Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience (Q57316356)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

title

Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

Idiopathic dilated cardiomyopathy

22 February 2020

main subject

patient

0 references

dilated cardiomyopathy

1 reference

based on heuristic

inferred from title

1 reference

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

10

Arthur A M Wilde

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

author name string

Imke Christiaans

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Karin Y van Spaendonck-Zwarts

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Ingrid A W van Rijsingen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Maarten P van den Berg

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Ronald H Lekanne Deprez

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Jan G Post

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Anneke M van Mil

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Irene M van Langen

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Rudolf A de Boer

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Jan D H Jongbloed

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

Yigal M Pinto

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

J Peter van Tintelen

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

publication date

24 January 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

European Journal of Heart Failure

22 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

volume

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

page(s)

628-636

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

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

22 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Dilated cardiomyopathy: a tale of cytoskeletal proteins and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Inherited Cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Genetic testing for dilated cardiomyopathy in clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Clinical and genetic issues in familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

DNA analysis in inherited cardiomyopathies: current status and clinical relevance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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/10.1093/EURJHF/HFT013

Mutations of presenilin genes in dilated cardiomyopathy and heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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/10.1093/EURJHF/HFT013

Genetic and phenotypic analysis of dilated cardiomyopathy with conduction system disease: demand for strategies in the management of presymptomatic lamin A/C mutant carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Truncations of titin causing dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Long-Term Outcome and Risk Stratification in Dilated Cardiolaminopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Haplotype sharing test maps genes for familial cardiomyopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Hereditary muscular dystrophies and the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093/EURJHF/HFT013

21 January 2018

Identifiers

DOI

10.1093/EURJHF/HFT013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23349452 AND SRC:MED&resulttype=core&format=json

22 February 2020

1 reference