Cargando…
The contributions of rare inherited and polygenic risk to ASD in multiplex families
Autism spectrum disorder (ASD) has a complex genetic architecture involving contributions from both de novo and inherited variation. Few studies have been designed to address the role of rare inherited variation or its interaction with common polygenic risk in ASD. Here, we performed whole-genome se...
Autores principales: | Cirnigliaro, Matilde, Chang, Timothy S., Arteaga, Stephanie A., Pérez-Cano, Laura, Ruzzo, Elizabeth K., Gordon, Aaron, Bicks, Lucy K., Jung, Jae-Yoon, Lowe, Jennifer K., Wall, Dennis P., Geschwind, Daniel H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400943/ https://www.ncbi.nlm.nih.gov/pubmed/37506195 http://dx.doi.org/10.1073/pnas.2215632120 |
Ejemplares similares
-
Neuronal protein interaction networks in autism spectrum disorder
por: Bicks, Lucy K., et al.
Publicado: (2023) -
A polygenic risk score analysis of ASD and ADHD across emotion recognition subtypes
por: Waddington, Francesca, et al.
Publicado: (2020) -
Increased Sensory Processing Atypicalities in Parents of Multiplex ASD Families Versus Typically Developing and Simplex ASD Families
por: Donaldson, Chelsea K., et al.
Publicado: (2016) -
Does the cognitive architecture of simplex and multiplex ASD families differ?
por: Oerlemans, Anoek M., et al.
Publicado: (2015) -
Polygenic risk for ADHD and ASD and their relation with cognitive measures in school children
por: Aguilar-Lacasaña, Sofía, et al.
Publicado: (2022)