Cargando…
Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data
BACKGROUND: Numerous genes are implicated in autism spectrum disorder (ASD). ASD encompasses a wide-range and severity of symptoms and co-occurring conditions; however, the details of how genetic variation contributes to phenotypic differences are unclear. This creates a challenge for translating ge...
Autores principales: | Veatch, Olivia J., Mazzotti, Diego R., Schultz, Robert T., Abel, Ted, Michaelson, Jacob J., Brodkin, Edward S., Tunc, Birkan, Assouline, Susan G., Nickl-Jockschat, Thomas, Malow, Beth A., Sutcliffe, James S., Pack, Allan I. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233372/ https://www.ncbi.nlm.nih.gov/pubmed/35751013 http://dx.doi.org/10.1186/s11689-022-09448-8 |
Ejemplares similares
-
Characterization of genetic and phenotypic heterogeneity of obstructive sleep apnea using electronic health records
por: Veatch, Olivia J., et al.
Publicado: (2020) -
Dissecting 16p11.2 hemi-deletion to study sex-specific striatal phenotypes of neurodevelopmental disorders
por: Abel, Ted, et al.
Publicado: (2023) -
An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder
por: Veatch, Olivia J., et al.
Publicado: (2020) -
Pleiotropic effects of a high confidence Autism Spectrum Disorder gene, arid1b, on zebrafish sleep
por: Doldur-Balli, Fusun, et al.
Publicado: (2023) -
Spatial transcriptomics reveals unique gene expression changes in different brain regions after sleep deprivation
por: Vanrobaeys, Yann, et al.
Publicado: (2023)