(Q58451547)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

An association study between 5-HTTLPR polymorphism, COMT polymorphism, and Tourette's syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

Maria Cristina Cavallini

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Daniela Di Bella

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

author name string

M Catalano

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

L Bellodi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

language of work or name

English

0 references

publication date

1 December 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

97

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

2-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

page(s)

93-100

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

Brain monoamines and amino acids in Gilles de la Tourette's syndrome: a preliminary study of subcortical regions

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Catechol-O-methyltransferase and Gilles de la Tourette syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Citalopram and fluvoxamine in Tourette's disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Association of the serotonin transporter promoter regulatory region polymorphism and obsessive-compulsive disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Obsessive compulsive disorder, response to serotonin reuptake inhibitors and the serotonin transporter gene

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

The functional neuroanatomy of Tourette's syndrome: an FDG-PET study. I. Regional changes in cerebral glucose metabolism differentiating patients and controls

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

The genetic susceptibility to Gilles de la Tourette syndrome in a large multiple affected British kindred: linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and ty

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Lack of association between obsessive-compulsive disorder and the dopamine D3 receptor gene: Some preliminary considerations

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

5HT2C CYS23/SER23 polymorphism is not associated with obsessive–compulsive disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Chronic, multiple tics of Gilles de la Tourette's disease. CSF acid monoamine metabolites after probenecid administration

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: the additive and subtractive effect of the three dopaminergic genes--DRD2, D beta H, and DAT1.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Functional promoter polymorphism of the human serotonin transporter

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Evidence for autosomal dominant transmission in Tourette's syndrome. United Kingdom cohort study

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Gilles de la Tourette Syndrome Is Not Linked to D2-Dopamine Receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Serotonin-dopamine interaction and its relevance to schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

The Yale Global Tic Severity Scale: initial testing of a clinician-rated scale of tic severity

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Extending levodopa action: COMT inhibition

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Whole blood serotonin relates to violence in an epidemiological study.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

A Molecular Investigation Suggests No Relationship between Obsessive-Compulsive Disorder and the Dopamine D 2 Receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Psychiatric genetics: back to the future

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

The inheritance of Gilles de la Tourette's syndrome and associated behaviors. Evidence for autosomal dominant transmission

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

Tics in a patient with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2800%2900220-1

7 January 2021

10.1016/S0165-1781(00)00220-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11166081%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference