Scn2a deletion improves survival and brain–heart dynamics in the Kcna1-null mouse model of sudden unexpected death in epilepsy (SUDEP)

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

(2016) Richard D. Bagnall et al.   ANNALS OF NEUROLOGY

Differential impact of type-1 and type-2 diabetes on control of heart rate in mice

(2016) Catherine L. Stables et al.   AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL

Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention

(2016) Alica M. Goldman et al.   EPILEPSIA

Ketogenic diet treatment increases longevity inKcna1-null mice, a model of sudden unexpected death in epilepsy

(2016) Kristina A. Simeone et al.   EPILEPSIA

Uncovering brain–heart information through advanced signal and image processing

(2016) Gaetano Valenza et al.   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES

Orexin Receptor Antagonism Improves Sleep and Reduces Seizures in Kcna1-null Mice

(2016) Harrison M. Roundtree et al.   SLEEP

Orexin Receptor Antagonism Improves Sleep and Reduces Seizures in Kcna1-null Mice

(2016) Harrison M. Roundtree et al.   SLEEP

Spontaneous seizures in Kcna1 -null mice lacking voltage-gated Kv1.1 channels activate Fos expression in select limbic circuits

(2015) Nicole M. Gautier et al.   JOURNAL OF NEUROCHEMISTRY

Pathway-driven discovery of epilepsy genes

(2015) Jeffrey Noebels   NATURE NEUROSCIENCE

SCN2Aencephalopathy

(2015) Katherine B. Howell et al.   NEUROLOGY

Spreading depolarization in the brainstem mediates sudden cardiorespiratory arrest in mouse SUDEP models

(2015) Isamu Aiba et al.   Science Translational Medicine

New insights into the pathogenesis and therapeutics of episodic ataxia type 1

(2015) Maria Cristina D’Adamo et al.   Frontiers in Cellular Neuroscience

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

(2015) Costin Leu et al.   EBioMedicine

Sodium Channels, Inherited Epilepsy, and Antiepileptic Drugs

(2014) William A. Catterall   Annual Review of Pharmacology and Toxicology

Sudden unexpected death in epilepsy: Assessing the public health burden

(2014) David J. Thurman et al.   EPILEPSIA

The Kv1.1 null mouse, a model of sudden unexpected death in epilepsy (SUDEP)

(2014) Brian M. Moore et al.   EPILEPSIA

Voltage-gated sodium channels

(2013) Mena Abdelsayed et al.   Channels

Kubios HRV – Heart rate variability analysis software

(2013) Mika P. Tarvainen et al.   COMPUTER METHODS AND PROGRAMS IN BIOMEDICINE

High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile

(2013) Tara L. Klassen et al.   EPILEPSIA

Genomic biomarkers of SUDEP in brain and heart

(2013) Edward Glasscock   EPILEPSY & BEHAVIOR

Localization of sodium channel subtypes in mouse ventricular myocytes using quantitative immunocytochemistry

(2013) Ruth E. Westenbroek et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Tau Loss Attenuates Neuronal Network Hyperexcitability in Mouse and Drosophila Genetic Models of Epilepsy

(2013) J. K. Holth et al.   JOURNAL OF NEUROSCIENCE

Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective study

(2013) Philippe Ryvlin et al.   LANCET NEUROLOGY

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

(2013) Gemma L Carvill et al.   NATURE GENETICS

Spectral and spatial shifts of post-ictal slow waves in temporal lobe seizures

(2012) Lin Yang et al.   BRAIN

Kv1.1 and Kv1.2: Similar channels, different seizure models

(2012) Carol A. Robbins et al.   EPILEPSIA

Sodium channels and the neurobiology of epilepsy

(2012) Megan Oliva et al.   EPILEPSIA

Voltage-gated potassium channels and the diversity of electrical signalling

(2012) Lily Yeh Jan et al.   JOURNAL OF PHYSIOLOGY-LONDON

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

(2012) Anita Rauch et al.   LANCET

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

(2012) Stephan J. Sanders et al.   NATURE

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

(2012) Joep de Ligt et al.   NEW ENGLAND JOURNAL OF MEDICINE

Exome Sequencing of Ion Channel Genes Reveals Complex Profiles Confounding Personal Risk Assessment in Epilepsy

(2011) Tara Klassen et al.   CELL

Genetic modifiers of neurological disease

(2011) Jennifer A Kearney   CURRENT OPINION IN GENETICS & DEVELOPMENT

Unifying the definitions of sudden unexpected death in epilepsy

(2011) Lina Nashef et al.   EPILEPSIA

Improving early seizure detection

(2011) Christophe C. Jouny et al.   EPILEPSY & BEHAVIOR

The Many Faces of Tau

(2011) Meaghan Morris et al.   NEURON

Seizure Prediction and its Applications

(2011) Leon D. Iasemidis   NEUROSURGERY CLINICS OF NORTH AMERICA

Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy

(2010) Yunxiang Liao et al.   BRAIN

Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Nav1.1

(2010) Wei-Ping Liao et al.   EPILEPSIA

Kv1.1 Potassium Channel Deficiency Reveals Brain-Driven Cardiac Dysfunction as a Candidate Mechanism for Sudden Unexplained Death in Epilepsy

(2010) E. Glasscock et al.   JOURNAL OF NEUROSCIENCE

Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins

(2010) T. D. Graves et al.   NEUROLOGY

Ketogenic diet treatment abolishes seizure periodicity and improves diurnal rhythmicity in epilepticKcna1-null mice

(2009) Kristina A. Fenoglio-Simeone et al.   EPILEPSIA

Information Flow and Application to Epileptogenic Focus Localization From Intracranial EEG

(2009) S. Sabesan et al.   IEEE TRANSACTIONS ON NEURAL SYSTEMS AND REHABILITATION ENGINEERING

A novelKCNA1mutation associated with global delay and persistent cerebellar dysfunction

(2009) Michelle K. Demos et al.   MOVEMENT DISORDERS

Impaired NaV1.2 function and reduced cell surface expression in benign familial neonatal-infantile seizures

(2008) Sunita N. Misra et al.   EPILEPSIA

Molecular genetics of sudden cardiac death

(2008) María Sol Rodríguez-Calvo et al.   FORENSIC SCIENCE INTERNATIONAL