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List of works by Tiina Heliö

2069 Assessment of genetic dilated cardiomyopathy in LMNA-mutation carriers by cardiac MRI

A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

article

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

scientific article

Characteristics of Atrial Fibrillation and Comorbidities in Familial Atrial Fibrillation

scientific article published on 29 March 2013

Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in Finland

scientific article published in January 2007

Concept of VNTR alleles: Comparison of apolipoprotein B 3′ hypervariable region genotyping results obtained by three methods ⬇️

scientific article published on December 16, 1991

Description of A/C gene mutation related dilated cardiomyopathy with gadolinium- enhanced magnetic resonance imaging

scientific article published on 2 February 2011

Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry

scientific article published on 11 November 2020

ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients

scientific article published on 07 August 2020

Early familial dilated cardiomyopathy: identification with determination of disease state parameter from cine MR image data

scientific article

Electrocardiographic ventricular repolarization during cardiovascular autonomic function testing in patients with arrhythmogenic right ventricular cardiomyopathy

scientific article published in December 2008

Genetic Variants of Apolipoprotein B: Relation to Serum Lipid Levels and Coronary Artery Disease Among the Finns

scientific article published on 01 October 1992

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21

scientific article published on 01 May 2001

Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy

Genome-wide search in Finnish families with inflammatory bowel disease provides evidence for novel susceptibility loci

scientific article published on 01 February 2003

Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy

scientific article published in January 2005

Lamin A/C mutation affecting primarily the right side of the heart

Left ventricular mechanical dispersion is associated with nonsustained ventricular tachycardia in hypertrophic cardiomyopathy

scientific article published in June 2016

Modeling of LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cells

scientific article published on 15 June 2019

Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy

scientific article

Pregnancy and childbirth in carriers of the lamin A/C-gene mutation

article

Screening for mutations in the exon 26 of the apolipoprotein B gene in hypercholesterolemic Finnish families by the single-strand conformation polymorphism method.

scientific article published on January 1994

Screening of tumor necrosis factor receptor-associated factor 6 as a candidate gene for inflammatory bowel disease

article

Searching for Linear Dependencies between Heart Magnetic Resonance Images and Lipid Profiles

Serum lipidomics meets cardiac magnetic resonance imaging: profiling of subjects at risk of dilated cardiomyopathy

scientific article

The Metabolome in Finnish Carriers of the MYBPC3-Q1061X Mutation for Hypertrophic Cardiomyopathy

scientific article published on 12 August 2015

The effects of the apolipoprotein B signal peptide (ins/del) and XbaI polymorphisms on plasma lipid responses to dietary change

article

Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population

scientific article published on 2 April 2012

Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy

scientific article published in December 2004

Use of home telemonitoring to support multidisciplinary care of heart failure patients in Finland: randomized controlled trial.

scientific article

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