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Cited by 464

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14

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St George-Hyslop, P., Haines, J., Rogaev, E., Mortilla, M., Vaula, G., Pericak-Vance, M., Foncin, J-F, Montesi, M., Bruni, A., Sorbi, S., Rainero, I., Pinessi, L., Pollen, D., Polinsky, R., Nee, L., Kennedy, J., Macciardi, F., Rogaeva, E., Liang, Y., Alexandrova, N., Lukiw, W., Schlumpf, K., Tanzi, R., Tsuda, T., Farrer, L., Cantu, J-M, Duara, R., Amaducci, L., Bergamini, L., Gusella, J., Roses, A., Crapper McLachlan, D.·1992·Nature Genetics
DOI 10.1038/ng1292-330
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Research works printed but not linked: 31

  1. Katzman, R. Alzheimer's Disease. New Engl. J. Med. 314, 964–973 (1986). · DOI · Paper page
  2. St George-Hyslop, P.H. et al. Familial Alzheimer's Disease: Progress and Problems. Neurobiol. Aging. 10, 417–425 (1989). · DOI
  3. St George-Hyslop, P.H. et al. The genetic defect causing Familial Alzheimer Disease Maps on chromosome 21. Science 235, 885–889 (1987). · DOI · Paper page
  4. St George-Hyslop, P.H. et al. Genetic Linkage studies suggest that Alzheimer's Disease is not a single homogeneous disorder. Nature. 347, 194–197 (1991). · DOI · Paper page
  5. Karlinsky, H. et al. Molecular and prospective phenotypic characterization of a pedigree with Familial Alzheimer Disease and a missense mutation in codon 717 of the B-Amyloid Precursor Protein (APP) gene. Neurology 42, 1445–1453 (1992). · DOI
  6. Murrell, J., Farlow, M., Ghetti, B. & Benson, M.D. A mutation in the amyloid precursor protein associated with hereditary Alzheimer's Disease. Science 254, 97–99 (1991). · DOI · Paper page
  7. Pericak-Vance, M.A., Bedout, J.L., Gaskell, P.C. & Roses, A.D. Linkage studies in Familial Alzheimer Disease - evidence for chromosome 19 linkage. Am. J. hum. Genet. 48, 1034–1050 (1991).
  8. Pericak-Vance, M.A., Yamoaka, L.H. & Haynes, C.S. Genetic Linkage Studies in Alzheimer's Disease Families. Exp. Neurol. 102, 271–279 (1988). · DOI · Paper page
  9. Tanzi, R.E. et al. Assessment of amyloid B protein gene mutations in a large set of familial and sporadic Alzheimer Disease cases. Am. J. hum. Genet. 51, 273–282 (1992).
  10. Wisneiwski, H.M., Currie, J.R., Barchikowska, M., Robakis, N.K. & Miller, D.L. Alzheimer's Disease, a form of cerebral amyloidosis. In Immunology and Alzheimer Disease. (eds Pouplard-Barthelaix, A., Emile, J. & Christen, Y.) 1–6 (Springer, Berlin, 1988).
  11. Gadjusek, D.C. et al. Regulation and genetic control of brain amyloid. Brain Res. 16, 83–114 (1991). · DOI
  12. Beyreuther, K. et al. Mechanisms of amyloid deposition in Alzheimer Disease. Ann. N.Y. Acad. Sci. 640, 129–139 (1991). · DOI
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  14. Joachim, C.L. & Selkoe, D.J. The seminal role of beta amyloid in the pathogenesis of Alzheimer Disease. Alzheimer Dis. Ass. Disord. 6, 7–34 (1992). · DOI · Paper page
  15. Cox, D.W., Nakamura, Y., Gedde-Dahl, T. Report of the committee on the genetic constitution of chromosome 14. Cytogenet. cell Genet. 55, 183–188 (1990). · doi:10.1159/000133010
  16. Heyman, A. et al. Alzheimer's disease: genetic aspects and associated clinical disorders. Ann. Neurol. 14, 507–515 (1983). · DOI · Paper page
  17. Wang, Z., Weber, J.L. Continuous Linkage Map of human chromosome 14 short tandem repeat polymorphisms. Genomics 13, 532–536 (1992). · doi:10.1016/0888-7543(92)90121-8
  18. Lathrop, G.M., Lalouel, J.M., Julier, C., Ott, J. Multi-locus linkage analysis in humans: detection of linkage and estimation of recombination. Am. J. hum. Genet. 37, 482–498 (1985).
  19. Schellenberg, G.D. et al. Absence of linkage of chromosome 21q21 markers to Familial Alzheimer Disease. Science 241, 1507–1510 (1988). · DOI · Paper page
  20. Schellenberg, G.D. et al. Linkage analysis of familial Alzheimer Disease using chromosome 21 markers. Am. J. hum. Genet. 48, 563–583 (1991).
  21. Haines, J.L. The genetics of Alzheimer Disease a teasing problem. Am. J. hum. Genet. 48, 1021–1025 (1991).
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  23. Hendriks, L. et al. Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β Amyloid Precursor Protein gene. Nature Genet. 1, 218–221 (1992). · DOI · Paper page
  24. Roses, A.D. et al. Locus heterogeneity in Alzheimer Disease. In Heterogeneity in Alzheimer Disease. (eds Boeller, F., Forette, F., Khachaturian, Z., Poncet, M. & Christien, Y.) (Springer, Berlin, in the press).
  25. Carter, D.A. et al. More missense in amyloid gene. Nature Genet. 2, (1992). · DOI
  26. Heston, L.L., Orr, H.T., Rich, S.S. & White, J.A. Linkage of Alzheimer Disease susceptibility locus to markers on human chromosome 21. Am. J. hum. Genet. 40, 449–453 (1991). · DOI
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  28. Hofker, M.H., Smith, S., Nakamura, Y., Teshima, I., White, R., Cox, D.W. Physical mapping of probes within 14q32, a subtelomeric region showing high recombination frequency. Genomics 6, 33–38 (1990). · doi:10.1016/0888-7543(90)90445-z
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  30. Pollwein, P., Masters, C.L. & Beyreuther, K. The expression of the amyloid precursor protein (APP) is regulated by two GC-elements in the promoter. Nucl. Acid Res. 20, 63–68 (1991). · DOI
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Metadata

Authors
St George-Hyslop, P., Haines, J., Rogaev, E., Mortilla, M., Vaula, G., Pericak-Vance, M., Foncin, J.-F., Montesi, M., Bruni, A., Sorbi, S., Rainero, I., Pinessi, L., Pollen, D., Polinsky, R., Nee, L., Kennedy, J., Macciardi, F., Rogaeva, E., Liang, Y., Alexandrova, N., Lukiw, W., Schlumpf, K., Tanzi, R., Tsuda, T., Farrer, L., Cantu, J.-M., Duara, R., Amaducci, L., Bergamini, L., Gusella, J., Roses, A., & Crapper McLachlan, D.
Venue
Nature Genetics
Publisher
Springer Science and Business Media LLC
Published
1992-12
Volume
2
Issue
4
Pages
330-334
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
DOI
10.1038/ng1292-330
OpenAlex
W2090390963
Cited by
464
References
2
FWCI
30.87
Type
journal article
Language
en
Open access
bronze
Licence
www.springer.com/tdm (tdm)

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CoChat. (2026). Citation check: Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. https://app.cochat.ai/papers/10.1038/ng1292-330
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St George-Hyslop, P., Haines, J., Rogaev, E., Mortilla, M., Vaula, G., Pericak-Vance, M., Foncin, J.-F., Montesi, M., Bruni, A., Sorbi, S., Rainero, I., Pinessi, L., Pollen, D., Polinsky, R., Nee, L., Kennedy, J., Macciardi, F., Rogaeva, E., Liang, Y., . . . Crapper McLachlan, D. (1992). Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nature Genetics. https://doi.org/10.1038/ng1292-330

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.