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GABRB3 gene

Known as: GABRB3, GAMMA-AMINOBUTYRIC ACID RECEPTOR, BETA-3, GABA(A) receptor, beta 3 
National Institutes of Health

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Related topics

1 relation
GABRE gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Genetic analysis of GABRB3 at 15q12 as a candidate gene of schizophrenia
Objective Copy number variations encompassing the chromosome 15q11-q13 region have been implicated in the pathogenesis of several… 
Highly Cited
2007
Highly Cited
2007
Association of GABRB3 Polymorphisms with Autism Spectrum Disorders in Korean Trios
Background/Aims: Autism spectrum disorders (ASD) are complex neuropsychiatric disorders having a genetic risk factor. The… 
Review
2005
Review
2005
GABRB3 gene deficient mice: a potential model of autism spectrum disorder.
2004
2004
Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.
BACKGROUND Childhood absence epilepsy (CAE) is one of the most frequently recognized syndromes among the idiopathic generalized… 
2002
2002
Prader Willi/Angelman and DiGeorge/velocardiofacial syndrome deletions: diagnosis by primed in situ labeling (PRINS).
A recently developed methodology-primed in situ labeling (PRINS)-can be used in place of fluorescence in situ hybridization (FISH… 
2000
2000
Association and linkage studies of candidate genes involved in GABAergic neurotransmission in lithium-responsive bipolar disorder.
OBJECTIVE To test for genetic linkage and association with GABAergic candidate genes in lithium-responsive bipolar disorder… 
2000
2000
Modification in the inherent mode of allelic replication in lymphocytes of patients suffering from renal cell carcinoma: A novel genetic alteration associated with malignancy
Using fluorescence in situ hybridization (FISH) to interphase nuclei, we examined the replication timing of 1 allele relative to… 
1995
1995
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
We have studied a patient with Angelman syndrome (AS) and a 47,XY,+inv dup(15) (pter-->q11::q11-->pter) karyotype. Molecular… 
1993
1993
Linkage analysis in familial Angelman syndrome.
Familial Angelman syndrome (AS) can result from mutations in chromosome 15q11q13 that, when transmitted from father to child… 
Highly Cited
1991
Highly Cited
1991
The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7.
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