The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients (Q60687066)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

The Cys282Tyr polymorphism in the HFE gene in Australian Parkinson's disease patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

David Le Couteur

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

George D. Mellick

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

P A Silburn

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

J B Chalk

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

language of work or name

English

0 references

publication date

1 July 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

327

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

91-94

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

Genetic association studies of bronchial asthma--a need for Bonferroni correction?

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

The significance of haemochromatosis gene mutations in the general population: implications for screening

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Is hemochromatosis a risk factor for Alzheimer's disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Increased iron-related MRI contrast in the substantia nigra in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Replication validity of genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Correcting for multiple testing in genetic association studies: the legend lives on

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Altered systemic iron metabolism in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Are hereditary hemochromatosis mutations involved in Alzheimer disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

Relation between HFE mutations and mild iron-overload expression

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

The hemochromatosis gene affects the age of onset of sporadic Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

The future of genetic case-control studies

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2802%2900398-1

7 January 2021

10.1016/S0304-3940(02)00398-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12098643%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference