Published in Meta Gene on July 21, 2015
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics (2004) 125.23
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature (2009) 33.26
Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature (2008) 20.31
Biological insights from 108 schizophrenia-associated genetic loci. Nature (2014) 16.13
Genome-wide association study identifies five new schizophrenia loci. Nat Genet (2011) 9.07
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet (2013) 7.44
WGAViewer: software for genomic annotation of whole genome association studies. Genome Res (2008) 7.15
Schizophrenia: a common disease caused by multiple rare alleles. Br J Psychiatry (2007) 7.00
A polygenic burden of rare disruptive mutations in schizophrenia. Nature (2014) 5.99
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet (2012) 5.78
CNVs: harbingers of a rare variant revolution in psychiatric genetics. Cell (2012) 4.81
Balancing structure and function at hippocampal dendritic spines. Annu Rev Neurosci (2008) 4.38
Do thin spines learn to be mushroom spines that remember? Curr Opin Neurobiol (2007) 3.63
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia. Nat Genet (2012) 3.49
Immune involvement in schizophrenia and autism: etiology, pathology and animal models. Behav Brain Res (2008) 3.12
Dendritic spine "dysgenesis" and mental retardation. Science (1974) 2.44
Rho GTPases, dendritic structure, and mental retardation. J Neurobiol (2005) 2.19
Molecular characterization of bipolar disorder by comparing gene expression profiles of postmortem brains of major mental disorders. Mol Psychiatry (2004) 1.95
MHCI negatively regulates synapse density during the establishment of cortical connections. Nat Neurosci (2011) 1.20
A polymorphism in the PDLIM5 gene associated with gene expression and schizophrenia. Biol Psychiatry (2005) 1.11
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders. Mol Autism (2014) 1.10
708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. Mol Psychiatry (2013) 1.05
Major histocompatibility complex I in brain development and schizophrenia. Biol Psychiatry (2013) 0.99
The genomics of schizophrenia: update and implications. J Clin Invest (2013) 0.98
Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism. Transl Psychiatry (2012) 0.98
Neuregulin 3 genetic variations and susceptibility to schizophrenia in a Chinese population. Biol Psychiatry (2008) 0.95
Genome-wide association studies of schizophrenia: does bigger lead to better results? Curr Opin Psychiatry (2012) 0.94
Genetics of schizophrenia. Curr Psychiatry Rep (2014) 0.92
Consanguinity and increased risk for schizophrenia in Egypt. Schizophr Res (2010) 0.92
Balance within the Neurexin Trans-Synaptic Connexus Stabilizes Behavioral Control. Front Hum Neurosci (2014) 0.90
Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample. FASEB J (2011) 0.89
MHC class I protein is expressed by neurons and neural progenitors in mid-gestation mouse brain. Mol Cell Neurosci (2012) 0.88
The rate of consanguineous marriages among parents of schizophrenic patients in the Arab Bedouin population in Southern Israel. World J Biol Psychiatry (2009) 0.86
Postsynaptic PDLIM5/Enigma Homolog binds SPAR and causes dendritic spine shrinkage. Mol Cell Neurosci (2009) 0.85
Does consanguinity increase the risk of schizophrenia? Study based on primary health care centre visits. Ment Health Fam Med (2012) 0.79
Schizophrenia spectrum psychosis in a Croatian genetic isolate: genealogical reconstructions. Psychiatr Danub (2010) 0.76
Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy. Invest Ophthalmol Vis Sci (2014) 0.82
A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract. Meta Gene (2016) 0.79
A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement. Orphanet J Rare Dis (2016) 0.75