Cargando…
Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk
BACKGROUND: Autism is a complex disorder characterized by deficits involving communication, social interaction, and repetitive and restrictive patterns of behavior. Twin studies have shown that autism is strongly heritable, suggesting a strong genetic component. In other disease states with a comple...
Autores principales: | Carayol, Jerome, Schellenberg, Gerard D, Tores, Frederic, Hager, Jörg, Ziegler, Andreas, Dawson, Geraldine |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907567/ https://www.ncbi.nlm.nih.gov/pubmed/20678243 http://dx.doi.org/10.1186/2040-2392-1-4 |
Ejemplares similares
-
Autism risk assessment in siblings of affected children using sex-specific genetic scores
por: Carayol, Jerome, et al.
Publicado: (2011) -
A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism
por: Carayol, Jérôme, et al.
Publicado: (2014) -
Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis
por: Philippi, Anne, et al.
Publicado: (2007) -
Are There Cultural Differences in Parental Interest in Early Diagnosis and Genetic Risk Assessment for Autism Spectrum Disorder?
por: Amiet, Claire, et al.
Publicado: (2014) -
Common genetic variants, acting additively, are a major source of risk for autism
por: Klei, Lambertus, et al.
Publicado: (2012)