Found: 9
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Identification of Rare Copy Number Variants in High Burden Schizophrenia Families.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 3, p. 273, doi. 10.1002/ajmg.b.32146
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- Article
Rare Copy Number Variants in Neuropsychiatric Disorders: Specific Phenotype or Not?
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 7, p. 812, doi. 10.1002/ajmg.b.32088
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- Article
Identification of a CACNA2D4 Deletion in Late Onset Bipolar Disorder Patients and Implications for the Involvement of Voltage-Dependent Calcium Channels in Psychiatric Disorders.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 4, p. 465, doi. 10.1002/ajmg.b.32053
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- Article
Subclinical epileptiform activity and sleep disturbances in Alzheimer's disease.
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- Brain & Behavior, 2023, v. 13, n. 12, p. 1, doi. 10.1002/brb3.3306
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- Article
Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023450
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- Article
Toward Quantification of Agitation in People With Dementia Using Multimodal Sensing.
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- Innovation in Aging, 2022, v. 6, n. 7, p. 1, doi. 10.1093/geroni/igac064
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- Article
Hippocampal volume change following ECT is mediated by rs699947 in the promotor region of VEGF.
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- Translational Psychiatry, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41398-019-0530-6
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- Article
Facial expression recognition deficits in frontotemporal dementia and Alzheimer's disease: a meta-analytic investigation of effects of phenotypic variant, task modality, geographical region and symptomatic specificity.
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- Journal of Neurology, 2023, v. 270, n. 12, p. 5731, doi. 10.1007/s00415-023-11927-4
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- Article
A paleo-neurologic investigation of the social brain hypothesis in frontotemporal dementia.
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- Cerebral Cortex, 2023, v. 33, n. 3, p. 622, doi. 10.1093/cercor/bhac089
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- Article