Genetic localization of the familial adult myoclonic epilepsy ( FAME ) gene to chromosome 8q24

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1998 • 1,191 citations

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1995 • 1,112 citations

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

1998 • 1,003 citations

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1998 • 937 citations

Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)

1996 • 542 citations

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

1998 • 475 citations

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

1988 • 317 citations

Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q

1997 • 256 citations

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

1999 • 220 citations

Classification of progressive myoclonus epilepsies and related disorders

1990 • 153 citations

A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q.

1996 • 123 citations

Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy

1996 • 58 citations

Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region.

1996 • 58 citations