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130: Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype. Results of an 8-center international study

American journal of obstetrics and gynecology, 2018-01, Vol.218 (1), p.S93-S93

2018

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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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Assays of Variant Effect and Automated Patch Clamping Improve KCNH2 -LQTS Variant Classification and Cardiac Event Risk Stratification

Circulation (New York, N.Y.), 2024-09

2024

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Assessment and Support? AI,R – A Pilot Project on Support Systems for Innovation in Automation Industry

Procedia, social and behavioral sciences, 2015-07, Vol.195, p.103-112

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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Bromine number determination by coulometric flow-injection titration

Talanta (Oxford), 1992-07, Vol.39 (7), p.789-794

1992

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Brugada Syndrome in New Zealand: The Experience of the National Cardiac Inherited Disease Group

Heart, lung & circulation, 2022, Vol.31, p.S7-S7

2022

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The Cardiac Inherited Disease Group's Experience of Brugada Syndrome in New Zealand

Heart, lung & circulation, 2021, Vol.30, p.S68

2021

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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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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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Cause-specific stillbirth and neonatal death in Sweden: a catchment area-based analysis

Acta Paediatrica, 2001-09, Vol.90 (9), p.1054-1061

2001

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Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects

Heart, lung & circulation, 2019-01, Vol.28 (1), p.22-30

2019

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ChemInform Abstract: Crystal Structure of the Double Carbonate K2Ca2(CO3)3

ChemInform, 1997-09, Vol.28 (38), p.no-no

1997

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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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A computer-based method for cause of death classification in stillbirths and neonatal deaths

International journal of epidemiology, 1997-12, Vol.26 (6), p.1298-1306

1997

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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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Crystal structure of the double carbonate K2Ca2(CO3)(3)

Acta Chemica Scandinavica, 1997-03, Vol.51 (3), p.387

1997

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Crystal Structure of the Double Carbonate K2Ca2(CO3)3

Acta chemica Scandinavica (Copenhagen. 1989), 1997, Vol.51, p.387-391

1997

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Differential expression profile of microRNA in yak skeletal muscle and adipose tissue during development

Genes & Genomics, 2020, 42(11), , pp.1347-1359

2020

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Dynamic composite hydrogels of gelatin methacryloyl (GelMA) with supramolecular fibers for tissue engineering applications

Biomaterials Advances, 2024-10, Vol.163, p.213957, Article 213957

2024

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Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

Europace (London, England), 2023-11, Vol.25 (11)

2023

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Effet fondateur et estimation de l’âge de la mutation fondatrice dans trois pays maghrébins : à propos de 66 patients atteints du syndrome d’Allgrove

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.309-310

2016

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

Genetics in medicine, 2020-09

2020

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130: Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype. Results of an 8-center international study

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

Assays of Variant Effect and Automated Patch Clamping Improve KCNH2 -LQTS Variant Classification and Cardiac Event Risk Stratification

Assessment and Support? AI,R – A Pilot Project on Support Systems for Innovation in Automation Industry

The Brain-Heart Connection in Sympathetically Triggered Inherited Arrhythmia Syndromes

Bromine number determination by coulometric flow-injection titration

Brugada Syndrome in New Zealand: The Experience of the National Cardiac Inherited Disease Group

BS-469619-003 GRANULAR VARIANT-SPECIFIC FEATURES IMPROVE KCNH2-LONG QT SYNDROME RISK STRATIFICATION

The Cardiac Inherited Disease Group's Experience of Brugada Syndrome in New Zealand

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

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

Cause-specific stillbirth and neonatal death in Sweden: a catchment area-based analysis

Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects

ChemInform Abstract: Crystal Structure of the Double Carbonate K2Ca2(CO3)3

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

A computer-based method for cause of death classification in stillbirths and neonatal deaths

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

Crystal structure of the double carbonate K2Ca2(CO3)(3)

Crystal Structure of the Double Carbonate K2Ca2(CO3)3

Differential expression profile of microRNA in yak skeletal muscle and adipose tissue during development

Dynamic composite hydrogels of gelatin methacryloyl (GelMA) with supramolecular fibers for tissue engineering applications

Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

Effet fondateur et estimation de l’âge de la mutation fondatrice dans trois pays maghrébins : à propos de 66 patients atteints du syndrome d’Allgrove

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

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

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