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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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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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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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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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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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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

2009

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

Läkartidningen, 2021, Vol.118 (40)

2021

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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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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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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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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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Longer QTc in Y111C Carriers

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

2011

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Experiences from a multidisciplinary cardiogenetic clinic

Experiences from a multidisciplinary cardiogenetic clinic

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

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

Longer QTc in Y111C Carriers

Vectorcardiographic recordings of QT interval predicts long QT syndrome

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