CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 23, Issue 6, Pages 1669-1676
Publisher
Oxford University Press (OUP)
Online
2013-10-27
DOI
10.1093/hmg/ddt540
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder
- (2013) Santhosh Girirajan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family
- (2013) Marina Myles-Worsley et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- The genomic psychiatry cohort: Partners in discovery
- (2013) Michele T. Pato et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- The SLC1 high-affinity glutamate and neutral amino acid transporter family
- (2013) Yoshikatsu Kanai et al. MOLECULAR ASPECTS OF MEDICINE
- Copy Number Variants in German Patients with Schizophrenia
- (2013) Lutz Priebe et al. PLoS One
- Implication of a Rare Deletion at Distal 16p11.2 in Schizophrenia
- (2013) Saurav Guha JAMA Psychiatry
- Cingulin, paracingulin, and PLEKHA7: signaling and cytoskeletal adaptors at the apical junctional complex
- (2012) Sandra Citi et al. Annals of the New York Academy of Sciences
- Genome-Wide Association Study Implicates HLA-C*01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia
- (2012) BIOLOGICAL PSYCHIATRY
- CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
- (2012) Dheeraj Malhotra et al. CELL
- Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
- (2012) Santhosh Girirajan et al. NEW ENGLAND JOURNAL OF MEDICINE
- Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
- (2011) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants
- (2011) Elliott Rees et al. BIOLOGICAL PSYCHIATRY
- High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy
- (2011) Larissa R Stewart et al. BMC Medical Genetics
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
- (2011) G Kirov et al. MOLECULAR PSYCHIATRY
- Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
- (2011) Vladimir Vacic et al. NATURE
- A copy number variation morbidity map of developmental delay
- (2011) Gregory M Cooper et al. NATURE GENETICS
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle et al. AMERICAN JOURNAL OF HUMAN GENETICS
- De novo rates and selection of large copy number variation
- (2010) A. Itsara et al. GENOME RESEARCH
- Phenotypic variability and genetic susceptibility to genomic disorders
- (2010) S. Girirajan et al. HUMAN MOLECULAR GENETICS
- Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
- (2010) Nigel M Williams et al. LANCET
- A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
- (2010) Francesca Antonacci et al. NATURE GENETICS
- A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
- (2010) Santhosh Girirajan et al. NATURE GENETICS
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- Disruption of the neurexin 1 gene is associated with schizophrenia
- (2008) Dan Rujescu et al. HUMAN MOLECULAR GENETICS
- Paracingulin Regulates the Activity of Rac1 and RhoA GTPases by Recruiting Tiam1 and GEF-H1 to Epithelial Junctions
- (2008) Laurent Guillemot et al. MOLECULAR BIOLOGY OF THE CELL
- 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
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started