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 Experiment Videos

Medical genetics in Israel

J Zlotogora1, J Chemke

  • 1Department of Human Genetics, Hadassah University Hospital, Jerusalem, Israel.

European Journal of Human Genetics : EJHG
|January 1, 1995
PubMed
Summary
This summary is machine-generated.

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

The Effect of Genetic Counseling on Knowledge and Perceptions Regarding Risks for Breast Cancer.

Journal of genetic counseling·2015
Same author

Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.

Journal of medical genetics·2010
Same author

A mutation analysis of the phenylalanine hydroxylase (PAH) gene in the Israeli population.

Annals of human genetics·2008
Same author

The fate of 12 recessive mutations in a single village.

Annals of human genetics·2007
Same author

Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.

Hearing research·2003
Same author

Changing family structure in a modernizing society: a study of marriage patterns in a single Muslim village in Israel.

American journal of human biology : the official journal of the Human Biology Council·2002
Same journal

Australian parents' perspectives on extended genomic screening: what information to return and when?

European journal of human genetics : EJHG·2026
Same journal

Perspectives on phenotype in genetic testing for early-onset atrial fibrillation.

European journal of human genetics : EJHG·2026
Same journal

Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders.

European journal of human genetics : EJHG·2026
Same journal

Decoding splicing variants in high-throughput sequencing: a functional validation approach integrating deep learning tools.

European journal of human genetics : EJHG·2026
Same journal

How parents decide whether to have genomic newborn screening: experiences from BabyScreen.

European journal of human genetics : EJHG·2026
Same journal

Psychosocial outcomes of reproductive genetic carrier screening up to five years post-result.

European journal of human genetics : EJHG·2026
See all related articles

Genetic origins in Israel are crucial for understanding hereditary disorders. Identifying specific subgroups aids in medical genetics, enabling targeted screening and research for rare diseases.

Area of Science:

  • Human Genetics
  • Medical Genetics
  • Population Genetics

Background:

  • Israel's population comprises diverse subgroups, including Jewish and non-Jewish communities.
  • Subgroups within Jewish and non-Jewish populations are distinguished by country of origin, religion, or village.
  • Certain hereditary disorders occur with increased frequency in specific Israeli subgroups.

Purpose of the Study:

  • To highlight the importance of precise patient origin in medical genetics within Israel.
  • To underscore the role of genetic origins in identifying and managing hereditary disorders.
  • To inform preventive genetic screening strategies based on population-specific risks.

Main Methods:

  • Analysis of population structure in Israel, considering Jewish and non-Jewish communities.

Related Experiment Videos

  • Review of reported hereditary disorders and their frequencies within distinct subgroups.
  • Examination of genetic factors such as founder effect, genetic drift, and selection.
  • Main Results:

    • Patient's precise origin is critical for medical geneticists in Israel.
    • Increased frequencies of specific mendelian disorders are observed in various Israeli communities.
    • Founder effect, genetic drift, and selection contribute to high frequencies of genetic disorders.

    Conclusions:

    • Understanding genetic origins is vital for medical geneticists in Israel.
    • Knowledge of subgroup-specific hereditary disorders facilitates targeted genetic screening and research.
    • Israel's medical genetics infrastructure supports both clinical service and research in human genetics.