×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
De novo GRIN1 mutations: An emerging cause of severe early infantile encephalopathy.
28389307
2017
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Novel homozygous missense variant of GRIN1 in two sibs with intellectual disability and autistic features without epilepsy.
28051072
2017
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
27164704
2016
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.
25864721
2015
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
The GluN2B subunit of N-methy-D-asparate receptor regulates the radial migration of cortical neurons in vivo.
25838242
2015
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.
25167861
2014
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
The NMDA receptor as a target for cognitive enhancement.
22796429
2013
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
De novo mutations in epileptic encephalopathies.
23934111
2013
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
23933818
2013
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Integrative mechanisms of oriented neuronal migration in the developing brain.
23937349
2013
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Functional insights from glutamate receptor ion channel structures.
22974439
2013
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Overstimulation of NMDA receptors impairs early brain development in vivo.
22606296
2012
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.
21376300
2011
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
The NCBI BioSystems database.
19854944
2010
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
20890276
2010
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Model of infantile spasms induced by N-methyl-D-aspartic acid in prenatally impaired brain.
17315208
2007
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
The chromosome 9q subtelomere deletion syndrome.
17910072
2007
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
NMDA receptors, glial cells, and clinical medicine.
16600850
2006
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Knocking-down the NMDAR1 subunit in a limited amount of neurons in the rat hippocampus impairs learning.
16635252
2006
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
The glutamate story.
16402093
2006
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Evidence for a tetrameric structure of recombinant NMDA receptors.
9526012
1998
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Molecular cloning and chromosomal localization of the key subunit of the human N-methyl-D-aspartate receptor.
7679115
1993
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Molecular cloning and characterization of the rat NMDA receptor.
1834949
1991
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Luteinizing hormone and follicle stimulating hormone secretion patterns in boys throughout puberty measured using highly sensitive immunoradiometric assays.
2516786
1989
×
Entrez Id:
2902
Gene Symbol:
GRIN1
GRIN1
Movement Disorders
0.130
GeneticVariation
CLINVAR
Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus.
6306230
1983