(Q35512313)

8 August 2017

5 references

25 April 2019

15 December 2019

19 December 2019

23 July 2020

10 September 2020

TMEM106B a novel risk factor for frontotemporal lobar degeneration (English)

1 reference

frontotemporal lobar degeneration

8 August 2017

0 references

3 references

15 December 2019

19 December 2019

23 July 2020

1 reference

15 December 2019

1 reference

19 December 2019

genetic predisposition to disease

2 references

23 July 2020

10 September 2020

1

Julie van der Zee

0 references

Christine Van Broeckhoven

series ordinal

2

object named as

Christine Van Broeckhoven

0 references

publication date

26 May 2011

1 reference

Journal of Molecular Neuroscience

8 August 2017

1 November 2011

4 references

25 April 2019

15 December 2019

19 December 2019

23 July 2020

5 references

8 August 2017

25 April 2019

15 December 2019

19 December 2019

23 July 2020

45

1 reference

8 August 2017

issue

3

1 reference

8 August 2017

page(s)

516-521

1 reference

TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Role of progranulin as a biomarker for Alzheimer's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Genome-wide association study reveals genetic risk underlying Parkinson's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Loss of progranulin function in frontotemporal lobar degeneration

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3207134

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

12 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

Serum biomarker for progranulin-associated frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

ALS predisposition modifiers: knock NOX, who's there? SOD1 mice still are.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9555-X

10.1007/S12031-011-9555-X

21 January 2018

Identifiers

DOI

1 reference

8 August 2017

1 reference

8 August 2017

1 reference