(Q44765961)

English

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

scientific article published in February 2004

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scholarly article

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23 November 2019

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD (English)

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23 November 2019

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23 November 2019

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23 November 2019

Michael C O'Donovan

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23 November 2019

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23 November 2019

Marianne Bernadette van den Bree

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23 November 2019

9

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N Craddock

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23 November 2019

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D Turic

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23 November 2019

S Mills

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23 November 2019

M Stephens

4

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23 November 2019

D Lawson

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23 November 2019

C Govan

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23 November 2019

N Williams

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23 November 2019

M Owen

11

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23 November 2019

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publication date

1 February 2004

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23 November 2019

Molecular Psychiatry

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23 November 2019

9

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23 November 2019

2

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23 November 2019

169-173

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23 November 2019

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001387

0 references

Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

On the role of cortical glutamate in obsessive-compulsive disorder and attention-deficit hyperactivity disorder, two phenomenologically antithetical conditions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Glutamatergic modulation of hyperactivity in mice lacking the dopamine transporter

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Mice with reduced NMDA receptor expression display behaviors related to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Reduced spontaneous activity of mice defective in the epsilon 4 subunit of the NMDA receptor channel

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Reduced hippocampal LTP and spatial learning in mice lacking NMDA receptor epsilon 1 subunit

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Autism screening questionnaire: diagnostic validity.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

21 January 2018

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

1 reference

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21 January 2018

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

1 reference

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21 January 2018

Neuropsychological analyses of impulsiveness in childhood hyperactivity.

1 reference

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21 January 2018

Developmental trajectories of brain volume abnormalities in children and adolescents with attention-deficit/hyperactivity disorder.

1 reference

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21 January 2018

Interactions between glutamatergic and monoaminergic systems within the basal ganglia-implications for schizophrenia and Parkinson's disease

1 reference

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21 January 2018

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

1 reference

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21 January 2018

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

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21 January 2018

Glutamate receptors: brain function and signal transduction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

7 January 2021

based on heuristic

inferred from DOI database lookup

Attention-deficit hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

7 January 2021

based on heuristic

inferred from DOI database lookup

A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001387

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.MP.4001387

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23 November 2019

1 reference

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23 November 2019

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