Skip to main content
CMAJ : Canadian Medical Association Journal logoLink to CMAJ : Canadian Medical Association Journal
. 1993 Nov 1;149(9):1285–1289.

Finding the genes of neurologic and psychiatric illnesses: variations on a theme.

A Robinson
PMCID: PMC1485703  PMID: 8221484

Full text

PDF
1285

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abdalla J. A., Casley W. L., Cousin H. K., Hudson A. J., Murphy E. G., Cornélis F. C., Hashimoto L., Ebers G. C. Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35. Am J Hum Genet. 1992 Sep;51(3):579–584. [PMC free article] [PubMed] [Google Scholar]
  2. Bassett A. S. Linkage analysis of schizophrenia: challenges and promise. Soc Biol. 1991 Fall-Winter;38(3-4):189–196. doi: 10.1080/19485565.1991.9988787. [DOI] [PubMed] [Google Scholar]
  3. Ebers G. C., Bulman D. E., Sadovnick A. D., Paty D. W., Warren S., Hader W., Murray T. J., Seland T. P., Duquette P., Grey T. A population-based study of multiple sclerosis in twins. N Engl J Med. 1986 Dec 25;315(26):1638–1642. doi: 10.1056/NEJM198612253152603. [DOI] [PubMed] [Google Scholar]
  4. Ebers G. C., George A. L., Barchi R. L., Ting-Passador S. S., Kallen R. G., Lathrop G. M., Beckmann J. S., Hahn A. F., Brown W. F., Campbell R. D. Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene. Ann Neurol. 1991 Dec;30(6):810–816. doi: 10.1002/ana.410300610. [DOI] [PubMed] [Google Scholar]
  5. George A. L., Jr, Crackower M. A., Abdalla J. A., Hudson A. J., Ebers G. C. Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita). Nat Genet. 1993 Apr;3(4):305–310. doi: 10.1038/ng0493-305. [DOI] [PubMed] [Google Scholar]
  6. Hayden M. R. On planting alfalfa and growing orchids: the cloning of the gene causing Huntington disease. Clin Genet. 1993 May;43(5):217–222. doi: 10.1111/j.1399-0004.1993.tb03806.x. [DOI] [PubMed] [Google Scholar]
  7. Karlinsky H., Vaula G., Haines J. L., Ridgley J., Bergeron C., Mortilla M., Tupler R. G., Percy M. E., Robitaille Y., Noldy N. E. Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene. Neurology. 1992 Aug;42(8):1445–1453. doi: 10.1212/wnl.42.8.1445. [DOI] [PubMed] [Google Scholar]
  8. Rommens J. M., Lin B., Hutchinson G. B., Andrew S. E., Goldberg Y. P., Glaves M. L., Graham R., Lai V., McArthur J., Nasir J. A transcription map of the region containing the Huntington disease gene. Hum Mol Genet. 1993 Jul;2(7):901–907. doi: 10.1093/hmg/2.7.901. [DOI] [PubMed] [Google Scholar]
  9. Saunders A. M., Strittmatter W. J., Schmechel D., George-Hyslop P. H., Pericak-Vance M. A., Joo S. H., Rosi B. L., Gusella J. F., Crapper-MacLachlan D. R., Alberts M. J. Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease. Neurology. 1993 Aug;43(8):1467–1472. doi: 10.1212/wnl.43.8.1467. [DOI] [PubMed] [Google Scholar]
  10. St George-Hyslop P. H., Haines J. L., Farrer L. A., Polinsky R., Van Broeckhoven C., Goate A., McLachlan D. R., Orr H., Bruni A. C., Sorbi S. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 1990 Sep 13;347(6289):194–197. doi: 10.1038/347194a0. [DOI] [PubMed] [Google Scholar]
  11. St George-Hyslop P., Haines J., Rogaev E., Mortilla M., Vaula G., Pericak-Vance M., Foncin J. F., Montesi M., Bruni A., Sorbi S. Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nat Genet. 1992 Dec;2(4):330–334. doi: 10.1038/ng1292-330. [DOI] [PubMed] [Google Scholar]

Articles from CMAJ: Canadian Medical Association Journal are provided here courtesy of Canadian Medical Association

RESOURCES