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

Genetic markers in Finland

H R Nevanlinna

    Haematologia
    |January 1, 1980
    PubMed
    Summary
    This summary is machine-generated.

    Finland exhibits a growing number of unique monogenic markers and rare recessive diseases, likely due to founder effects from early settlers. Common genetic markers suggest significant eastern European and Siberian population influences.

    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 population genetic study in Finland: comparison of the Finnish- and Swedish-speaking populations.

    Human heredity·1991
    Same author

    Low prevalence of antibodies against human immunodeficiency virus in Finnish haemophiliacs.

    Vox sanguinis·1991
    Same author

    WES, a 'new' infrequent blood group antigen in Finns.

    Vox sanguinis·1987
    Same author

    Classification principles and genetics of chronic gastritis.

    Scandinavian journal of gastroenterology. Supplement·1987
    Same author

    Joint phenotype distributions at the glyoxalase I and haptoglobin loci in Finland.

    Human heredity·1987
    Same author

    Perinatal mortality from Rh(D) hemolytic disease in Finland, 1975-1984.

    Acta obstetricia et gynecologica Scandinavica·1986

    Area of Science:

    • Population Genetics
    • Human Genetics
    • Medical Genetics

    Background:

    • Finland shows an increasing discovery rate of novel monogenic markers, many rare in other European populations.
    • Numerous rare recessive diseases, characteristic of the Finnish population, have been identified over the past two decades.
    • These genetic findings suggest potential founder effects from a numerically limited ancestral population during Finland's settlement.

    Purpose of the Study:

    • To investigate the genetic landscape of the Finnish population.
    • To understand the origins of rare monogenic markers and diseases in Finland.
    • To analyze the population structure and historical influences on Finnish genetics.

    Main Methods:

    • Analysis of monogenic markers and rare recessive diseases.

    Related Experiment Videos

  • Comparative population genetics studies.
  • Genetic marker distribution analysis.
  • Main Results:

    • A significant number of Finnish-specific monogenic markers and rare diseases have been identified.
    • Genetic data suggests these rare variants likely arose by chance in the early Finnish population.
    • Common polymorphic markers indicate a strong eastern influence, with similarities to Estonian and Siberian populations.

    Conclusions:

    • Finland's genetic makeup is shaped by both unique founder effects and historical eastern admixture.
    • Understanding these genetic patterns is crucial for diagnosing and managing rare diseases in Finland.
    • The study highlights the value of population-specific genetic research in uncovering disease origins and migration histories.