Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

(2015) Andrew J. Pocklington et al.   NEURON

The genomic and functional characteristics of disease genes

(2014) A. Collins   BRIEFINGS IN BIOINFORMATICS

Association of SLC18A1, TPH1, and RELN gene polymorphisms with risk of paranoid schizophrenia

(2014) D. Yu. Galaktionova et al.   MOLECULAR BIOLOGY

Copy number variation in schizophrenia in Sweden

(2014) J P Szatkiewicz et al.   MOLECULAR PSYCHIATRY

De novo mutations in schizophrenia implicate synaptic networks

(2014) Menachem Fromer et al.   NATURE

A polygenic burden of rare disruptive mutations in schizophrenia

(2014) Shaun M. Purcell et al.   NATURE

Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family

(2013) Marina Myles-Worsley et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Analysis of copy number variations at 15 schizophrenia-associated loci

(2013) Elliott Rees et al.   BRITISH JOURNAL OF PSYCHIATRY

Reelin, an extracellular matrix protein linked to early onset psychiatric diseases, drives postnatal development of the prefrontal cortex via GluN2B-NMDARs and the mTOR pathway

(2013) J Iafrati et al.   MOLECULAR PSYCHIATRY

Support for the N -Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex Families

(2013) Andrew E. Timms et al.   JAMA Psychiatry

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

(2012) Dheeraj Malhotra et al.   CELL

Epigenetic modifications of GABAergic interneurons are associated with the schizophrenia-like phenotype induced by prenatal stress in mice

(2012) Francesco Matrisciano et al.   NEUROPHARMACOLOGY

A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han

(2011) W.J. Kuang et al.   GENETICS AND MOLECULAR RESEARCH

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

(2011) G Kirov et al.   MOLECULAR PSYCHIATRY

Exome sequencing supports a de novo mutational paradigm for schizophrenia

(2011) Bin Xu et al.   NATURE GENETICS

Increased exonic de novo mutation rate in individuals with schizophrenia

(2011) Simon L Girard et al.   NATURE GENETICS

Impairment of cognitive performance after reelin knockdown in the medial prefrontal cortex of pubertal or adult rats

(2011) Jan Brosda et al.   NEUROBIOLOGY OF DISEASE

Overexpression of Reelin Prevents the Manifestation of Behavioral Phenotypes Related to Schizophrenia and Bipolar Disorder

(2011) Cátia M Teixeira et al.   NEUROPSYCHOPHARMACOLOGY

Reelin deficiency causes specific defects in the molecular composition of the synapses in the adult brain

(2011) A. Ventruti et al.   NEUROSCIENCE

Analysis of common genetic variants identifiesRELNas a risk gene for schizophrenia in Chinese population

(2011) Ming Li et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia

(2009) Jessica E. van Schijndel et al.   JOURNAL OF PSYCHIATRIC RESEARCH

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

(2009) Paul Lichtenstein et al.   LANCET

A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder

(2009) Anne Pisanté et al.   PSYCHIATRIC GENETICS

The Reelin Signaling Pathway Promotes Dendritic Spine Development in Hippocampal Neurons

(2008) S. Niu et al.   JOURNAL OF NEUROSCIENCE

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women

(2008) Sagiv Shifman et al.   PLoS Genetics

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE