(Q73222818)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

Genetic association analysis between CYP2D6*2 allele and tardive dyskinesia in schizophrenic patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

Ohmori O

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Kojima H

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Shinkai T

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Terao T

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Suzuki T

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Abe K

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

language of work or name

English

0 references

publication date

1 October 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

87

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

issue

2-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

239-244

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

Non-functional CYP2D6 alleles and risk for neuroleptic-induced movement disorders in schizophrenic patients

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Mutant debrisoquine hydroxylation genes in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Antipsychotic drug-induced movement disorders in schizophrenics in relation to CYP2D6 genotype

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Tardive dyskinesia in CYP2D6 polymorphism in Chinese

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Nomenclature for human CYP2D6 alleles.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

"It's the genes, stupid". Molecular bases and clinical consequences of genetic cytochrome P450 2D6 polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Polymorphism of the cytochrome P450 CYP2D6 gene in a European population: characterization of 48 mutations and 53 alleles, their frequencies and evolution.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Hereditary Predisposition in Drug-Induced Parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Tardive dyskinesia and debrisoquine 4-hydroxylase (CYP2D6) genotype in Japanese schizophrenics.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

CYP2D6 polymorphism in a Gabonese population: contribution of the CYP2D6*2 and CYP2D6*17 alleles to the high prevalence of the intermediate metabolic phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Research Diagnoses for Tardive Dyskinesia

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

The inter-relationships of tardive dyskinesia, parkinsonism, akathisia and tardive dystonia: the Curaçao Extrapyramidal Syndromes Study II

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

R296C and other CYP2D6 mutations in Chinese

1 reference

https://api.crossref.org/works/10.1016%2FS0165-1781%2899%2900065-7

7 January 2021

10.1016/S0165-1781(99)00065-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10579557%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference