Cargando…

A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease

Epidemiological and genetic studies suggest that schizophrenia and autism may share genetic links. Besides common single nucleotide polymorphisms, recent data suggest that some rare copy number variants (CNVs) are risk factors for both disorders. Because we have previously found that schizophrenia a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zheng, Xiaojing, Demirci, F. Yesim, Barmada, M. Michael, Richardson, Gale A., Lopez, Oscar L., Sweet, Robert A., Kamboh, M. Ilyas, Feingold, Eleanor
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224411/ https://www.ncbi.nlm.nih.gov/pubmed/25379732 http://dx.doi.org/10.1371/journal.pone.0111462

Ejemplares similares

Genome-wide copy-number variation study of psychosis in Alzheimer's disease
por: Zheng, X, et al.
Publicado: (2015)

Sensory processing in 16p11.2 deletion and 16p11.2 duplication
por: Smith, Harriet, et al.
Publicado: (2022)

Paroxysmal Kinesigenic Dyskinesia in Twins With Chromosome 16p11.2 Duplication Syndrome
por: Ueda, Keisuke, et al.
Publicado: (2021)

Connecting the Dots: Potential of Data Integration to Identify Regulatory SNPs in Late-Onset Alzheimer's Disease GWAS Findings
por: Rosenthal, Samantha L., et al.
Publicado: (2014)

Psychiatric disorders in children with 16p11.2 deletion and duplication
por: Niarchou, Maria, et al.
Publicado: (2019)

Gene Expression and Cardiometabolic Phenotypes of Vitamin D-Deficient Overweight and Obese Black Children
por: Rajakumar, Kumaravel, et al.
Publicado: (2019)

Association of VPREB1 Gene Copy Number Variation and Rheumatoid Arthritis Susceptibility
por: Aslam, Muhammad Muaaz, et al.
Publicado: (2020)

Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication
por: Niarchou, Maria, et al.
Publicado: (2019)

Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion
por: Wang, You, et al.
Publicado: (2022)

Association of Fc Gamma Receptor 3B Gene Copy Number Variation with Rheumatoid Arthritis Susceptibility
por: Aslam, M. Muaaz, et al.
Publicado: (2022)

Transposition of the great arteries - a phenotype associated with 16p11.2 duplications?
por: Karunanithi, Zarmiga, et al.
Publicado: (2017)

Neuro-Behavioral Phenotype in 16p11.2 Duplication: A Case Series
por: Posar, Annio, et al.
Publicado: (2020)

Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population
por: Aslam, Muhammad Muaaz, et al.
Publicado: (2019)

A sequencing study of CTLA4 in Pakistani rheumatoid arthritis cases
por: Aslam, Muhammad Muaaz, et al.
Publicado: (2020)

Case Report: Autoimmune Psychosis in Chromosome 22q11.2 Deletion Syndrome
por: Ciano-Petersen, Nicolás Lundahl, et al.
Publicado: (2021)

Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population
por: Cheema, Asma Naseer, et al.
Publicado: (2020)

Chromosome 22q11.2 Duplication Syndrome and Diagnostic Overshadowing: A Case Report
por: Singh, Ashok, et al.
Publicado: (2023)

Investigating the GWAS-Implicated Loci for Rheumatoid Arthritis in the Pakistani Population
por: Aslam, Muhammad Muaaz, et al.
Publicado: (2020)

Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications
por: Hudac, Caitlin M., et al.
Publicado: (2015)

Deletion and duplication of 16p11.2 are associated with opposing effects on visual evoked potential amplitude
por: LeBlanc, Jocelyn J., et al.
Publicado: (2016)

Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region
por: Moufawad El Achkar, Christelle, et al.
Publicado: (2022)

Genome-Wide Association Study of Antiphospholipid Antibodies
por: Kamboh, M. Ilyas, et al.
Publicado: (2013)

Resequencing of LPL in African Blacks and associations with lipoprotein–lipid levels
por: Pirim, Dilek, et al.
Publicado: (2015)

Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study
por: Niemsiri, Vipavee, et al.
Publicado: (2015)

Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes
por: Arbogast, Thomas, et al.
Publicado: (2016)

Genetic association between APOE*4 and neuropsychiatric symptoms in patients with probable Alzheimer's disease is dependent on the psychosis phenotype
por: Christie, Drew, et al.
Publicado: (2012)

Chromosome 16p11.2 deletions: another piece in the genetic puzzle of childhood obesity
por: Perrone, Laura, et al.
Publicado: (2010)

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2
por: Li, Meihua, et al.
Publicado: (2022)

Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups
por: Pirim, Dilek, et al.
Publicado: (2019)

Evidence that duplications of 22q11.2 protect against schizophrenia
por: Rees, E, et al.
Publicado: (2014)

22q11.2 Deletion and Duplication Syndromes and COVID-19
por: Crowley, T. Blaine, et al.
Publicado: (2022)

The application of network label propagation to rank biomarkers in genome-wide Alzheimer’s data
por: Stokes, Matthew E, et al.
Publicado: (2014)

Case Report: Novel Copy Number Variant 16p11.2 Duplication Associated With Prune Belly Syndrome
por: Talluri, Sriharsha, et al.
Publicado: (2021)

Reciprocal Deletion and Duplication of 17p11.2-11.2: Korean Patients with Smith-Magenis Syndrome and Potocki-Lupski Syndrome
por: Lee, Cha Gon, et al.
Publicado: (2012)

Identifying genetic interactions associated with late-onset Alzheimer’s disease
por: Floudas, Charalampos S, et al.
Publicado: (2014)

Clinical management of psychosis in 22q11.2 deletion syndrome
por: Iftimovici, Anton, et al.
Publicado: (2022)

Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers
por: Vergés, Laia, et al.
Publicado: (2014)

Exposure, entropion, and bilateral corneal ulceration in a newborn as a manifestation of chromosome 22 q11.2 duplication syndrome
por: Moein, Hamid-Reza, et al.
Publicado: (2018)

A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2
por: Walters, R. G., et al.
Publicado: (2010)

Copy number variation and brain structure: lessons learned from chromosome 16p11.2
por: Stein, Jason L
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_v1fbch2nua17fdpjkrel9n431a