Published in Hum Mol Genet on May 20, 2008
Kinase associated-1 domains drive MARK/PAR1 kinases to membrane targets by binding acidic phospholipids. Cell (2010) 2.83
Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis. Mol Psychiatry (2011) 2.28
A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Res Hum Genet (2010) 1.30
A review of the evidence for the canonical Wnt pathway in autism spectrum disorders. Mol Autism (2012) 0.97
Genome-wide association study in bipolar patients stratified by co-morbidity. PLoS One (2011) 0.89
LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules. Scientifica (Cairo) (2013) 0.85
The polarity protein partitioning-defective 1 (PAR-1) regulates dendritic spine morphogenesis through phosphorylating postsynaptic density protein 95 (PSD-95). J Biol Chem (2012) 0.83
Autism risk assessment in siblings of affected children using sex-specific genetic scores. Mol Autism (2011) 0.82
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Transcriptional responses of cultured rat sympathetic neurons during BMP-7-induced dendritic growth. PLoS One (2011) 0.80
Dendrite and spine modifications in autism and related neurodevelopmental disorders in patients and animal models. Dev Neurobiol (2016) 0.80
Novel inter-hemispheric white matter connectivity in the BTBR mouse model of autism. Brain Res (2013) 0.79
Suppression of adipogenesis by pathogenic seipin mutant is associated with inflammatory response. PLoS One (2013) 0.77
Proteomic Analysis of Mouse Cortex Postsynaptic Density following Neonatal Brain Hypoxia-Ischemia. Dev Neurosci (2017) 0.76
Molecular determinants of KA1 domain-mediated autoinhibition and phospholipid activation of MARK1 kinase. Biochem J (2016) 0.75
Active zone proteins are transported via distinct mechanisms regulated by Par-1 kinase. PLoS Genet (2017) 0.75
Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors. Nat Nanotechnol (2016) 0.75
Bio-collections in autism research. Mol Autism (2017) 0.75
Potential Role of Microtubule Stabilizing Agents in Neurodevelopmental Disorders. Int J Mol Sci (2017) 0.75
Neuronal Polarity in the Embryonic Mammalian Cerebral Cortex. Front Cell Neurosci (2017) 0.75
Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet (2012) 7.59
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet (2003) 3.96
Structural clusters of evolutionary trace residues are statistically significant and common in proteins. J Mol Biol (2002) 2.50
Cognitive dysfunction in psychiatric disorders: characteristics, causes and the quest for improved therapy. Nat Rev Drug Discov (2012) 2.44
A hepatocellular carcinoma 5-gene score associated with survival of patients after liver resection. Gastroenterology (2013) 2.37
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA. Science (2011) 2.04
Hox paralog group 2 genes control the migration of mouse pontine neurons through slit-robo signaling. PLoS Biol (2008) 1.85
Neogenin mediates the action of repulsive guidance molecule. Nat Cell Biol (2004) 1.77
Genetics of dopamine receptors and drug addiction: a comprehensive review. Behav Pharmacol (2009) 1.72
Evolutionary trace of G protein-coupled receptors reveals clusters of residues that determine global and class-specific functions. J Biol Chem (2003) 1.65
Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain. J Neurosci (2007) 1.52
VEGF mediates commissural axon chemoattraction through its receptor Flk1. Neuron (2011) 1.45
Is DSM-IV bereavement exclusion for major depression relevant to treatment response? A case-control, prospective study. J Clin Psychiatry (2010) 1.45
The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules. Hum Mol Genet (2007) 1.36
Genome-wide population-based association study of extremely overweight young adults--the GOYA study. PLoS One (2011) 1.34
Modulation of the respiratory rhythm generator by the pontine noradrenergic A5 and A6 groups in rodents. Respir Physiol Neurobiol (2004) 1.31
Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. Hum Mol Genet (2004) 1.20
DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome. Hum Mol Genet (2009) 1.19
Estimating cancer risk in HNPCC by the GRL method. Eur J Hum Genet (2007) 1.13
Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations. Eur J Hum Genet (2005) 1.13
Altered axonal targeting and short-term plasticity in the hippocampus of Disc1 mutant mice. Proc Natl Acad Sci U S A (2011) 1.09
Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism. Am J Med Genet B Neuropsychiatr Genet (2008) 1.08
Large scale association analysis identifies three susceptibility loci for coronary artery disease. PLoS One (2011) 1.07
SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution. Hum Mol Genet (2010) 1.07
Evolution of neural precursor selection: functional divergence of proneural proteins. Development (2004) 1.07
The etiology of behavioral problems and competencies in very young twins. J Abnorm Psychol (2008) 1.06
Matrix-binding vascular endothelial growth factor (VEGF) isoforms guide granule cell migration in the cerebellum via VEGF receptor Flk1. J Neurosci (2010) 1.05
Massively multiplayer online role-playing games: comparing characteristics of addict vs non-addict online recruited gamers in a French adult population. BMC Psychiatry (2011) 1.05
DSM bereavement exclusion for major depression and objective cognitive impairment. J Affect Disord (2010) 1.05
Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis. PLoS One (2012) 1.03
Murine peripherin gene sequences direct Cre recombinase expression to peripheral neurons in transgenic mice. FEBS Lett (2002) 1.03
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. Am J Hum Genet (2013) 1.02
RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects. J Med Genet (2011) 1.01
Negative affectivity, self-referential processing and the cortical midline structures. Soc Cogn Affect Neurosci (2010) 1.01
Expression of netrin-1, slit-1 and slit-3 but not of slit-2 after cerebellar and spinal cord lesions. Eur J Neurosci (2005) 1.00
Improving treatment adherence in your patients with schizophrenia: the STAY initiative. Clin Drug Investig (2013) 0.99
The CNR1 gene as a pharmacogenetic factor for antipsychotics rather than a susceptibility gene for schizophrenia. Eur Neuropsychopharmacol (2007) 0.98
The 3' region of the DRD2 gene is involved in genetic susceptibility to schizophrenia. Schizophr Res (2004) 0.98
Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1. BMC Med Genet (2007) 0.98
Nrxn3 upregulation in the globus pallidus of mice developing cocaine addiction. Neuroreport (2008) 0.97
Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse). Hum Mol Genet (2003) 0.97
Lifetime positive symptoms in patients with schizophrenia and cannabis abuse are partially explained by co-morbid addiction. Schizophr Res (2006) 0.96
TFAP2B -dietary protein and glycemic index interactions and weight maintenance after weight loss in the DiOGenes trial. Hum Hered (2013) 0.95
Genetic polymorphisms of MMP1, MMP3 and MMP7 gene promoter and risk of colorectal adenoma. BMC Cancer (2006) 0.94
Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects. Biol Psychiatry (2011) 0.93
Slit1 and slit2 proteins control the development of the lateral olfactory tract. J Neurosci (2002) 0.93
Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders. Biol Psychiatry (2009) 0.92
The 3' part of the dopamine transporter gene DAT1/SLC6A3 is associated with withdrawal seizures in patients with alcohol dependence. Alcohol Clin Exp Res (2007) 0.91
The role of brief motivational intervention on self-efficacy and abstinence in a cohort of patients with alcohol dependence. Int J Psychiatry Med (2009) 0.91
Family trios analysis of common polymorphisms in the obestatin/ghrelin, BDNF and AGRP genes in patients with Anorexia nervosa: association with subtype, body-mass index, severity and age of onset. Psychoneuroendocrinology (2007) 0.90
Molecular genetics of alcohol dependence and related endophenotypes. Curr Genomics (2008) 0.90
First positive reactions to cannabis constitute a priority risk factor for cannabis dependence. Addiction (2009) 0.90
A new definition of early age at onset in alcohol dependence. Drug Alcohol Depend (2009) 0.89
TFAP2B influences the effect of dietary fat on weight loss under energy restriction. PLoS One (2012) 0.89
Genetics of dopamine receptors and drug addiction. Hum Genet (2012) 0.89
Evolutionary traces of functional surfaces along G protein signaling pathway. Methods Enzymol (2002) 0.89
The short allele of the serotonin transporter promoter polymorphism influences relapse in alcohol dependence. Alcohol Alcohol (2008) 0.89
The role of genes involved in neuroplasticity and neurogenesis in the observation of a gene-environment interaction (GxE) in schizophrenia. Curr Mol Med (2009) 0.89
The executive control of attention differentiates patients with schizophrenia, their first-degree relatives and healthy controls. Neuropsychologia (2010) 0.89
Survival motor neuron SMN1 and SMN2 gene promoters: identical sequences and differential expression in neurons and non-neuronal cells. Eur J Hum Genet (2004) 0.88
Association between dopamine receptor D1 gene DdeI polymorphism and sensation seeking in alcohol-dependent men. Alcohol Clin Exp Res (2003) 0.88
Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk. Mol Autism (2010) 0.88
Genetics and early disturbances of breathing control. Pediatr Res (2004) 0.88
A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL). Blood (2002) 0.87
A haplotype of the norepinephrine transporter (Net) gene Slc6a2 is associated with clinical response to atomoxetine in attention-deficit hyperactivity disorder (ADHD). Neuropsychopharmacology (2009) 0.87
Intraretinal RGMa is involved in retino-tectal mapping. Mol Cell Neurosci (2008) 0.87
Single KTP nanocrystals as second-harmonic generation biolabels in cortical neurons. Nanoscale (2013) 0.87
Psychiatrists' awareness of adherence to antipsychotic medication in patients with schizophrenia: results from a survey conducted across Europe, the Middle East, and Africa. Patient Prefer Adherence (2013) 0.87
Association study of polymorphisms in the human estrogen receptor alpha gene and prostate cancer risk. Eur Urol (2003) 0.87
Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis. BMC Med Genet (2007) 0.86
A genetic schizophrenia-susceptibility region located between the ANKK1 and DRD2 genes. Prog Neuropsychopharmacol Biol Psychiatry (2010) 0.86
Genetics and personality affect visual perspective in autobiographical memory. Conscious Cogn (2009) 0.86
Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors. Psychiatr Genet (2006) 0.86