Multiplex gene and phenotype network to characterize shared genetic pathways of epilepsy and autism
Abstract It is well established that epilepsy and autism spectrum disorder (ASD) commonly co-occur; however, the underlying biological mechanisms of the co-occurence from their genetic susceptibility are not well understood. Our aim in this study is to characterize genetic modules of subgroups of ep...
Guardado en:
Autores principales: | Jacqueline Peng, Yunyun Zhou, Kai Wang |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/538145d3e7294c148050618d6296d848 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Phenotypic analysis of catastrophic childhood epilepsy genes
por: Aliesha Griffin, et al.
Publicado: (2021) -
Text mining of gene–phenotype associations reveals new phenotypic profiles of autism-associated genes
por: Sijie Li, et al.
Publicado: (2021) -
Quantitative and multiplexed chemical-genetic phenotyping in mammalian cells with QMAP-Seq
por: Sonia Brockway, et al.
Publicado: (2020) -
Multiplexed histology analyses for the phenotypic and spatial characterization of human innate lymphoid cells
por: Anna Pascual-Reguant, et al.
Publicado: (2021) -
Chromosomal barcoding as a tool for multiplexed phenotypic characterization of laboratory evolved lineages
por: Leonie Johanna Jahn, et al.
Publicado: (2018)