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Tunable reflection minima of nanostructured antireflective surfaces

Applied physics letters, 2008-09, Vol.93 (13), p.133108-133108-3

2008

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Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young

Heart rhythm, 2014-04, Vol.11 (4), p.655-662

2014

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A Prospective Study of Sudden Cardiac Death among Children and Young Adults

The New England journal of medicine, 2016-06, Vol.374 (25), p.2441-2452

2016

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Improved Optimization Strategy for Irradiance Equalization in Dynamic Photovoltaic Arrays

IEEE transactions on power electronics, 2013-06, Vol.28 (6), p.2946-2956

2013

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Global microRNA profiling of the mouse ventricles during development of severe hypertrophic cardiomyopathy and heart failure

PloS one, 2012-09, Vol.7 (9), p.e44744-e44744

2012

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Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy

Annals of neurology, 2016-04, Vol.79 (4), p.522-534

2016

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Optical properties of gold and aluminium nanoparticles for silicon solar cell applications

Journal of applied physics, 2011-04, Vol.109 (8), p.084343-084343-13

2011

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Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases

Brain pathology (Zurich, Switzerland), 2011-03, Vol.21 (2), p.201-208

2011

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Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention

Epilepsia (Copenhagen), 2016-01, Vol.57 (S1), p.17-25

2016

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Genetic Basis of Sudden Unexpected Death in Epilepsy

Frontiers in neurology, 2017-07, Vol.8, p.348-348

2017

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Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease

Journal of molecular and cellular cardiology, 2012-08, Vol.53 (2), p.277-281

2012

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Recommendations for clinical interpretation of variants found in non-coding regions of the genome

Genome medicine, 2022-07, Vol.14 (1), p.73-73, Article 73

2022

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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

Genetics in medicine, 2019-03, Vol.21 (3), p.650-662

2019

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Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

Genetics in medicine, 2014-04, Vol.16 (4), p.286-293

2014

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Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome

PloS one, 2018-04, Vol.13 (4), p.e0195594-e0195594

2018

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Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review

Human pathology, 2013-09, Vol.44 (9), p.1730-1736

2013

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Acceleration and mitigation of carrier-induced degradation in p-type multi-crystalline silicon

Physica status solidi. PSS-RRL. Rapid research letters, 2016-03, Vol.10 (3), p.237-241

2016

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Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A

Blood, 2002-01, Vol.99 (1), p.168-174

2002

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Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392 + 3A > G splice-site variant

Stem cell research, 2023-09, Vol.71, p.103153-103153, Article 103153

2023

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Fabrication and characterization of n-ZnO/p-AlGaN heterojunction light-emitting diodes on 6H-SiC substrates

Applied physics letters, 2003-12, Vol.83 (23), p.4719-4721

2003

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A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

Heart rhythm, 2016-08, Vol.13 (8), p.1652-1660

2016

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Optical manifestations of planar chirality

Physical review letters, 2003-03, Vol.90 (10), p.107404-107404, Article 107404

2003

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Genetic architecture of left ventricular noncompaction in adults

Human genome variation, 2020-10, Vol.7 (1), p.33-33, Article 33

2020

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Genetic basis of familial valvular heart disease

Circulation. Cardiovascular genetics, 2012-10, Vol.5 (5), p.569

2012

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Genetic Analysis of Hyperpolarization-Activated Cyclic Nucleotide-Gated Cation Channels in Sudden Unexpected Death in Epilepsy Cases

Brain pathology (Zurich, Switzerland), 2011-11, Vol.21 (6), p.692-698

2011

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Tunable reflection minima of nanostructured antireflective surfaces

Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young

A Prospective Study of Sudden Cardiac Death among Children and Young Adults

Improved Optimization Strategy for Irradiance Equalization in Dynamic Photovoltaic Arrays

Global microRNA profiling of the mouse ventricles during development of severe hypertrophic cardiomyopathy and heart failure

Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy

Optical properties of gold and aluminium nanoparticles for silicon solar cell applications

Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases

Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention

Genetic Basis of Sudden Unexpected Death in Epilepsy

Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease

Recommendations for clinical interpretation of variants found in non-coding regions of the genome

Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy

Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment

Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome

Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review

Acceleration and mitigation of carrier-induced degradation in p-type multi-crystalline silicon

Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A

Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392 + 3A > G splice-site variant

Fabrication and characterization of n-ZnO/p-AlGaN heterojunction light-emitting diodes on 6H-SiC substrates

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

Optical manifestations of planar chirality

Genetic architecture of left ventricular noncompaction in adults

Genetic basis of familial valvular heart disease

Genetic Analysis of Hyperpolarization-Activated Cyclic Nucleotide-Gated Cation Channels in Sudden Unexpected Death in Epilepsy Cases

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