Published in Mol Psychiatry on February 26, 2013
Genetic studies in intellectual disability and related disorders. Nat Rev Genet (2015) 1.40
The discovery of integrated gene networks for autism and related disorders. Genome Res (2014) 1.35
Intellectual disability and autism spectrum disorders: causal genes and molecular mechanisms. Neurosci Biobehav Rev (2014) 1.14
Serum microRNA profiles in children with autism. Mol Autism (2014) 1.08
Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders. Mol Syndromol (2015) 1.00
Thalamic reticular impairment underlies attention deficit in Ptchd1(Y/-) mice. Nature (2016) 0.98
Integrated systems analysis reveals a molecular network underlying autism spectrum disorders. Mol Syst Biol (2014) 0.97
The Role of Epigenetic Change in Autism Spectrum Disorders. Front Neurol (2015) 0.95
The molecular genetic architecture of attention deficit hyperactivity disorder. Mol Psychiatry (2015) 0.94
Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach. Transl Psychiatry (2014) 0.89
Genome-wide association study of autistic-like traits in a general population study of young adults. Front Hum Neurosci (2013) 0.89
MeCP2 regulates the synaptic expression of a Dysbindin-BLOC-1 network component in mouse brain and human induced pluripotent stem cell-derived neurons. PLoS One (2013) 0.87
Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database. Mol Psychiatry (2015) 0.84
A conserved BDNF, glutamate- and GABA-enriched gene module related to human depression identified by coexpression meta-analysis and DNA variant genome-wide association studies. PLoS One (2014) 0.84
Identifying novel interventional strategies for psychiatric disorders: integrating genomics, 'enviromics' and gene-environment interactions in valid preclinical models. Br J Pharmacol (2014) 0.82
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach. Am J Med Genet B Neuropsychiatr Genet (2016) 0.81
Coexpression networks identify brain region-specific enhancer RNAs in the human brain. Nat Neurosci (2015) 0.81
Decanalization mediating gene-environment interactions in schizophrenia and other psychiatric disorders with neurodevelopmental etiology. Front Behav Neurosci (2013) 0.81
An assessment of sex bias in neurodevelopmental disorders. Genome Med (2015) 0.81
Pathway Network Analyses for Autism Reveal Multisystem Involvement, Major Overlaps with Other Diseases and Convergence upon MAPK and Calcium Signaling. PLoS One (2016) 0.79
Transcriptome Analysis of Honeybee (Apis Mellifera) Haploid and Diploid Embryos Reveals Early Zygotic Transcription during Cleavage. PLoS One (2016) 0.78
Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes. Transl Psychiatry (2013) 0.78
A neuroligin-3 mutation implicated in autism causes abnormal aggression and increases repetitive behavior in mice. Mol Autism (2015) 0.77
Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants. Hum Mol Genet (2015) 0.77
An overview of the neurobiology of suicidal behaviors as one meta-system. Mol Psychiatry (2014) 0.77
Receptor Tyrosine Kinase MET Interactome and Neurodevelopmental Disorder Partners at the Developing Synapse. Biol Psychiatry (2016) 0.77
Circulating microRNAs and Bioinformatics Tools to Discover Novel Diagnostic Biomarkers of Pediatric Diseases. Genes (Basel) (2017) 0.77
Co-morditities of environmental diseases: A common cause. Interdiscip Toxicol (2014) 0.76
Modeling anorexia nervosa: transcriptional insights from human iPSC-derived neurons. Transl Psychiatry (2017) 0.75
Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample. Ann Neurosci (2014) 0.75
Psychiatric gene discoveries shape evidence on ADHD's biology. Mol Psychiatry (2015) 0.75
Network Diffusion-Based Prioritization of Autism Risk Genes Identifies Significantly Connected Gene Modules. Front Genet (2017) 0.75
DNA methylation in schizophrenia in different patient-derived cell types. NPJ Schizophr (2017) 0.75
Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders. Mol Psychiatry (2017) 0.75
Genetic tests in major psychiatric disorders-integrating molecular medicine with clinical psychiatry-why is it so difficult? Transl Psychiatry (2017) 0.75
MicroRNAs: target recognition and regulatory functions. Cell (2009) 92.17
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature (2007) 75.09
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature (2009) 33.26
Community structure in social and biological networks. Proc Natl Acad Sci U S A (2002) 29.77
Strong association of de novo copy number mutations with autism. Science (2007) 27.84
miRBase: integrating microRNA annotation and deep-sequencing data. Nucleic Acids Res (2010) 25.85
Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nat Genet (2008) 24.51
BioGRID: a general repository for interaction datasets. Nucleic Acids Res (2006) 22.41
The endophenotype concept in psychiatry: etymology and strategic intentions. Am J Psychiatry (2003) 21.70
TRANSFAC: an integrated system for gene expression regulation. Nucleic Acids Res (2000) 15.70
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature (2012) 14.76
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature (2012) 13.71
De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature (2012) 13.61
Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med (1995) 12.70
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet (2011) 11.94
Rate of de novo mutations and the importance of father's age to disease risk. Nature (2012) 11.92
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. N Engl J Med (2008) 10.88
Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch Gen Psychiatry (2003) 10.44
Common variants conferring risk of schizophrenia. Nature (2009) 10.37
De novo gene disruptions in children on the autistic spectrum. Neuron (2012) 9.69
Neuroligins and neurexins link synaptic function to cognitive disease. Nature (2008) 9.23
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat Genet (2008) 8.44
Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature (2009) 8.12
Genomics of microRNA. Trends Genet (2006) 7.75
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature (2009) 7.39
Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter. Nature (1996) 7.26
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database. Nat Genet (2008) 6.71
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet (2003) 6.63
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet (2010) 5.78
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet (2012) 5.78
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Brain Res (2010) 5.50
Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics. Am J Med Genet (2000) 5.07
Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature (2011) 4.85
A genome-wide linkage and association scan reveals novel loci for autism. Nature (2009) 4.76
Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity. Science (1999) 4.70
A new generation of JASPAR, the open-access repository for transcription factor binding site profiles. Nucleic Acids Res (2006) 4.32
Human Proteinpedia enables sharing of human protein data. Nat Biotechnol (2008) 4.21
Neurobiology of schizophrenia. Neuron (2006) 3.69
Candidate gene studies of ADHD: a meta-analytic review. Hum Genet (2009) 3.56
Attention-deficit hyperactivity disorder: a category or a continuum? Genetic analysis of a large-scale twin study. J Am Acad Child Adolesc Psychiatry (1997) 3.56
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genet (2008) 3.33
AutDB: a gene reference resource for autism research. Nucleic Acids Res (2008) 2.62
The genetic basis of complex human behaviors. Science (1994) 2.62
Genome-wide association studies in ADHD. Hum Genet (2009) 2.58
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Am J Psychiatry (2012) 2.48
Genome-wide association scan of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet (2008) 2.40
Human Proteinpedia: a unified discovery resource for proteomics research. Nucleic Acids Res (2008) 2.30
Autism spectrum disorders--a genetics review. Genet Med (2011) 2.29
Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry (2008) 2.07
XLMR genes: update 2007. Eur J Hum Genet (2008) 2.07
Case-control genome-wide association study of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry (2010) 1.86
Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry (2010) 1.79
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. Schizophr Res (2010) 1.60
A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case. Bioinformatics (2009) 1.50
Fragile X and X-linked intellectual disability: four decades of discovery. Am J Hum Genet (2012) 1.50
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia. Am J Hum Genet (2012) 1.47
SZGR: a comprehensive schizophrenia gene resource. Mol Psychiatry (2010) 1.36
Candidate genes for schizophrenia: a survey of association studies and gene ranking. Am J Med Genet B Neuropsychiatr Genet (2008) 1.31
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet (2008) 1.30
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. PLoS Genet (2012) 1.25
Gene expression studies in autism: moving from the genome to the transcriptome and beyond. Neurobiol Dis (2011) 1.09
Genetic basis of autism: is there a way forward? Curr Opin Psychiatry (2011) 1.07
Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism. Transl Psychiatry (2012) 0.98
Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders. PLoS One (2011) 0.96
Human Proteinpedia as a resource for clinical proteomics. Mol Cell Proteomics (2008) 0.87
Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variants. Eur J Med Genet (2012) 0.84
Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach. Transl Psychiatry (2014) 0.89
The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome. Clin Genet (2014) 0.84