Cargando…

Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits

IMPORTANCE: Psychotic experiences, such as hallucinations and delusions, are reported by approximately 5% to 10% of the general population, although only a small proportion develop psychotic disorders such as schizophrenia. Studying the genetic causes of psychotic experiences in the general populati...

Descripción completa

Detalles Bibliográficos
Autores principales:	Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M., Pardiñas, Antonio F., Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina A. S., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Zammit, Stanley, Walters, James T. R.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	American Medical Association 2019
Materias:	Original Investigation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764002/ https://www.ncbi.nlm.nih.gov/pubmed/31553412 http://dx.doi.org/10.1001/jamapsychiatry.2019.2508

Ejemplares similares

Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank
por: Dennison, Charlotte A., et al.
Publicado: (2021)

Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia
por: Legge, Sophie E., et al.
Publicado: (2021)

Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank
por: Bracher-Smith, Matthew, et al.
Publicado: (2022)

Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study
por: Kendall, Kimberley M., et al.
Publicado: (2020)

Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder
por: Allardyce, Judith, et al.
Publicado: (2017)

Association of Rare Copy Number Variants With Risk of Depression
por: Kendall, Kimberley Marie, et al.
Publicado: (2019)

S178. SHOULD SCHIZOAFFECTIVE DISORDER DEPRESSED-TYPE BE DISTINCT FROM SCHIZOPHRENIA? ANALYSIS OF GENETIC LIABILITY AND LIFETIME CLINICAL CHARACTERISTICS
por: Dennison, Charlotte, et al.
Publicado: (2020)

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank
por: Kendall, Kimberley M., et al.
Publicado: (2019)

Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank
por: Caseras, Xavier, et al.
Publicado: (2021)

Gender differences in CNV burden do not confound schizophrenia CNV associations
por: Han, Jun, et al.
Publicado: (2016)

Effects of pathogenic CNVs on physical traits in participants of the UK Biobank
por: Owen, David, et al.
Publicado: (2018)

Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance
por: Caseras, Xavier, et al.
Publicado: (2022)

Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia
por: Rammos, Alexandros, et al.
Publicado: (2023)

Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach
por: Vivian‐Griffiths, Timothy, et al.
Publicado: (2018)

S134. INCIDENCE, IMPACT AND TRAJECTORIES OF PSYCHOTIC EXPERIENCES FROM CHILDHOOD TO ADULTHOOD, AND PREDICTION OF PSYCHOTIC DISORDER
por: Zammit, Stanley, et al.
Publicado: (2020)

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci
por: Escott-Price, Valentina, et al.
Publicado: (2015)

Ultrarare Coding Variants and Cognitive Function in Schizophrenia
por: Creeth, Hugo D. J., et al.
Publicado: (2022)

Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder
por: Richards, Alexander L., et al.
Publicado: (2022)

A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia
por: Hall, Lynsey S, et al.
Publicado: (2020)

Risk Factors, Clinical Features, and Polygenic Risk Scores in Schizophrenia and Schizoaffective Disorder Depressive-Type
por: Dennison, Charlotte A, et al.
Publicado: (2021)

Genetic association of FMRP targets with psychiatric disorders
por: Clifton, Nicholas E., et al.
Publicado: (2020)

Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis
por: Rees, Elliott, et al.
Publicado: (2019)

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia
por: Rees, Elliott, et al.
Publicado: (2020)

Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort
por: Grama, Steluta, et al.
Publicado: (2020)

A data‐driven investigation of relationships between bipolar psychotic symptoms and schizophrenia genome‐wide significant genetic loci
por: Leonenko, Ganna, et al.
Publicado: (2018)

Age-dependent effect of APOE and polygenic component on Alzheimer's disease
por: Bellou, Eftychia, et al.
Publicado: (2020)

A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents
por: Zammit, Stanley, et al.
Publicado: (2014)

POLARIS: Polygenic LD‐adjusted risk score approach for set‐based analysis of GWAS data
por: Baker, Emily, et al.
Publicado: (2018)

Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
por: Rees, Elliott, et al.
Publicado: (2021)

Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer’s disease
por: Creese, Byron, et al.
Publicado: (2019)

Comparison of Genetic Liability for Sleep Traits Among Individuals With Bipolar Disorder I or II and Control Participants
por: Lewis, Katie J. S., et al.
Publicado: (2020)

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia
por: Pocklington, Andrew J., et al.
Publicado: (2015)

The Duffy-null genotype and risk of infection
por: Legge, Sophie E, et al.
Publicado: (2020)

Common alleles contribute to schizophrenia in CNV carriers
por: Tansey, K E, et al.
Publicado: (2016)

Erratum: Common alleles contribute to schizophrenia in CNV carriers
por: Tansey, K E, et al.
Publicado: (2015)

Early manifestations of genetic liability for ADHD, autism and schizophrenia at ages 18 and 24 months
por: Riglin, Lucy, et al.
Publicado: (2022)

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk
por: Chapman, Jade, et al.
Publicado: (2013)

Using Genetics to Examine a General Liability to Childhood Psychopathology
por: Riglin, Lucy, et al.
Publicado: (2019)

Association of copy number variation across the genome with neuropsychiatric traits in the general population
por: Guyatt, Anna L., et al.
Publicado: (2018)

Clinical Indicators of Symptom Dimensions and Cognitive Ability in Schizophrenia
por: Farakish, L., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_td4k5t0rcpr9rvpvhnj8m1bqhq