Navigating the channels and beyond: unravelling the genetics of the epilepsies
Top Cited Papers
- 1 March 2008
- journal article
- review article
- Published by Elsevier in The Lancet Neurology
- Vol. 7 (3) , 231-245
- https://doi.org/10.1016/s1474-4422(08)70039-5
Abstract
No abstract availableKeywords
This publication has 176 references indexed in Scilit:
- Genome-wide association study identifies novel breast cancer susceptibility lociNature, 2007
- A genome-wide association study identifies novel risk loci for type 2 diabetesNature, 2007
- Global variation in copy number in the human genomeNature, 2006
- CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degenerationNature Genetics, 2006
- Infantile seizures and other epileptic phenotypes in a Chinese family with a missense mutation of KCNQ2European Journal of Pediatrics, 2006
- Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of InfancyBiochemical and Biophysical Research Communications, 2006
- Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsyBrain & Development, 2006
- A haplotype map of the human genomeNature, 2005
- Benign familial infantile seizuresBrain & Development, 2005
- Factors Prognostic of Unprovoked Seizures after Febrile ConvulsionsNew England Journal of Medicine, 1987