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ICD harm and benefit: risk scores applied to the Swedish ICD-treated LQTS population

Scandinavian cardiovascular journal : SCJ, 2022-12, Vol.56 (1), p.48-55

2022

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To Modify or Not to Modify: Allele-Specific Effects of 3'UTR- KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation

Journal of the American Heart Association, 2022-09, Vol.11 (18), p.e025981-e025981

2022

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Experiences from a multidisciplinary cardiogenetic clinic

Läkartidningen, 2021-10, Vol.118

2021

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Experiences from a multidisciplinary cardiogenetic clinic

Läkartidningen, 2021-10, Vol.118

2021

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QT correction using Bazett’s formula remains preferable in long QT syndrome type 1 and 2

Annals of noninvasive electrocardiology, 2021-01, Vol.26 (1), p.e12804-n/a

2021

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Ärftliga hjärt–kärlsjukdomar – ett multidisciplinärt arbetssätt krävs: Experiences from a multidisciplinary cardiogenetic clinic

Läkartidningen, 2021, Vol.118 (40)

2021

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LQTS founder population in Northern Sweden - the natural history of a potentially fatal inherited cardiac disorder

Biodemography and social biology, 2020-10, Vol.66 (3-4), p.191-207

2020

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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Circulation (New York, N.Y.), 2020-07, Vol.142, p.324-338

2020

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The prevalence of prolonged QTc increases by GOLD stage, and is associated with worse survival among subjects with COPD

Heart & lung, 2019-03, Vol.48 (2), p.148-154

2019

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Implantable cardioverter defibrillator treatment in long QT syndrome patients: a national study on adherence to international guidelines

Scandinavian cardiovascular journal : SCJ, 2017-04, Vol.51 (2), p.88-94

2017

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Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2015-08, Vol.8 (4), p.806-814

2015

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Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1families

BMC cardiovascular disorders, 2014-02, Vol.14 (1), Article 22

2014

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Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families

BMC cardiovascular disorders, 2014-02, Vol.14 (1), p.22-22

2014

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Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene

Journal of applied physiology (1985), 2013-11, Vol.115 (10), p.1423-1432

2013

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Instability of repolarization in LQTS mutation carriers compared to healthy control subjects assessed by vectorcardiography

Heart rhythm, 2013-08, Vol.10 (8), p.1169-1175

2013

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Vectorcardiographic Recordings of the Q-T Interval in a Pediatric Long Q-T Syndrome Population

Pediatric cardiology, 2013-02, Vol.34 (2), p.245-249

2013

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Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden

Europace (London, England), 2012-12, Vol.14 (12), p.1799-1806

2012

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Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

BMC cardiovascular disorders, 2012-10, Vol.12 (1), p.95-95, Article 95

2012

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Origin of the Swedish long QT syndrome Y111C/ KCNQ1 founder mutation

Heart rhythm, 2011-04, Vol.8 (4), p.541-547

2011

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Longer QTc in Y111C Carriers

Journal of electrocardiology, 2011-03, Vol.44 (2), p.e54-e55

2011

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Age and origin of the Y111C/KCNQ1 founder mutation—a major cause of the long-QT syndrome in Sweden

Journal of electrocardiology, 2011-03, Vol.44 (2), p.e14-e14

2011

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Two automatic QT algorithms compared with manual measurement in identification of long QT syndrome

Journal of electrocardiology, 2010, Vol.43 (1), p.25-30

2010

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Low Incidence of Sudden Cardiac Death in a Swedish Y111C Type 1 Long-QT syndrome Population

Circulation. Cardiovascular genetics, 2009-12, Vol.2 (6), p.558-564

2009

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Vectorcardiographic recordings of QT interval predicts long QT syndrome

Journal of electrocardiology, 2007-07, Vol.40 (4), p.S63-S64

2007

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ICD harm and benefit: risk scores applied to the Swedish ICD-treated LQTS population

To Modify or Not to Modify: Allele-Specific Effects of 3'UTR- KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation

Experiences from a multidisciplinary cardiogenetic clinic

Experiences from a multidisciplinary cardiogenetic clinic

QT correction using Bazett’s formula remains preferable in long QT syndrome type 1 and 2

Ärftliga hjärt–kärlsjukdomar – ett multidisciplinärt arbetssätt krävs: Experiences from a multidisciplinary cardiogenetic clinic

LQTS founder population in Northern Sweden - the natural history of a potentially fatal inherited cardiac disorder

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

The prevalence of prolonged QTc increases by GOLD stage, and is associated with worse survival among subjects with COPD

Implantable cardioverter defibrillator treatment in long QT syndrome patients: a national study on adherence to international guidelines

Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome

Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1families

Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families

Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene

Instability of repolarization in LQTS mutation carriers compared to healthy control subjects assessed by vectorcardiography

Vectorcardiographic Recordings of the Q-T Interval in a Pediatric Long Q-T Syndrome Population

Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

Origin of the Swedish long QT syndrome Y111C/ KCNQ1 founder mutation

Longer QTc in Y111C Carriers

Age and origin of the Y111C/KCNQ1 founder mutation—a major cause of the long-QT syndrome in Sweden

Two automatic QT algorithms compared with manual measurement in identification of long QT syndrome

Low Incidence of Sudden Cardiac Death in a Swedish Y111C Type 1 Long-QT syndrome Population

Vectorcardiographic recordings of QT interval predicts long QT syndrome

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