The DOI matches its Crossref record; 95 of the 95 references it cites were found in a registry or an index.
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond
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Citations
Cites
MACDONALD, M. (1993) · Cell · doi:10.1016/0092-8674(93)90585-e · Cited by 8,366
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
Spada, A. R. L., Wilson, E. M., Lubahn, D. B., Harding, A. E., & Fischbeck, K. H. (1991) · Nature · doi:10.1038/352077a0 · Cited by 2,784
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis
Schöls, L., Bauer, P., Schmidt, T., Schulte, T., & Riess, O. (2004) · The Lancet Neurology · doi:10.1016/s1474-4422(04)00737-9 · Cited by 1,058
CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS
Harding, A. E. (1983) · The Lancet · doi:10.1016/s0140-6736(83)92879-9 · Cited by 965
Repeat instability: mechanisms of dynamic mutations
Pearson, C. E., Edamura, K. N., & Cleary, J. D. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1689 · Cited by 924
Repeat instability : mechanisms of dynamic mutations
Pearson, C. E. (2005) · Medical Entomology and Zoology · Cited by 711
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
Koob, M. D., Moseley, M. L., Schut, L. J., Benzow, K. A., Bird, T. D., Day, J. W., & Ranum, L. P. W. (1999) · Nature Genetics · doi:10.1038/7710 · Cited by 638
Distinct molecular mechanisms and divergent endocytotic pathways of AMPA receptor internalization
Lin, J. W., Ju, W., Foster, K., Lee, S. H., Ahmadian, G., Wyszynski, M., Wang, Y. T., & Sheng, M. (2000) · Nature Neuroscience · doi:10.1038/81814 · Cited by 557
Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12
Holmes, S. E., O'Hearn, E. E., McInnis, M. G., Gorelick-Feldman, D. A., Kleiderlein, J. J., Callahan, C., Kwak, N. G., Ingersoll-Ashworth, R. G., Sherr, M., Sumner, A. J., et al. (1999) · Nature Genetics · doi:10.1038/70493 · Cited by 488
Durr, A., Stevanin, G., Cancel, G., Duyckaerts, C., Abbas, N., Didierjean, O., Chneiweiss, H., Benomar, A., Lyon‐Caen, O., Julien, J., et al. (1996) · Annals of Neurology · doi:10.1002/ana.410390411 · Cited by 437
Self-citation
Cited by
Klockgether, T., Mariotti, C., & Paulson, H. L. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0074-3 · Cited by 696
Brain pathology of spinocerebellar ataxias
Seidel, K., Siswanto, S., Brunt, E. R. P., den Dunnen, W., Korf, H.-W., & Rüb, U. (2012) · Acta Neuropathologica · doi:10.1007/s00401-012-1000-x · Cited by 403
Polyglutamine spinocerebellar ataxias — from genes to potential treatments
Paulson, H. L., Shakkottai, V. G., Clark, H. B., & Orr, H. T. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.92 · Cited by 373
The autosomal recessive cerebellar ataxias.
Anheim, M., Tranchant, C., & Koenig, M. (2012) · New England Journal of Medicine · doi:10.1056/nejmra1006610 · Cited by 356
Loy, C. T., Schofield, P. R., Turner, A. M., & Kwok, J. B. (2014) · The Lancet · doi:10.1016/s0140-6736(13)60630-3 · Cited by 342
Metadata
- Authors
- Durr, A.
- Venue
- The Lancet Neurology
- Publisher
- Elsevier BV
- Published
- 2010-09
- Volume
- 9
- Issue
- 9
- Pages
- 885-894
- ISSN
- 1474-4422 (ISSN-L)
- OpenAlex
- W2051186583
- Cited by
- 656
- References
- 95
- FWCI
- 19.67
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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Cite CoChat for the checks on this page, and the paper for its own findings.
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- CoChat. (2026). Citation check: Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. https://app.cochat.ai/papers/10.1016/s1474-4422(10)70183-6
- The paper
- Durr, A. (2010). Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. The Lancet Neurology. https://doi.org/10.1016/s1474-4422(10)70183-6
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
