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By Kevin J. Mitchell

Neurodevelopmental issues come up from disturbances to numerous strategies of mind improvement, that can happen in various methods. They surround many infrequent genetic syndromes in addition to universal, heritable stipulations akin to highbrow incapacity, autism, ADHD, schizophrenia and plenty of different types of epilepsy.The Genetics of Neurodevelopmental Disordersexaminesrecent innovative advances in our knowing of the Read more...

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Neurodevelopmental problems come up from disturbances to numerous strategies of mind improvement, which could appear in diversified methods. They surround many infrequent genetic syndromes in addition to common, Read more...

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The Genetics of Neurodevelopmental Disorders

Neurodevelopmental issues come up from disturbances to numerous approaches of mind improvement, that may occur in different methods. They surround many infrequent genetic syndromes in addition to universal, heritable stipulations corresponding to highbrow incapacity, autism, ADHD, schizophrenia and lots of varieties of epilepsy.

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Behav Brain Sci 29, 385–404; discussion 405–352. , et al. (2013). Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders. Mol Psychiatry. C. (2009). Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum Mol Genet 18, 1497–1503. , et al. (2014). The penetrance of copy number variations for schizophrenia and developmental delay. Biol Psychiatry 75, 378–385. , et al. (2012). Common genetic variants, acting additively, are a major source of risk for autism.

C. (2013). Emerging roles of metaplasticity in behaviour and disease. Trends Neurosci 36, 353–362. , et al. (2013). Negligible impact of rare autoimmune-locus coding-region variants on missing heritability. Nature 498, 232–235. , and Verma, R. (2014). Sex differences in the structural connectome of the human brain. Proc Natl Acad Sci U S A 111, 823–828. K. (2011). The false-positive to false-negative ratio in epidemiologic studies. Epidemiology 22, 450–456. , et al. (2012). De novo gene disruptions in children on the autistic spectrum.

2012). Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism 3, 9. , et al. (2014). Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition. Am J Med Genet Part B, Neuropsychiatric Genet: Off Publ Int Soc Psychiatric Genet 165, 84–95. R. (2007). Most rare missense alleles are deleterious in humans: implications for complex disease 24 THE GENETICS OF NEURODEVELOPMENTAL DISORDERS and association studies.

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