The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Quantitative assessment of cortical synaptic density in Alzheimer's disease
Abstract
Significant progress has been made over the last decade in delineating the neuropathological and neurochemical changes in the brains of patients with Alzheimer's disease (AD). Less well studied are the actual synaptic connections of affected areas of the brain, such as the cerebral cortex. Because the final common pathway for neurotransmission involves synaptic integrity, we quantitatively assessed synaptic number and synapse size in lamina III and V of human frontal cortex (Brodmann area 9) in patients with AD and age-matched controls. Samples were also matched for postmortem interval, and artifacts associated with postmortem change were eliminated. We found a significant decrease in synaptic number per unit volume in both lamina, more marked in lamina III (-42%) than V (-29%). In both normal controls and AD brains, there was a negative correlation between synapse number and synapse size as indexed by the length of the postsynaptic density (PSD); cortical samples with fewer synapses had larger synapse size. This appeared to be a compensatory response, rather than a selective loss of small synapses, since the total amount of synaptic contact area per unit volume did not decline in lamina V (despite a 29% loss of synapses); in lamina III it was reduced 11% despite a 42% loss of synapses. The loss of synapses in AD is widespread and significant in frontal cortex; there is observable compensation by enlargement of synaptic size. This compensatory effort is overcome by the continuing loss of synapses in areas most affected by the degeneration.
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
“Other previous transcriptomic studies and investigations into cortical synaptic density in AD have underscored the link between synaptic transmission and AD pathogenesis, demonstrating that disruptions in synaptic integrity contribute to cortical thinning in AD [74, 75].”
From Association of APOC1 with cortical atrophy during conversion to Alzheimer’s disease (2025) · cites this paper as [75]
In the citing paper
“Our findings, consistent with previous studies [72, 74–76], reinforce the connection between synaptic dysfunction and AD pathogenesis, suggesting that disruptions in synaptic integrity contribute to cortical thinning and cognitive decline.”
From Association of APOC1 with cortical atrophy during conversion to Alzheimer’s disease (2025) · cites this paper as [75]
In the citing paper
“Nonetheless, in the absence of more definitive premortem cognitive status data, the present research focuses on a correlate of dementia that is quantifiable postmortem, synapse loss, 11,12 and not on dementia itself.”
From Soluble Amyloid β Peptide Concentration as a Predictor of Synaptic Change in Alzheimer's Disease (1999) · cites this paper as [11]
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
Statistical principles in experimental design.
Winer, B. J. (1962) · McGraw-Hill Book Company · doi:10.1037/11774-000 · Cited by 27,137
Statistical Principles in Experimental Design
Myers, J. L., & Winer, B. J. (1964) · The American Journal of Psychology · doi:10.2307/1419292 · Cited by 8,111
The cholinergic hypothesis of geriatric memory dysfunction
Bartus, R. T., Dean, R. L., Beer, B., & Lippa, A. S. (1982) · Science · doi:10.1126/science.7046051 · Cited by 5,545
Alzheimer's Disease: A Disorder of Cortical Cholinergic Innervation
Coyle, J. T., Price, D. L., & DeLong, M. R. (1983) · Science · doi:10.1126/science.6338589 · Cited by 3,052
Synaptic density in human frontal cortex —Developmental changes and effects of aging
Peter R., H. (1979) · Brain Research · doi:10.1016/0006-8993(79)90349-4 · Cited by 2,645
Diagnosis of Alzheimer's Disease
Khachaturian, Z. S. (1985) · Archives of Neurology · doi:10.1001/archneur.1985.04060100083029 · Cited by 2,499
The Clinical Diagnosis of Alzheimer's Disease
Wade, J. P. H., Mirsen, T. R., Hachinski, V. C., Fisman, M., Lau, C. S., & Merskey, H. (1987) · Archives of Neurology · doi:10.1001/archneur.1987.00520130016010 · Cited by 1,416
Davies, P., Katzman, R., & Terry, R. D. (1980) · Nature · doi:10.1038/288279a0 · Cited by 882
Some morphometric aspects of the brain in senile dementia of the alzheimer type
Terry, R. D., Peck, A., DeTeresa, R., Schechter, R., & Horoupian, D. S. (1981) · Annals of Neurology · doi:10.1002/ana.410100209 · Cited by 801
Cited by
Sorted by citations
Items 201–300 of 445
Pathophysiology of Parkinson's disease behavior – a view from the network
Caviness, J. N. (2013) · Parkinsonism & Related Disorders · doi:10.1016/s1353-8020(13)70012-9 · Cited by 50
Intrinsic Bioenergetic Properties and Stress Sensitivity of Dopaminergic Synaptosomes
Choi, S. W., Gerencser, A. A., Lee, D. W., Rajagopalan, S., Nicholls, D. G., Andersen, J. K., & Brand, M. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5817-10.2011 · Cited by 51
Proctor, D. T., Coulson, E. J., & Dodd, P. R. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.02.002 · Cited by 53
Tu, Z., Efange, S. M. N., Xu, J., Li, S., Jones, L. A., Parsons, S. M., & Mach, R. H. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm8012344 · Cited by 50
Altered dopamine modulation of LTD-like plasticity in Alzheimer's disease patients.
Koch, G., Esposito, Z., Codecà, C., Mori, F., Kusayanagi, H., Monteleone, F., Lorenzo, F. D., Bernardi, G., & Martorana, A. (2011) · Clinical Neurophysiology · doi:10.1016/j.clinph.2010.10.033 · Cited by 51
Liu, X., Hua, F., Yang, D., Lin, Y., Zhang, L., Ying, J., Sheng, H., & Wang, X. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03625-y · Cited by 50
Tau Causes Synapse Loss without Disrupting Calcium Homeostasis in the rTg4510 Model of Tauopathy
Kopeikina, K. J., Wegmann, S., Pitstick, R., Carlson, G. A., Bacskai, B. J., Betensky, R. A., Hyman, B. T., & Spires‐Jones, T. L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080834 · Cited by 48
Repeated cognitive stimulation alleviates memory impairments in an Alzheimer’s disease mouse model
Yeung, S. T., Martínez‐Coria, H., Ager, R. R., Rodríguez‐Ortiz, C. J., Baglietto‐Vargas, D., & LaFerla, F. M. (2015) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2015.07.001 · Cited by 50
Emerging insights into synapse dysregulation in Alzheimer’s disease
Martínez-Serra, R., Alonso‐Nanclares, L., Cho, K., & Giese, K.-P. (2022) · Brain Communications · doi:10.1093/braincomms/fcac083 · Cited by 49
Postmortem changes in brain cell structure: a reviewPreprint
Krassner, M. M., Kauffman, J., Sowa, A., Cialowicz, K. I., Walsh, S., Farrell, K. W., Crary, J. F., & McKenzie, A. T. (2023) · OSF Preprints (OSF Preprints) · doi:10.17879/freeneuropathology-2023-4790 · Cited by 73
Tiernan, C. T., Combs, B., Cox, K. K., Morfini, G. A., Brady, S. T., Counts, S., & Kanaan, N. M. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.06.030 · Cited by 46
Cisternas, P., Oliva, C. A., Torres, V. I., Barrera, D. P., & Inestrosa, N. C. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00295 · Cited by 45
Parkinson's Disease Dementia and Potential Therapeutic Strategies
Caviness, J. N., Lue, L., Adler, C. H., & Walker, D. G. (2010) · CNS Neuroscience & Therapeutics · doi:10.1111/j.1755-5949.2010.00216.x · Cited by 46
A Longitudinal Study of Behavioral Deficits in an AβPP Transgenic Mouse Model of Alzheimer's Disease
Havas, D., Hutter‐Paier, B., Ubhi, K. K., Rockenstein, E. M., Crailsheim, K., Masliah, E., & Windisch, M. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101866 · Cited by 45
Steele, J., Brautigam, H., Short, J. A., Sowa, A., Shi, M., Yadav, A., Weaver, C. M., Westaway, D. A., Fraser, P. E., George‐Hyslop, P. S., et al. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23536 · Cited by 45
Bazrgar, M., Khodabakhsh, P., Prudencio, M., Mohagheghi, F., & Ahmadiani, A. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105805 · Cited by 45
Enhanced degradation of synaptophysin by the proteasome in mucopolysaccharidosis type IIIB
Vitry, S., Ausseil, J., Hocquemiller, M., Bigou, S., Coura, R., & Heard, J. M. (2009) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2009.01.001 · Cited by 46
Naito, Y., Tanabe, Y., Lee, A. K., Hamel, E., & Takahashi, H. (2017) · Scientific Reports · doi:10.1038/srep42548 · Cited by 42
Rockenstein, E. M., Desplats, P., Ubhi, K. K., Mante, M., Florio, J. B., Adame, A., Winter, S., Brandstaetter, H., Meier, D., & Masliah, E. (2015) · Stem Cell Research · doi:10.1016/j.scr.2015.04.008 · Cited by 42
Early Alzheimer-type lesions in cognitively normal subjects
Tsartsalis, S., Xekardaki, A., Hof, P. R., Kövari, E., & Bouras, C. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.10.002 · Cited by 41
Alzheimer’s disease as a disorder of dynamic brain self-organization
Arendt, T. (2004) · Progress in brain research · doi:10.1016/s0079-6123(04)47025-3 · Cited by 43
Song, C., Perides, G., Wang, D., & Liu, Y. F. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01182.x · Cited by 41
Arendt, T., Marcova, L., Bigl, V., & Brückner, M. K. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903510202 · Cited by 42
Developmental neurotoxicity of PFOA exposure on hiPSC-derived cortical neurons
Wu, S., Xie, J., Zhao, H., Zhao, X., Sánchez, O. F., Rochet, J., Freeman, J. L., & Yuan, C. (2024) · Environment International · doi:10.1016/j.envint.2024.108914 · Cited by 41
Compensating for synaptic loss in Alzheimer’s disease
Abuhassan, K., Coyle, D., Belatreche, A., & Maguire, L. (2013) · Journal of Computational Neuroscience · doi:10.1007/s10827-013-0462-8 · Cited by 43
Rapoport, S. I. (2003) · Neurotoxicity Research · doi:10.1007/bf03033167 · Cited by 42
Coleman, P. D., Kazee, A. M., Lapham, L. W., Eskin, T. A., & Rogers, K. E. (1992) · Neurobiology of Aging · doi:10.1016/0197-4580(92)90085-c · Cited by 41
Antioxidants have a rapid and long-lasting effect on neuritic abnormalities in APP:PS1 mice
Garcı́a-Alloza, M., Borrelli, L. A., Hyman, B. T., & Bacskai, B. J. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.11.006 · Cited by 44
Axonal Transport and Mitochondrial Dysfunction in Alzheimer's Disease
Riemer, J., & Kins, S. (2012) · Neurodegenerative Diseases · doi:10.1159/000342020 · Cited by 39
Brokaw, D. L., Piras, I. S., Mastroeni, D., Weisenberger, D. J., Nolz, J., Delvaux, E., Serrano, G. E., Beach, T. G., Huentelman, M. J., & Coleman, P. D. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.06.022 · Cited by 38
Synapses, Microglia, and Lipids in Alzheimer’s Disease
Paasila, P. J., Aramideh, J. A., Sutherland, G. T., & Graeber, M. B. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.778822 · Cited by 40
Immunotherapy alleviates amyloid-associated synaptic pathology in an Alzheimer’s disease mouse model
Dorostkar, M. M., Burgold, S., Filser, S., Barghorn, S., Schmidt, B., Anumala, U. R., Hillen, H., Klein, C., & Herms, J. W. (2014) · Brain · doi:10.1093/brain/awu280 · Cited by 40
Wan, L., Ai, J.-Q., Yang, C. G., Jiang, J., Zhang, Q., Luo, Z., Huang, R., Tu, T., Pan, A., Tu, E., et al. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.717263 · Cited by 37
Rusu, P. M., Jansen, A., Soba, P., Kirsch, J., Loewer, A., Merdes, G., Kuan, Y., Jung, A. G., Beyreuther, K. T., Kjærulff, O., et al. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05341.x · Cited by 40
Nakamura, K., Zhou, X. Z., & Lu, K. P. (2013) · Prion · doi:10.4161/pri.22849 · Cited by 36
Wang, Z., Fan, J., Wang, J., Li, Y., Duan, D., Du, G., & Wang, Q. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.12.047 · Cited by 37
Rapoport, S. I. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb07823.x · Cited by 38
What are the facts and artifacts of the pathogenensis and etiology of Alzheimer disease?
Smith, M. A., & Perry, G. L. (1998) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(98)00061-1 · Cited by 36
Ongoing Research on the Role of Gintonin in the Management of Neurodegenerative Disorders
Ikram, M. A., Ullah, R., Khan, A., & Kim, M. O. (2020) · Cells · doi:10.3390/cells9061464 · Cited by 36
Rapoport, S. I., & Grady, C. L. (1993) · International Journal of Neuroscience · doi:10.3109/00207459309000559 · Cited by 35
Hippocampus-related cognitive impairments in young apoE4 targeted replacement mice
Salomon-Zimri, S., Boehm-Cagan, A., Liraz, O., & Michaelson, D. M. (2013) · Neurodegenerative Diseases · doi:10.1159/000354777 · Cited by 34
Otoki, Y., Kato, S., Nakagawa, K., Harvey, D. J., Jin, L., Dugger, B. N., & Taha, A. Y. (2021) · NeuroMolecular Medicine · doi:10.1007/s12017-020-08636-w · Cited by 34
Diagnosis of Alzheimer's Disease
Reisberg, ., Burns, A. S., Brodaty, H., Eastwood, R., Rossor, M. N., Sartorius, N., & Winblad, B. G. (1997) · International Psychogeriatrics · doi:10.1017/s1041610297004675 · Cited by 36
The pathology of Alzheimer's disease: Numbers count
Terry, R. D. (1997) · Annals of Neurology · doi:10.1002/ana.410410104 · Cited by 34
3D Analysis of the Synaptic Organization in the Entorhinal Cortex in Alzheimer’s Disease
Domínguez-Álvaro, M., Montero‐Crespo, M., Blázquez‐Llorca, L., Plaza‐Alonso, S., Cano‐Astorga, N., DeFelipe, J., & Alonso‐Nanclares, L. (2021) · eNeuro · doi:10.1523/eneuro.0504-20.2021 · Cited by 35
Abnormal brain spectrin immunoreactivity in sprouting neurons in Alzheimer disease
Masliah, E., Hansen, L. A., Mallory, M. E., Albright, T., & Terry, R. D. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90707-z · Cited by 33
Carmo, S. D., Crynen, G. C., Paradis, T., Reed, J. M., Iulita, M. F., Ducatenzeiler, A., Crawford, F., & Cuello, A. C. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0580-9 · Cited by 31
Lan, G., Li, A., Liu, Z., Ma, S., Guo, T., & Initiative, A. D. N. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12890 · Cited by 31
Woelfle, S., Deshpande, D., Feldengut, S., Braak, H., Tredici, K. D., Roselli, F., Deisseroth, K. A., Michaelis, J., Boeckers, T. M., & Schön, M. (2023) · BMC Biology · doi:10.1186/s12915-023-01582-6 · Cited by 35
Uncovering Neurodegenerative Protein Modifications via Proteomic Profiling
Gallart‐Palau, X., Serra, A., & Sze, S. K. (2015) · International review of neurobiology · doi:10.1016/bs.irn.2015.06.002 · Cited by 29
Efange, S. M. N., Khare, A. B., von Hohenberg, K., Mach, R. H., Parsons, S. M., & Tu, Z. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm9017916 · Cited by 31
Neuronal thread protein over-expression in brains with Alzheimer's disease lesions
de la Monte, S. M., & Wands, J. R. (1992) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(92)90243-e · Cited by 30
Boutté, A. M., Woltjer, R. L., Zimmerman, L. J., Stamer, S. L., Montine, K. S., Manno, M. V., Cimino, P. J., Liebler, D. C., & Montine, T. J. (2006) · The FASEB Journal · doi:10.1096/fj.06-5920com · Cited by 30
Use of bomb pulse carbon-14 to age senile plaques and neurofibrillary tangles in Alzheimer’s disease
Lovell, M. A., Robertson, J. D., Buchholz, B. A., Xie, C., & Markesbery, W. R. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00281-0 · Cited by 29
Katsuse, O., Lin, W.-L., Lewis, J. M., Hutton, M. L., & Dickson, D. W. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.09.021 · Cited by 30
Bertoni–Freddari, C., Mocchegiani, E., Malavolta, M., Casoli, T., Stefano, G. D., & Fattoretti, P. (2006) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2006.01.019 · Cited by 30
Tcf4 regulates dendritic spine density and morphology in the adult brain
Crux, S., Herms, J. W., & Dorostkar, M. M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199359 · Cited by 29
The Role of Glial Cells and Synapse Loss in Mouse Models of Alzheimer’s Disease
Ziegler-Waldkirch, S., & Meyer-Luehmann, M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00473 · Cited by 21
Soricelli, A., Postiglione, A., Fojaja, M. R. G., Mainenti, P. P., Discepolo, A., Varrone, A., Salvatore, M., & Lassen, N. A. (1996) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/bf01367587 · Cited by 29
Thy1-ApoE4/C/EBPβ double transgenic mice act as a sporadic model with Alzheimer’s disease
Qian, Z., Wang, Z., Li, B., Meng, X., Kuang, Z., Li, Y., Yang, Y., & Ye, K. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02565-x · Cited by 28
Heiss, J. K., Barrett, J., Yu, Z., Haas, L. T., Kostylev, M. A., & Strittmatter, S. M. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw188 · Cited by 30
Factors Affecting Ultrastructural Quality in the Prefrontal Cortex of the Postmortem Human Brain
Glausier, J. R., Konanur, A., & Lewis, D. A. (2018) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155418819481 · Cited by 28
Targeted quantitative analysis of synaptic proteins in Alzheimer’s disease brain
Chang, R. Y. K., Etheridge, N., Dodd, P. R., & Nouwens, A. S. (2014) · Neurochemistry International · doi:10.1016/j.neuint.2014.05.011 · Cited by 28
Bavarsad, M. S., Spina, S., Oehler, A., Allen, I. E., Suemoto, C. K., Leite, R. E. P., Seeley, W. S., Green, A., Jagust, W., Rabinovici, G. D., et al. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02816-9 · Cited by 29
Neuroimmune nexus of depression and dementia: Shared mechanisms and therapeutic targets
Herman, F. J., Simkovic, S. J., & Pasinetti, G. M. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14569 · Cited by 29
Haas, U., & Sparks, D. L. (1996) · Molecular and Chemical Neuropathology · doi:10.1007/bf02815189 · Cited by 27
Garza-Manero, S., Pichardo‐Casas, I., Arias, C., Vaca, L. A., & Zepeda, A. (2013) · Brain Research · doi:10.1016/j.brainres.2013.12.009 · Cited by 28
Reekes, T. H., Ledbetter, C. R., Alexander, J., Stokes, K. Y., Pardue, S., Bhuiyan, M. A. N., Patterson, J. C., Lofton, K. T., Kevil, C. G., & Disbrow, E. A. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102633 · Cited by 26
Reactive Synaptogenesis in Aging and Alzheimer's Disease: Lessons Learned in the Cotman Laboratory
Scheff, S. W. (2003) · Neurochemical Research · doi:10.1023/a:1026048619220 · Cited by 26
Seeing Early Signs of Alzheimer's Disease Through the Lens of the Eye
Reed, B., Béhar‐Cohen, F., & Krantic, S. M. (2016) · Current Alzheimer Research · doi:10.2174/1567205013666160819131904 · Cited by 26
Edaravone injection reverses learning and memory deficits in a rat model of vascular dementia
Xu, L., Fen, L., Li, W., Qin, L., Yao, Y., Ge, X., Yu, Q.-K., Liang, X., Zhao, D., Li, X., et al. (2016) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmw116 · Cited by 24
Intermediary metabolism disturbance in AD/SDAT and its relation to molecular events
Hoyer, S. (1993) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/0278-5846(93)90043-r · Cited by 26
Structural plasticity of synapses in Alzheimer's disease
Adams, I. (1991) · Molecular Neurobiology · doi:10.1007/bf02935562 · Cited by 25
Shah, R. M. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00166-0 · Cited by 25
Mikkelsen, J. D., Kaad, S., Aripaka, S. S., & Finsen, B. R. (2023) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2023.05.003 · Cited by 24
Choi, J. G., Moon, M., Kim, H. G., Mook‐Jung, I., Chung, S.-Y., Kang, T. H., Kim, S. Y., Lee, E. H., & Oh, M. S. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.06.004 · Cited by 24
Bories, C., Arsenault, D., Lemire, M., Tremblay, C., Koninck, Y. D., & Calon, F. (2017) · Aging · doi:10.18632/aging.101239 · Cited by 25
Synaptic environment and extrasynaptic glutamate signals: The quest continues
Rusakov, D. A., & Stewart, M. G. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108688 · Cited by 23
Tau-Mediated Dysregulation of Neuroplasticity and Glial Plasticity
Koller, E. J., & Chakrabarty, P. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00151 · Cited by 23
Neuro-modulation, aminergic neuro-disinhibition and neuro-degeneration.
Schmitt, H. P. (2005) · Medical Hypotheses · doi:10.1016/j.mehy.2005.06.018 · Cited by 23
Nie, Y., Yang, W., Liu, Y., Yang, J., Lei, X., Gerwick, W. H., & Zhang, Y. (2020) · Marine Life Science & Technology · doi:10.1007/s42995-020-00065-9 · Cited by 22
Targeting Tau to Treat Clinical Features of Huntington's Disease
Masnata, M., Salem, S., Jacquet, A. D. R., Anwer, M., & Cicchetti, F. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.580732 · Cited by 25
Dai, X., Lin, A., Zhuang, L.-P., Zeng, Q., Cai, L., Wei, Y., Liang, H., Gao, W., Zhang, J., & Chen, X. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01775-1 · Cited by 24
Chen, X., Zuo, X., Becker, A., Head, E., & Mobley, W. C. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12835 · Cited by 23
Rockenstein, E. M., Ubhi, K. K., Pham, E., Michael, S. A., Doppler, E., Novak, P. H., Inglis, C. A., Mante, M., Adame, A., Alvarez, X. A., et al. (2011) · Journal of Neuroscience Research · doi:10.1002/jnr.22712 · Cited by 21
Animal models of olfactory dysfunction in neurodegenerative diseases
Prediger, R. D., Schamne, M. G., Sampaio, T. B., Moreira, E. L. G., & Rial, D. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63855-7.00024-1 · Cited by 21
Bachmann, C., Tetzlaff, T., Duarte, R., & Morrison, A. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007790 · Cited by 19
Cortical atrophy in Alzheimer's disease unmasks electrically silent sulci and lowers EEG dipolarity
Hara, J., Shankle, W. R., & Musha, T. (1999) · IEEE Transactions on Biomedical Engineering · doi:10.1109/10.775399 · Cited by 19
Colom‐Cadena, M., Davies, C., Sirisi, S., Lee, J.-E., Simzer, E. M., Tzioras, M., Querol‐Vilaseca, M., Sánchez‐Aced, É., Chang, Y. Y., Holt, K., et al. (2023) · medRxiv · doi:10.1101/2023.03.15.23287268 · Cited by 19
P-tau subgroups in AD relate to distinct amyloid production and synaptic integrity profiles
Wesenhagen, K. E. J., Tijms, B. M., Boonkamp, L., Hoede, P. L., Goossens, J., Dewit, N., Scheltens, P., Vanmechelen, E., Visser, P. J., & Teunissen, C. E. (2022) · Alzheimer s Research & Therapy · doi:10.1186/s13195-022-01038-z · Cited by 18
Lefort, R. (2015) · Neurotherapeutics · doi:10.1007/s13311-014-0328-4 · Cited by 17
Role of the dorsomedial nucleus of the thalamus in Alzheimer's disease.
Paskavitz, J., Lippa, C. F., Hamos, J. E., Pulaski-Salo, D., & Drachman, D. A. (1995) · PubMed · Cited by 18
Plasticity in Alzheimer's disease: Too much or not enough?
Geddes, J. W., & Cotman, C. W. (1991) · Neurobiology of Aging · doi:10.1016/0197-4580(91)90011-8 · Cited by 18
Developmental patterns of neuronal thread protein gene expression in Down syndrome
de la Monte, S. M., Xu, Y., Hutchins, G. M., & Wands, J. R. (1996) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(95)00257-3 · Cited by 18
Romero-García, R., Atienza, M., & Cantero, J. L. (2015) · International Journal of Neural Systems · doi:10.1142/s0129065716500039 · Cited by 17
Rockenstein, E. M., Ubhi, K. K., Trejo, M., Mante, M., Patrick, C., Adame, A., Novak, P. H., Jech, M., Doppler, E., Moessler, H., et al. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-90 · Cited by 18
RetractedRanBP9 overexpression accelerates loss of dendritic spines in a mouse model of Alzheimer's disease
Wang, R., Palavicini, J. P., Wang, H., Maiti, P., Bianchi, E., Xu, S., Lloyd, B. N., Dawson-Scully, K. D., Kang, D. E., & Lakshmana, M. K. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.05.029 · Cited by 17
Systematic Review on the Impact of Intelligence on Cognitive Decline and Dementia Risk
Rodriguez, F. S., & Lachmann, T. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00658 · Cited by 18
Synaptopathy Mechanisms in ALS Caused by C9orf72 Repeat Expansion
Nishimura, A. L., & Arias, N. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.660693 · Cited by 17
Preserved synaptic vesicle recycling in hippocampal neurons in a mouse Alzheimer’s disease model
Yao, P. J., Bushlin, I., & Furukawa, K. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.02.121 · Cited by 17
Metadata
- Authors
- Scheff, S. W., DeKosky, S. T., & Price, D. A.
- Affiliations
- University of Kentucky (US)
- Corresponding author
- Scheff, Stephen W.
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 1990-01
- Volume
- 11
- Issue
- 1
- Pages
- 29-37
- ISSN
- 0197-4580 (ISSN-L)
- OpenAlex
- W2083752135
- Cited by
- 446
- References
- 41
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 14 · 2023: 19 · 2022: 16 · 2021: 14 · 2020: 19 · 2019: 14 · 2018: 15 · 2017: 12 · 2016: 17 · 2015: 21 · 2014: 13 · 2013: 16 · 2012: 16
- FWCI
- 9.93
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Kentucky
- National Institute on Aging (P50AG005144, AG-05144, P01AG005119, AG0 5119)
- 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 › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- Alzheimer's disease, synaptic density, synapse size, postsynaptic density, frontal cortex, Brodmann area 9, cortical layers, synaptic loss, postmortem interval, neuropathology
- MeSH terms
- Aged, Aged, 80 and over, Alzheimer Disease, Cell Count, Cerebral Cortex, Female, Humans, Male, Middle Aged, Nerve Degeneration, Synapses, In Vitro Techniques
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