Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy (Q24288778)

Idiopathic dilated cardiomyopathy

inferred from title

1 reference

inferred from title

author

Christian Hengstenberg

38

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Thomas Meitinger

32

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Thomas Illig

26

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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

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Richard Isnard

Richard Isnard

7

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Inke R. König

Inke R König

34

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Vera Regitz-Zagrosek

37

Vera Regitz-Zagrosek

0 references

Michel Komajda

6

Michel Komajda

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Wolfgang Koenig

30

Wolfgang Koenig

0 references

Thomas Wichter

19

Thomas Wichter

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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

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François Cambien

10

François Cambien

0 references

Laurence Tiret

11

Laurence Tiret

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Marie-Claude Aumont

12

Marie-Claude Aumont

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Jean-Noël Trochu

14

Jean-Noël Trochu

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Ulrike B Esslinger

2

Ulrike B Esslinger

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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

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author name string

Olivier Dubourg

13

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Pascal Degroote

16

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Anette Richter

17

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Bernhard Maisch

18

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Christa Zollbrecht

20

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Martina Grassl

Creative Commons Attribution 4.0 International

21

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language of work or name

English

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publication date

October 2010

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published in

PLOS Genetics

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volume

6

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issue

10

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

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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

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27 September 2017

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

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Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

21 January 2018

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

21 January 2018

1 reference

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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

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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

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[Familial dilated cardiomyopathy].

21 January 2018

1 reference

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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