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CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
INCREASED INFLAMMATION AND MACROPHAGE INFILTRATION IS ASSOCIATED WITH ALTERED SUBEPENDYMAL ZONE NEUROGENESIS IN SCHIZOPHRENIA BUT NOT BIPOLAR DISORDER.
- Published in:
- Schizophrenia Bulletin, 2020, v. 46, p. S28, doi. 10.1093/schbul/sbaa028.065
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- Publication type:
- Article
White Matter Disruptions in Schizophrenia Are Spatially Widespread and Topologically Converge on Brain Network Hubs.
- Published in:
- Schizophrenia Bulletin, 2017, v. 43, n. 2, p. 425, doi. 10.1093/schbul/sbw100
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- Publication type:
- Article
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007535
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- Publication type:
- Article
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1851, doi. 10.3390/jcm9061851
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- Publication type:
- Article
Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 8, p. 485, doi. 10.1002/ajmg.b.32879
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- Publication type:
- Article
Cover Image, Volume 186B, Number 8, December 2021.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 8, p. 1, doi. 10.1002/ajmg.b.32803
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- Publication type:
- Article
Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2020, v. 183, n. 5, p. 277, doi. 10.1002/ajmg.b.32786
- By:
- Publication type:
- Article
Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 7, p. 617, doi. 10.1002/ajmg.b.32344
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- Publication type:
- Article
Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy: Additional information.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1424, doi. 10.1002/ajmg.a.36846
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- Publication type:
- Article
Characterization of a 520 kb deletion on chromosome 15q26.1 including ST8SIA2 in a patient with behavioral disturbance, autism spectrum disorder, and epilepsy.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 782, doi. 10.1002/ajmg.a.36345
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- Publication type:
- Article
Wellbeing and brain structure: A comprehensive phenotypic and genetic study of image‐derived phenotypes in the UK Biobank.
- Published in:
- Human Brain Mapping, 2022, v. 43, n. 17, p. 5180, doi. 10.1002/hbm.25993
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- Publication type:
- Article
Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores.
- Published in:
- Genes, Brain & Behavior, 2020, v. 19, n. 8, p. 1, doi. 10.1111/gbb.12694
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- Publication type:
- Article
Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.
- Published in:
- Frontiers in Psychiatry, 2018, p. 1, doi. 10.3389/fpsyt.2018.00207
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- Publication type:
- Article
Characterisation of Genetic Variation in <i>ST8SIA2</i> and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092556
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- Publication type:
- Article
Identification of Sialyltransferase 8B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15q25-26.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0038172
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- Publication type:
- Article
Glucocorticoid Receptor 1B and 1C mRNA Transcript Alterations in Schizophrenia and Bipolar Disorder, and Their Possible Regulation by GR Gene Variants.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0031720
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- Publication type:
- Article
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
- Published in:
- Journal of Psychiatry & Neuroscience, 2021, v. 46, n. 2, p. E247, doi. 10.1503/jpn.200083
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- Publication type:
- Article
Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
- Published in:
- Journal of Psychiatry & Neuroscience, 2019, v. 44, n. 5, p. 350, doi. 10.1503/jpn.180184
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- Publication type:
- Article
RNA-sequencing suggests extracellular matrix and vasculature dysregulation could impair neurogenesis in schizophrenia cases with elevated inflammation.
- Published in:
- Schizophrenia (2754-6993), 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41537-024-00466-0
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- Publication type:
- Article
Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02079-6
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- Publication type:
- Article
Genetic and environment effects on structural neuroimaging endophenotype for bipolar disorder: a novel molecular approach.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01892-3
- By:
- Publication type:
- Article
Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01874-5
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- Publication type:
- Article
A schizophrenia subgroup with elevated inflammation displays reduced microglia, increased peripheral immune cell and altered neurogenesis marker gene expression in the subependymal zone.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01742-8
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- Publication type:
- Article
Does perfectionism in bipolar disorder pedigrees mediate associations between anxiety/stress and mood symptoms?
- Published in:
- International Journal of Bipolar Disorders, 2017, v. 5, n. 1, p. 1, doi. 10.1186/s40345-017-0102-8
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- Publication type:
- Article
An examination of multiple classes of rare variants in extended families with bipolar disorder.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0113-y
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- Publication type:
- Article
Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls.
- Published in:
- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-017-0052-z
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- Publication type:
- Article
Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder.
- Published in:
- BMC Psychiatry, 2012, v. 12, n. 1, p. 84, doi. 10.1186/1471-244X-12-84
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- Publication type:
- Article
Family environment and polygenic risk in the bipolar high-risk context.
- Published in:
- JCPP Advances, 2023, v. 3, n. 2, p. 1, doi. 10.1002/jcv2.12143
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- Publication type:
- Article
De Novo Gene Variants and Familial Bipolar Disorder.
- Published in:
- JAMA Network Open, 2020, v. 3, n. 5, p. e203382, doi. 10.1001/jamanetworkopen.2020.3382
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- Publication type:
- Article
Prediction of lithium response using genomic data.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-80814-z
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- Publication type:
- Article
Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer.
- Published in:
- International Journal of Cancer, 2020, v. 146, n. 6, p. 1568, doi. 10.1002/ijc.32683
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- Publication type:
- Article
Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 4, p. 523, doi. 10.1007/s00401-013-1078-9
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- Publication type:
- Article
Assessing oxidative pathway genes as risk factors for bipolar disorder.
- Published in:
- Bipolar Disorders, 2010, v. 12, n. 5, p. 550, doi. 10.1111/j.1399-5618.2010.00834.x
- By:
- Publication type:
- Article
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
- Published in:
- Neurogenetics, 2013, v. 14, n. 1, p. 11, doi. 10.1007/s10048-012-0349-2
- By:
- Publication type:
- Article
Predictors of functional impairment in bipolar disorder: Results from 13 cohorts from seven countries by the global bipolar cohort collaborative.
- Published in:
- Bipolar Disorders, 2022, v. 24, n. 7, p. 709, doi. 10.1111/bdi.13208
- By:
- Publication type:
- Article
Diagnosis of bipolar disorders and body mass index predict clustering based on similarities in cortical thickness—ENIGMA study in 2436 individuals.
- Published in:
- Bipolar Disorders, 2022, v. 24, n. 5, p. 509, doi. 10.1111/bdi.13172
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- Publication type:
- Article