A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression. (Q47620193)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29056226%20AND%20SRC:MED&resulttype=core&format=json

7 April 2020

title

A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression (English)

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7 April 2020

0 references

8

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7 April 2020

Struan F.A. Grant

10

1 reference

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7 April 2020

author name string

Michael D Gallagher

1

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7 April 2020

Marijan Posavi

2

1 reference

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7 April 2020

Peng Huang

3

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7 April 2020

Travis L Unger

4

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7 April 2020

Yosef Berlyand

5

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7 April 2020

Analise L Gruenewald

6

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7 April 2020

Alessandra Chesi

7

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7 April 2020

Andrew D Wells

9

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7 April 2020

Gerd A Blobel

11

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7 April 2020

Christopher D Brown

12

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7 April 2020

Alice S Chen-Plotkin

13

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7 April 2020

language of work or name

English

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publication date

19 October 2017

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American Journal of Human Genetics

7 April 2020

published in

1 reference

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7 April 2020

volume

101

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7 April 2020

issue

5

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7 April 2020

page(s)

643-663

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Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data

7 April 2020

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

26 August 2018

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26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

A unique chromatin signature uncovers early developmental enhancers in humans

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Histone H3K27ac separates active from poised enhancers and predicts developmental state

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

A map of human genome variation from population-scale sequencing

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Integrating common and rare genetic variation in diverse human populations

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

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

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Common regulatory variation impacts gene expression in a cell type-dependent manner

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

A genome-wide association study of global gene expression

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS)

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

Haploview: analysis and visualization of LD and haplotype maps

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

The extent of linkage disequilibrium in four populations with distinct demographic histories

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5673619

10.1016/J.AJHG.2017.09.004

26 August 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29056226%20AND%20SRC:MED&resulttype=core&format=json

7 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29056226%20AND%20SRC:MED&resulttype=core&format=json

7 April 2020

PubMed publication ID

29056226

1 reference