The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.
Molecular drivers and cortical spread of lateral entorhinal cortex dysfunction in preclinical Alzheimer's disease
Open accessAbstract
The entorhinal cortex has been implicated in the early stages of Alzheimer's disease, which is characterized by changes in the tau protein and in the cleaved fragments of the amyloid precursor protein (APP). We used a high-resolution functional magnetic resonance imaging (fMRI) variant that can map metabolic defects in patients and mouse models to address basic questions about entorhinal cortex pathophysiology. The entorhinal cortex is divided into functionally distinct regions, the medial entorhinal cortex (MEC) and the lateral entorhinal cortex (LEC), and we exploited the high-resolution capabilities of the fMRI variant to ask whether either of them was affected in patients with preclinical Alzheimer's disease. Next, we imaged three mouse models of disease to clarify how tau and APP relate to entorhinal cortex dysfunction and to determine whether the entorhinal cortex can act as a source of dysfunction observed in other cortical areas. We found that the LEC was affected in preclinical disease, that LEC dysfunction could spread to the parietal cortex during preclinical disease and that APP expression potentiated tau toxicity in driving LEC dysfunction, thereby helping to explain regional vulnerability in the disease.
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
“the hippocampal region is important to short-term memory loss in AD and is the earliest region involved in the progression of the disease”
From AAVrh.10-Mediated APOE2 Central Nervous System Gene Therapy for APOE4-Associated Alzheimer's Disease (2018) · cites this paper as [40]
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
McKhann, G., Drachman, D., Folstein, M., Katzman, R., Price, D., & Stadlan, E. M. (1984) · Neurology · doi:10.1212/wnl.34.7.939 · Cited by 27,915
Hirono, N., Mori, E., Ikejiri, Y., Imamura, T., Shimomura, T., Hashimoto, M., Yamashita, H., & Ikeda, M. (1997) · PubMed · Cited by 21,012
Desikan, R. S., Ségonne, F., Fischl, B., Quinn, B. T., Dickerson, B. C., Blacker, D., Buckner, R. L., Dale, A. M., Maguire, R. P., Hyman, B. T., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.021 · Cited by 13,324
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859
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
Sperling, R. A., Aisen, P. S., Beckett, L. A., Bennett, D. A., Craft, S., Fagan, A. M., Iwatsubo, T., Jack, C. R., Kaye, J., Montine, T. J., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.003 · Cited by 7,155
A New Clinical Scale for the Staging of Dementia
Hughes, C. P., Berg, L., Danziger, W., Coben, L. A., & Martin, R. L. (1982) · British Journal of Psychiatry · doi:10.1192/bjp.140.6.566 · Cited by 7,056
N4ITK: Improved N3 Bias Correction
Tustison, N. J., Avants, B., Cook, P. A., Zheng, Y., Egan, A., Yushkevich, P. A., & Gee, J. C. (2010) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2010.2046908 · Cited by 6,119
Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B
Klunk, W. E., Engler, H., Nordberg, A., Wang, Y., Blomqvist, G., Holt, D. P., Bergström, M., Savitcheva, I., Huang, G., Estrada, S., et al. (2004) · Annals of Neurology · doi:10.1002/ana.20009 · Cited by 4,496
Alzheimer's Disease Is a Synaptic Failure
Selkoe, D. J. (2002) · Science · doi:10.1126/science.1074069 · Cited by 4,420
Flagged first, then by citations
Research works printed but not linked: 2
- Kageyama, G.H. & Wong-Riley, M.T. Histochemical localization of cytochrome oxidase in the hippocampus: correlation with specific neuronal types and afferent pathways. Neuroscience 7, 2337–2361 (1982). · DOI
- Moreno, H., Hua, F., Brown, T. & Small, S. Longitudinal mapping of mouse cerebral blood volume with MRI. NMR Biomed. 19, 535–543 (2006). · DOI
Cited by
Sorted by citations
Items 201–300 of 558
Genetic underpinnings in Alzheimer’s disease – a review
Moustafa, A. A., Hassan, M., Hewedi, D. H., Hewedi, I. H., Garami, J. K., Alashwal, H., Zaki, N., Seo, S., Cutsuridis, V., Angulo, S. L., et al. (2017) · Reviews in the Neurosciences · doi:10.1515/revneuro-2017-0036 · Cited by 37
Lander, S. S., Khan, U., Lewandowski, N. M., Chakraborty, D., Provenzano, F. A., Mingote, S., Chornyy, S., Frigerio, F., Maechler, P., Kaphzan, H., et al. (2018) · Schizophrenia Bulletin · doi:10.1093/schbul/sby011 · Cited by 38
Self-citationAssessing mild cognitive impairment using object‐location memory in immersive virtual environments
Castegnaro, A., Howett, D., Li, A., Harding, E. M., Chan, D., Burgess, N., & King, J. A. (2022) · Hippocampus · doi:10.1002/hipo.23458 · Cited by 37
Salimi, M., Tabasi, F., Abdolsamadi, M., Dehghan, S., Dehdar, K., Nazari, M., Javan, M., Mirnajafi‐Zadeh, J., & Raoufy, M. R. (2022) · Scientific Reports · doi:10.1038/s41598-022-08528-y · Cited by 40
Hurtado, M. L., Fuller, H. R., Wong, A. M. S., Eaton, S. L., Gillingwater, T. H., Pennetta, G., Cooper, J. D., & Wishart, T. M. (2017) · Scientific Reports · doi:10.1038/s41598-017-12603-0 · Cited by 33
Maharjan, A., Wang, E., Peng, M., & Çakmak, Y. Ö. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00225 · Cited by 39
Peleh, T., Ike, K. G. O., Wams, E. J., Lebois, E. P., & Hengerer, B. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.018 · Cited by 39
Key Disease Mechanisms Linked to Alzheimer’s Disease in the Entorhinal Cortex
Bottero, V., Powers, D., Yalamanchi, A., Quinn, J. P., & Potashkin, J. A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22083915 · Cited by 35
Early cognitive decline in older adults better predicts object than scene recognition performance
Fidalgo, C., Changoor, A. T., Page‐Gould, E., Lee, A. C. H., & Barense, M. D. (2016) · Hippocampus · doi:10.1002/hipo.22658 · Cited by 36
Park, H. Y., Suh, C. H., Heo, H., Shim, W. H., & Kim, S. J. (2022) · European Radiology · doi:10.1007/s00330-022-08838-9 · Cited by 35
Early hippocampal hyperexcitability in PS2APP mice: role of mutant PS2 and APP
Fontana, R., Agostini, M., Murana, E., Mahmud, M., Scremin, E., Rubega, M., Sparacino, G., Vassanelli, S., & Fasolato, C. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.10.027 · Cited by 35
Rapid Aging in the Perforant Path Projections to the Rodent Dentate Gyrus
Amani, M., Lauterborn, J. C., Le, A. A., Cox, B. M., Wang, W., Quintanilla, J., Cox, C. D., Gall, C. M., & LYNCH, G. S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2376-20.2021 · Cited by 37
Probabilistic Modeling of Imaging, Genetics and Diagnosis
Batmanghelich, K. N., Dalca, A. V., Quon, G., Sabuncu, M. R., & Golland, P. (2016) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2016.2527784 · Cited by 36
Visualization of Altered Hippocampal Connectivity in an Animal Model of Alzheimer’s Disease
Jeon, S. G., Kim, Y. J., Kim, K. A., Mook‐Jung, I., & Moon, M. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-0918-y · Cited by 33
Rad, K. R., & Maleki, A. (2020) · Journal of the Royal Statistical Society Series B (Statistical Methodology) · doi:10.1111/rssb.12374 · Cited by 68
Altered Cerebro-Cerebellar Limbic Network in AD Spectrum: A Resting-State fMRI Study
Qi, Z., An, Y., Zhang, M., Li, H., & Lu, J. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00072 · Cited by 35
Adams, J. N., Maaß, A., Berron, D., Harrison, T. M., Baker, S. L., Thomas, W. P., Stanfill, M., & Jagust, W. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2504-20.2021 · Cited by 34
Lateral entorhinal cortex dysfunction in amnestic mild cognitive impairment
Tran, T., Speck, C. L., Gallagher, M., & Bakker, A. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.12.008 · Cited by 34
Modeling Alzheimer’s Disease Progression with Fused Laplacian Sparse Group Lasso
Liu, X., Cao, P., Gonçalves, A. R., Zhao, D., & Banerjee, A. (2018) · ACM Transactions on Knowledge Discovery from Data · doi:10.1145/3230668 · Cited by 33
Shi, A., Petrache, A. L., Shi, J., & Ali, A. B. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz165 · Cited by 36
Chen, P.-Z., Jiang, H., Wen, B., Ren, S., Chen, Y., Ji, W.-G., Hu, B., Zhang, J., Xu, F., & Zhu, Z.-R. (2014) · Neural Plasticity · doi:10.1155/2014/320937 · Cited by 32
Ground zero in Alzheimer's disease
Yassa, M. A. (2014) · Nature Neuroscience · doi:10.1038/nn.3631 · Cited by 32
Dynamic Cortico-hippocampal Networks Underlying Memory and Cognition: The PMAT Framework
Inhoff, M. C., & Ranganath, C. (2017) · Springer eBooks · doi:10.1007/978-3-319-50406-3_18 · Cited by 41
Tanninen, S. E., Nouriziabari, B., Morrissey, M. D., Bakir, R., Dayton, R. D., Klein, R. L., & Takehara‐Nishiuchi, K. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.06.024 · Cited by 32
Leal, S. L., Ferguson, L. A., Harrison, T. M., & Jagust, W. J. (2019) · Learning & Memory · doi:10.1101/lm.048967.118 · Cited by 32
The hippocampal longitudinal axis—relevance for underlying tau and TDP-43 pathology
Lladó, A., Tort‐Merino, A., Sánchez‐Valle, R., Falgàs, N., Balasa, M., Bosch, B., Castellvı́, M., Olives, J., Antonell, A., & Hornberger, M. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.05.035 · Cited by 30
Leparulo, A., Mahmud, M., Scremin, E., Pozzan, T., Vassanelli, S., & Fasolato, C. (2019) · Cells · doi:10.3390/cells9010054 · Cited by 31
Coughlan, G., Zhukovsky, P., Puthusseryppady, V., Gillings, R., Minihane, A. M., Cameron, D., & Hornberger, M. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.02.007 · Cited by 36
Yan, Y., Aierken, A., Wang, C., Song, D. F., Ni, J., Wang, Z., Quan, Z., & Qing, H. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.009 · Cited by 32
Hernández‐Frausto, M., Bilash, O. M., Masurkar, A. V., & Basu, J. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1223891 · Cited by 35
Family C G-Protein-Coupled Receptors in Alzheimer’s Disease and Therapeutic Implications
Prà, I. D., Armato, U., & Chiarini, A. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01282 · Cited by 31
Entorhinal cortex vulnerability to human APP expression promotes hyperexcitability and tau pathology
Goettemoeller, A. M., Banks, E., Kumar, P., Olah, V. J., McCann, K. E., South, K., Ramelow, C. C., Eaton, A., Duong, D. M., Seyfried, N. T., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52297-3 · Cited by 30
Fu, H., Hussaini, S. A., Wegmann, S., Profaci, C. P., Daniels, J. D., Herman, M., Emrani, S., Figueroa, H. Y., Hyman, B. T., Davies, P., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159463 · Cited by 28
Self-citationChronic Lyme Disease: A Working Case Definition
Stricker, R. B., & Fesler, M. C. (2018) · American Journal of Infectious Diseases · doi:10.3844/ajidsp.2018.1.44 · Cited by 30
Object and object‐memory representations across the proximodistal axis of CA1
Vandrey, B., Duncan, S., & Ainge, J. A. (2021) · Hippocampus · doi:10.1002/hipo.23331 · Cited by 28
Snytte, J., Fenerci, C., Rajagopal, S., Beaudoin, C., Hooper, K., Sheldon, S., Olsen, R. K., & Rajah, M. N. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119164 · Cited by 34
The amyloid state of proteins: A boon or bane?
Hassan, M. N., Nabi, F., Khan, A. N., Hussain, M. S., Siddiqui, W. A., Uversky, V. N., & Khan, R. H. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2022.01.115 · Cited by 30
Jiang, Z., Wang, J., Qin, Y., Liu, S., Luo, B., Bai, F., Wei, H., Zhang, S., Wei, J., Ding, G., et al. (2024) · Alzheimer s Research & Therapy · doi:10.1186/s13195-024-01392-0 · Cited by 32
Aβ1–42 triggers the generation of a retrograde signaling complex from sentinel mRNAs in axons
Walker, C. A., Randolph, L. K., Matute, C., Alberdi, E. M., Baleriola, J., & Hengst, U. (2018) · EMBO Reports · doi:10.15252/embr.201745435 · Cited by 28
Zimmer‐Bensch, G., & Zempel, H. (2021) · Cells · doi:10.3390/cells10113064 · Cited by 33
Castro, M. A. D., & Volterra, A. (2021) · Glia · doi:10.1002/glia.24128 · Cited by 27
Tarawneh, H. Y., Jayakody, D. M. P., Sohrabi, H. R., Martins, R. N., & Mulders, W. H. A. M. (2022) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-220035 · Cited by 30
Galizzi, G., Palumbo, L., Amato, A., Conigliaro, A., Nuzzo, D., Terzo, S., Caruana, L., Picone, P., Alessandro, R., Mulè, F., et al. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.08.014 · Cited by 28
D’Angelo, M. C., Kacollja, A., Rabin, J. S., Rosenbaum, R. S., & Ryan, J. D. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.07.025 · Cited by 27
The antimicrobial protein, CAP37, is upregulated in pyramidal neurons during Alzheimer’s disease
Brock, A. J., Kasus‐Jacobi, A., Lerner, M. R., Logan, S., Adesina, A. M., & Pereira, H. A. (2015) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1347-x · Cited by 26
Wang, X., Song, R., Lu, W., Liu, Z., Wang, L., Zhu, X., Liu, Y., Sun, Z., Li, J., & Li, X. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00157 · Cited by 27
Feng, X., Yang, J., Lipton, Z. C., Small, S. A., & Provenzano, F. A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/456277 · Cited by 27
Self-citationRaeper, R., Lisowska, A., & Rekik, I. (2018) · IEEE Access · doi:10.1109/access.2018.2863657 · Cited by 26
Tran, T., Bridi, M., Koh, M. T., Gallagher, M., & Kirkwood, A. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.07.010 · Cited by 26
Hrybouski, S., Das, S. R., Xie, L., Wisse, L. E. M., Kelley, M., Lane, J., Sherin, M., DiCalogero, M., Nasrallah, I. M., Detre, J. A., et al. (2023) · Brain Communications · doi:10.1093/braincomms/fcad245 · Cited by 38
Changes in the EEG amplitude as a biomarker for early detection of Alzheimer's disease
Al-Nuaimi, A. H. H., Jammeh, E., Sun, L., & Ifeachor, E. (2016) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2016.7590869 · Cited by 26
Impairment of entorhinal cortex network activity in Alzheimer’s disease
Karimani, F., Taei, A. A., Abolghasemi-Dehaghani, M.-R., Safari, M.-S., & Dargahi, L. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1402573 · Cited by 27
Capilla-López, M. D., Deprada-Fernandez, Á., Andrade‐Talavera, Y., Martínez‐Gallego, I., Coatl-Cuaya, H., Sotillo, P. S., Rodríguez-Álvarez, J., Moreno, A. R., Parra‐Damas, A., & Saura, C. A. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-02901-9 · Cited by 33
Gaynor, L. S., Curiel, R. E., Peñate, A., Rosselli, M., Burke, S. N., Wicklund, M. R., Loewenstein, D., & Bauer, R. M. (2019) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617719000316 · Cited by 25
Neurogenesis Makes a Crucial Contribution to the Neuropathology of Alzheimer’s Disease
Young, J. K. (2020) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-200218 · Cited by 28
Das, S. R., Mancuso, L., Olson, I. R., Arnold, S. E., & Wolk, D. A. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv022 · Cited by 22
Ramanan, S., Marstaller, L., Hodges, J. R., Piguet, O., & Irish, M. (2020) · Cortex · doi:10.1016/j.cortex.2019.12.026 · Cited by 24
Persistent firing in LEC III neurons is differentially modulated by learning and aging
Lin, C., Sherathiya, V. N., Oh, M. M., & Disterhoft, J. F. (2020) · eLife · doi:10.7554/elife.56816 · Cited by 23
Fung, C., Guo, J., Fu, H., Figueroa, H. Y., Konofagou, E. E., & Duff, K. (2020) · Science Advances · doi:10.1126/sciadv.abc8098 · Cited by 26
Self-citationZhou, R., Bernard, T. B., & Wolbers, T. (2022) · Topics in Cognitive Science · doi:10.1111/tops.12608 · Cited by 27
How the sense of smell influences cognition throughout life
Kostka, J. K., & Bitzenhofer, S. H. (2022) · e-Neuroforum · doi:10.1515/nf-2022-0007 · Cited by 26
Rodríguez, J. L., Oltmer, J., Marshall, M., Champion, S. N., Frosch, M. P., & Augustinack, J. C. (2023) · Brain Pathology · doi:10.1111/bpa.13159 · Cited by 22
Ferris, C. F., Kulkarni, P. P., Yee, J. R., Nedelman, M. A., & de Jong, I. E. M. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00279 · Cited by 24
Villamil-Ortiz, J. G., Barrera-Ocampo, A., Arias-Londoño, J. D., Villegas, A., Lopera, F., & Cardona-Gómez, G. P. (2018) · Journal of Alzheimer’s Disease · doi:10.3233/jad-170554 · Cited by 24
Cytoarchitectonic Areas of the Gyrus ambiens in the Human Brain
Insausti, R., Parada, M. C., Ubero, M., Rodado, A., Serrano, A. M. I., & Muñoz, M. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00021 · Cited by 22
Olajide, O. J., Rue, C. L., Bergdahl, A., & Chapman, C. A. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.960314 · Cited by 24
Dong, Q., Cui, Z., Wu, X., Li, L., Lu, F., & Liu, F. (2024) · Food & Function · doi:10.1039/d3fo05566c · Cited by 23
Kong, W., Mou, X., Zhang, N., Zeng, W., Li, S., & Yang, Y. (2015) · BioMed Research International · doi:10.1155/2015/394260 · Cited by 23
Disentangling associations between complex traits and cell types with seismic
Lai, Q., Dannenfelser, R., Roussarie, J.-P., & Yao, V. (2025) · Nature Communications · doi:10.1038/s41467-025-63753-z · Cited by 26
Experimental Models of Tauopathy – From Mechanisms to Therapies
Götz, J. J., & Götz, J. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-32-9358-8_28 · Cited by 24
Sex effects on cortical morphological networks in healthy young adults
Ge, R., Liu, X., Long, D., Frangou, S., & Vila‐Rodriguez, F. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117945 · Cited by 20
Chen, Z., Chen, K., Li, Y., Geng, D., Li, X., Liang, X., Lu, H., Ding, S., Xiao, Z., Ma, X., et al. (2023) · Human Brain Mapping · doi:10.1002/hbm.26529 · Cited by 21
Shahidi, ., Hashemi-Firouzi, N., Asl, S. S., & Komaki, A. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.02.004 · Cited by 23
Substituting Gadolinium in Brain MRI Using DeepContrast
Sun, H., Liu, X., Feng, X., Liu, C., Zhu, N., Gjerswold-Selleck, S., Wei, H.-J., Upadhyayula, P. S., Mela, A., Wu, C., et al. (2020) · IEEE International Symposium on Biomedical Imaging (ISBI) · doi:10.1109/isbi45749.2020.9098323 · Cited by 22
Self-citationOptogenetic stimulation: Understanding memory and treating deficits
Barnett, S. C., Perry, B. A. L., Dalrymple‐Alford, J. C., & Parr‐Brownlie, L. C. (2018) · Hippocampus · doi:10.1002/hipo.22960 · Cited by 23
Reale, M., D’Angelo, C., Costantini, E., Nicola, M. D., Yarla, N. S., Kamal, M. A., Salvador, N., & Perry, G. L. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-170999 · Cited by 21
Besson, G., Simon, J., Salmon, É., & Bastin, C. (2020) · Cortex · doi:10.1016/j.cortex.2020.02.022 · Cited by 21
Structural connectivity-based segmentation of the human entorhinal cortex
Syversen, I. F., Witter, M. P., Kobro‐Flatmoen, A., Goa, P. E., Schröder, T. N., & Doeller, C. F. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118723 · Cited by 22
Funane, T., Jun, H., Sutoko, S., Saido, T. C., Kandori, A., & Igarashi, K. M. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.955178 · Cited by 19
Fang, C., Li, C., Cabrerizo, M., Barreto, A. B., Andrian, J. H., Rishe, N. D., Loewenstein, D., Duara, R., & Adjouadi, M. (2018) · International Journal of Neural Systems · doi:10.1142/s012906571850017x · Cited by 20
Entorhinal cortex volume, thickness, surface area and curvature trajectories over the adult lifespan
Wang, Y., Lei, H. C., Zhang, Y., Zuo, C., & Wang, D. (2019) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2019.09.002 · Cited by 19
Entorhinal cortex-based metabolic profiling of chronic restraint stress mice model of depression
Chen, X., Lan, T., Wang, Y., He, Y., Wu, Z., Tian, Y., Li, Y., Bai, M., Zhou, W., Zhang, H., et al. (2020) · Aging · doi:10.18632/aging.102798 · Cited by 19
Cortical amyloid burden and age moderate hippocampal activity in cognitively-normal adults
Song, Z., McDonough, I. M., Liu, P., Lu, H., & Park, D. C. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.05.013 · Cited by 19
Gonçalves, M. M., Pinho, M. S., & Simões, M. R. (2017) · Aging Neuropsychology and Cognition · doi:10.1080/13825585.2017.1294651 · Cited by 19
Aldabbagh, Y., Islam, A., Zhang, W., Whiting, P. J., & Ali, A. B. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.822499 · Cited by 20
Selective vulnerabilities and biomarkers in neurocognitive aging
Reagh, Z. M., & Yassa, M. A. (2017) · F1000Research · doi:10.12688/f1000research.10652.1 · Cited by 18
Of mice and motion: Behavioural-EEG phenotyping of Alzheimer’s disease mouse models
Crouch, B., Yeap, J., Pais, B., Riedel, G., & Platt, B. (2018) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2018.06.028 · Cited by 17
Interaction of selected biomolecules and metabolites with amyloidogenic proteins
Kundu, D., Umesh, & Dubey, V. K. (2020) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2020.1760138 · Cited by 18
A scalable estimate of the extra-sample prediction error via approximate leave-one-outPreprint
Rad, K. R., & Maleki, A. (2018) · arXiv (Cornell University) · doi:10.48550/arxiv.1801.10243 · Cited by 18
Islam, A., Saito, T., Saido, T., & Ali, A. B. (2023) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2022.03.001 · Cited by 17
Levendovszky, S. R., Talati, P., Donahue, M. J., & Heckers, S. (2015) · Magnetic Resonance in Medicine · doi:10.1002/mrm.25836 · Cited by 16
Maurer, A. P., Burke, S. N., Diba, K., & Barnes, C. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0531-17.2017 · Cited by 16
Liu, D., Dai, S., He, K., Li, G., Liu, J., Liu, L. G., Huang, J., Xu, L., & Li, W. (2021) · Science Progress · doi:10.1177/00368504211001146 · Cited by 17
Self-citationA Network Explanation of Alzheimer's Regional VulnerabilityPreprint
Small, S. A., & Swanson, L. W. (2018) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2018.83.036889 · Cited by 17
Self-citationOlfactory bulb integrity in frontotemporal dementia and Alzheimer’s disease
Carnemolla, S. E., Kumfor, F., Liang, C. T., Foxe, D., Ahmed, R. M., & Piguet, O. (2022) · Journal of Alzheimer’s Disease · doi:10.3233/jad-220080 · Cited by 16
Computer-aided diagnosis of Alzheimer’s disease by MRI analysis and evolutionary computing
de Souza, R. G., Silva, G. D. S. L. E., dos Santos, W. P., de Lima, M. E., & Initiative, A. D. N. (2021) · Research on Biomedical Engineering · doi:10.1007/s42600-021-00160-5 · Cited by 15
Mandino, F., Yeow, L. Y., Bi, R., Sejin, L., Bae, H. G., Baek, S. H., Lee, C.-Y., Mohammad, H., Teoh, C. L., Horien, C. L., et al. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221082016 · Cited by 17
Borcuk, C., Héraud, C., Herbeaux, K., Diringer, M., Panzer, É., Scuto, J., Hashimoto, S., Saido, T. C., Saito, T., Goutagny, R., et al. (2022) · Aging Brain · doi:10.1016/j.nbas.2022.100042 · Cited by 18
Li, M., Wu, S., Song, B., Yang, J., Fan, L., Yang, Y., Wang, Y., Yang, J.-H., & Xu, Y. (2022) · Aging Cell · doi:10.1111/acel.13723 · Cited by 15
Sex-specific transcriptional rewiring in the brain of Alzheimer’s disease patients
Santiago, J. A., Quinn, J. P., & Potashkin, J. A. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1009368 · Cited by 16
Metadata
- Authors
- Khan, U. A., Liu, L., Provenzano, F. A., Berman, D. E., Profaci, C. P., Sloan, R., Mayeux, R., Duff, K. E., & Small, S. A.
- Affiliations
- SUNY Downstate Health Sciences University (US)
- Columbia University (US)
- Corresponding author
- Duff, Karen E
- Small, Scott A
- ORCID
- Venue
- Nature Neuroscience
- Published
- 2013-12-22
- Volume
- 17
- Issue
- 2
- Pages
- 304-311
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC4044925
- OpenAlex
- W1966100017
- Cited by
- 561
- References
- 60
- Citations by year
- 2026: 23 · 2025: 33 · 2024: 38 · 2023: 52 · 2022: 56 · 2021: 48 · 2020: 51 · 2019: 54 · 2018: 59 · 2017: 54 · 2016: 36 · 2015: 31 · 2014: 23 · 2013: 1
- FWCI
- 21.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Ministerio de Economía y Competitividad
- National Institute on Aging (R01AG034618, R01AG037212, P01AG007232, AG 07232, AG025161, R01AG025161, P50AG008702, AG037212, AG034618)
- National Heart, Lung, and Blood Institute (R01HL094423, HL094423)
- National Institute of Neurological Disorders and Stroke (NS074874, R01NS074874)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD007430)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- preclinical Alzheimer's disease, lateral entorhinal cortex, medial entorhinal cortex, amyloid precursor protein, tau protein, parietal cortex, regional vulnerability, mouse models of Alzheimer's disease
- MeSH terms
- Age Factors, Aged, Aged, 80 and over, Alzheimer Disease, Analysis of Variance, Animals, Brain Mapping, Cognition Disorders, Female, Humans, Image Processing, Computer-Assisted, Functional Laterality, Magnetic Resonance Imaging, Male, Mice, Transgenic, Mutation, Nerve Tissue Proteins, Oxygen, Cortical Spreading Depression, Gene Expression, Amyloid beta-Peptides, Amyloid beta-Protein Precursor, tau Proteins, Disease Progression, Entorhinal Cortex, Mice
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