Genetic evaluation of dilated cardiomyopathy (Q38107893)

29 August 2017

Genetic evaluation of dilated cardiomyopathy (English)

1 reference

29 August 2017

Ana Morales

1

1 reference

PubMed ID

23686784

29 August 2017

Ray E Hershberger

series ordinal

2

1 reference

29 August 2017

1 July 2013

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Current cardiology reports

29 August 2017

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29 August 2017

15

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29 August 2017

375

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29 August 2017

7

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https://scigraph.springernature.com/pub.10.1007/s11886-013-0375-1

29 August 2017

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cites work

Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals

1 reference

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Dominant missense mutations in ABCC9 cause Cantú syndrome.

21 January 2018

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Distribution and categorization of echocardiographic measurements in relation to reference limits: the Framingham Heart Study: formulation of a height- and sex-specific classification and its prospective validation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Clinical and genetic issues in familial dilated cardiomyopathy

21 January 2018

1 reference

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Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

21 January 2018

1 reference

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Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.

21 January 2018

1 reference

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Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation

21 January 2018

1 reference

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Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

21 January 2018

1 reference

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The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy

21 January 2018

1 reference

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Arrhythmogenic right ventricular cardiomyopathy: clinical presentation, diagnosis, and management

21 January 2018

1 reference

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The changing spectrum of arrhythmogenic (right ventricular) cardiomyopathy

21 January 2018

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21 January 2018

1 reference

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy

21 January 2018

1 reference

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Dilated cardiomyopathy presenting during fetal life

21 January 2018

1 reference

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Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

21 January 2018

1 reference

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Clinical characteristics of peripartum cardiomyopathy in the United States: diagnosis, prognosis, and management

21 January 2018

1 reference

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Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience

21 January 2018

1 reference

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Frequency and phenotypes of familial dilated cardiomyopathy.

21 January 2018

1 reference

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Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy

21 January 2018

1 reference

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A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy

21 January 2018

1 reference

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Desmosomal protein gene mutations in patients with idiopathic dilated cardiomyopathy undergoing cardiac transplantation: a clinicopathological study

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

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Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny

21 January 2018

1 reference

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Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy

21 January 2018

1 reference

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Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

21 January 2018

1 reference

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Truncations of titin causing dilated cardiomyopathy.

21 January 2018

1 reference

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Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.

21 January 2018

1 reference

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Mutation in BAG3 causes severe dominant childhood muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

21 January 2018

1 reference

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Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy.

21 January 2018

1 reference

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Titin mutations as the molecular basis for dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

A glimpse into multigene rare variant genetics: triple mutations in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Multiple mutations in genetic cardiovascular disease: a marker of disease severity?

21 January 2018

1 reference

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Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

21 January 2018

1 reference

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Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.

21 January 2018

1 reference

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HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

21 January 2018

1 reference

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Genetic testing for dilated cardiomyopathy in clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Family history: an essential tool for cardiovascular genetic medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

The family history as a tool to identify patients at risk for dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-013-0375-1

Features of left ventricular noncompaction in peripartum cardiomyopathy: a case series

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Psychological issues in genetic testing for inherited cardiovascular diseases

1 reference

12 December 2020

Left-dominant arrhythmogenic cardiomyopathy: an under-recognized clinical entity

1 reference

12 December 2020

Familial dilated cardiomyopathy: cardiac abnormalities are common in asymptomatic relatives and may represent early disease

1 reference

12 December 2020

Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families

1 reference

12 December 2020

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

1 reference

12 December 2020

Titin diversity--alternative splicing gone wild

1 reference

12 December 2020

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation

1 reference

12 December 2020

10.1007/S11886-013-0375-1

Identifiers

DOI

1 reference

PubMed ID

23686784

Dimensions Publication ID

29 August 2017

0 references

1 reference

PubMed ID

23686784