Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

doi:10.1002/ajmg.b.31007

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 5 Mar 2010

Ludwig Kerstin U, Roeske Darina, Herms Stefan, Schumacher Johannes, Warnke Andreas, Plume Ellen, Neuhoff Nina, Bruder Jennifer, Remschmidt Helmut, Schulte-Körne Gerd, Müller-Myhsok Bertram, Nöthen Markus M, Hoffmann Per

Abstract excerpt

A multi-marker haplotype within GRIN2B, a gene coding for a subunit of the ionotropic glutamate receptor, has recently been found to be associated with variation in human memory performance [de Quervain and Papassotiropoulos, 2006]. The gene locus is located within a region that has been linked to a phonological memory phenotype in a recent genome scan in families with dyslexia [Brkanac et al., 2008]. These...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Attention Deficit Disorder with Hyperactivity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cognition Disorders

Share to Comorbidity

Share to Dyslexia

Share to Language

Share to Memory, Short-Term

Share to Reading

Share to Receptors, N-Methyl-D-Aspartate

Source

Open in PubMed

Identifiers

PMID: 19591125
DOI: 10.1002/ajmg.b.31007

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.PMID 19591125Read ↗

GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia.Semantic proximity Read ↗

Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder.Semantic proximity Read ↗

Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia.Semantic proximity Read ↗

Combined effect of genetic variants in the GluN2B coding gene (GRIN2B) on prefrontal function during working memory performance.Semantic proximity Read ↗

A genome-wide survey of human short-term memory.Semantic proximity Read ↗

Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.Semantic proximity Read ↗

Functional human GRIN2B promoter polymorphism and variation of mental processing speed in older adults.Semantic proximity Read ↗

Genetic polymorphisms of GRIN2A and GRIN2B modify the neurobehavioral effects of low-level lead exposure in children.Semantic proximity Read ↗

GRIN2B predicts attention problems among disadvantaged children.Semantic proximity Read ↗

Dopamine D2 receptor and N-methyl-D-aspartate receptor 2B subunit genetic variants and intelligence.Semantic proximity Read ↗

The GRIN2B and GRIN2A Gene Variants Are Associated With Continuous Performance Test Variables in ADHD.Semantic proximity Read ↗

Impact of GRIK4 gene polymorphisms on cognitive dysfunction in patients with major depression.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.