The DOI matches its Crossref record; 31 of the 32 references it cites were found in a registry or an index.
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
Abstract
Objective To analyze the association of polymorphisms in the tau gene with pathologically confirmed corticobasal degeneration (CBD). Background The authors previously described an extended tau haplotype (H1) that covers the human tau gene and is associated with the development of progressive supranuclear palsy (PSP). The authors now extend this analysis to CBD, a neurodegenerative condition with clinical and neuropathologic similarities to PSP. Like PSP, CBD is associated with accumulation of aggregates containing the 4-repeat isoforms of tau. Because of difficulty in diagnosis of CBD, the authors only analyzed cases with pathologically confirmed CBD. Methods The authors collected 57 unrelated, neuropathologically confirmed cases of CBD. Tau sequencing in these cases failed to show the presence of pathogenic mutations. Polymorphisms that spanned the tau gene were analyzed in all CBD cases and controls. Results Analyzing tau polymorphisms in CBD cases showed that the frequency of H1 and H1/H1 was significantly increased when analyzing all cases and when separating by country of origin. H1 frequency in all CBD cases was 0.921, compared with a control frequency of 0.766 (X(2) = 9.1, p = 0.00255 [1df], OR 3.56 [8.43 > CI 95% > 1.53]). The H1/H1 frequency was also significantly higher at 0.842 compared with 0.596 in age-matched controls (X(2) = 17.42, p = 0.00016, 2df), OR 3.61 [7.05 > CI 95% > 1.85]). Conclusions The CBD tau association described here suggests that PSP and CBD sh…
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“An association of CBD with the H1 haplotype was first reported in a series of 18 cases (16 corticobasal syndrome patients and two autopsy-confirmed CBD cases)15 and subsequently confirmed in a larger autopsy series of 57 cases16.”
From Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy (2015) · cites this paper as [16]
Citations
Cites
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
Hutton, M., Lendon, C. L., Rizzu, P., Baker, M., Froelich, S., Houlden, H., Pickering-Brown, S., Chakraverty, S., Isaacs, A., Grover, A., et al. (1998) · Nature · doi:10.1038/31508 · Cited by 3,498
Self-citationLitvan, I., Agid, Y., Calne, D., Campbell, G., Dubois, B., Duvoisin, R. C., Goetz, C. G., Golbe, L. I., Grafman, J., Growdon, J. H., et al. (1996) · Neurology · doi:10.1212/wnl.47.1.1 · Cited by 2,538
Self-citationGoedert, M., Spillantini, M. G., Jakes, R., Rutherford, D., & Crowther, R. A. (1989) · Neuron · doi:10.1016/0896-6273(89)90210-9 · Cited by 2,492
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
Spillantini, M. G., Murrell, J. R., Goedert, M., Farlow, M. R., Klug, A., & Ghetti, B. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.13.7737 · Cited by 1,474
Tau is a candidate gene for chromosome 17 frontotemporal dementia
Poorkaj, P., Bird, T. D., Wijsman, E., Nemens, E., Garruto, R. M., Anderson, L., Andreadis, A., Wiederholt, W. C., Raskind, M., & Schellenberg, G. D. (1998) · Annals of Neurology · doi:10.1002/ana.410430617 · Cited by 1,374
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.
Hong, M., Zhukareva, V., Vogelsberg-Ragaglia, V., Wszolek, Z., Reed, L., Miller, B., Geschwind, D., Bird, T., McKeel, D., Goate, A., et al. (1998) · Science · doi:10.1126/science.282.5395.1914 · Cited by 1,024
Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy
Baker, M., Litvan, I., Houlden, H., Adamson, J., Dickson, D., Perez-Tur, J., Hardy, J., Lynch, T., Bigio, E., & Hutton, M. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.4.711 · Cited by 781
Self-citationTau protein pathology in neurodegenerative diseases
Spillantini, M. G., & Goedert, M. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01337-x · Cited by 683
Structure and novel exons of the human .tau. gene
Andreadis, A., Brown, W. M., & Kosik, K. S. (1992) · Biochemistry · doi:10.1021/bi00158a027 · Cited by 659
Corticodentatonigral Degeneration With Neuronal Achromasia
Rebeiz, J. J., Kolodny, E. H., & Richardson, E. P. (1968) · Archives of Neurology · doi:10.1001/archneur.1968.00470310034003 · Cited by 627
Cited by
Sorted by citations
Items 301–400 of 409
Caribbean parkinsonism and other atypical Parkinsonian disorders
TOLOSA, E. S., Calandrella, D., & Gallardo, M. (2004) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2004.02.003 · Cited by 5
Biomarkers to Identify the Pathological Basis for Frontotemporal Lobar Degeneration
Grossman, M. (2011) · Journal of Molecular Neuroscience · doi:10.1007/s12031-011-9597-0 · Cited by 5
Tau gene promoter rs242557 and allele-specific protein binding
Anaya, F., Lees, A. J., & de Silva, R. (2011) · Translational Neuroscience · doi:10.2478/s13380-011-0021-6 · Cited by 5
Self-citationGenetics of Frontotemporal Dementia
Heetveld, S., Rizzu, P., & Heutink, P. (2015) · Springer eBooks · doi:10.1007/978-3-319-17223-1_5 · Cited by 5
Naasan, G., Shany‐Ur, T., Sidhu, M., Barton, C., Ketelle, R., Shdo, S. M., Kramer, J. H., Miller, B. L., & Seeley, W. W. (2019) · Neurocase · doi:10.1080/13554794.2019.1604973 · Cited by 5
Wauters, E., Sleegers, K., Cruts, M., & Broeckhoven, C. V. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805120-7.00009-9 · Cited by 6
Progressive Supranuclear Palsy and Corticobasal Degeneration
Litvan, I. (2005) · Elsevier eBooks · doi:10.1016/b978-012088382-0/50046-3 · Cited by 5
Self-citationMitsumori, R., Ozaki, K., Saito, Y., Shigemizu, D., Iwata, A., Murayama, S., Akishita, M., Arai, T., Niida, S., & Toba, K. (2025) · Journal of Human Genetics · doi:10.1038/s10038-025-01438-7 · Cited by 4
Frontotemporal Lobar Degeneration: New Understanding Brings New Approaches
Tartaglia, M. C. (2012) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2011.11.009 · Cited by 4
Han, X., Zhang, Y., Petrosky, J. N., Bald, S., Sherva, R., Labadorf, A. T., Cherry, J. D., Chung, J., Farrell, K. W., Abdolmohammadi, B., et al. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102084 · Cited by 4
Atypical Parkinsonian Disorders
Olfati, N., Akhoundi, F. H., & Litvan, I. (2025) · Neurologic Clinics · doi:10.1016/j.ncl.2024.12.006 · Cited by 4
Self-citationZecca, C., Tortelli, R., Carrera, P., Dell’Abate, M. T., Logroscino, G., & Ferrari, M. (2022) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2022.2150833 · Cited by 6
Rini, J. F., Asken, B. M., Geier, E. G., Rankin, K. P., Kramer, J. H., Boxer, A. L., Miller, B. L., Yokoyama, J. S., & Spina, S. (2021) · Neurocase · doi:10.1080/13554794.2021.1879869 · Cited by 4
Armstrong, M. J., & Lang, A. E. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511920936.006 · Cited by 4
Self-citationTauopathies: A Distinct Class of Neurodegenerative Diseases
Ozansoy, M., & Başak, A. N. (2007) · Balkan Journal of Medical Genetics · doi:10.2478/v10034-008-0001-5 · Cited by 4
Role of tau in Alzheimer's dementia and other neurodegenerative diseases
Quadros, A., Weeks, O. I., & Ait‐Ghezala, G. (2007) · Journal of Applied Biomedicine · doi:10.32725/jab.2007.001 · Cited by 4
Mathematical topology and geometry-based classification of tauopathies
Sugiyama, M., Kosik, K. S., & Panagiotou, E. (2024) · Scientific Reports · doi:10.1038/s41598-024-58221-5 · Cited by 4
Bansal, A., Salaria, M., & Singh, T. R. (2018) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/978-1-5225-5282-6.ch010 · Cited by 3
Parkinsonism-Plus Syndromes and Secondary Parkinsonian Disorders
Fahn, S., Jankovic, J. J., Hallett, M., & Jenner, P. G. (2007) · Elsevier eBooks · doi:10.1016/b978-0-443-07941-2.50013-9 · Cited by 3
Parkinsonism and akinetic–rigid disorders
Ellison, D., Love, S., Chimelli, L. M. C., Harding, B. N., Lowe, J. S., Vinters, H. V., Brandner, S., & Yong, W. H. (2013) · Elsevier eBooks · doi:10.1016/b978-0-7234-3515-0.00028-3 · Cited by 3
Progressive Supranuclear Palsy and Corticobasal Degeneration
Geser, F., Scholz, S. W., & Wenning, G. K. (2007) · Springer eBooks · doi:10.1007/978-0-387-30377-2_8 · Cited by 3
Storch, A., & Schwarz, J. (2009) · Springer eBooks · doi:10.1007/978-3-540-29676-8_418 · Cited by 3
Describing the diversity of MAPT transcripts in the parietal cortex of Pick’s disease patients
Tamvaka, N., Stuber, M. G., Gavrielatos, M., Soto‐Beasley, A. I., Heckman, M. G., Murray, M. E., Boeve, B. F., Josephs, K. A., Roemer, S. F., Graff‐Radford, N. R., et al. (2025) · npj Dementia · doi:10.1038/s44400-025-00027-x · Cited by 2
Self-citationChapter 6 Progressive Supranuclear Palsy and Corticobasal Degeneration
Lees, A. J. (2007) · Blue books of neurology · doi:10.1016/s1877-184x(09)70057-7 · Cited by 2
Self-citationAlzheimer's disease pathology in aged chimpanzees
Edler, M. K. (2016) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 2
Neuropathology and genetics of corticobasal degeneration
Hazrati, L., & Bergeron, C. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)01248-1 · Cited by 2
Self-citationBhatia, K. P., & Lang, A. E. (2005) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544873.046 · Cited by 2
Self-citationGenetics of Parkinson Disease and Related Diseases
Goldman, J. S., & Fahn, S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-410529-4.00068-1 · Cited by 2
Josephs, K. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405195-9.00053-6 · Cited by 2
Atypical parkinsonism, parkinsonism-plus syndromes, and secondary parkinsonian disorders
Fahn, S., Jankovic, J. J., & Hallett, M. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4377-2369-4.00009-3 · Cited by 2
Neurodegeneration and the Ordered Assembly of Tau
Goedert, M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811304-2.00004-3 · Cited by 3
Neuropathology of Movement Disorders
Jellinger, K. A. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00076-9 · Cited by 2
Jung, Y. L., & Josephs, K. A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00078-6 · Cited by 2
Takeda, A., & Miller, B. L. (2020) · doi:10.1093/med/9780198713005.003.0041 · Cited by 2
A 74-year-old woman with progressive right-hand tremor and inability to use her right side
KERTESZ, A. E., Fealey, R. D., Keegan, B. M., & Parisi, J. E. (2009) · Neurology · doi:10.1212/wnl.0b013e3181bd80fe · Cited by 2
Self-citationTau kinases and Parkinson's disease: Guilt by association?
Dickson, D. W., & Farrer, M. J. (2005) · Annals of Neurology · doi:10.1002/ana.20764 · Cited by 2
Self-citationParkinson disease and related disorders
Goldman, J. S., & Fahn, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813866-3.00002-3 · Cited by 2
Genetics of Alzheimer’s Disease and Related Disorders
Hardy, J. (2004) · Humana Press eBooks · doi:10.1007/978-1-59259-661-4_1 · Cited by 2
Self-citationAtypical Parkinsonian Disorders
Duyckaerts, C. J. (2005) · Humana Press eBooks · doi:10.1385/1-59259-834-x:111 · Cited by 2
Boxer, A. L. (2011) · Wiley eBooks · doi:10.1002/9781444344110.ch4 · Cited by 3
Progressive Supranuclear Palsy
Morris, H. R. (2017) · Neurodegeneration · doi:10.1002/9781118661895.ch8 · Cited by 2
Self-citationValentino, R. R., Scotton, W. J., Roemer, S. F., Lashley, T., Heckman, M. G., Shoai, M., Martínez-Carrasco, A., Tamvaka, N., Walton, R. L., Baker, M., et al. (2023) · medRxiv · doi:10.1101/2023.04.17.23288471 · Cited by 2
Self-citationGenetics of progressive supranuclear palsy
Pittman, A. M., de Silva, R., Lees, A. J., & Wood, N. W. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)01244-4 · Cited by 1
Self-citationTermsarasab, P., & Riley, D. E. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511977749.004 · Cited by 1
From Protein Tangles to Genetic Variants: The Central Role of Tau in Neurodegenerative Disease
Julia, H., & Wade‐Martins, R. (2011) · InTech eBooks · doi:10.5772/29839 · Cited by 1
Venkatesan, E., Ramasamy, B., Kalidoss, R., & Raza, A. (2016) · Muller Journal of Medical Sciences and Research · doi:10.4103/0975-9727.185021 · Cited by 1
LeDoux, M. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405195-9.00024-x · Cited by 1
Molecular Imaging and Precision Medicine in Dementia and Movement Disorders
Mallik, A. K., Drzezga, A. E., & Minoshima, S. (2016) · PET Clinics · doi:10.1016/j.cpet.2016.08.003 · Cited by 1
Majidi, M., Rajabi, A., & Ahmadi, S. (2021) · Scientific Journal of Kurdistan University of Medical Sciences · doi:10.52547/sjku.26.3.129 · Cited by 1
DeKosky, S. T., Kaufer, D., Hamilton, R. L., Wolk, D. A., & López, O. L. (2008) · Elsevier eBooks · doi:10.1016/b978-0-7506-7525-3.50108-4 · Cited by 1
Tolnay, M., & Paulus, W. (2011) · Springer eBooks · doi:10.1007/978-3-642-02324-8_9 · Cited by 1
Frontotemporal Dementia (FTD) 2011
Kertesz, A. (2011) · Acta Neuropsychologica · doi:10.5604/01.3001.0001.0773 · Cited by 3
Self-citationOverview of frontotemporal dementia and its relationship to other neurodegenerative disorders
Mcmonagle, P., & Kertesz, A. (2016) · Cambridge University Press eBooks · doi:10.1017/cbo9781316091586.005 · Cited by 2
Self-citationBonavita, V., Caltagirone, C., Mariani, C. B., Padovani, A., Scarpini, E. A., & Sorbi, S. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-1433 · Cited by 1
Phenomenology of Atypical Parkinsonism
Frucht, S. J., & Termsarasab, P. (2020) · Springer eBooks · doi:10.1007/978-3-030-36975-0_4 · Cited by 1
Genetics of Atypical Parkinsonism
Gasser, T. (2005) · Humana Press eBooks · doi:10.1385/1-59259-834-x:139 · Cited by 1
Regulation des alternativen Spleißens von Tau Exon 10 durch Phosphorylierung von Spleißfaktoren
Hartmann, A. M. (2003) · doi:10.5282/edoc.1675 · Cited by 1
Genetic Characterisation of Neurodegenerative disorders
Fung, H. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique) · Cited by 1
Therapeutic Potential of Small Interfering RNA for Brain Diseases
Lovett-Racke, A. (2009) · Springer eBooks · doi:10.1007/978-3-642-00475-9_13 · Cited by 1
TAU Mutations are not a Predominant Cause of Frontotemporal Dementia in Canadian Patients
Levchenko, А., Robitaille, Y., Strong, M. J., & Rouleau, G. A. (2004) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100003450 · Cited by 1
The Clinical Spectrum of Dementia in Movement Disorders
KERTESZ, A. E. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-326-2_17 · Cited by 1
Self-citationCorticobasal degeneration and progressive supranuclear palsy
Lee, S. E., & Miller, B. L. (2016) · Wiley eBooks · doi:10.1002/9781118797662.ch7 · Cited by 1
Homologies Between the Genetic Etiology and Pathogenesis of the Synucleinopathies and Tauopathies
Hardy, J. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-326-2_19 · Cited by 1
Self-citationNeuropathology of frontotemporal lobar degenerations
Cairns, N. J. (2006) · CRC Press eBooks · doi:10.1201/b14376-13 · Cited by 1
Higgins, J. J. (2003) · Elsevier eBooks · doi:10.1016/b978-012566652-7/50032-0
Wenning, G. K., Colosimo, C., & Riley, D. E. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511920936.002
Etiologic and diagnostic facets of Creutzfeldt-Jakob disease: The effect of genes and environment
Sánchez‐Juan, P. (2007) · RePub (Erasmus University Rotterdam)
Cognitive Impairment and the Dementias
Duara, R., Rodriguez, M. J., Loewenstein, D., Farlow, M. R., Ballard, C. G., Chui, H. C., Segal‐Gidan, F., Perry, D. C., Rosen, H. J., Henry, M. L., et al. (2014) · Wiley eBooks · doi:10.1002/9781118730676.ch9 · Cited by 1
Chapter 4 Tau Protein and the Dementias
Goedert, M., & Spillantini, M. G. (2007) · Blue books of neurology · doi:10.1016/s1877-184x(09)70055-3
The neurobiology of the tauopathies
Spillantini, M. G., & Goedert, M. (2003) · Cambridge University Press eBooks · doi:10.1017/cbo9780511550072.013
Demencias degenerativas distintas de la enfermedad de alzheimer
García, D. M., Robert, M. F., & Pareja, D. B. (2003) · Medicine - Programa de Formación Médica Continuada Acreditado · doi:10.1016/s0304-5412(03)71010-5
Progressive Supranuclear Palsy and Corticobasal Degeneration: Similarities and Differences
Chand, P., & Litvan, I. (2008) · Future Neurology · doi:10.2217/14796708.3.3.299
Self-citationCampdelacreu, J., Ezquerra, M., Muñoz, E., Oliva, R., & TOLOSA, E. S. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00105-8
Diseases: New Concepts of Pathogenesis and Their Therapeutic Implications
Skovronsky, D., Lee, V. M. ‐., & Trojanowski, J. Q. (2006)
[Parkinsonism: alternative diagnosis beyond idiopathic Parkinson's disease].
Gutierrez, J., & Singer, C. (2010) · PubMed
Functional implications of tau-fyn interactions in Alzheimer's disease
Lau, H. W. D. (2015)
Introduction to and brief history of FTD
Dickerson, B. C. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781316091586.004
Neuropathology of frontotemporal lobar degeneration
Cairns, N. J. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199590674.003.0018
Drzezga, A. E. (2016) · Springer eBooks · doi:10.1007/978-3-319-30081-8_26
Toft, M., Farrer, M. J., Aasly, J. O., Dickson, D. W., & Wszołek, Z. K. (2007) · Springer eBooks · doi:10.1007/978-0-387-30377-2_4
Self-citationThe cognitive neurology of corticobasal degeneration and progressive supranuclear palsy
Fredericks, C. A., & Lee, S. E. (2016) · Cambridge University Press eBooks · doi:10.1017/9781139924771.015
Protein Aggregation and Neurodegeneration: Tauopathies and Synucleinopathies
Goedert, M. (2017) · Neurodegeneration · doi:10.1002/9781118661895.ch2
Hategan, A., Bourgeois, J. A., Cheng, T. Z., & Young, J. A. (2018) · Springer eBooks · doi:10.1007/978-3-319-77128-1_10
Saccades in Alzheimer’s disease: an MRI study.
Wright, S. L. (2011) · Otago University Research Archive (University of Otago)
Gallo, J., Noble, W. J., & Martin, T. R. (2007)
Josephs, K. A. (2017) · Neurodegeneration · doi:10.1002/9781118661895.ch10
Swieten, J. C. V. (2005) · Neurological disease and therapy · doi:10.1201/9780849358364.ch26
Criteri diagnostici delle degenerazioni corticobasali
Bénatru, I., & Colin, O. (2019) · EMC - Neurologia · doi:10.1016/s1634-7072(19)43055-9
Association of Pick's disease with the MAPT H2 haplotype
Nicolas, G. (2024) · The Lancet Neurology · doi:10.1016/s1474-4422(24)00123-6
Long-read transcriptomics in neurodegeneration
Gustavsson, E. K., & Macpherson, H. L. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13550-7.00002-1 · Cited by 1
Parkinson's disease and related disorders
Agin‐Liebes, J., & Fahn, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-19176-3.00023-6
Criteri diagnostici delle degenerazioni corticobasali
Bénatru, I., & Colin, O. (2025) · EMC - Neurologia · doi:10.1016/s1634-7072(25)50692-x
Sadikoglou, E., Domingo‐Fernándéz, D., Savytska, N., Fernandes, N., Rizzu, P., Illarionova, A., Strauß, T., Schwarz, S. C., Kodamullil, A. T., Höglinger, G. U., et al. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-08147-1 · Cited by 1
The Cognitive Neurology of Corticobasal Degeneration and Progressive Supranuclear Palsy
Lee, S. E., & Fredericks, C. A. (2025) · Cambridge University Press eBooks · doi:10.1017/9781108985055.013
Kim, E., Vatsavayai, S. C., & Seeley, W. W. (2025) · Cambridge University Press eBooks · doi:10.1017/9781108985055.004
Additional file 1 of Differential vulnerability of the dentate gyrus to tauopathies in dementias
Kawles, A., Minogue, G., Zouridakis, A., Keszycki, R. M., Gill, N., Nassif, C., Coventry, C., Zhang, H., Rogalski, E., Flanagan, M. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26558966
Self-citationTauber, C. V., Schwarz, S. C., Rösler, T. W., Arzberger, T., Gentleman, S., Windl, O., Krumbiegel, M., Reis, A., Ruf, V., Herms, J. W., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26574607
Metadata
- Authors
- Houlden, H., Baker, M., Morris, H. R., MacDonald, N., Pickering–Brown, S., Adamson, J., Lees, A. J., Rossor, M. N., Quinn, N. P., Kertesz, A., Khan, M. N., Hardy, J., Lantos, P. L., St. George–Hyslop, P., Munoz, D. G., Mann, D., Lang, A. E., Bergeron, C., Bigio, E. H., Litvan, I., Bhatia, K. P., Dickson, D., Wood, N. W., & Hutton, M.
- Affiliations
- St Bartholomew's Hospital (GB)
- From Neurogenetics (Drs. Houlden, Morris, Lees, Rossor, Quinn, Khan, Lantos, and Bhatia), Clinical Neurology and Dementia Research Group, Institute of Neurology, London; Mayo Clinic Jacksonville (Dr. Dickson and M. Baker and J. Adamson), Jacksonville, FL; Department of Gynaecological Oncology (Dr. MacDonald), St. Bartholomew’s Hospital, London; School of Biological Sciences (Dr. Pickering–Brown) and Department of Medicine (Dr. Mann), University of Manchester; Department of Neuropathology (M.N. Khan...
- National Institutes of Health (US)
- ORCID
- Venue
- Neurology
- Published
- 2001-06-26
- Volume
- 56
- Issue
- 12
- Pages
- 1702-1706
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W2045671840
- Cited by
- 409
- References
- 32
- Citations by year
- 2026: 3 · 2025: 11 · 2024: 14 · 2023: 9 · 2022: 2 · 2021: 11 · 2020: 11 · 2019: 11 · 2018: 10 · 2017: 14 · 2016: 19 · 2015: 16 · 2014: 16 · 2013: 7 · 2012: 16
- FWCI
- 16.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- UCL Discovery (University College London) (submittedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- Research Explorer (The University of Manchester) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- corticobasal degeneration, progressive supranuclear palsy, tau gene, tau aggregation, genetic association, neurodegeneration
- MeSH terms
- Genotype, Haplotypes, Humans, Supranuclear Palsy, Progressive, Polymerase Chain Reaction, tau Proteins, Neurodegenerative Diseases
About these checks
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
