Jove
Visualize
Contact Us

Related Experiment Videos

Genetics of complex diseases.

Arno G Motulsky1

  • 1University of Washington, Seattle, WA 98195, USA. agmot@u.washington.edu

Journal of Zhejiang University. Science. B
|January 20, 2006
PubMed
Summary
This summary is machine-generated.

Understanding the genetic basis of complex diseases is crucial. While rare, single-gene disorders can reveal mechanisms for common diseases, and identifying specific genes and common polymorphisms aids in assessing disease risk.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

A German-Jewish refugee in Vichy France 1939-1941. Arno Motulsky's memoir of life in the internment camps at St. Cyprien and Gurs.

American journal of medical genetics. Part A·2018
Same author

The Great Adventure of an American Human Geneticist.

Annual review of genomics and human genetics·2016
Same author

Erythrokinetics: quantitative measurements of red cell production and destruction in normal subjects and patients with anemia.

Blood·2016
Same author

Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.

American journal of human genetics·2015
Same author

Genetic Counseling and Screening of Consanguineous Couples and Their Offspring: Recommendations of the National Society of Genetic Counselors.

Journal of genetic counseling·2015
Same author

Letter to the Editor: Reply to Becker and Morgan.

Journal of genetic counseling·2015
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

Area of Science:

  • Genetics
  • Complex Diseases
  • Clinical Applications

Background:

  • Investigating the genetic underpinnings of common complex diseases is essential for advancing clinical applications.
  • Monogenic Mendelian inheritance, though infrequent in these conditions, offers valuable insights into pathogenic mechanisms.
  • The polygenic nature of complex diseases presents challenges in isolating and identifying specific contributing genes.

Purpose of the Study:

  • To review current approaches for studying the genetic basis of common complex diseases.
  • To explore the clinical applications of genetic research in complex diseases.
  • To discuss the role of common polymorphisms in disease risk assessment.

Main Methods:

  • Literature review of genetic studies on complex diseases.

Related Experiment Videos

  • Analysis of the role of monogenic inheritance in understanding complex disease mechanisms.
  • Discussion of gene identification strategies and polymorphism analysis.
  • Main Results:

    • Elucidation of monogenic disorders can inform the study of complex diseases.
    • Identification of specific genes involved in complex diseases remains challenging.
    • Common polymorphisms serve as important indicators of disease risk.

    Conclusions:

    • Genetic research provides critical insights into the etiology of complex diseases.
    • Further research is needed to effectively isolate and identify genes contributing to complex diseases.
    • Utilizing common polymorphisms can enhance disease risk prediction and clinical management.