×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Identification of a novel hypertrophic cardiomyopathy-associated mutation using targeted next-generation sequencing.
28498465
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing.
28790153
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients.
28356264
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients.
28356264
2017
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy.
26914223
2016
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Restrictive Cardiomyopathy Troponin I R145W Mutation Does Not Perturb Myofilament Length-dependent Activation in Human Cardiac Sarcomeres.
27557662
2016
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.
25940119
2016
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
A Double Heterozygous Mutation of TNNI3 Causes Hypertrophic Cardiomyopathy in a Han Chinese Family.
26506446
2016
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
A Systematic Review of Phenotypic Features Associated With Cardiac Troponin I Mutations in Hereditary Cardiomyopathies.
26440512
2015
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
25611685
2015
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan.
25086479
2015
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Genetics of hypertrophic cardiomyopathy in Norway.
24111713
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.
25524337
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Abnormal cardiac formation in hypertrophic cardiomyopathy: fractal analysis of trabeculae and preclinical gene expression.
24704860
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy.
25132132
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy.
25132132
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
Genetics of hypertrophic cardiomyopathy in Norway.
24111713
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations.
25524337
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Advanced heart failure with preserved systolic function in nonobstructive hypertrophic cardiomyopathy: under-recognized subset of candidates for heart transplant.
25239116
2014
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Inherited cardiomyopathies caused by troponin mutations.
23610579
2013
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.
23283745
2013
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
CausalMutation
disease
CLINVAR
Dramatically different phenotypic expressions of hypertrophic cardiomyopathy in male cousins undergoing cardiac transplantation with identical disease-causing gene mutation.
23540544
2013
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
0.500
GeneticVariation
disease
CLINVAR
High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.
22876777
2012