Cargando…
Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry
Attention-deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder with poorly understood molecular mechanisms that results in significant impairment in children. In this study, we sought to assess the role of rare recurrent variants in non-European populations and outside of coding re...
Autores principales: | Liu, Yichuan, Chang, Xiao, Qu, Hui-Qi, Tian, Lifeng, Glessner, Joseph, Qu, Jingchun, Li, Dong, Qiu, Haijun, Sleiman, Patrick, Hakonarson, Hakon |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927037/ https://www.ncbi.nlm.nih.gov/pubmed/33671795 http://dx.doi.org/10.3390/genes12020310 |
Ejemplares similares
-
Non-coding structural variation differentially impacts attention-deficit hyperactivity disorder (ADHD) gene networks in African American vs Caucasian children
por: Liu, Yichuan, et al.
Publicado: (2020) -
Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans
por: Chang, Xiao, et al.
Publicado: (2020) -
An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities
por: Slaby, Isabella, et al.
Publicado: (2022) -
Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population
por: Liu, Yichuan, et al.
Publicado: (2022) -
Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients
por: Liu, Yichuan, et al.
Publicado: (2022)