(Q60627349)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Neuroreceptor subunit genes and the genetic susceptibility to Gilles de la Tourette syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

Brett PM

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Robertson MM

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Gurling HM

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

language of work or name

English

0 references

publication date

1 November 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

number of pages

7

1 reference

based on heuristic

inferred from page(s)

published in

Biological Psychiatry

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

941-947

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

Failure to find linkage and increased homozygosity for the dopamine D3 receptor gene in Tourette's syndrome

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Autosomal Dominant Gene Transmission in a Large Kindred with Gilles de la Tourette Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

A procedure for combining two-point lod scores into a summary multipoint map.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Glycine receptors: a startling connection

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Exclusion of close linkage of Tourette's syndrome to D1 dopamine receptor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation

7 January 2021

2 references

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

inferred from DOI database lookup

7 January 2021

based on heuristic

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Further evidence for clustering of human GABAA receptor subunit genes: localization of the alpha 6-subunit gene (GABRA6) to distal chromosome 5q by linkage analysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Gilles de la Tourette's syndrome in identical twins.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Confirmation of the localization of the human GABAA receptor alpha 1-subunit gene (GABRA1) to distal 5q by linkage analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Difficulties in gene localization for Tourette's syndrome. Clinical aspects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

The Gilles de la Tourette syndrome: the current status

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Familial Tourette's syndrome in a large British pedigree. Associated psychopathology, severity, and potential for linkage analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

The psychopathology of the Gilles de la Tourette syndrome. A phenomenological analysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Avoiding recomputation in linkage analysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Tourette syndrome and other tic disorders. Diagnosis, pathophysiology, and treatment.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Second messenger systems in Tourette's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

A human dopamine transporter cDNA predicts reduced glycosylation, displays a novel repetitive element and provides racially-dimorphic TaqI RFLPs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Radiation hybrid map of 13 loci on the long arm of chromosome 5

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

Gilles de la Tourette's syndrome in monozygotic twins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

A second-generation linkage map of the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900140-6

10.1016/S0006-3223(97)00140-6

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9359981%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference