SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:gup.ub.gu.se/143661"
 

Search: onr:"swepub:oai:gup.ub.gu.se/143661" > Analysis of ten can...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Analysis of ten candidate genes in autism by association and linkage

Philippe, Anne (author)
Guilloud-Bataille, Michel (author)
Martinez, Maria (author)
show more...
Gillberg, Christopher, 1950 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kvinnors och barns hälsa, Avdelningen för barn- och ungdomspsykiatri,Institute for the Health of Women and Children, Dept of Child and Adolescent Psychiatry
Råstam, Maria, 1948 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kvinnors och barns hälsa, Avdelningen för barn- och ungdomspsykiatri,Institute for the Health of Women and Children, Dept of Child and Adolescent Psychiatry
Sponheim, Eili (author)
Coleman, Mary (author)
Zappella, Michele (author)
Aschauer, Harald (author)
Penet, Christiane (author)
Feingold, Josué (author)
Brice, Alexis (author)
Leboyer, Marion (author)
show less...
 (creator_code:org_t)
2002-01-08
2002
English.
In: American Journal of Medical Genetics. - : Wiley. - 0148-7299. ; 114:2, s. 125-128
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • We studied the possible involvement of ten candidate genes in autism: proenkephalin, prodynorphin, and proprotein convertase subtilisin/kexin type 2 (opioid metabolism); tyrosine hydroxylase, dopamine receptors D2 and D5, monoamine oxidases A and B (monoaminergic system); brain-derived neurotrophic factor, and neural cell adhesion molecule (involved in neurodevelopment). Thirty-eight families with two affected siblings and one family with two affected half-siblings, recruited by the Paris Autism Research International Sibpair Study (PARIS), were tested using the transmission disequilibrium test and two-point affected sib-pair linkage analysis. We found no evidence for association or linkage with intragenic or linked markers. Our family sample has good power for detecting a linkage disequilibrium of 0.80. Thus, these genes are unlikely to play a major role in the families studied, but further studies in a much larger sample would be needed to highlight weaker genetic effects.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)

Keyword

Alleles
Autistic Disorder
Genetics
Chromosome Mapping
DNA
Genetics
Family Health
Female
Genetic Predisposition to Disease
Genetics
Genotype
Humans
Linkage Disequilibrium
Male
Microsatellite Repeats
Monoamine Oxidase
Genetics
Nuclear Family
Receptors
Dopamine
Genetics
Tyrosine 3-Monooxygenase
Genetics

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view