(Q55042376)

16 June 2018

title

Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder. (English)

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16 June 2018

obsessive-compulsive disorder

main subject

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J R Wendland

1

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16 June 2018

M R Kruse

series ordinal

2

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16 June 2018

D L Murphy

series ordinal

3

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16 June 2018

language of work or name

English

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publication date

1 September 2006

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16 June 2018

published in

Molecular Psychiatry

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16 June 2018

volume

11

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16 June 2018

issue

9

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16 June 2018

page(s)

802-804

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16 June 2018

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001848

exact match

0 references

cites work

Sequence variants in SLITRK1 are associated with Tourette's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Adulthood outcome of tic and obsessive-compulsive symptom severity in children with Tourette syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

A family study of obsessive-compulsive disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Diagnostic interview assessed neuropsychiatric disorder comorbidity in 334 individuals with obsessive-compulsive disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

Chromosomal abnormalities and mental illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001848

21 January 2018

Identifiers

DOI

10.1038/SJ.MP.4001848

1 reference

16 June 2018

Dimensions Publication ID

1032888477

0 references

1 reference

16 June 2018