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List of works by Jens Mogensen

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).

scientific article published on 29 August 2014

A Systematic Review of Phenotypic Features Associated With Cardiac Troponin I Mutations in Hereditary Cardiomyopathies.

scientific article published on 23 June 2015

A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.

scientific article published on 5 August 2016

An International External Validation Study of the 2014 European Society of Cardiology Guideline on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (Evidence from HCM).

scientific article

An improved method for chromosome-specific labeling of alpha satellite DNA in situ by using denatured double-stranded DNA probes as primers in a primed in situ labeling (PRINS) procedure.

scientific article

Assignment of the human cardiac troponin I gene (TNNI3) to chromosome 19q13.4 by radiation hybrid mapping ⬇️

scientific article published on January 1, 1997

Atlas of the clinical genetics of human dilated cardiomyopathy

scientific article (publication date: 7 May 2015)

Clinical utility gene card for: Dilated Cardiomyopathy (CMD) ⬇️

scientific article published on December 19, 2012

Current approaches to unravel the mystery of dilated cardiomyopathy, a common cause of hereditary heart failure

scientific article published on 01 December 2005

Current state of knowledge on aetiology, diagnosis, management, and therapy of myocarditis: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.

scientific article published on 03 July 2013

DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency

scientific article published on 07 June 2017

Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

scientific article published on 14 August 2019

Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotype

scientific article

Fast one-step procedure for the detection of nucleic acids in situ by primer-induced sequence-specific labeling with fluorescein-12-dUTP

scientific article published on 01 January 1992

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy

scientific article published on 01 November 2018

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

scientific article published on December 2004

Functional effects of the DCM mutant Gly159Asp Troponin C in skinned muscle fibres

article

Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers.

scientific article

Hypertrophic cardiomyopathy-the clinical challenge of managing a hereditary heart condition

scientific article published on 01 March 2003

Left ventricular longitudinal systolic function after alcohol septal ablation for hypertrophic obstructive cardiomyopathy: a long-term follow-up study focused on speckle tracking echocardiography.

scientific article published on 28 July 2010

Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy.

scientific article published on 5 June 2006

Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.

scientific article

Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy

scientific article

Nonradioactive, sequence-specific detection of RNA in situ by primed in situ labeling (PRINS)

scientific article published on 01 September 1991

Pathogenic RBM20-Variants Are Associated With a Severe Disease Expression in Male Patients With Dilated Cardiomyopathy

scientific article published on 01 March 2019

Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy

scientific article published in July 2005

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

article

Protein expression studies of desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms

scientific article published on 03 December 2012

Quantitative Expression of the Mutated Lamin A/C Gene in Patients With Cardiolaminopathy

article

Restrictive cardiomyopathy

scientific article published on 01 May 2009

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

scientific article published on 01 January 2012

Role of genotyping in risk factor assessment for sudden death in hypertrophic cardiomyopathy

scientific article published on 01 June 2002

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

scientific article

The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins

scientific article published on 31 August 2013

The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus

scientific article

The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope

scientific article published on 26 June 2018

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

Triage strategy for urgent management of cardiac tamponade: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

scientific article published on 7 July 2014

Troponin mutations in cardiomyopathies.

scientific article published on January 2007

Truncating Plakophilin-2 Mutations in Arrhythmogenic Cardiomyopathy Are Associated With Protein Haploinsufficiency in Both Myocardium and Epidermis

scientific article published on 04 April 2014

Wytyczne ESC dotyczące rozpoznawania i postępowania w kardiomiopatii przerostowej w 2014 roku

scientific article published on 01 January 2014

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