Literature DB >> 20100225

Genetic testing in the epilepsies--report of the ILAE Genetics Commission.

Ruth Ottman1, Shinichi Hirose, Satish Jain, Holger Lerche, Iscia Lopes-Cendes, Jeffrey L Noebels, José Serratosa, Federico Zara, Ingrid E Scheffer.   

Abstract

In this report, the International League Against Epilepsy (ILAE) Genetics Commission discusses essential issues to be considered with regard to clinical genetic testing in the epilepsies. Genetic research on the epilepsies has led to the identification of more than 20 genes with a major effect on susceptibility to idiopathic epilepsies. The most important potential clinical application of these discoveries is genetic testing: the use of genetic information, either to clarify the diagnosis in people already known or suspected to have epilepsy (diagnostic testing), or to predict onset of epilepsy in people at risk because of a family history (predictive testing). Although genetic testing has many potential benefits, it also has potential harms, and assessment of these potential benefits and harms in particular situations is complex. Moreover, many treating clinicians are unfamiliar with the types of tests available, how to access them, how to decide whether they should be offered, and what measures should be used to maximize benefit and minimize harm to their patients. Because the field is moving rapidly, with new information emerging practically every day, we present a framework for considering the clinical utility of genetic testing that can be applied to many different syndromes and clinical contexts. Given the current state of knowledge, genetic testing has high clinical utility in few clinical contexts, but in some of these it carries implications for daily clinical practice.

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Year:  2010        PMID: 20100225      PMCID: PMC2855784          DOI: 10.1111/j.1528-1167.2009.02429.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  114 in total

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3.  CLCN2 variants in idiopathic generalized epilepsy.

Authors:  Ailing Kleefuss-Lie; Waltraut Friedl; Sven Cichon; Karsten Haug; Maike Warnstedt; Alexi Alekov; Thomas Sander; Alfredo Ramirez; Barbara Poser; Snezana Maljevic; Simon Hebeisen; Christian Kubisch; Johannes Rebstock; Steve Horvath; Kerstin Hallmann; Jörn S Dullinger; Birgit Rau; Fritz Haverkamp; Stefan Beyenburg; Herbert Schulz; Dieter Janz; Bernd Giese; Gerhard Müller-Newen; Peter Propping; Christian E Elger; Christoph Fahlke; Holger Lerche
Journal:  Nat Genet       Date:  2009-09       Impact factor: 38.330

4.  A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.

Authors:  S M Zuberi; L H Eunson; A Spauschus; R De Silva; J Tolmie; N W Wood; R C McWilliam; J B Stephenson; J P Stephenson; D M Kullmann; M G Hanna
Journal:  Brain       Date:  1999-05       Impact factor: 13.501

5.  Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).

Authors:  Lisa J Strug; Tara Clarke; Theodore Chiang; Minchen Chien; Zeynep Baskurt; Weili Li; Ruslan Dorfman; Bhavna Bali; Elaine Wirrell; Steven L Kugler; David E Mandelbaum; Steven M Wolf; Patricia McGoldrick; Huntley Hardison; Edward J Novotny; Jingyue Ju; David A Greenberg; James J Russo; Deb K Pal
Journal:  Eur J Hum Genet       Date:  2009-01-28       Impact factor: 4.246

Review 6.  Epilepsy pharmacogenetics.

Authors:  Dalia Kasperaviciūte; Sanjay M Sisodiya
Journal:  Pharmacogenomics       Date:  2009-05       Impact factor: 2.533

Review 7.  Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

Authors:  Ingrid E Scheffer; Yue-Hua Zhang; Floor E Jansen; Leanne Dibbens
Journal:  Brain Dev       Date:  2009-02-08       Impact factor: 1.961

8.  Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.

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Journal:  J Med Genet       Date:  2008-10-17       Impact factor: 6.318

9.  Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy.

Authors:  Cécile Saint-Martin; Grégory Gauvain; Georgeta Teodorescu; Isabelle Gourfinkel-An; Estelle Fedirko; Yvonne G Weber; Snezana Maljevic; Jan-Peter Ernst; Jennie Garcia-Olivares; Christoph Fahlke; Rima Nabbout; Eric LeGuern; Holger Lerche; Jean Christophe Poncer; Christel Depienne
Journal:  Hum Mutat       Date:  2009-03       Impact factor: 4.878

10.  15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.

Authors:  Ingo Helbig; Heather C Mefford; Andrew J Sharp; Michel Guipponi; Marco Fichera; Andre Franke; Hiltrud Muhle; Carolien de Kovel; Carl Baker; Sarah von Spiczak; Katherine L Kron; Ines Steinich; Ailing A Kleefuss-Lie; Costin Leu; Verena Gaus; Bettina Schmitz; Karl M Klein; Philipp S Reif; Felix Rosenow; Yvonne Weber; Holger Lerche; Fritz Zimprich; Lydia Urak; Karoline Fuchs; Martha Feucht; Pierre Genton; Pierre Thomas; Frank Visscher; Gerrit-Jan de Haan; Rikke S Møller; Helle Hjalgrim; Daniela Luciano; Michael Wittig; Michael Nothnagel; Christian E Elger; Peter Nürnberg; Corrado Romano; Alain Malafosse; Bobby P C Koeleman; Dick Lindhout; Ulrich Stephani; Stefan Schreiber; Evan E Eichler; Thomas Sander
Journal:  Nat Genet       Date:  2009-01-11       Impact factor: 38.330

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  53 in total

1.  Genetic testing in epilepsy: what should you be doing?

Authors:  Ingrid E Scheffer
Journal:  Epilepsy Curr       Date:  2011-07       Impact factor: 7.500

Review 2.  Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing.

Authors:  Jodi Warman Chardon; Chandree Beaulieu; Taila Hartley; Kym M Boycott; David A Dyment
Journal:  Curr Neurol Neurosci Rep       Date:  2015-09       Impact factor: 5.081

3.  Genetics of Epilepsy in Clinical Practice.

Authors:  Samuel F Berkovic
Journal:  Epilepsy Curr       Date:  2015 Jul-Aug       Impact factor: 7.500

4.  Recurrent Nonconvulsive Status Epilepticus in a Patient with Coffin-Lowry Syndrome.

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Review 5.  Ethics and neuropsychiatric genetics: a review of major issues.

Authors:  Steven K Hoge; Paul S Appelbaum
Journal:  Int J Neuropsychopharmacol       Date:  2012-01-25       Impact factor: 5.176

Review 6.  Genetic Testing in Pediatric Epilepsy.

Authors:  Tristan T Sands; Hyunmi Choi
Journal:  Curr Neurol Neurosci Rep       Date:  2017-05       Impact factor: 5.081

Review 7.  The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.

Authors:  Davide Mei; Elena Parrini; Carla Marini; Renzo Guerrini
Journal:  Mol Diagn Ther       Date:  2017-08       Impact factor: 4.074

Review 8.  The genetics of the epilepsies.

Authors:  Christelle M El Achkar; Heather E Olson; Annapurna Poduri; Phillip L Pearl
Journal:  Curr Neurol Neurosci Rep       Date:  2015-07       Impact factor: 5.081

9.  Psychiatrists' views of the genetic bases of mental disorders and behavioral traits and their use of genetic tests.

Authors:  Robert Klitzman; Kristopher J Abbate; Wendy K Chung; Karen Marder; Ruth Ottman; Katherine Johansen Taber; Cheng-Shiun Leu; Paul S Appelbaum
Journal:  J Nerv Ment Dis       Date:  2014-07       Impact factor: 2.254

10.  Presence of epilepsy-associated variants in large exome databases.

Authors:  Natalya S Cherepanova; Elizabeth Leslie; Polly J Ferguson; Michael J Bamshad; Alexander G Bassuk
Journal:  J Neurogenet       Date:  2013-03-25       Impact factor: 1.250

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