253 related articles for article (PubMed ID: 25194493)
1. New technologies in molecular genetics: the impact on epilepsy research.
Helbig I
Prog Brain Res; 2014; 213():253-78. PubMed ID: 25194493
[TBL] [Abstract][Full Text] [Related]
2. The contribution of next generation sequencing to epilepsy genetics.
Møller RS; Dahl HA; Helbig I
Expert Rev Mol Diagn; 2015; 15(12):1531-8. PubMed ID: 26565596
[TBL] [Abstract][Full Text] [Related]
3. Microdeletion and microduplication syndromes.
Vissers LE; Stankiewicz P
Methods Mol Biol; 2012; 838():29-75. PubMed ID: 22228006
[TBL] [Abstract][Full Text] [Related]
4. Recent advances in the molecular genetics of epilepsy.
Hildebrand MS; Dahl HH; Damiano JA; Smith RJ; Scheffer IE; Berkovic SF
J Med Genet; 2013 May; 50(5):271-9. PubMed ID: 23468209
[TBL] [Abstract][Full Text] [Related]
5. Unraveling the genetics of common epilepsies: approaches, platforms, and caveats.
Petrovski S; Kwan P
Epilepsy Behav; 2013 Mar; 26(3):229-33. PubMed ID: 23103323
[TBL] [Abstract][Full Text] [Related]
6. Genetics of idiopathic epilepsies.
Nabbout R; Scheffer IE
Handb Clin Neurol; 2013; 111():567-78. PubMed ID: 23622204
[TBL] [Abstract][Full Text] [Related]
7. Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies.
Jähn JA; von Spiczak S; Muhle H; Obermeier T; Franke A; Mefford HC; Stephani U; Helbig I
Epilepsy Res; 2014 Jan; 108(1):109-16. PubMed ID: 24246141
[TBL] [Abstract][Full Text] [Related]
8. Genetic investigations of the epileptic encephalopathies: Recent advances.
Myers CT; Mefford HC
Prog Brain Res; 2016; 226():35-60. PubMed ID: 27323938
[TBL] [Abstract][Full Text] [Related]
9. Epilepsy genetics: the ongoing revolution.
Lesca G; Depienne C
Rev Neurol (Paris); 2015; 171(6-7):539-57. PubMed ID: 26003806
[TBL] [Abstract][Full Text] [Related]
10. Progress from genome-wide association studies and copy number variant studies in epilepsy.
Leu C; Coppola A; Sisodiya SM
Curr Opin Neurol; 2016 Apr; 29(2):158-67. PubMed ID: 26886358
[TBL] [Abstract][Full Text] [Related]
11. Advancing epilepsy genetics in the genomic era.
Myers CT; Mefford HC
Genome Med; 2015 Aug; 7(1):91. PubMed ID: 26302787
[TBL] [Abstract][Full Text] [Related]
12. New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies.
Magalhães PHM; Moraes HT; Athie MCP; Secolin R; Lopes-Cendes I
Epilepsy Behav; 2021 Aug; 121(Pt B):106428. PubMed ID: 31400936
[TBL] [Abstract][Full Text] [Related]
13. Epilepsy genetics revolutionizes clinical practice.
Scheffer IE
Neuropediatrics; 2014 Apr; 45(2):70-4. PubMed ID: 24615646
[TBL] [Abstract][Full Text] [Related]
14. Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.
Mulley JC; Scheffer IE; Desai T; Bayly MA; Grinton BE; Vears DF; Berkovic SF; Dibbens LM
Epilepsia; 2011 Oct; 52(10):e139-42. PubMed ID: 21777232
[TBL] [Abstract][Full Text] [Related]
15. Genetic contribution to common epilepsies.
Sisodiya SM; Mefford HC
Curr Opin Neurol; 2011 Apr; 24(2):140-5. PubMed ID: 21252662
[TBL] [Abstract][Full Text] [Related]
16. Detection of microchromosomal aberrations in refractory epilepsy: a pilot study.
McMahon JM; Scheffer IE; Nicholl JK; Waters W; Eyre H; Hinton L; Nelson P; Yu S; Dibbens LM; Berkovic SF; Mulley JC
Epileptic Disord; 2010 Sep; 12(3):192-8. PubMed ID: 20643615
[TBL] [Abstract][Full Text] [Related]
17. Molecular biology of epilepsy genes.
Williams CA; Battaglia A
Exp Neurol; 2013 Jun; 244():51-8. PubMed ID: 22178301
[TBL] [Abstract][Full Text] [Related]
18. Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.
Poot M; van der Smagt JJ; Brilstra EH; Bourgeron T
Cytogenet Genome Res; 2011; 135(3-4):228-40. PubMed ID: 22085975
[TBL] [Abstract][Full Text] [Related]
19. Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.
Hochstenbach R; Buizer-Voskamp JE; Vorstman JA; Ophoff RA
Cytogenet Genome Res; 2011; 135(3-4):174-202. PubMed ID: 22056632
[TBL] [Abstract][Full Text] [Related]
20. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
Zucca C; Redaelli F; Epifanio R; Zanotta N; Romeo A; Lodi M; Veggiotti P; Airoldi G; Panzeri C; Romaniello R; De Polo G; Bonanni P; Cardinali S; Baschirotto C; Martorell L; Borgatti R; Bresolin N; Bassi MT
Arch Neurol; 2008 Apr; 65(4):489-94. PubMed ID: 18413471
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
