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Genomic biomarkers of SUDEP in brain and heart

published in: Epilepsy Behavior

date of publication: 2013-10-17

main subject: biomarker, epilepsy, heart disease, sudden death

Cites articles 150

Date

Title

Authors

2013-03-25

Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation

Antonio Oliva, Oscar Campuzano, Federico Zara, Carlo A Tassinari, Ramon Brugada, Sara Partemi, Vincenzo L Pascali, Pasquale Striano, Monica Coll Vidal
2013-01-01

Tau loss attenuates neuronal network hyperexcitability in mouse and Drosophila genetic models of epilepsy

Jeffrey L. Noebels, Steven G. Younkin, Linda H Younkin
2013-01

BioGPS and MyGene.info: organizing online, gene-centric information

Andrew I. Su, Chunlei Wu
2013-01-23

Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy

Sarah E Heron, Leanne Dibbens
2013-01-23

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP

Angelo Labate, Francesca Cavalcanti, Umberto Aguglia, Antonio Gambardella
2012-09-04

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Albena Jordanova, Peter De Jonghe, Franz Rüschendorf, Tobias Balschun, Christian Gieger, Ulrich Stephani, Hiltrud Muhle, Dorothée Kasteleijn-Nolst Trenité, Felix Rosenow, Dick Lindhout, Verena Gaus, Rainer Surges, Peter Nürnberg, Heinz Erich Wichmann, Holger Lerche, Pasquale Striano, Antonio Gambardella, Anna-Elina Lehesjoki, Sarah von Spiczak, Ann-Kathrin Ruppert, Martha Feucht, Fritz Zimprich, Carla Marini, David Ellinghaus, Claudia Kapser, Arvid Suls, Susannah T Bellows, Karen Oliver, Michael Steffens, Gerrit-Jan de Haan, Ingrid Scheffer, Wolfram S. Kunz, Federico Zara, Paolo Tinuper, Samuel Berkovic, Rikke S Møller, Andre Franke, Carolien G de Kovel, Christian E Elger, Thomas F Wienker, Mohammad Reza Toliat, EPICURE Consortium, EMINet Consortium, Bernhard Steinhoff, Michel Guipponi, Alain Malafosse, Christoph J Schankin, Bobby Koeleman, Leanne Dibbens, Saul A Mullen, Angela Robbiano, Dieter Janz, Ailing A Kleefuss-Lie, Stéphanie Baulac, Anne Hempelmann, Rima Nabbout, José M Serratosa, Philipp Reif
2012-07-01

Advances in epilepsy genetics and genomics

Jennifer A. Kearney
2012-08-14

Epilepsy is a risk factor for sudden cardiac arrest in the general population

Roland D Thijs, Ley Sander
2012-08-20

Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome
2012-04-19

KCNH2 gene mutation: a potential link between epilepsy and long QT-2 syndrome

Antonio Lopez Farre
2012-03-09

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP

Evan E. Eichler
2012-01-01

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

Jozef Gécz, Hadassa Goldberg-Stern, Sarah E Heron, Eric Herlenius, Ingrid Scheffer, Samuel Berkovic, Amos D. Korczyn, Sameer M Zuberi, Lynette Sadleir, Leanne Dibbens
2012-02

Unifying the definitions of sudden unexpected death in epilepsy

Torbjörn Tomson
2012-03-19

Voltage-gated potassium channels and the diversity of electrical signalling
2012-10-22

Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice.

Jernej Ule
2012-10-13

QT and P wave dispersion and heart rate variability in patients with Dravet syndrome
2012-05-21

Targeted next generation sequencing as a diagnostic tool in epileptic disorders
2012-05-28

Transcompartmental reversal of single fibre hyperexcitability in juxtaparanodal Kv1.1-deficient vagus nerve axons by activation of nodal KCNQ channels

Matthew J Kole, Jeffrey L. Noebels
2011-12-15

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions

Anne M. Bowcock, Patrice Roll, Elisha Roberson, Kailash Phatechand Bhatia, Steven Frucht, Gabrielle Rudolf, Nicholas W. Wood, Susan Bressman, Kathryn J Swoboda, Michael Hanna
2011-12

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia
2011-09-24

A null mutation of the neuronal sodium channel NaV1.6 disrupts action potential propagation and excitation-contraction coupling in the mouse heart

David S. Auerbach, Philip Furspan, Kuljeet Kaur, José Jalife, Todd J Herron, Sami F Noujaim, Michelle L Milstein
2011-07-01

Genetic testing in epilepsy: what should you be doing?

Ingrid Scheffer
2011-07-11

Genomic biomarkers in predictive medicine: an interim analysis
2011-04-30

Altered ryanodine receptor expression in mild cognitive impairment and Alzheimer's disease

David A Bennett, Michelle L. Hastings
2011-04-01

Dravet syndrome: the long-term outcome
2011-01-01

The serotonin axis: Shared mechanisms in seizures, depression, and SUDEP

George B Richerson, Gordon F Buchanan
2011-06-01

Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy

John McPherson, Donna Muzny, Caleb F Davis, Jeffrey L. Noebels, David A. Wheeler, Richard A Gibbs, Margaret B Morgan, Lora Lewis
2011-12-22

Sudden unexpected death in epilepsy: people with nocturnal seizures may be at highest risk.

Ley Sander, Roland D Thijs
2011-11-01

Recessive loss-of-function mutation in the pacemaker HCN2 channel causing increased neuronal excitability in a patient with idiopathic generalized epilepsy

Andrea Barbuti, Annalisa Bucchi, Benedetta Terragni, Mirko Baruscotti
2011-04-01

Electrical and autonomic cardiac function in patients with Dravet syndrome.
2011-08-16

Genetic analysis of hyperpolarization-activated cyclic nucleotide-gated cation channels in sudden unexpected death in epilepsy cases

Johan Duflou, Richard D Bagnall, Christopher Semsarian
2010-05-01

Molecular identity of dendritic voltage-gated sodium channels

Article - wd:Q37707209

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