rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population. (Q53315769)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Ming-Jang Chiu

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Ming-Jen Lee

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

author name string

Ting-Wen Cheng

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

7 January 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

Neurodegenerative Diseases

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

216-220

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

19 January 2020

cites work

1 reference

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

21 January 2018

1 reference

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

21 January 2018

1 reference

Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.

21 January 2018

1 reference

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

21 January 2018

1 reference

Hardy-Weinberg equilibrium testing of biological ascertainment for Mendelian randomization studies

21 January 2018

1 reference

Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms

21 January 2018

1 reference

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models

21 January 2018

1 reference

Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly

21 January 2018

1 reference

Different models and single-nucleotide polymorphisms signal the simulated weak gene-gene interaction for a quantitative trait using haplotype-based and mixed models testing

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000322538

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21212639%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference