1p34.3 deletion involvingGRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay

Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

(2012) Rui Luo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

(2012) Dheeraj Malhotra et al.   CELL

Association study of GRIK1 gene polymorphisms in schizophrenia: case-control and family-based studies

(2012) Yuko Hirata et al.   HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

(2012) Christelle Golzio et al.   NATURE

Genome-wide association study on bipolar disorder in the Bulgarian population

(2011) A. Yosifova et al.   GENES BRAIN AND BEHAVIOR

Overview of glutamatergic neurotransmission in the nervous system

(2011) Mark J. Niciu et al.   PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR

Pharmacology of ionotropic glutamate receptors: A structural perspective

(2010) Philipp Stawski et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Association Between Polymorphisms in GRIK2 Gene and Obsessive-Compulsive Disorder: A Family-Based Study

(2010) Aline S. Sampaio et al.   CNS Neuroscience & Therapeutics

A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21

(2009) Chad R. Haldeman-Englert et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

(2009) R. A. Kumar et al.   JOURNAL OF MEDICAL GENETICS

Atypical Functional Properties of GluK3-Containing Kainate Receptors

(2009) D. Perrais et al.   JOURNAL OF NEUROSCIENCE

Microduplications of 16p11.2 are associated with schizophrenia

(2009) Shane E McCarthy et al.   NATURE GENETICS

High-Affinity Kainate Receptor Subunits Are Necessary for Ionotropic but Not Metabotropic Signaling

(2009) Herman B. Fernandes et al.   NEURON

Comparative genomics of autism and schizophrenia

(2009) B. Crespi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Are GRIK3 (T928G) gene variants in schizophrenia patients different from those intheir first-degree relatives?

(2009) Gamze Kilic et al.   PSYCHIATRY RESEARCH

Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype

(2008) Maria Clara Bonaglia et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

(2008) Xue-Zhong Liu et al.   HUMAN GENETICS

Association between Microdeletion and Microduplication at 16p11.2 and Autism

(2008) Lauren A. Weiss et al.   NEW ENGLAND JOURNAL OF MEDICINE