Cargando…
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
Attention-deficit/hyperactivity disorder (ADHD) is a common and highly heritable disorder, but specific genetic factors underlying risk remain elusive. To assess the role of structural variation in ADHD, we identified 222 inherited copy number variations (CNVs) within 335 ADHD patients and their par...
Autores principales: | Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877197/ https://www.ncbi.nlm.nih.gov/pubmed/19546859 http://dx.doi.org/10.1038/mp.2009.57 |
Ejemplares similares
-
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
por: Elia, J, et al.
Publicado: (2010) -
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
por: Gai, Xiaowu, et al.
Publicado: (2010) -
Rare structural variation of synapse and neurotransmission genes in autism
por: Gai, X, et al.
Publicado: (2012) -
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders
por: Glessner, Joseph T., et al.
Publicado: (2023) -
Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
por: Glessner, Joseph T., et al.
Publicado: (2010)