The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
Frontotemporal dementia and its subtypes: a genome-wide association study
Open accessAbstract
Background Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological signatures, and genetic variability. Mutations in three genes-MAPT, GRN, and C9orf72--have been associated with FTD. We sought to identify novel genetic risk loci associated with the disorder. Methods We did a two-stage genome-wide association study on clinical FTD, analysing samples from 3526 patients with FTD and 9402 healthy controls. To reduce genetic heterogeneity, all participants were of European ancestry. In the discovery phase (samples from 2154 patients with FTD and 4308 controls), we did separate association analyses for each FTD subtype (behavioural variant FTD, semantic dementia, progressive non-fluent aphasia, and FTD overlapping with motor neuron disease [FTD-MND]), followed by a meta-analysis of the entire dataset. We carried forward replication of the novel suggestive loci in an independent sample series (samples from 1372 patients and 5094 controls) and then did joint phase and brain expression and methylation quantitative trait loci analyses for the associated (p<5 × 10(-8)) single-nucleotide polymorphisms. Findings We identified novel associations exceeding the genome-wide significance threshold (p<5 × 10(-8)). Combined (joint) analyses of discovery and replication phases showed genome-wide significant association at 6p21.3, HLA locus (immune system), for rs9268877 (p=1·05 × 10(-8); odds ratio=1·204 [95% CI 1·11-1·30]), rs9268856 (p=5·51 × 10(-9); 0·809 [0·76-0·86]) and rs1980493 (p value=1·57 × 10(-8), 0·775 [0·69-0·86]) in the entire cohort. We also identified a potential novel locus at 11q14, encompassing RAB38/CTSC (the transcripts of which are related to lysosomal biology), for the behavioural FTD subtype for which joint analyses showed suggestive association for rs302668 (p=2·44 × 10(-7); 0·814 [0·71-0·92]). Analysis of expression and methylation quantitative trait loci data suggested that these loci might affect expression and methylation in cis. Interpretation Our findings suggest that immune system processes (link to 6p21.3) and possibly lysosomal and autophagy pathways (link to 11q14) are potentially involved in FTD. Our findings need to be replicated to better define the association of the newly identified loci with disease and to shed light on the pathomechanisms contributing to FTD. Funding The National Institute of Neurological Disorders and Stroke and National Institute on Aging, the Wellcome/MRC Centre on Parkinson's disease, Alzheimer's Research UK, and Texas Tech University Health Sciences Center.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“MAPT mutations drive tau pathology”
From The Role of Retrotransposons and Endogenous Retroviruses in Age-Dependent Neurodegenerative Disorders (2024) · cites this paper as Ferrari et al. 2014
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Age-dependent neurodegenerative disorders are clinically diverse but exhibit significant comorbidity and heterogeneous pathology both within and across disorders”
From The Role of Retrotransposons and Endogenous Retroviruses in Age-Dependent Neurodegenerative Disorders (2024) · cites this paper as Ferrari et al. 2014
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Exploration, normalization, and summaries of high density oligonucleotide array probe level data
Irizarry, R. A. (2003) · Biostatistics · doi:10.1093/biostatistics/4.2.249 · Cited by 10,603
Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
Principal components analysis corrects for stratification in genome-wide association studies
Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., & Reich, D. (2006) · Nature Genetics · doi:10.1038/ng1847 · Cited by 10,248
An integrated map of genetic variation from 1,092 human genomes
The 1000 Genomes Project Consortium (2012) · Nature · doi:10.1038/nature11632 · Cited by 7,711
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Rascovsky, K., Hodges, J. R., Knopman, D., Mendez, M. F., Kramer, J. H., Neuhaus, J., van Swieten, J. C., Seelaar, H., Dopper, E. G. P., Onyike, C. U., et al. (2011) · Brain · doi:10.1093/brain/awr179 · Cited by 5,221
Self-citationClassification of primary progressive aphasia and its variants
Gorno-Tempini, M. L., Hillis, A. E., Weintraub, S., Kertesz, A., Mendez, M., Cappa, S. F., Ogar, J. M., Rohrer, J. D., Black, S., Boeve, B. F., et al. (2011) · Neurology · doi:10.1212/wnl.0b013e31821103e6 · Cited by 5,141
Self-citationFrontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
Neary, D., Snowden, J. S., Gustafson, L., Passant, U., Stuss, D., Black, S., Freedman, M., Kertesz, A., Robert, P. H., Albert, M., et al. (1998) · Neurology · doi:10.1212/wnl.51.6.1546 · Cited by 5,047
Self-citationDeJesus-Hernandez, M., Mackenzie, I. R., Boeve, B. F., Boxer, A. L., Baker, M., Rutherford, N. J., Nicholson, A. M., Finch, N. A., Flynn, H., Adamson, J., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.011 · Cited by 4,936
Self-citationA Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Renton, A. E., Majounie, E., Waite, A., Simón-Sánchez, J., Rollinson, S., Gibbs, J. R., Schymick, J. C., Laaksovirta, H., van Swieten, J. C., Myllykangas, L., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.010 · Cited by 4,409
Self-citationMeta-Analysis of 74,046 Individuals Identifies 11 New Susceptibility Loci for Alzheimer’s Disease
(EADI), E. A. D. I., Lambert, J.-C., (GERAD), G. A. E. R. I. A. D., Alzheimer's Disease Genetic Consortium (ADGC), (CHARGE), C. F. H. A. A. R. I. G. E., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., et al. (2013) · Nature Genetics · doi:10.1038/ng.2802 · Cited by 4,336
Self-citation
Cited by
Sorted by citations
Items 301–386 of 386
The Development of Drug Therapies for Frontotemporal Dementia Caused by Progranulin Mutations
Muynck, L. D., & Damme, P. V. (2015) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9781681080680115030007 · Cited by 2
Arrant, A. E., & Roberson, E. D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801942-9.00006-9 · Cited by 3
Manzoni, C., & Ferrari, R. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-51140-1_17 · Cited by 2
Self-citationImmunogenetic mechanism driving neurological and neurodegenerative disorders
Hajam, Y. A., Premlata, P., Rani, R., Sharma, R., Sharma, P., & Kumar, R. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90250-2.00001-7 · Cited by 2
Rossi, G., Salvi, E., Benussi, L., Mehmeti, E., Geviti, A., Bellini, S., Longobardi, A., Facconi, A., Carrara, M., Bonvicini, C., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232112847 · Cited by 2
Self-citationZhu, Y., Mao, L., Wang, H., Yang, F., Du, R., Pang, X., Bai, J., & Huang, X. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03817-7 · Cited by 2
Genetic factors influencing a neurobiological substrate for psychiatric disordersPreprint
Andlauer, T. F. M., Mühleisen, T. W., Hoffstaedter, F., Teumer, A., Wittfeld, K., Teuber, A., Reinbold, C. S., Grotegerd, D., Bülow, R., Caspers, S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/774463 · Cited by 2
Gene expression imputation provides insight into the genetic architecture of frontotemporal dementiaPreprint
Reus, L. M., Paşaniuc, B., Posthuma, D., Boltz, T. A., Pijnenburg, Y. A. L., & Ophoff, R. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.23.166355 · Cited by 2
Self-citationEditorial: Multi-omics, Epigenomics, and Computational Analysis of Neurodegenerative Disorders
Jaiswal, M. K. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.930425 · Cited by 2
Spargo, T. P., Gilchrist, L., Hunt, G. P., Dobson, R., Proitsi, P., Al‐Chalabi, A., Pain, O., & Iacoangeli, A. (2023) · eLife · doi:10.7554/elife.88768 · Cited by 3
The genetics of TDP43-Type-C neurodegeneration: a whole genome sequencing studyPreprint
Nassan, M. M., Ayala, I. A. D. L., Sloan, J., Bonfitto, A., Stark, B., Song, S., Naymik, M., Geula, C., Gefen, T. D., Barbieri, E., et al. (2025) · medRxiv · doi:10.1101/2025.01.25.25320561 · Cited by 2
Genetic structure of different ethnic populations at the frontotemporal dementia risk loci
Mavrych, V., Alamil, M., Bolgova, O., & Dvornyk, V. (2025) · PLoS ONE · doi:10.1371/journal.pone.0329809 · Cited by 2
Khamkar, A. S., Jha, S., Bakhla, A. K., & Chauhan, G. (2025) · International Journal of Stroke · doi:10.1177/17474930251377513 · Cited by 1
Stiglitz, S., Leitha, T., Krampla, W. W., & Fischer, P. Q. (2018) · psychopraxis neuropraxis · doi:10.1007/s00739-018-0484-0 · Cited by 1
Clinical and pathological phenotypes in dementia
Rainero, I., Vacca, A., & Rubino, E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815854-8.00010-0 · Cited by 1
Self-citationSawyer, R. P., Stone, H. K., Salim, H., Lu, X., Weirauch, M. T., & Kottyan, L. C. (2022) · Medicine · doi:10.1097/md.0000000000031078 · Cited by 1
Autoimmunity and Frontotemporal Lobar Degeneration: From Laboratory Study to Clinical Practice
Sun, Y., Zhang, L., Liu, P., & Peng, G. (2023) · Clinical Interventions in Aging · doi:10.2147/cia.s394286 · Cited by 1
Role of Retroelements in Frontotemporal Dementia Development
Mustafin, R. N. (2025) · Frontiers in Bioscience-Scholar · doi:10.31083/fbs25922 · Cited by 2
DNA Methylation in Cellular Mechanisms of Neurodegeneration
Neidhart, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-420194-1.00018-x · Cited by 1
Genetic contributions to sporadic frontotemporal dementia
Carr, J. S., Sirkis, D. W., & Yokoyama, J. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815868-5.00005-0 · Cited by 1
I.S., C., Hochsprung, M. E., K., L., & Bergamaschi, E. D. N. C. (2023) · EDITORA CRV eBooks · doi:10.24824/978652513581.6.541-547 · Cited by 1
Hagenaars, S. P., Radaković, R., Crockford, C., Fawns‐Ritchie, C., Harris, S. E., Galé, C. R., & Deary, I. J. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/219345 · Cited by 1
Beaton, D., Rieck, J. R., Alhazmi, F. H., ADNI, & Abdi, H. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/235945 · Cited by 1
The TMEM106B rs1990621 protective variant is also associated with increased neuronal proportionPreprint
Li, Z., Farias, F. G., Dube, U., Del‐Aguila, J. L., Mihindukulasuriya, K. A., Fernández, M. V., Ibáñez, L., Budde, J., Wang, F., Lake, A. M., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/583286 · Cited by 1
Self-citationCXCR4 involvement in neurodegenerative diseasesPreprint
Bonham, L. W., Karch, C. M. M., Fan, C. C., Tan, C. H., Geier, E. G., Wang, Y., Wen, N., Broce, I., Li, Y., Barkovich, M. J., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/181693 · Cited by 1
Self-citationLona‐Durazo, F., Reynolds, R. H., Scholz, S. W., Ryten, M., & Taliun, S. A. G. (2022) · medRxiv · doi:10.1101/2022.12.07.22283179 · Cited by 1
Spargo, T. P., Gilchrist, L., Hunt, G. P., Dobson, R., Proitsi, P., Al‐Chalabi, A., Pain, O., & Iacoangeli, A. (2023) · eLife · doi:10.7554/elife.88768.1 · Cited by 1
Matsuda, K. M., Umeda‐Kameyama, Y., Iwadoh, K., Miyawaki, M., Yakabe, M., Ishii, M., Ogawa, S., Akishita, M., Sato, S., & Yoshizaki, A. (2024) · medRxiv · doi:10.1101/2024.09.20.24313547 · Cited by 1
Rambarack, N., Fodder, K., Murthy, M. N., Toomey, C. E., de Silva, R., Heutink, P., Humphrey, J., Raj, T., Lashley, T., & Bettencourt, C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.21.634065 · Cited by 1
Self-citationCorrection to “Unlocking the Therapeutic Potential of Natural Products for Alzheimer’s Disease”
Li, Z., Zhang, Z., & Yu, B. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c00926 · Cited by 1
Gong, W., Lan, F., Ren, P., Hu, H., Su, W., Hu, H., Li, Q.-Y., Hou, X., Huang, L.-Y., Hao, Q., et al. (2025) · medRxiv · doi:10.64898/2025.12.19.25342615 · Cited by 1
Genetica delle demenze degenerative
Wallon, D., & Nicolas, G. (2015) · EMC - Neurologia · doi:10.1016/s1634-7072(15)73962-0
[Clinical effectiveness of Duracef in children with ENT inflammation].
Богомильский, М. Р., & Vr, C. (2001) · PubMed
Combining controls can improve power in two-stage association studies
Liley, J. (2018) · BMC Genetics · doi:10.1186/s12863-018-0675-y
Bani‐Fatemi, A., Tasmim, S., Santos, T., Araújo, J. P., & Luca, V. D. (2018) · Neuromethods · doi:10.1007/978-1-4939-7647-8_12
Partitioning the genetic architecture of amyotrophic lateral sclerosisPreprint
Broce, I., Fan, C. C., Olney, N. T., Lomen‐Hoerth, C., Finkbeiner, S. M., Atassi, N., Cudkowicz, M., Paganoni, S., Yokoyama, J. S., Kao, A. W., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/505693 · Cited by 1
Self-citationNeurochemical Aspects of Frontotemporal Dementia
Farooqui, A. A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816347-4.00006-4
Combining controls can improve power in two-stage association studiesPreprint
Liley, J. (2017) · arXiv (Cornell University) · doi:10.17863/cam.30543
Shadrin, A. A., Mucha, S., Ellinghaus, D., Makarious, M. B., Blauwendraat, C., Sreelatha, A. A. K., Heras‐Garvin, A., Ding, J., Hammer, M. B., Foubert‐Samier, A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/751354
Self-citationA Multi-omics Data Resource for Frontotemporal Dementia Research
Heutink, P., Menden, K., & Dalmia, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-51140-1_16
Self-citationLill, C. M. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.02.010
Neuropsychology, social cognition, and loss of insight in frontotemporal dementia
O’Keeffe, F. M., & McCormack, D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818000-6.00012-3
TREM2 Limits Progression of Deficits and Spreading of Tau Pathology in MicePreprint
Feiten, A., Au, C. G., van Hummel, A., van der Hoven, J., Deng, Y., Przybyla, M., Bright, F., Butler, T. A., Delerue, F., Toutonji, A., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-741896/v1
Genetic regulation of gene expression in brain and blood
de Klein, N. (2021) · University of Groningen research database (University of Groningen / Centre for Information Technology) · doi:10.33612/diss.178049845
Delgado, F. R., Rubio, R. D., Barahona‐Hernando, R., & Rodríguez‐Gómez, O. (2015) · Medicine - Programa de Formación Médica Continuada Acreditado · doi:10.1016/j.med.2015.01.001
Renton, A. E., & Goate, A. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190681425.003.0051
Faculty Opinions recommendation of The genetic architecture of the human cerebral cortex.
Konopka, G. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737584496.793573108
TREM2 limits progression of deficits and spreading of tau pathology in micePreprint
Feiten, A., Au, C. G., Sabale, M., van Hummel, A., van der Hoven, J., Deng, Y., Przybyla, M., Bright, F., Butler, T., Delerue, F., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-741896/v2
(2023) · Advances in magnetic resonance technology and applications · doi:10.1016/b978-0-323-91771-1.00026-5
Immune dysregulation and neurodegenerative diseases
Cipollini, V., Troili, F., & Giubilei, F. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-85841-0.00015-8
Spargo, T. P., Gilchrist, L., Hunt, G. P., et al. (2023) · eLife · doi:10.7554/elife.88768.1.sa0
Spargo, T. P., Gilchrist, L., Hunt, G. P., et al. (2023) · eLife · doi:10.7554/elife.88768.1.sa1
Strauss, A., Swann, P., Kigar, S. L., Christou, R., Yarkoni, N. S., Murley, A. G., Chouliaras, L., Savulich, G., Bevan-Jones, W. R., Surendranthan, A., et al. (2024) · medRxiv · doi:10.1101/2024.01.16.24301348
Self-citationMultiomic Analyses Direct Hypotheses for Creutzfeldt-Jakob Disease Risk GenesPreprint
Küçükali, F., Hill, E., Watzeels, T., Hummerich, H., Campbell, T., Darwent, L., Collins, S. J., Stehmann, C., Kovács, G. G., Geschwind, M. D., et al. (2024) · medRxiv · doi:10.1101/2024.07.19.24310476
Self-citationSpargo, T. P., Gilchrist, L., Hunt, G. P., et al. (2024) · eLife · doi:10.7554/elife.88768.2.sa2
Spargo, T. P., Gilchrist, L., Hunt, G. P., et al. (2024) · eLife · doi:10.7554/elife.88768.2.sa1
Spargo, T. P., Gilchrist, L., Hunt, G. P., Dobson, R., Proitsi, P., Al‐Chalabi, A., Pain, O., & Iacoangeli, A. (2024) · eLife · doi:10.7554/elife.88768.2.sa0
Spargo, T. P., Gilchrist, L., Hunt, G. P., Dobson, R., Proitsi, P., Al‐Chalabi, A., Pain, O., & Iacoangeli, A. (2024) · eLife · doi:10.7554/elife.88768.2
Integrative analysis of causal associations between neurodegenerative diseases and colorectal cancer
Wang, F., Chen, L., Nie, M., & Li, Z. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e35432
Gallucci, M., Ronch, C. D., Bendini, M., Fiore, V., Turolla, L., Ferrarini, M., Fabrizi, G. M., & Tiraboschi, P. (2024) · Journal of Alzheimer s Disease Reports · doi:10.1177/25424823241302743
Zorkina, Y., Berdalin, A. B., Morozova, I., Andryushchenko, A., Ka, P., Pavlova, O., Abramova, O. V., Ushakova, V. M., Zeltser, A., Kurmishev, M., et al. (2025) · Psychiatry International · doi:10.3390/psychiatryint6020064
Han, X., Rosenberg, G. M., Kisling, V. M., Zhang, T., Lee, C., Ravi, A., Melnik, M., Bilousova, T., Spina, S., Nana, A. L., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73007-1
Self-citationThe Search for Answers: Causes, Risk Factors, and Current Research in Neurodegenerative Disorders
Kajrolkar, A. (2025) · Premier Journal of Neuroscience · doi:10.70389/pjn.100013
Novel insight into genetic impacts on neurodegenerative dementia
Xiao, X., Luo, S., Li, J., Jiao, B., & Shen, L. (2025) · Ageing and Neurodegenerative Diseases · doi:10.20517/and.2025.04
Woollacott, I., Toomey, C. E., Strand, C., Courtney, R. J., Benson, B. C., Rohrer, J. D., & Lashley, T. (2020) · Figshare · doi:10.6084/m9.figshare.12788931
Self-citationChen, Q., Zhang, C., Wu, S., He, Y., Liu, Y., Zheng, L., Li, B., Liu, G., & Liu, L. (2024) · Figshare · doi:10.6084/m9.figshare.26195748
Woollacott, I., Toomey, C. E., Strand, C., Courtney, R. J., Benson, B. C., Rohrer, J. D., & Lashley, T. (2020) · Figshare · doi:10.6084/m9.figshare.12788937
Self-citationZhao, L., Tang, Y., Tu, Y., & Cao, J. (2024) · Figshare · doi:10.6084/m9.figshare.26729974
Guo, T., Sun, M., Jia, G., Liu, D., Liu, X., & Xie, H. (2025) · Critical Public Health · doi:10.1080/09581596.2025.2605781
Scotton, W. J., Valentino, R. R., Martínez-Carrasco, A., Real, R., Macpherson, H. L., Tamvaka, N., Mok, K. Y., Heckman, M. G., Kobylecki, C., Escott‐Price, V., et al. (2025) · medRxiv · doi:10.64898/2025.12.21.25342758
Self-citationBrain patterns linked to neuropsychiatric genetic risk mirror those seen in disease
Chou, C.-J., del Re, E. C., Wang, H., Hamada, K., Tian, X., Iakunchykova, O. P., Wang, Y., Fiecas, M. J. A., & Chen, C. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1152
Gao, S., Wu, S., Liu, F., Zhu, P., He, Y., He, Y., Wang, R., Yang, J., Zhao, L., Liu, X., et al. (2026) · medRxiv · doi:10.64898/2026.02.27.26345967
The Genetics of TDP-43 Type C Neurodegeneration
Nassan, M. M., Ayala, I. A., Sloan, J., Bonfitto, A., Stark, B., Song, S., Naymik, M., Geula, C., Gefen, T. D., Barbieri, E., et al. (2026) · Neurology Genetics · doi:10.1212/nxg.0000000000200369 · Cited by 3
Integrative genomic and functional analyses reveal NINL as a modulator of tau aggregation
Swift, S. K., Huang, G., Cochran, J. N., Albanus, R. D., Minaya, M., Castruita, P. A., Zhang, R., Miller, K. J., Starr, E., Galasso, G., et al. (2026) · Alzheimer s & Dementia · doi:10.1002/alz.71352 · Cited by 1
Husén, E., Cai, Z., Gerrits, E., Sjöstedt, E., Mitsios, N., Zheng, T., Skarwan, E., Uhlén, M., Sivertsson, Å., & Mulder, J. (2026) · eLife · doi:10.64898/2026.06.11.731645
Mekkes, N., Kumar, U., Hoekstra, E., Marmolejo-Garza, A., Dagkesamanskaia, E., Wever, D. D., de Groot, M., Kreft, K. L., Rajicic, A., Seelaar, H., et al. (2026) · medRxiv · doi:10.64898/2026.06.30.26356924 · Cited by 1
Self-citationProteome-wide Mendelian randomization identifies causal plasma proteins in frontotemporal dementia
Yao, Y., Zou, Q., & Chen, K. (2026) · Neurological Sciences · doi:10.1007/s10072-026-09249-0
From biology to therapy: advances in progranulin-related neurodegenerative diseases
Hu, S., Qiu, K., Zhen, F., & Zhou, X. (2026) · Molecular Neurodegeneration Advances · doi:10.1186/s44477-026-00042-z
Zheng, C., Shivakumar, M., Shen, L., & Kim, D. (2026) · medRxiv · doi:10.64898/2026.08.24.26361271
Wolozin, B. L., Best, M. N., Ellini, M., Ma, Y., Bok, S., Hwang, D., & Filipponi, C. (2026) · Cells · doi:10.3390/cells15171596
Laureyssen, C., Thal, D. R., & Sleegers, K. (2026) · Acta Neuropathologica · doi:10.1007/s00401-026-03085-4
e/pQTL-GWAS coloc and TWAS/PWAS results for sCJD GWAS
Küçükali, F., & Sleegers, K. (2025) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.12507354
BindingDB (2026) · UC San Diego · doi:10.7270/q2cz3d17
Metadata
- Authors
- Ferrari, R., Hernandez, D. G., Nalls, M. A., Rohrer, J. D., Ramasamy, A., Kwok, J. B. J., Dobson-Stone, C., Brooks, W. S., Schofield, P. R., Halliday, G. M., Hodges, J. R., Piguet, O., Bartley, L., Thompson, E., Haan, E., Hernández, I., Ruiz, A., Boada, M., Borroni, B., Padovani, A., Cruchaga, C., Cairns, N. J., Benussi, L., Binetti, G., Ghidoni, R., Forloni, G., Galimberti, D., Fenoglio, C., Serpente, M., Scarpini, E., Clarimón, J., Lleó, A., Blesa, R., Waldö, M. L., Nilsson, K., Nilsson, C., Mackenzie, I. R. A., Hsiung, G.-Y. R., Mann, D. M. A., Grafman, J., Morris, C. M., Attems, J., Griffiths, T. D., McKeith, I. G., Thomas, A. J., Pietrini, P., Huey, E. D., Wassermann, E. M., Baborie, A., Jaros, E., Tierney, M. C., Pastor, P., Razquin, C., Ortega-Cubero, S., Alonso, E., Perneczky, R., Diehl-Schmid, J., Alexopoulos, P., Kurz, A., Rainero, I., Rubino, E., Pinessi, L., Rogaeva, E., St George-Hyslop, P., Rossi, G., Tagliavini, F., Giaccone, G., Rowe, J. B., Schlachetzki, J. C. M., Uphill, J., Collinge, J., Mead, S., Danek, A., Van Deerlin, V. M., Grossman, M., Trojanowski, J. Q., van der Zee, J., Deschamps, W., Van Langenhove, T., Cruts, M., Van Broeckhoven, C., Cappa, S. F., Le Ber, I., Hannequin, D., Golfier, V., Vercelletto, M., Brice, A., Nacmias, B., Sorbi, S., Bagnoli, S., Piaceri, I., Nielsen, J. E., Hjermind, L. E., Riemenschneider, M., Mayhaus, M., Ibach, B., Gasparoni, G., Pichler, S., Gu, W., Rossor, M. N., Fox, N. C., Warren, J. D., Spillantini, M. G., Morris, H. R., Rizzu, P., Heutink, P., Snowden, J. S., Rollinson, S., Richardson, A., Gerhard, A., Bruni, A. C., Maletta, R., Frangipane, F., Cupidi, C., Bernardi, L., Anfossi, M., Gallo, M., Conidi, M. E., Smirne, N., Rademakers, R., Baker, M., Dickson, D. W., Graff-Radford, N. R., Petersen, R. C., Knopman, D., Josephs, K. A., Boeve, B. F., Parisi, J. E., Seeley, W. W., Miller, B. L., Karydas, A. M., Rosen, H., van Swieten, J. C., Dopper, E. G. P., Seelaar, H., Pijnenburg, Y. A. L., Scheltens, P., Logroscino, G., Capozzo, R., Novelli, V., Puca, A. A., Franceschi, M., Postiglione, A., Milan, G., Sorrentino, P., Kristiansen, M., Chiang, H.-H., Graff, C., Pasquier, F., Rollin, A., Deramecourt, V., Lebert, F., Kapogiannis, D., Ferrucci, L., Pickering-Brown, S., Singleton, A. B., Hardy, J., & Momeni, P.
- Affiliations
- Texas Tech University (US)
- National Institutes of Health (US)
- National Hospital for Neurology and Neurosurgery (GB)
- Guy's Hospital (GB)
- UNSW Sydney (AU)
- Neuroscience Research Australia (AU)
- South Australia Pathology (AU)
- Fundació ACE (ES)
- University of Brescia (IT)
- Washington University in St. Louis (US)
- Centro San Giovanni di Dio Fatebenefratelli (IT)
- Mario Negri Institute for Pharmacological Research (IT)
- University of Milan (IT)
- Universitat Autònoma de Barcelona (ES)
- Lund University (SE)
- University of British Columbia (CA)
- University of Manchester (GB)
- Northwestern University (US)
- Newcastle University (GB)
- University of Pisa (IT)
- Columbia University (US)
- Walton Centre (GB)
- Royal Victoria Infirmary (GB)
- Centro de Investigación Médica Aplicada (ES)
- West London Mental Health NHS Trust (GB)
- Technical University of Munich (DE)
- Azienda Ospedaliera Citta' della Salute e della Scienza di Torino (IT)
- University of Toronto (CA)
- Fondazione IRCCS Istituto Neurologico Carlo Besta (IT)
- MRC Cognition and Brain Sciences Unit (GB)
- University of Freiburg (DE)
- MRC Prion Unit (GB)
- German Center for Neurodegenerative Diseases (DE)
- University of Pennsylvania (US)
- University of Antwerp (BE)
- Vita-Salute San Raffaele University (IT)
- Inserm (FR)
- Centre Hospitalier de Saint-Brieuc (FR)
- Centre Hospitalier Universitaire de Nantes (FR)
- Centre National de la Recherche Scientifique (FR)
- University of Florence (IT)
- University of Copenhagen (DK)
- Saarland University (DE)
- University of Regensburg (DE)
- University of Luxembourg (LU)
- University of Cambridge (GB)
- Cardiff University (GB)
- Presidio Ospedaliero Lamezia Terme (IT)
- Mayo Clinic (US)
- University of California, San Francisco (US)
- Erasmus MC (NL)
- Amsterdam UMC Location Vrije Universiteit Amsterdam (NL)
- University of Bari Aldo Moro (IT)
- Istituti Clinici Scientifici Maugeri (IT)
- University of Salerno (IT)
- MultiMedica (IT)
- Federico II University Hospital (IT)
- University College London (GB)
- Karolinska University Hospital (SE)
- Université Lille Nord de France (FR)
- National Institute on Aging (US)
- UCL Queen Square Institute of Neurology (GB)
- Corresponding author
- Hardy, John
- ORCID
- Ferrari, Raffaele
- Hernandez, Dena G
- Rohrer, Jonathan D
- Ramasamy, Adaikalavan
- Kwok, John B J
- Brooks, William S
- Schofield, Peter R
- Halliday, Glenda M
- Hodges, John R
- Piguet, Olivier
- Haan, Eric
- Borroni, Barbara
- Padovani, Alessandro
- Cruchaga, Carlos
- Cairns, Nigel J
- Benussi, Luisa
- Binetti, Giuliano
- Ghidoni, Roberta
- Forloni, Gianluigi
- Galimberti, Daniela
- Fenoglio, Chiara
- Scarpini, Elio
- Clarimón, Jordi
- Lleó, Alberto
- Blesa, Rafael
- Waldö, Maria Landqvist
- Nilsson, Karin
- Nilsson, Christer
- Mackenzie, Ian R A
- Hsiung, Ging-Yuek R
- Mann, David M A
- Grafman, Jordan
- Morris, Christopher M
- Attems, Johannes
- Griffiths, Timothy D
- McKeith, Ian G
- Thomas, Alan J
- Pietrini, P
- Huey, Edward D
- Wassermann, Eric M
- Perneczky, Robert
- Alexopoulos, Panagiotis
- Kurz, Alexander
- Rainero, Innocenzo
- Rubino, Elisa
- Pinessi, Lorenzo
- Rogaeva, Ekaterina
- Rossi, Giacomina
- Tagliavini, Fabrizio
- Giaccone, Giorgio
- Rowe, James B
- Schlachetzki, Johannes C M
- Collinge, John
- Mead, Simon
- Danek, Adrian
- Grossman, Murray
- Trojanowski, John Q
- van der Zee, Julie
- Cruts, Marc
- Cappa, Stefano F
- Hannequin, Didier
- Brice, Alexis
- Nacmias, Benedetta
- Sorbi, Sandro
- Bagnoli, Silvia
- Piaceri, Irene
- Nielsen, Jørgen E
- Hjermind, Lena E
- Gasparoni, Gilles
- Gu, Wei
- Rossor, Martin N
- Fox, Nick C
- Warren, Jason D
- Spillantini, Maria Grazia
- Morris, Huw R
- Rizzu, Patrizia
- Heutink, Peter
- Snowden, Julie S
- Rollinson, Sara
- Richardson, Anna
- Gerhard, Alexander
- Bruni, Amalia C
- Maletta, Raffaele
- Cupidi, Chiara
- Bernardi, Livia
- Anfossi, Maria
- Gallo, Maura
- Smirne, Nicoletta
- Rademakers, Rosa
- Baker, Matt
- Dickson, Dennis W
- Petersen, Ronald C
- Knopman, David
- Josephs, Keith A
- Boeve, Bradley F
- Seeley, William W
- Miller, Bruce L
- Dopper, Elise G P
- Seelaar, Harro
- Pijnenburg, Yolande A L
- Scheltens, Philip
- Logroscino, Giancarlo
- Capozzo, Rosa
- Novelli, Valeria
- Puca, Annibale A
- Franceschi, Massimo
- Milan, Graziella
- Pasquier, Florence
- Deramecourt, Vincent
- Lebert, Florence
- Kapogiannis, Dimitrios
- Ferrucci, Luigi
- Pickering-Brown, Stuart
- Singleton, Andrew B
- Hardy, John
- Venue
- The Lancet Neurology
- Publisher
- Elsevier BV
- Published
- 2014-07
- Volume
- 13
- Issue
- 7
- Pages
- 686-699
- ISSN
- 1474-4422 (ISSN-L)
- PMC
- PMC4112126
- OpenAlex
- W2152748843
- Cited by
- 383
- References
- 61
- Citations by year
- 2026: 17 · 2025: 29 · 2024: 48 · 2023: 44 · 2022: 32 · 2021: 39 · 2020: 32 · 2019: 28 · 2018: 33 · 2017: 27 · 2016: 26 · 2015: 19 · 2014: 8
- FWCI
- 20.36
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Lancet Neurology (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- IMT Institutional Repository (IMT School for Advanced Studies Lucca) (acceptedVersion)
- PubMed Central (acceptedVersion)
- University of Regensburg Publication Server (University of Regensburg) (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
- UNSWorks (UNSW Sydney) (submittedVersion, cc-by-nc-nd)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) (submittedVersion, other-oa)
- CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion)
- Adelaide Research & Scholarship (AR&S) (University of Adelaide) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Florence Research (University of Florence) (submittedVersion)
- Institutional Research Information System (Università degli Studi di Brescia) (submittedVersion)
- Lund University Publications (Lund University) (submittedVersion)
- mediaTUM (Technical University of Munich) (submittedVersion)
- Open Repository and Bibliography (University of Luxembourg) (submittedVersion, cc-by-nc-sa)
- DZNE Pub (submittedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- CINECA IRIS Institutional Research Information System (University of Bari Aldo Moro) (submittedVersion)
- UNSWorks (University of New South Wales, Sydney, Australia) (submittedVersion, cc-by-nc-nd)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Funders
- ARUK (ARUK-PG2012-18)
- MRC Sudden Death Brain Bank (CS) (G0901254 to JH and MW)
- Fellowship award (G0802462 to MR)
- National Health and Medical Resarch Council (NHMRC), Australia (510217 and 1005769)
- NHMRC (630428 and 1005769, 510217 and 1005769, 1029538, 1037746)
- NHMRC Enabling (401184)
- NHMRC Research Fellowship 630434 (1029538, and Program Grant 1037746)
- NHMRC Career Development Fellowship 1022684 (1003139)
- NIH (P50 AG05681, P01 AG03991, and P01 AG026276, AG023501, AG019724)
- Fondazione CARIPLO (2009-2633, 2009–2633)
- CIHR (74580)
- PARF (C06-01)
- Newcastle Brain Tissue Resource (G0400074 and G1100540)
- BMBF (FKZ 01GI1007A)
- Cambridge NIHR Biomedical Research Centre and Wellcome Trust (088324)
- VMVD and JQT (AG032953, AG017586 and AG010124)
- MG (AG032953, AG017586, AG010124, and NS044266)
- German Ministry for Education and Research (01GS0465)
- MRC (G0301152)
- Motor Neuron Disease Association (6057)
- RR (P50 AG016574, R01 NS080882, R01 NS065782, P50 NS72187)
- DWD (P50NS072187, P50AG016574)
- State of Florida Alzheimer Disease Initiative, and CurePSP Inc. NRGR, JEP, RCP, DK, and BFB (P50 AG016574)
- KAJ (R01 AG037491)
- BLM (P50AG023501, P01AG019724)
- HR (AG032306)
- Stichting Dioraphte Foundation (11 02 03 00)
- Nuts Ohra Foundation (0801-69)
- Hersenstichting Nederland (BG 2010-02)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Keywords
- frontotemporal dementia, genetic susceptibility loci, semantic dementia, progressive nonfluent aphasia, HLA, 6p21.3, MAPT, gene regulatory networks, C9orf72, methylation quantitative trait loci
- MeSH terms
- Adult, Aged, Aged, 80 and over, Female, Genotype, Humans, Male, Middle Aged, Genome-Wide Association Study, Frontotemporal Dementia
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