Impairments in dendrite morphogenesis as etiology for neurodevelopmental disorders and implications for therapeutic treatments
- 1 September 2016
- journal article
- review article
- Published by Elsevier BV in Neuroscience & Biobehavioral Reviews
- Vol. 68, 946-978
- https://doi.org/10.1016/j.neubiorev.2016.04.008
Abstract
No abstract availableThis publication has 100 references indexed in Scilit:
- DISC1 genetics, biology and psychiatric illnessFrontiers in Biology, 2012
- Cognitive, Behavioural and Psychiatric Phenotype in 22q11.2 Deletion SyndromeBehavior Genetics, 2011
- Targeted treatments for fragile X syndromeJournal of Neurodevelopmental Disorders, 2011
- Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disordersNeuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG), 2010
- Hooks and comets: The story of microtubule polarity orientation in the neuronDevelopmental Neurobiology, 2010
- The Basics of Brain DevelopmentNeuropsychology Review, 2010
- Association of Anxiety and Depression With Microtubule-Associated Protein 2– and Synaptopodin-Immunolabeled Dendrite and Spine Densities in Hippocampal CA3 of Older HumansArchives of General Psychiatry, 2010
- The Role of MeCP2 in Brain Development and Neurodevelopmental DisordersCurrent Psychiatry Reports, 2010
- Velo‐cardio‐facial syndrome: 30 Years of studyDevelopmental Disabilities Research Reviews, 2008
- Angelman syndrome 2005: Updated consensus for diagnostic criteriaAmerican Journal of Medical Genetics Part A, 2006