(Q41595939)

4 October 2017

0 references

Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis (English)

1 reference

4 October 2017

1 reference

Yongdui Chen

1

1 reference

4 October 2017

Siqi Li

2

1 reference

4 October 2017

Liling Su

3

1 reference

4 October 2017

Jinghao Sheng

4

1 reference

4 October 2017

Wen Lv

5

1 reference

4 October 2017

Guangdi Chen

6

1 reference

4 October 2017

Zhengping Xu

7

1 reference

4 October 2017

language of work or name

1 reference

13 January 2015

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4 October 2017

1 reference

4 October 2017

262

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4 October 2017

4

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4 October 2017

814-822

1 reference

https://scigraph.springernature.com/pub.10.1007/s00415-014-7630-2

4 October 2017

0 references

cites work

Neurodegenerative diseases: an overview of environmental risk factors

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Towards unveiling the genetics of neurodegenerative diseases

21 January 2018

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Rethinking ALS: the FUS about TDP-43.

21 January 2018

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The heritability and genetics of frontotemporal lobar degeneration.

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

21 January 2018

1 reference

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Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.

21 January 2018

1 reference

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Potential mechanisms of progranulin-deficient FTLD

21 January 2018

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Progranulin mutations as risk factors for Alzheimer disease

21 January 2018

1 reference

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Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Loss of progranulin function in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Operating characteristics of a rank correlation test for publication bias

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Progranulin variability has no major role in Parkinson disease genetic etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

The granulin gene family: from cancer to dementia

21 January 2018

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Progranulin: an emerging target for FTLD therapies

21 January 2018

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Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-014-7630-2

Systematic evaluation and comparison of statistical tests for publication bias

21 January 2018

1 reference

12 December 2020

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

1 reference

12 December 2020

GRN variability contributes to sporadic frontotemporal lobar degeneration

1 reference

12 December 2020

GRN variant rs5848 reduces plasma and brain levels of granulin in Alzheimer's disease patients.

1 reference

12 December 2020

10.1007/S00415-014-7630-2

Identifiers

DOI

1 reference

4 October 2017

1 reference