(Q24288778)

Idiopathic dilated cardiomyopathy

inferred from title

1 reference

inferred from title

author

Christian Hengstenberg

38

0 references

Thomas Meitinger

32

0 references

Thomas Illig

26

0 references

Heribert Schunkert

22

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Jeanette Erdmann

24

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Heinz Erich Wichmann

28

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Christa Meisinger

29

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Peter Lichtner

31

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Patrick Linsel-Nitschke

23

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George Petrov

George Petrov

4

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Eric Villard

Eric Villard

9

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Philippe Charron

Philippe Charron

8

0 references

Richard Isnard

Richard Isnard

7

0 references

Inke R. König

Inke R König

34

0 references

Vera Regitz-Zagrosek

37

Vera Regitz-Zagrosek

0 references

Michel Komajda

6

Michel Komajda

0 references

Wolfgang Koenig

30

Wolfgang Koenig

0 references

Thomas Wichter

19

Thomas Wichter

0 references

Roland Hetzer

35

Roland Hetzer

0 references

Norman Klopp

27

Norman Klopp

0 references

Laurent Fauchier

15

Laurent Fauchier

0 references

Klaus Stark

1

Klaus Stark

0 references

François Cambien

10

François Cambien

0 references

Laurence Tiret

11

Laurence Tiret

0 references

Marie-Claude Aumont

12

Marie-Claude Aumont

0 references

Jean-Noël Trochu

14

Jean-Noël Trochu

0 references

Ulrike B Esslinger

2

Ulrike B Esslinger

0 references

Thomas W Winkler

5

Thomas Winkler

0 references

Wibke Reinhard

3

Wibke Reinhard

0 references

Iris M Heid

36

Iris M Heid

0 references

Jens Baumert

25

Jens Baumert

0 references

Arne Schillert

33

Arne Schillert

0 references

author name string

Olivier Dubourg

13

0 references

Pascal Degroote

16

0 references

Anette Richter

17

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Bernhard Maisch

18

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Christa Zollbrecht

20

0 references

Martina Grassl

Creative Commons Attribution 4.0 International

21

0 references

language of work or name

English

0 references

publication date

October 2010

0 references

published in

PLOS Genetics

0 references

volume

6

0 references

issue

10

0 references

page(s)

e1001167

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copyright license

start time

21 October 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

19 March 2017

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Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

19 March 2017

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Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

19 March 2017

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Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

19 March 2017

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Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

19 March 2017

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ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

19 March 2017

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The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

19 March 2017

1 reference

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Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

19 March 2017

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A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16

19 March 2017

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Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

19 March 2017

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Identification and characterization of cvHsp. A novel human small stress protein selectively expressed in cardiovascular and insulin-sensitive tissues

19 March 2017

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Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

19 March 2017

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Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy

19 March 2017

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A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy

19 March 2017

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Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

19 March 2017

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Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy

19 March 2017

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

19 March 2017

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Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

19 March 2017

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27 September 2017

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Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy

27 September 2017

1 reference

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27 September 2017

1 reference

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Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control study

27 September 2017

1 reference

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27 September 2017

1 reference

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De novo identification of MIZ-1 (ZBTB17) encoding a MYC-interacting zinc-finger protein as a new favorable neuroblastoma gene

27 September 2017

1 reference

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Heat shock factor 1 as a coordinator of stress and developmental pathways

27 September 2017

1 reference

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Mutations of presenilin genes in dilated cardiomyopathy and heart failure

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

The Spen homolog Msx2-interacting nuclear target protein interacts with the E2 ubiquitin-conjugating enzyme UbcH8.

27 September 2017

1 reference

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27 September 2017

1 reference

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Clinical and genetic issues in familial dilated cardiomyopathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

In vivo role of CLC chloride channels in the kidney

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

Desmin mutation responsible for idiopathic dilated cardiomyopathy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

Frequency of development of idiopathic dilated cardiomyopathy among relatives of patients with idiopathic dilated cardiomyopathy.

27 September 2017

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001167

[Familial dilated cardiomyopathy].

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2958814

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20975947

12 December 2020

inferred from PubMed ID database lookup

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20975947

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1371/JOURNAL.PGEN.1001167

1 reference

1 reference

1 reference

PubMed publication ID

20975947

1 reference