Published in Sci Rep on June 17, 2011
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The ZIC gene family in development and disease. Clin Genet (2005) 1.66
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Zic2 controls cerebellar development in cooperation with Zic1. J Neurosci (2002) 1.42
Slitrk1-deficient mice display elevated anxiety-like behavior and noradrenergic abnormalities. Mol Psychiatry (2008) 1.41
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Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination. Hum Mol Genet (2001) 1.38
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Loss of M5 muscarinic acetylcholine receptors leads to cerebrovascular and neuronal abnormalities and cognitive deficits in mice. Neurobiol Dis (2006) 1.23
Zic deficiency in the cortical marginal zone and meninges results in cortical lamination defects resembling those in type II lissencephaly. J Neurosci (2008) 1.23
Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients. Am J Med Genet C Semin Med Genet (2010) 1.23
Zic1 and Zic3 regulate medial forebrain development through expansion of neuronal progenitors. J Neurosci (2007) 1.19
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. J Med Genet (2009) 1.10
Research review: Cholinergic mechanisms, early brain development, and risk for schizophrenia. J Child Psychol Psychiatry (2009) 1.06
A wide-range phylogenetic analysis of Zic proteins: implications for correlations between protein structure conservation and body plan complexity. Genomics (2006) 1.03
Mice mutant for genes associated with schizophrenia: common phenotype or distinct endophenotypes? Behav Brain Res (2009) 0.97
Behavioral abnormalities of Zic1 and Zic2 mutant mice: implications as models for human neurological disorders. Behav Genet (2001) 0.97
Zic2 and Zic3 synergistically control neurulation and segmentation of paraxial mesoderm in mouse embryo. Dev Biol (2007) 0.97
Medial amygdala lesions in male rats reduce aggressive behavior: interference with experience. Physiol Behav (1987) 0.95
Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly. Hum Genet (2001) 0.93
Expression of ZIC family genes in meningiomas and other brain tumors. BMC Cancer (2010) 0.93
Myogenic repressor I-mfa interferes with the function of Zic family proteins. Biochem Biophys Res Commun (2004) 0.91
Neural inputs of the hypothalamic "aggression area" in the rat. Behav Brain Res (2010) 0.88
ZIC2-dependent transcriptional regulation is mediated by DNA-dependent protein kinase, poly(ADP-ribose) polymerase, and RNA helicase A. J Biol Chem (2007) 0.84
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet (2009) 8.11
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet (2003) 3.02
IP3 receptor types 2 and 3 mediate exocrine secretion underlying energy metabolism. Science (2005) 2.53
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients. J Clin Invest (2007) 2.45
Adult neurogenesis modulates the hippocampus-dependent period of associative fear memory. Cell (2009) 2.43
Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype. PLoS Biol (2007) 1.88
Zic2 patterns binocular vision by specifying the uncrossed retinal projection. Cell (2003) 1.81
Potent amyloidogenicity and pathogenicity of Aβ43. Nat Neurosci (2011) 1.76
Novel 18F-labeled arylquinoline derivatives for noninvasive imaging of tau pathology in Alzheimer disease. J Nucl Med (2013) 1.58
Comparison of patients with Kawasaki disease with retropharyngeal edema and patients with retropharyngeal abscess. Eur J Pediatr (2013) 1.50
All-trans retinoic acid and a novel synthetic retinoid tamibarotene (Am80) differentially regulate CD38 expression in human leukemia HL-60 cells: possible involvement of protein kinase C-delta. J Leukoc Biol (2011) 1.50
Selective control of inhibitory synapse development by Slitrk3-PTPδ trans-synaptic interaction. Nat Neurosci (2012) 1.50
DNA methylation status of SOX10 correlates with its downregulation and oligodendrocyte dysfunction in schizophrenia. J Neurosci (2005) 1.49
Genetic analysis of the calcineurin pathway identifies members of the EGR gene family, specifically EGR3, as potential susceptibility candidates in schizophrenia. Proc Natl Acad Sci U S A (2007) 1.46
Extracellular signal-regulated kinase 2 (ERK2) knockdown mice show deficits in long-term memory; ERK2 has a specific function in learning and memory. J Neurosci (2007) 1.41
Two genetic variants of CD38 in subjects with autism spectrum disorder and controls. Neurosci Res (2010) 1.35
Prdm proto-oncogene transcription factor family expression and interaction with the Notch-Hes pathway in mouse neurogenesis. PLoS One (2008) 1.28
Loss of M5 muscarinic acetylcholine receptors leads to cerebrovascular and neuronal abnormalities and cognitive deficits in mice. Neurobiol Dis (2006) 1.23
Zic deficiency in the cortical marginal zone and meninges results in cortical lamination defects resembling those in type II lissencephaly. J Neurosci (2008) 1.23
A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia. Biol Psychiatry (2005) 1.20
Genetic analyses of roundabout (ROBO) axon guidance receptors in autism. Am J Med Genet B Neuropsychiatr Genet (2008) 1.19
Zic1 and Zic3 regulate medial forebrain development through expansion of neuronal progenitors. J Neurosci (2007) 1.19
Identification of multiple serine racemase (SRR) mRNA isoforms and genetic analyses of SRR and DAO in schizophrenia and D-serine levels. Biol Psychiatry (2005) 1.18
Comparison of the binding characteristics of [18F]THK-523 and other amyloid imaging tracers to Alzheimer's disease pathology. Eur J Nucl Med Mol Imaging (2012) 1.18
Delphilin: a novel PDZ and formin homology domain-containing protein that synaptically colocalizes and interacts with glutamate receptor delta 2 subunit. J Neurosci (2002) 1.17
ERK2 contributes to the control of social behaviors in mice. J Neurosci (2011) 1.17
Association between polymorphisms in the promoter region of the sialyltransferase 8B (SIAT8B) gene and schizophrenia. Biol Psychiatry (2005) 1.15
Pax6 is required for production and maintenance of progenitor cells in postnatal hippocampal neurogenesis. Genes Cells (2005) 1.13
Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p. Am J Hum Genet (2005) 1.11
Distinguishable haplotype blocks in the HTR3A and HTR3B region in the Japanese reveal evidence of association of HTR3B with female major depression. Biol Psychiatry (2006) 1.07
Low serum levels of brain-derived neurotrophic factor and epidermal growth factor in patients with chronic schizophrenia. Schizophr Res (2008) 1.07
Genome-wide expression analysis detects eight genes with robust alterations specific to bipolar I disorder: relevance to neuronal network perturbation. Hum Mol Genet (2006) 1.07
Neuronal functions of the novel serine/threonine kinase Ndr2. J Biol Chem (2004) 1.06
Association study of polymorphisms in the 5' upstream region of human DISC1 gene with schizophrenia. Neurosci Lett (2004) 1.06
Association between schizophrenia with ocular misalignment and polyalanine length variation in PMX2B. Hum Mol Genet (2004) 1.05
Elucidation of penetrance variability of a ZIC3 mutation in a family with complex heart defects and functional analysis of ZIC3 mutations in the first zinc finger domain. Hum Mutat (2007) 1.05
Reduction in memory in passive avoidance learning, exploratory behaviour and synaptic plasticity in mice with a spontaneous deletion in the ubiquitin C-terminal hydrolase L1 gene. Eur J Neurosci (2008) 1.04
Functional and structural basis of the nuclear localization signal in the ZIC3 zinc finger domain. Hum Mol Genet (2008) 1.03
Genome-wide association study of schizophrenia in Japanese population. PLoS One (2011) 1.02
Altered RNA editing of serotonin 2C receptor in a rat model of depression. Neurosci Res (2005) 1.01
Comparison of mice deficient in the high- or low-affinity neurotensin receptors, Ntsr1 or Ntsr2, reveals a novel function for Ntsr2 in thermal nociception. Brain Res (2004) 1.01
Rines/RNF180, a novel RING finger gene-encoded product, is a membrane-bound ubiquitin ligase. Genes Cells (2008) 0.99
Failure to support a genetic contribution of AKT1 polymorphisms and altered AKT signaling in schizophrenia. J Neurochem (2006) 0.99
Enhanced carbonyl stress in a subpopulation of schizophrenia. Arch Gen Psychiatry (2010) 0.99
Arachidonic acid drives postnatal neurogenesis and elicits a beneficial effect on prepulse inhibition, a biological trait of psychiatric illnesses. PLoS One (2009) 0.99
Further evidence for the role of MET in autism susceptibility. Neurosci Res (2010) 0.98
The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment. Neuropsychobiology (2010) 0.98
Evaluation of Pax6 mutant rat as a model for autism. PLoS One (2010) 0.98
The effects of Fabp7 and Fabp5 on postnatal hippocampal neurogenesis in the mouse. Stem Cells (2012) 0.98
Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder. Genomics (2004) 0.98
Inducible cAMP early repressor acts as a negative regulator for kindling epileptogenesis and long-term fear memory. J Neurosci (2008) 0.98
Zic2 and Zic3 synergistically control neurulation and segmentation of paraxial mesoderm in mouse embryo. Dev Biol (2007) 0.97
Disorganized innervation and neuronal loss in the inner ear of Slitrk6-deficient mice. PLoS One (2009) 0.97
Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism. Biochem Biophys Res Commun (2007) 0.97
Neutrophil-mediated inflammation in respiratory syncytial viral bronchiolitis. Pediatr Int (2005) 0.97
Activin plays a key role in the maintenance of long-term memory and late-LTP. Learn Mem (2010) 0.97
Important role of heparan sulfate in postnatal islet growth and insulin secretion. Biochem Biophys Res Commun (2009) 0.96
Genetic analysis of a functional GRIN2A promoter (GT)n repeat in bipolar disorder pedigrees in humans. Neurosci Lett (2003) 0.96
A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient. Neurosci Lett (2009) 0.96
A population-specific uncommon variant in GRIN3A associated with schizophrenia. Biol Psychiatry (2012) 0.96
Age dependence of diffusion-weighted magnetic resonance imaging findings in maple syrup urine disease encephalopathy. J Comput Assist Tomogr (2005) 0.96
FKBP12.6 disruption impairs glucose-induced insulin secretion. Biochem Biophys Res Commun (2008) 0.95
Genetic and expression analyses of the STOP (MAP6) gene in schizophrenia. Schizophr Res (2006) 0.95
[(18)F]THK-5117 PET for assessing neurofibrillary pathology in Alzheimer's disease. Eur J Nucl Med Mol Imaging (2015) 0.95