Cargando…
A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism
Autism spectrum disorders (ASD) are highly heritable complex neurodevelopmental disorders with a 4:1 male: female ratio. Common genetic variation could explain 40–60% of the variance in liability to autism. Because of their small effect, genome-wide association studies (GWASs) have only identified a...
Autores principales: | Carayol, Jérôme, Schellenberg, Gerard D., Dombroski, Beth, Amiet, Claire, Génin, Bérengère, Fontaine, Karine, Rousseau, Francis, Vazart, Céline, Cohen, David, Frazier, Thomas W., Hardan, Antonio Y., Dawson, Geraldine, Rio Frio, Thomas |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927086/ https://www.ncbi.nlm.nih.gov/pubmed/24600472 http://dx.doi.org/10.3389/fgene.2014.00033 |
Ejemplares similares
-
Autism risk assessment in siblings of affected children using sex-specific genetic scores
por: Carayol, Jerome, et al.
Publicado: (2011) -
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) -
Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk
por: Carayol, Jerome, et al.
Publicado: (2010) -
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) -
Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
por: Amiet, Claire, et al.
Publicado: (2013)