Localization of a gene for partial epilepsy to chromosome 10q (original) (raw)
References
Hauser, W.A., Annegers, J.F. & Kurland, L.T. Prevalence of epilepsy in Rochester, Minnesota, 1940–1980. Epilepsia31, 429–445 (1991). Article Google Scholar
Hauser, W.A., Annegers, J.F. & Kurland, L.T. Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935–1984. Epilepsia34, 453–468 (1993). ArticleCASPubMed Google Scholar
Leppert, M. et al. Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Nature337, 647–648 (1989). ArticleCASPubMed Google Scholar
Lewis, T.B., Leach, R.J., Ward, K., O'Connell, P. & Ryan, S.G. Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q. Am. J. hum. Genet.53, 670–675 (1993). CASPubMedPubMed Central Google Scholar
Steinlein, O. et al. Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) to human chromosome 20q13.2–q13.3. Genomics22, 493–495 (1994). ArticleCASPubMed Google Scholar
Lehesjoki, A.-E. et al. Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22. Proc. natn. Acad. Sci. U.S.A.88, 3696–3699 (1991). ArticleCAS Google Scholar
Greenberg, D.A. et al. Juvenile myoclonic epilepsy may be linked to the BF and HLA loci on human chromosome 6. Am. J. Med. Genet.31, 185–192 (1988). ArticleCASPubMed Google Scholar
Weissbecker, K.A., Durner, M., Janz, D., Scaramelli, A., Sparkes, R.S. & Spence, M.A. Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6. Am. J. Med. Genet.38, 32–86 (1991). ArticleCASPubMed Google Scholar
Durner, M., Sander, T., Greenberg, D.A., Johnson, K., Beck-Mannagetta, G. & Janz, D. Localization of idiopathic generalized epilepsy on chromosome 6p in families ascertained through juvenile myoclonic epilepsy patients. Neurology41, 1651–1655 (1991). ArticleCASPubMed Google Scholar
Whitehouse, W.P. et al. Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region. Am. J. hum. Genet.53, 652–662 (1993). CASPubMedPubMed Central Google Scholar
Commission on Classification and Terminololgy of the International League Against Epilepsy. Proposal for revised clinical and electroencephalographic classification of epileptic seizures. Epilepsia22, 489–501 (1981).
Commission on Classification and Terminology of the International League Against Epilepsy. A revised proposal for the classification of epilepsy and epileptic syndromes. Epilepsia30, 268–278 (1989).
Ottman, R., Annegers, J.F., Hauser, W.A. & Kurland, L.T. Seizure risk in offspring of parents with generalized vs. partial epilepsy. Epilepsia30, 157–161 (1989). ArticleCASPubMed Google Scholar
Heijbel, J., Blom, S. & Rasmuson, M. Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study. Epilepsia16, 285–93 (1975). ArticleCASPubMed Google Scholar
Scheffer, I.E. et al. Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder. Lancet343, 515–517 (1994). ArticleCASPubMed Google Scholar
Ottman, R. & Susser, M. Data collection strategies in genetic epidemiology: the Epilepsy Family Study of Columbia University. J. din. Epidemiol.45, 721–727 (1992). ArticleCAS Google Scholar
Lathrop, G.M. & Lalouel, J.M. Easy calculations of lod scores and genetic risks on small computers. Am. J. hum. Genet.36, 460–465 (1984). CASPubMedPubMed Central Google Scholar
Lathrop, G.M. & Lalouel, J.M. Efficient computations in multilocus linkage analysis. Am. J. hum. Genet.42, 498–505 (1988). CASPubMedPubMed Central Google Scholar
Cottingham, R.W., Jr Idury, R.M. & Schaffer, A.A. Faster sequential genetic linkage computations. Am. J. hum. Genet.53, 252–263 (1993). PubMedPubMed Central Google Scholar
Ottman, R. & Sherman, S. Genetic analysis of epilepsy in families ascertained from voluntary organizations [abstract]. Epilepsia31, 611 (1990). Article Google Scholar
Gyapay, G. et al. The 1993–94 Genethon human genetic linkage map. Nature Genet.7, 246–339 (1994). ArticleCASPubMed Google Scholar
Ottman, R., Lee, J.H., Hauser, W.A. & Risch, N. Birth cohort and familial risk of epilepsy: the effect of diminished recall in studies of lifetime prevalence. Am. J. Epidemiol. (in the press).
Weber, J.L. & May, P.E. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. hum. Genet.44, 388–396 (1989). CASPubMedPubMed Central Google Scholar