Cargando…
ADGRL3 (LPHN3) variants are associated with a refined phenotype of ADHD in the MTA study
BACKGROUND: ADHD is the most common neuropsychiatric condition affecting individuals of all ages. Long‐term outcomes of affected individuals and association with severe comorbidities as SUD or conduct disorders are the main concern. Genetic associations have been extensively described. Multiple stud...
Autores principales: | Acosta, Maria T., Swanson, James, Stehli, Annamarie, Molina, Brooke S. G., Martinez, Ariel F., Arcos‐Burgos, Mauricio, Muenke, Maximilian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023939/ https://www.ncbi.nlm.nih.gov/pubmed/27652281 http://dx.doi.org/10.1002/mgg3.230 |
Ejemplares similares
-
ADGRL3 (LPHN3) variants predict substance use disorder
por: Arcos-Burgos, Mauricio, et al.
Publicado: (2019) -
A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome
por: Acosta, M T, et al.
Publicado: (2011) -
ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP
por: Vidal, Oscar M., et al.
Publicado: (2022) -
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD
por: Jain, M, et al.
Publicado: (2012) -
ADGRL3, FGF1 and DRD4: Linkage and Association with Working Memory and Perceptual Organization Candidate Endophenotypes in ADHD
por: Cervantes-Henriquez, Martha L., et al.
Publicado: (2021)