A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease
Authors
Keywords
-
Journal
PLoS One
Volume 9, Issue 11, Pages e111462
Publisher
Public Library of Science (PLoS)
Online
2014-11-08
DOI
10.1371/journal.pone.0111462
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genetics of Psychosis in Alzheimer's Disease: A Review
- (2017) Mary Ann DeMichele-Sweet et al. JOURNAL OF ALZHEIMERS DISEASE
- Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease
- (2017) Erin L. Heinzen et al. JOURNAL OF ALZHEIMERS DISEASE
- An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis
- (2014) D. W. Morris et al. HUMAN MOLECULAR GENETICS
- Common variant at 16p11.2 conferring risk of psychosis
- (2012) S Steinberg et al. MOLECULAR PSYCHIATRY
- KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
- (2012) Christelle Golzio et al. NATURE
- Downregulation of extracellular signal-regulated kinase 1/2 activity by calmodulin KII modulates p21Cip1 levels and survival of immortalized lymphocytes from Alzheimer’s disease patients
- (2012) Noemí Esteras et al. NEUROBIOLOGY OF AGING
- Simons Variation in Individuals Project (Simons VIP): A Genetics-First Approach to Studying Autism Spectrum and Related Neurodevelopmental Disorders
- (2012) The Simons VIP Consortium NEURON
- Copy number variations in neurodevelopmental disorders
- (2012) Hannah M. Grayton et al. PROGRESS IN NEUROBIOLOGY
- Genome-wide association study of Alzheimer's disease
- (2012) M I Kamboh et al. Translational Psychiatry
- Genome-wide association study of Alzheimer's disease with psychotic symptoms
- (2011) P Hollingworth et al. MOLECULAR PSYCHIATRY
- Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- (2010) Daniel Moreno-De-Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review
- (2010) Fabiola Quintero-Rivera et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
- (2010) R. G. Walters et al. NATURE
- No association of psychosis in Alzheimer disease with neurodegenerative pathway genes
- (2010) Mary Ann A. DeMichele-Sweet et al. NEUROBIOLOGY OF AGING
- Uncovering Molecular Biomarkers That Correlate Cognitive Decline with the Changes of Hippocampus' Gene Expression Profiles in Alzheimer's Disease
- (2010) Martín Gómez Ravetti et al. PLoS One
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
- (2009) Audrey Guilmatre et al. ARCHIVES OF GENERAL PSYCHIATRY
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
- (2009) M. Shinawi et al. JOURNAL OF MEDICAL GENETICS
- Effect of quinolinic acid on human astrocytes morphology and functions: implications in Alzheimer's disease
- (2009) Ka Ting et al. Journal of Neuroinflammation
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Genetic overlap between autism, schizophrenia and bipolar disorder
- (2009) Liam S Carroll et al. Genome Medicine
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
- (2008) Nicola Brunetti-Pierri et al. NATURE GENETICS
- Alterations in kynurenine precursor and product levels in schizophrenia and bipolar disorder
- (2008) Christine L. Miller et al. NEUROCHEMISTRY INTERNATIONAL
- Genetic Variation in the α7 Nicotinic Acetylcholine Receptor is Associated with Delusional Symptoms in Alzheimer’s Disease
- (2008) Robyn Carson et al. NEUROMOLECULAR MEDICINE
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started