(Q34300747)

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A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability (English)

1 reference

Europe PubMed Central

1 August 2017

1

1 reference

Europe PubMed Central

1 August 2017

Michael C O'Donovan

8

1 reference

Europe PubMed Central

1 August 2017

author name string

D M Turic

2

1 reference

Europe PubMed Central

1 August 2017

L Hill

3

1 reference

Europe PubMed Central

1 August 2017

D E Turic

4

1 reference

Europe PubMed Central

1 August 2017

M Stephens

5

1 reference

Europe PubMed Central

1 August 2017

J Williams

6

1 reference

Europe PubMed Central

1 August 2017

M J Owen

7

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Europe PubMed Central

1 August 2017

language of work or name

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publication date

1 June 2004

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Europe PubMed Central

1 August 2017

Molecular Psychiatry

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Europe PubMed Central

1 August 2017

9

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Europe PubMed Central

1 August 2017

6

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Europe PubMed Central

1 August 2017

582-586

1 reference

Europe PubMed Central

1 August 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001441

0 references

Genetics, genes, genomics and g

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001441

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Role of the cholinergic muscarinic 2 receptor (CHRM2) gene in cognition.

1 reference

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A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition

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The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function

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Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoforms

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001441

21 January 2018

Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001441

21 January 2018

4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001441

21 January 2018

A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups.

1 reference

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21 January 2018

Top 1 in 10,000: a 10-year follow-up of the profoundly gifted.

1 reference

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Searching for justice: The discovery of IQ gains over time

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DNA by mail: an inexpensive and noninvasive method for collecting DNA samples from widely dispersed populations.

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

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Purification from human brain and some properties of two NADPH-linked aldehyde reductases which reduce succinic semialdehyde to 4-hydroxybutyrate

1 reference

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21 January 2018

The transmission/disequilibrium test: history, subdivision, and admixture

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Facilitation of the induction of long-term potentiation by GABAB receptors.

1 reference

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A model of hippocampal memory encoding and retrieval: GABAergic control of synaptic plasticity.

1 reference

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Ionic mechanisms of GABA-induced long-term potentiation in the rat superior colliculus

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Kindling suppresses primed-burst-induced long-term potentiation in hippocampal CA1.

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Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1

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Replication validity of genetic association studies

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Association study designs for complex diseases

1 reference

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Association analysis of candidate genes for neuropsychiatric disease: the perpetual campaign

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

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21 January 2018

Genetics and general cognitive ability (g).

1 reference

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21 January 2018

Genetic influences on brain structure

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001441

21 January 2018

Neural mechanisms of general fluid intelligence

1 reference

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21 January 2018

Genetics and general cognitive ability

1 reference

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Cathepsin D exon 2 polymorphism associated with general intelligence in a healthy older population

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Genetic research on general cognitive ability as a model for mild mental retardation

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Comparative sequencing of the proneurotensin gene and association studies in schizophrenia

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Cis-acting variation in the expression of a high proportion of genes in human brain

1 reference

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7 January 2021

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Dominant inheritance in two families with familial Mediterranean fever (FMF)

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Identifiers

10.1038/SJ.MP.4001441

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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