No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy

[1]  Daniel Rabinowitz,et al.  A Unified Approach to Adjusting Association Tests for Population Admixture with Arbitrary Pedigree Structure and Arbitrary Missing Marker Information , 2000, Human Heredity.

[2]  S Shinnar,et al.  Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy. , 2000, American journal of human genetics.

[3]  D. Clayton,et al.  A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. , 1999, American journal of human genetics.

[4]  K. Flanigan,et al.  Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24 , 1999, Neurology.

[5]  D. A. Brown,et al.  Two Types of K+ Channel Subunit, Erg1 and KCNQ2/3, Contribute to the M-Like Current in a Mammalian Neuronal Cell , 1999, The Journal of Neuroscience.

[6]  C. Marescaux,et al.  [Benign familial neonatal convulsions: a model of idiopathic epilepsy]. , 1999, Revue neurologique.

[7]  J. McNamara Emerging insights into the genesis of epilepsy , 1999, Nature.

[8]  L. Kruglyak Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.

[9]  Martin Schoell,et al.  Diamondoids and oil are not forever , 1999, Nature.

[10]  S. Moshé,et al.  Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity. , 1999, American journal of human genetics.

[11]  O. Steinlein,et al.  The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy. , 1999, Neuroreport.

[12]  M Knapp,et al.  The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/ disequilibrium test. , 1999, American journal of human genetics.

[13]  P. Coumel,et al.  Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome. , 1999, Circulation research.

[14]  C. Kubisch,et al.  Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy , 1998, Nature.

[15]  B S Brown,et al.  KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel. , 1998, Science.

[16]  M. T. Medina,et al.  Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24. , 1998, American journal of human genetics.

[17]  S. Berkovic,et al.  Epilepsies in twins: Genetics of the major epilepsy syndromes , 1998, Annals of neurology.

[18]  Hao Wang,et al.  Deletion of the KV1.1 Potassium Channel Causes Epilepsy in Mice , 1998, Neuron.

[19]  J. Doyle,et al.  Ataxia, arrhythmia and ion-channel gene defects. , 1998, Trends in genetics : TIG.

[20]  S. Berkovic,et al.  A potassium channel mutation in neonatal human epilepsy. , 1998, Science.

[21]  D. Curtis,et al.  Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. , 1997, Human molecular genetics.

[22]  L. Jan,et al.  Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[23]  S. Berkovic,et al.  Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21. , 1996, Journal of medical genetics.

[24]  N. Risch,et al.  A comparison of linkage disequilibrium measures for fine-scale mapping. , 1995, Genomics.

[25]  P. Patel,et al.  Mapping of genes predisposing to idiopathic generalized epilepsy. , 1995, Human molecular genetics.

[26]  M. Owen,et al.  Association and linkage: complementary strategies for complex disorders. , 1993, Journal of medical genetics.

[27]  W. Ewens,et al.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). , 1993, American journal of human genetics.

[28]  Jorge Eslava‐Cobos,et al.  Experience with the International League Against Epilepsy Proposals for Classification of Epileptic Seizures and the Epilepsies and Epileptic Syndromes in a Pediatric Outpatient Epilepsy Clinic , 1989, Epilepsia.

[29]  Shirley A. Miller,et al.  A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.

[30]  M. Owen,et al.  Psychiatric genetics: back to the future , 2000, Molecular Psychiatry.

[31]  M. T. Medina,et al.  Mapping and positional cloning of common idiopathic generalized epilepsies: juvenile myoclonus epilepsy and childhood absence epilepsy. , 1999, Advances in neurology.

[32]  Robin J. Leach,et al.  A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family , 1998, Nature Genetics.

[33]  L. Jan,et al.  Epilepsy genes: excitement traced to potassium channels , 1998, Nature Genetics.