerio
12:31

In Vivo Modeling of the Morbid Human Genome using Danio rerio

Published on: August 24, 2013

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry
05:53

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

Published on: June 21, 2018

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
09:37

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information

Published on: August 15, 2019

  • Discussion of spontaneous mutation rates, insertion elements, and repair enzyme induction.
  • Main Results:

    • The doubling-dose method relies on mouse data and has limitations with recent findings.
    • The direct method uses induced dominant mutations in mice and translocations in monkeys.
    • The parallelogram approach integrates data from various cell types and species for improved estimates.

    Conclusions:

    • Current methods for estimating radiation genetic risk have underlying assumptions that need re-evaluation.
    • New data on spontaneous mutations and repair mechanisms may refine risk assessments.
    • Developing comprehensive databases on somatic cell mutations is crucial for accurate human germ cell risk estimation.