Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. (Q29417073)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21623375%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone (English)

1 reference

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genome-wide association study

2 February 2020

main subject

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2 February 2020

Timothy Cundy

7

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2 February 2020

Alberto Falchetti

11

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2 February 2020

Fernando Gianfrancesco

14

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2 February 2020

Wim Van Hul

16

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2 February 2020

Geoffrey C. Nicholson

18

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2 February 2020

Sarah L. Rea

23

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2 February 2020

John P. Walsh

28

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2 February 2020

6

Maria Luisa Brandi

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2 February 2020

29

Stuart H Ralston

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2 February 2020

author name string

Sachin E Wani

2

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2 February 2020

Micaela R Visconti

3

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2 February 2020

Nerea Alonso

4

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2 February 2020

Kirsteen Goodman

5

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2 February 2020

Pui Yan Jenny Chung

8

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2 February 2020

Rosemary Dargie

9

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2 February 2020

Jean-Pierre Devogelaer

10

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2 February 2020

William D Fraser

12

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2 February 2020

Luigi Gennari

13

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2 February 2020

Michael J Hooper

15

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2 February 2020

Gianluca Isaia

17

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2 February 2020

Ranuccio Nuti

19

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2 February 2020

Socrates Papapoulos

20

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2 February 2020

Javier del Pino Montes

21

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2 February 2020

Thomas Ratajczak

22

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2 February 2020

Domenico Rendina

24

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2 February 2020

Rogelio Gonzalez-Sarmiento

25

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2 February 2020

Marco Di Stefano

26

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2 February 2020

Lynley C Ward

27

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2 February 2020

Genetic Determinants of Paget's Disease (GDPD) Consortium

30

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2 February 2020

language of work or name

English

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publication date

29 May 2011

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2 February 2020

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2 February 2020

volume

43

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2 February 2020

page(s)

685-689

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2 February 2020

issue

7

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DC-STAMP is essential for cell-cell fusion in osteoclasts and foreign body giant cells

2 February 2020

cites work

1 reference

RANKL-induced DC-STAMP is essential for osteoclastogenesis

21 April 2017

1 reference

A novel binding protein composed of homophilic tetramer exhibits unique properties for the small GTPase Rab5

21 April 2017

1 reference

Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans

21 April 2017

1 reference

Cytoplasmic PML function in TGF-beta signalling

21 April 2017

1 reference

Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210

21 April 2017

1 reference

Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin

21 April 2017

1 reference

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

21 April 2017

1 reference

Genetics and beyond--the transcriptome of human monocytes and disease susceptibility

21 April 2017

1 reference

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

21 April 2017

1 reference

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

21 April 2017

1 reference

Mapping the genetic architecture of gene expression in human liver

21 April 2017

1 reference

Meta-analysis in clinical trials

21 April 2017

1 reference

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

21 April 2017

1 reference

Population structure, differential bias and genomic control in a large-scale, case-control association study

21 April 2017

1 reference

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

21 April 2017

1 reference

LocusZoom: regional visualization of genome-wide association scan results

21 April 2017

1 reference

Population genomics of human gene expression

21 April 2017

1 reference

Transcriptome genetics using second generation sequencing in a Caucasian population

21 April 2017

1 reference

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone

21 April 2017

1 reference

The epidemiology of Paget's disease in Britain: is the prevalence decreasing?

21 January 2018

1 reference

Frequency and characteristics of familial aggregation of Paget's disease of bone

21 January 2018

1 reference

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone

21 January 2018

1 reference

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

21 January 2018

1 reference

CCN family 2/connective tissue growth factor (CCN2/CTGF) promotes osteoclastogenesis via induction of and interaction with dendritic cell-specific transmembrane protein (DC-STAMP).

21 January 2018

1 reference

Nup93, a vertebrate homologue of yeast Nic96p, forms a complex with a novel 205-kDa protein and is required for correct nuclear pore assembly

21 January 2018

1 reference

RIN3: a novel Rab5 GEF interacting with amphiphysin II involved in the early endocytic pathway

21 January 2018

1 reference

The role of prenylated small GTP-binding proteins in the regulation of osteoclast function

21 January 2018

1 reference

Familial aggregation of Paget's disease of bone

21 January 2018

1 reference

Randomized trial of intensive bisphosphonate treatment versus symptomatic management in Paget's disease of bone.

21 January 2018

1 reference

Genetic epidemiology of Paget's disease of bone in italy: sequestosome1/p62 gene mutational test and haplotype analysis at 5q35 in a large representative series of sporadic and familial Italian cases of Paget's disease of bone

21 January 2018

1 reference

Paget's disease of bone in The Netherlands: a population-based radiological and biochemical survey--the Rotterdam Study

21 January 2018

1 reference

ProbABEL package for genome-wide association analysis of imputed data

21 January 2018

1 reference

High-resolution mapping of expression-QTLs yields insight into human gene regulation

21 January 2018

1 reference

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

21 January 2018

1 reference

The majority of the genetic risk for Paget’s disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes

21 January 2018

1 reference

DC-STAMP, a novel multimembrane-spanning molecule preferentially expressed by dendritic cells

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21623375

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations of SQSTM1 are associated with severity and clinical outcome in paget disease of bone

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21623375

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

SQSTM1 gene analysis and gene-environment interaction in Paget's disease of bone

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21623375

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.845

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21623375%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

2 February 2020

0 references

1 reference

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