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Cardiac response to water activities in children with Long QT syndrome type 1

PloS one, 2023-12, Vol.18 (12), p.e0295431-e0295431

2023

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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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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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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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Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

BMC medical genetics, 2017-07, Vol.18 (1), p.74-74, Article 74

2017

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Combining tissue engineering and optical imaging approaches to explore interactions along the neuro-cardiac axis

Royal Society open science, 2020-06, Vol.7 (6), p.200265-200265

2020

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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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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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Modelling neurocardiac physiology and diseases using human pluripotent stem cells: current progress and future prospects

The Journal of physiology, 2024-09

2024

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Functional hyperactivity in long OT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

American journal of physiology. Heart and circulatory physiology, 2021-07, Vol.321 (1), p.H217

2021

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Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells

American journal of physiology. Heart and circulatory physiology, 2020-11, Vol.319 (5), p.H927-H937

2020

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Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations

HeartRhythm case reports, 2018-06, Vol.4 (6), p.237-240

2018

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A Population-Based Registry of Patients With Inherited Cardiac Conditions and Resuscitated Cardiac Arrest

Journal of the American College of Cardiology, 2020-06, Vol.75 (21), p.2698-2707

2020

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Vestibular dysfunction is a clinical feature of the Jervell and Lange-Nielsen Syndrome

Scandinavian cardiovascular journal : SCJ, 2015-02, Vol.49 (1), p.7-13

2015

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The Brain-Heart Connection in Sympathetically Triggered Inherited Arrhythmia Syndromes

Heart, lung & circulation, 2020-04, Vol.29 (4), p.529-537

2020

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Neuroscience in the heart: Recent advances in neurocardiac communication and its role in cardiac arrhythmias

The international journal of biochemistry & cell biology, 2020-05, Vol.122, p.105737-105737, Article 105737

2020

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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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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Genetics in medicine, 2021-01, Vol.23 (1), p.47-58

2021

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Functional hyperactivity in long QT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

American journal of physiology. Heart and circulatory physiology, 2021-07, Vol.321 (1), p.H217-H227

2021

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Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

American journal of obstetrics and gynecology, 2020-03, Vol.222 (3), p.263.e1-263.e11

2020

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Molecular and cellular neurocardiology in heart disease

The Journal of physiology, 2024-05

2024

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Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry

Circulation. Heart failure, 2024-03, Vol.17 (3), p.e010970

2024

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Cardiac response to water activities in children with Long QT syndrome type 1

PloS one, 2023-01, Vol.18 (12), p.e0295431

2023

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Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes

Journal of molecular and cellular cardiology, 2016-11, Vol.100, p.25-34

2016

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Cardiac response to water activities in children with Long QT syndrome type 1

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

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

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

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

Combining tissue engineering and optical imaging approaches to explore interactions along the neuro-cardiac axis

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

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

Modelling neurocardiac physiology and diseases using human pluripotent stem cells: current progress and future prospects

Functional hyperactivity in long OT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells

Fetal heart rate reflects mutation burden and clinical outcome in twin probands with KCNQ1 mutations

A Population-Based Registry of Patients With Inherited Cardiac Conditions and Resuscitated Cardiac Arrest

Vestibular dysfunction is a clinical feature of the Jervell and Lange-Nielsen Syndrome

The Brain-Heart Connection in Sympathetically Triggered Inherited Arrhythmia Syndromes

Neuroscience in the heart: Recent advances in neurocardiac communication and its role in cardiac arrhythmias

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

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Functional hyperactivity in long QT syndrome type 1 pluripotent stem cell-derived sympathetic neurons

Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

Molecular and cellular neurocardiology in heart disease

Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups: Insights From a New Zealand National Registry

Cardiac response to water activities in children with Long QT syndrome type 1

Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes

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