相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease
Anne S. Bassett et al.
AMERICAN JOURNAL OF PSYCHIATRY (2010)
Copy Number Variation in Schizophrenia in the Japanese Population
Masashi Ikeda et al.
BIOLOGICAL PSYCHIATRY (2010)
Functional and Dysfunctional Synaptic Plasticity in Prefrontal Cortex: Roles in Psychiatric Disorders
Yukiori Goto et al.
BIOLOGICAL PSYCHIATRY (2010)
The role of copy number variation in schizophrenia
George Kirov
EXPERT REVIEW OF NEUROTHERAPEUTICS (2010)
Polymorphic CA repeat in IGF-I gene: lack of association with schizophrenia
Cristian Bonvicini et al.
PSYCHIATRIC GENETICS (2010)
The Role of DNA Copy Number Variation in Schizophrenia
Gloria W. C. Tam et al.
BIOLOGICAL PSYCHIATRY (2009)
GenotypeColour™: colour visualisation of SNPs and CNVs
Sergio Barlati et al.
BMC BIOINFORMATICS (2009)
Laser capture microdissection and cDNA array analysis for identification of mouse KIAA/FLJ genes differentially expressed in the embryonic dorsal spinal cord
Tomoyuki Masuda et al.
BRAIN RESEARCH (2009)
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
George Kirov et al.
HUMAN MOLECULAR GENETICS (2009)
A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia
Anna C. Need et al.
PLOS GENETICS (2009)
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
Maricela Alarcon et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
Terry Vrijenhoek et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Disruption of neurexin 1 associated with autism spectrum disorder
Hyung-Goo Kim et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area
Chiara Floris et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
An association analysis of synapse-associated protein 97 (SAP97) gene in schizophrenia
Junko Sato et al.
JOURNAL OF NEURAL TRANSMISSION (2008)
Rare chromosomal deletions and duplications increase risk of schizophrenia
Jennifer L. Stone et al.
NATURE (2008)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson et al.
NATURE (2008)
Strong association of de novo copy number mutations with sporadic schizophrenia
Bin Xu et al.
NATURE GENETICS (2008)
Del-1, an Endogenous Leukocyte-Endothelial Adhesion Inhibitor, Limits Inflammatory Cell Recruitment
Eun Young Choi et al.
SCIENCE (2008)
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Tom Walsh et al.
SCIENCE (2008)
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
George Kirov et al.
HUMAN MOLECULAR GENETICS (2008)
Copy-number variations measured by single-nucleotide polymorphism oligonucleotide Arrays in patients with mental retardation
Janine Wagenstaller et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
G308A tumor necrosis factor alpha functional polymorphism and schizophrenia risk: Meta-analysis plus association study
Emilio Sacchetti et al.
BRAIN BEHAVIOR AND IMMUNITY (2007)
Strong association of de novo copy number mutations with autism
Jonathan Sebat et al.
SCIENCE (2007)
Global variation in copy number in the human genome
Richard Redon et al.
NATURE (2006)
A worldwide survey of haplotype variation and linkage disequilibrium in the human genome
Donald F. Conrad et al.
NATURE GENETICS (2006)
Diagnostic genome profiling in mental retardation
BBA de Vries et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1
A Shimizu et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2003)
Identification of two new members of the CSMD gene family
WL Lau et al.
GENOMICS (2003)
beta-1,3-glucuronyltransferase-1 gene implicated as a candidate for a schizophrenia-like psychosis through molecular analysis of a balanced translocation
AR Jeffries et al.
MOLECULAR PSYCHIATRY (2003)
Mice deficient in nervous system-specific carbohydrate epitope HNK-1 exhibit impaired synaptic plasticity and spatial learning
S Yamamoto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
分享论文
