(Q34605483)

3 August 2017

title

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

1 reference

frontotemporal lobar degeneration

3 August 2017

1 reference

1 reference

based on heuristic

inferred from title

author

Christine Van Broeckhoven

16

Christine Van Broeckhoven

0 references

Julie van der Zee

1

Julie van der Zee

0 references

Kristel Sleegers

4

Kristel Sleegers

1 reference

3 August 2017

Sebastiaan Engelborghs

5

Sebastiaan Engelborghs

1 reference

3 August 2017

Rik Vandenberghe

6

0 references

Patrick Santens

Patrick Santens

7

0 references

Gernot Kleinberger

3

Gernot Kleinberger

1 reference

3 August 2017

14

Peter P De Deyn

1 reference

3 August 2017

15

Marc Cruts

1 reference

3 August 2017

11

Maria Mattheijssens

1 reference

3 August 2017

Marleen Van den Broeck

8

Marleen Van den Broeck

1 reference

3 August 2017

13

Patrick Cras

1 reference

3 August 2017

2

Tim Van Langenhove

1 reference

3 August 2017

Geert Joris

9

1 reference

3 August 2017

Jolien Brys

10

1 reference

3 August 2017

Karin Peeters

12

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 March 2011

1 reference

3 August 2017

1 reference

3 August 2017

volume

134

1 reference

3 August 2017

issue

Pt 3

1 reference

3 August 2017

page(s)

808-815

1 reference

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

3 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=3044834

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

PLINK: a tool set for whole-genome association and population-based linkage analyses

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

PMUT: a web-based tool for the annotation of pathological mutations on proteins.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

novoSNP, a novel computational tool for sequence variation discovery

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Markov chain Monte Carlo segregation and linkage analysis for oligogenic models

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

Diagnostic performance of a CSF-biomarker panel in autopsy-confirmed dementia.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044834

26 October 2018

Frontotemporal dementia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21354975

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21354975

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BRAIN/AWR007

1 reference

3 August 2017

1 reference

3 August 2017

1 reference