List of works - Petros Syrris

A microRNA Expression Profile as Non-Invasive Biomarker in a Large Arrhythmogenic Cardiomyopathy Cohort

scientific article published on 24 February 2020

A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity

scientific article published on 11 April 2012

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

scientific article

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

scientific article

Abnormal cardiac formation in hypertrophic cardiomyopathy: fractal analysis of trabeculae and preclinical gene expression.

scientific article published on 05 April 2014

Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.

scientific article published on 29 March 2015

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

scientific article

Arrhythmogenic right ventricular cardiomyopathy/dysplasia on the basis of the revised diagnostic criteria in affected families with desmosomal mutations

scientific article

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

scientific article

Atlas of the clinical genetics of human dilated cardiomyopathy

scientific article (publication date: 7 May 2015)

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

scientific article published on 20 January 2012

Carnosine protects proteins against in vitro glycation and cross-linking ⬇️

scientific article published on 01 November 1994

Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy

article

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

scientific article

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

scientific article

Common arterial trunk associated with a homeodomain mutation of NKX2.6

scientific article

Desmoglein-2 interaction is crucial for cardiomyocyte cohesion and function

scientific article (publication date: November 2014)

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

scientific article published on 10 May 2017

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

scientific article (publication date: November 2011)

Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.

scientific article

Dynamic conduction and repolarisation changes in early arrhythmogenic right ventricular cardiomyopathy versus benign outflow tract ectopy demonstrated by high density mapping & paced surface ECG analysis

scientific article

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

scientific article

Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathy.

scientific article

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

scientific article published on 6 July 2021

Familial Evaluation in Arrhythmogenic Right Ventricular Cardiomyopathy

article

Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation database

scientific article published on 25 May 2018

Genetic basis of arrhythmogenic cardiomyopathy

scientific article published on 14 March 2018

Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics

scientific article published on 27 January 2019

Hypertrophy Regression With N-Acetylcysteine in Hypertrophic Cardiomyopathy (HALT-HCM): A Randomized, Placebo-Controlled, Double-Blind Pilot Study

scientific article published on 14 March 2018

Lamin and the heart

scientific article published on 25 November 2017

Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature

scientific article published on 25 October 2018

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

scientific article

Mutational Heterogeneity, Modifier Genes, and Environmental Influences Contribute to Phenotypic Diversity of Arrhythmogenic Cardiomyopathy

article

No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

scientific article published on 30 August 2018

Non‐enzymatic glycosylation of the dipeptide l‐carnosine, a potential anti‐protein‐cross‐linking agent ⬇️

scientific article published on August 28, 1995

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

scientific article

Polymorphism in apolipoprotein(a) kringle IV 37 (Met/Thr): Frequency in a London population and its association with coronary artery disease ⬇️

scientific article published on 01 October 1997

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

article

Prevalence of F-fluorodeoxyglucose positron emission tomography abnormalities in patients with arrhythmogenic right ventricular cardiomyopathy

scientific article published on 26 October 2018

Proteomic Analysis of the Myocardium in Hypertrophic Obstructive Cardiomyopathy

scientific article published in December 2018

Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada.

scientific article

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

scientific article

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the

scientific article published on 05 April 2015

The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants.

scientific article

Unique epidermolytic bullous dermatosis with associated lethal cardiomyopathy related to novel desmoplakin mutations

scientific article published on 29 October 2008

Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy

scientific article

List of works by Petros Syrris

A microRNA Expression Profile as Non-Invasive Biomarker in a Large Arrhythmogenic Cardiomyopathy Cohort

A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

Abnormal cardiac formation in hypertrophic cardiomyopathy: fractal analysis of trabeculae and preclinical gene expression.

Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

Arrhythmogenic right ventricular cardiomyopathy/dysplasia on the basis of the revised diagnostic criteria in affected families with desmosomal mutations

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

Atlas of the clinical genetics of human dilated cardiomyopathy

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

Carnosine protects proteins against in vitro glycation and cross-linking ⬇️

Clinical Significance of Epsilon Waves in Arrhythmogenic Cardiomyopathy

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

Common arterial trunk associated with a homeodomain mutation of NKX2.6

Desmoglein-2 interaction is crucial for cardiomyocyte cohesion and function

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

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

Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.

Dynamic conduction and repolarisation changes in early arrhythmogenic right ventricular cardiomyopathy versus benign outflow tract ectopy demonstrated by high density mapping & paced surface ECG analysis

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathy.

Evidence-Based Assessment of Genes in Dilated Cardiomyopathy

Familial Evaluation in Arrhythmogenic Right Ventricular Cardiomyopathy

Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation database

Genetic basis of arrhythmogenic cardiomyopathy

Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics

Hypertrophy Regression With N-Acetylcysteine in Hypertrophic Cardiomyopathy (HALT-HCM): A Randomized, Placebo-Controlled, Double-Blind Pilot Study

Lamin and the heart

Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

Mutational Heterogeneity, Modifier Genes, and Environmental Influences Contribute to Phenotypic Diversity of Arrhythmogenic Cardiomyopathy

No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy

Non‐enzymatic glycosylation of the dipeptide l‐carnosine, a potential anti‐protein‐cross‐linking agent ⬇️

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

Polymorphism in apolipoprotein(a) kringle IV 37 (Met/Thr): Frequency in a London population and its association with coronary artery disease ⬇️

Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy

Prevalence of F-fluorodeoxyglucose positron emission tomography abnormalities in patients with arrhythmogenic right ventricular cardiomyopathy

Proteomic Analysis of the Myocardium in Hypertrophic Obstructive Cardiomyopathy

Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada.

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the

The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variants.

Unique epidermolytic bullous dermatosis with associated lethal cardiomyopathy related to novel desmoplakin mutations

Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy