The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Genetic prion disease: the EUROCJD experience
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Citations
Cites
Neurodegenerative Diseases and Prions
Prusiner, S. B. (2001) · New England Journal of Medicine · doi:10.1056/nejm200105173442006 · Cited by 772
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Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt–Jakob disease
Zerr, I., Pocchiari, M., Collins, S., Brandel, J. P., de Pedro Cuesta, J., Knight, R. S. G., Bernheimer, H., Cardone, F., Delasnerie-Lauprêtre, N., Cuadrado Corrales, N., et al. (2000) · Neurology · doi:10.1212/wnl.55.6.811 · Cited by 481
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Self-citationMortality from Creutzfeldt–Jakob disease and related disorders in Europe, Australia, and Canada
Ladogana, A., Puopolo, M., Croes, E. A., Budka, H., Jarius, C., Collins, S., Klug, G. M., Sutcliffe, T., Giulivi, A., Alperovitch, A., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000160117.56690.b2 · Cited by 387
Self-citationINSERTION IN PRION PROTEIN GENE IN FAMILIAL CREUTZFELDT-IAKOB DISEASE
Owen, F., Lofthouse, R., Crow, T. J., Baker, H. F., Poulter, M., Collinge, J., Risby, D., Ridley, R. M., Hsiao, K., & Prusiner, S. B. (1989) · The Lancet · doi:10.1016/s0140-6736(89)91713-3 · Cited by 305
Pocchiari, M. (2004) · Brain · doi:10.1093/brain/awh249 · Cited by 302
Self-citationMutations of the Prion Protein Gene
Kovács, G. G., Trabattoni, G., Hainfellner, J. A., Ironside, J. W., Knight, R. S. G., & Budka, H. (2002) · Journal of Neurology · doi:10.1007/s00415-002-0896-9 · Cited by 259
Self-citation
Research works printed but not linked: 6
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- Mayer V, Orolin D, Mitrova E (1977) Cluster of Creutzfeldt–Jakob disease and presenile dementia. Lancet 2:256 · doi:10.1016/s0140-6736(77)92881-1
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- Sasaki K, Doh-Ura K, Furuta A, Nakashima S, Morisada Y, Tateishi J, Iwaki T (2003) Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann–Straussler–Scheinker disease. Acta Neuropathol 106:92–96 · doi:10.1007/s00401-003-0697-y
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Cited by
Schulz-Schaeffer, W. J. (2010) · Acta Neuropathologica · doi:10.1007/s00401-010-0711-0 · Cited by 627
Quantifying prion disease penetrance using large population control cohorts
Minikel, E. V., Vallabh, S. M., Lek, M., Estrada, K., Samocha, K. E., Sathirapongsasuti, J. F., McLean, C. Y., Tung, J. Y., Yu, L. P. C., Gambetti, P., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad5169 · Cited by 442
Self-citationEEG in Creutzfeldt–Jakob disease
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YKL-40 in the brain and cerebrospinal fluid of neurodegenerative dementias
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Metadata
- Authors
- Kovács, G. G., Puopolo, M., Ladogana, A., Pocchiari, M., Budka, H., van Duijn, C., Collins, S. J., Boyd, A., Giulivi, A., Coulthart, M., Delasnerie-Laupretre, N., Brandel, J. P., Zerr, I., Kretzschmar, H. A., de Pedro-Cuesta, J., Calero-Lara, M., Glatzel, M., Aguzzi, A., Bishop, M., Knight, R., Belay, G., Will, R., & Mitrova, E.
- Venue
- Human Genetics
- Published
- 2005-09-27
- Volume
- 118
- Issue
- 2
- Pages
- 166-174
- ISSN
- 0018-7348 (ISSN-L)
- 0340-6717
- 1432-1203
- OpenAlex
- W2038096175
- Cited by
- 450
- References
- 32
- FWCI
- 5.65
- Type
- journal article
- Language
- en
- Open access
- green
- Licence
- www.springer.com/tdm (tdm)
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- CoChat. (2026). Citation check: Genetic prion disease: the EUROCJD experience. https://app.cochat.ai/papers/10.1007/s00439-005-0020-1
- The paper
- Kovács, G. G., Puopolo, M., Ladogana, A., Pocchiari, M., Budka, H., van Duijn, C., Collins, S. J., Boyd, A., Giulivi, A., Coulthart, M., Delasnerie-Laupretre, N., Brandel, J. P., Zerr, I., Kretzschmar, H. A., de Pedro-Cuesta, J., Calero-Lara, M., Glatzel, M., Aguzzi, A., Bishop, M., . . . Mitrova, E. (2005). Genetic prion disease: the EUROCJD experience. Human Genetics. https://doi.org/10.1007/s00439-005-0020-1
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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.
