Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3.
|
31568572 |
2019 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
RIKADA Study Reveals Risk Factors in Pediatric Primary Cardiomyopathy.
|
31333075 |
2019 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
|
28669108 |
2017 |
Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
BEFREE |
Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
|
28669108 |
2017 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.
|
29367539 |
2017 |
Cardiomyopathy, Dilated
|
0.630 |
Biomarker
|
group |
MGD |
Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium Desensitization.
|
27936050 |
2016 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
|
27153395 |
2016 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
|
24503780 |
2014 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
A novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM).
|
24992688 |
2014 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity.
|
23539503 |
2013 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Usefulness of running wheel for detection of congestive heart failure in dilated cardiomyopathy mouse model.
|
23383212 |
2013 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.
|
24205113 |
2013 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Effects of troponin T cardiomyopathy mutations on the calcium sensitivity of the regulated thin filament and the actomyosin cross-bridge kinetics of human β-cardiac myosin.
|
24367593 |
2013 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy.
|
24119082 |
2013 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.
|
22517884 |
2012 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates.
|
22675533 |
2012 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Cardiac structural and sarcomere genes associated with cardiomyopathy exhibit marked intolerance of genetic variation.
|
23074333 |
2012 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Genetic testing for dilated cardiomyopathy in clinical practice.
|
22464770 |
2012 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
BEFREE |
Genetic variation screening of TNNT2 gene in a cohort of patients with hypertrophic and dilated cardiomyopathy.
|
22292720 |
2012 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
|
21551322 |
2011 |
Cardiomyopathy, Dilated
|
0.630 |
GeneticVariation
|
group |
CLINVAR |
Dilated cardiomyopathy caused by a novel TNNT2 mutation-added value of genetic testing in the correct identification of affected subjects.
|
19324435 |
2010 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Cardiomyopathy-causing deletion K210 in cardiac troponin T alters phosphorylation propensity of sarcomeric proteins.
|
20079745 |
2010 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy.
|
20978592 |
2010 |
Cardiomyopathy, Dilated
|
0.630 |
CausalMutation
|
group |
CLINVAR |
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
|
20031601 |
2009 |