Selected Findings from the Religious Orders Study and Rush Memory and Aging Project

The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease

McKhann, G. M., Knopman, D. S., Chertkow, H., Hyman, B. T., Jack, C. R., Kawas, C. H., Klunk, W. E., Koroshetz, W. J., Manly, J. J., Mayeux, R., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.005 · Cited by 18,657 · see citing works

The diagnosis of mild cognitive impairment due to Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease

Albert, M. S., DeKosky, S. T., Dickson, D., Dubois, B., Feldman, H. H., Fox, N. C., Gamst, A., Holtzman, D. M., Jagust, W. J., Petersen, R. C., et al. (2011) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2011.03.008 · Cited by 10,152 · see citing works

Toward defining the preclinical stages of Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease

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 · see citing works

Forecasting the global burden of Alzheimer's disease

Brookmeyer, R., Johnson, E., Ziegler‐Graham, K., & Arrighi, H. M. (2007) · Alzheimer's & Dementia · doi:10.1016/j.jalz.2007.04.381 · Cited by 3,370 · see citing works

The Diagnosis of Mild Cognitive Impairment due to Alzheimer’s Disease: Recommendations from the National Institute on Aging-Alzheimer’s Association Workgroups on Diagnostic Guidelines for Alzheimer’s Disease

Albert, M., DeKosky, S. T., Dickson, D. W., Dubois, B., Feldman, H., Fox, N. C., Gamst, A. C., Holtzman, D. M., Jagust, W. J., Petersen, R. C., et al. (2013) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/appi.focus.11.1.96 · Cited by 2,630 · see citing works

Perceived social isolation and cognition

Cacioppo, J. T., & Hawkley, L. C. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.06.005 · Cited by 2,144 · see citing works

An active and socially integrated lifestyle in late life might protect against dementia

Fratiglioni, L., Paillard-Borg, S., & Winblad, B. (2004) · The Lancet Neurology · doi:10.1016/s1474-4422(04)00767-7 · Cited by 2,135 · see citing works

Loneliness and Risk of Alzheimer Disease

Wilson, R. S., Krueger, K. R., Arnold, S. E., Schneider, J. A., Kelly, J. F., Barnes, L. L., Tang, Y., & Bennett, D. A. (2007) · Archives of General Psychiatry · doi:10.1001/archpsyc.64.2.234 · Cited by 1,363 · see citing works

Neuropathology of older persons without cognitive impairment from two community-based studies

Bennett, D. A., Schneider, J. A., Arvanitakis, Z., Kelly, J. F., Aggarwal, N. T., Shah, R. C., & Wilson, R. S. (2006) · Neurology · doi:10.1212/01.wnl.0000219668.47116.e6 · Cited by 1,336 · see citing works

Diabetes mellitus and risk of Alzheimer disease and decline in cognitive function

Arvanitakis, Z., Wilson, R. S., Bienias, J. L., Evans, D. A., & Bennett, D. A. (2004) · Archives of Neurology · doi:10.1001/archneur.61.5.661 · Cited by 1,258 · see citing works

Type 2 Diabetes, APOE Gene, and the Risk for Dementia and Related Pathologies

Peila, R., Rodriguez, B. L., & Launer, L. J. (2002) · Diabetes · doi:10.2337/diabetes.51.4.1256 · Cited by 1,207 · see citing works

Natural history of mild cognitive impairment in older persons

Bennett, D. A., Wilson, R. S., Schneider, J. A., Evans, D. A., Beckett, L. A., Aggarwal, N. T., Barnes, L. L., Fox, J. H., & Bach, J. (2002) · Neurology · doi:10.1212/wnl.59.2.198 · Cited by 1,037 · see citing works

The neuropathology of probable Alzheimer disease and mild cognitive impairment

Schneider, J. A., Arvanitakis, Z., Leurgans, S. E., & Bennett, D. A. (2009) · Annals of Neurology · doi:10.1002/ana.21706 · Cited by 935 · see citing works

Age, Neuropathology, and Dementia

Savva, G. M., Wharton, S. B., Ince, P. G., Forster, G., Matthews, F. E., & Brayne, C. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0806142 · Cited by 900 · see citing works

Individual differences in rates of change in cognitive abilities of older persons.

Wilson, R. S., Beckett, L. A., Barnes, L. L., Schneider, J. A., Bach, J., Evans, D. A., & Bennett, D. A. (2002) · Psychology and Aging · doi:10.1037/0882-7974.17.2.179 · Cited by 842 · see citing works

Overview and Findings from the Rush Memory and Aging Project

Bennett, D. A., Schneider, J. A., Buchman, A. S., Barnes, L. L., Boyle, P. A., & Wilson, R. S. (2012) · Current Alzheimer Research · doi:10.2174/156720512801322663 · Cited by 837 · see citing works

Loneliness and the health of older people

Luanaigh, C. Ó., & LAWLOR, B. A. (2008) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.2054 · Cited by 750 · see citing works

Hippocampal and entorhinal atrophy in mild cognitive impairment

Devanand, D. P., Pradhaban, G., Liu, X., Khandji, A., Santi, S. D., Segal, S., Rusinek, H., Pelton, G. H., Honig, L. S., Mayeux, R. P., et al. (2007) · Neurology · doi:10.1212/01.wnl.0000256697.20968.d7 · Cited by 739 · see citing works

The effect of social networks on the relation between Alzheimer's disease pathology and level of cognitive function in old people: a longitudinal cohort study

Bennett, D. A., Schneider, J. A., Tang, Y., Arnold, S. E., & Wilson, R. S. (2006) · The Lancet Neurology · doi:10.1016/s1474-4422(06)70417-3 · Cited by 718 · see citing works

Overview and Findings from the Religious Orders Study

Bennett, D. A., Schneider, J. A., Arvanitakis, Z., & Wilson, R. S. (2012) · Current Alzheimer Research · doi:10.2174/156720512801322573 · Cited by 647 · see citing works

Frequency and course of mild cognitive impairment in a multiethnic community

Manly, J. J., Tang, M., Schupf, N., Stern, Y., Vonsattel, J., & Mayeux, R. P. (2008) · Annals of Neurology · doi:10.1002/ana.21326 · Cited by 592 · see citing works

Neurofibrillary tangles mediate the association of amyloid load with clinical Alzheimer disease and level of cognitive function

Bennett, D. A., Schneider, J. A., Wilson, R. S., Bienias, J. L., & Arnold, S. E. (2004) · Archives of Neurology · doi:10.1001/archneur.61.3.378 · Cited by 526 · see citing works

Diabetes, Alzheimer disease, and vascular dementia

Ahtiluoto, S., Polvikoski, T. M., Peltonen, M., Solomon, A., Tuomilehto, J., Winblad, B. G., Sulkava, R. O., & Kivipelto, M. (2010) · Neurology · doi:10.1212/wnl.0b013e3181f4d7f8 · Cited by 493 · see citing works

White matter changes in mild cognitive impairment and AD: a diffusion tensor imaging study

Medina, D., deToledo-Morrell, L., Urresta, F., Gabrieli, J. D. E., Moseley, M., Fleischman, D., Bennett, D. A., Leurgans, S., Turner, D. A., & Stebbins, G. T. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.03.026 · Cited by 492 · see citing works

Conversion from subtypes of mild cognitive impairment to Alzheimer dementia

Fischer, P., Jungwirth, S., Zehetmayer, S., Weissgram, S., Hoenigschnabl, S., Gelpi, E., Krampla, W., & Tragl, K. H. (2007) · Neurology · doi:10.1212/01.wnl.0000252358.03285.9d · Cited by 471 · see citing works

The Public Health Impact of Alzheimer's Disease, 2000–2050: Potential Implication of Treatment Advances

Sloane, P. D., Zimmerman, S. I., Suchindran, C., Reed, P. S., Wang, L., Boustani, M. A., & Sudha, S. (2002) · Annual Review of Public Health · doi:10.1146/annurev.publhealth.23.100901.140525 · Cited by 461 · see citing works

Pathological correlates of dementia in a longitudinal, population‐based sample of aging

Sonnen, J. A., Larson, E. B., Crane, P. K., Haneuse, S., Li, G., Schellenberg, G. D., Craft, S., Leverenz, J. B., & Montine, T. J. (2007) · Annals of Neurology · doi:10.1002/ana.21208 · Cited by 432 · see citing works

Decision Rules Guiding the Clinical Diagnosis of Alzheimer’s Disease in Two Community-Based Cohort Studies Compared to Standard Practice in a Clinic-Based Cohort Study

Bennett, D. A., Schneider, J. A., Aggarwal, N. T., Arvanitakis, Z., Shah, R. C., Kelly, J. F., Fox, J. H., Cochran, E. J., Arends, D., Treinkman, A., et al. (2006) · Neuroepidemiology · doi:10.1159/000096129 · Cited by 407 · see citing works

Microinfarct Pathology, Dementia, and Cognitive Systems

Arvanitakis, Z., Leurgans, S. E., Barnes, L. L., Bennett, D. A., & Schneider, J. A. (2011) · Stroke · doi:10.1161/strokeaha.110.595082 · Cited by 404 · see citing works

Neuropathologic Outcome of Mild Cognitive Impairment Following Progression to Clinical Dementia

Jicha, G. A., Parisi, J. E., Dickson, D. W., Johnson, K., Cha, R., Ivnik, R. J., Tangalos, E. G., Boeve, B. F., Knopman, D. S., Braak, H., et al. (2006) · Archives of Neurology · doi:10.1001/archneur.63.5.674 · Cited by 399 · see citing works

Prediction of conversion from mild cognitive impairment to Alzheimer's disease dementia based upon biomarkers and neuropsychological test performance

Ewers, M., Walsh, C., Trojanowski, J. Q., Shaw, L. M. J., Petersen, R. C., Jack, C. R., Feldman, H., Bokde, A. L. W., Alexander, G. E., Scheltens, P., et al. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.10.019 · Cited by 397 · see citing works

Social Network, Cognitive Function, and Dementia Incidence Among Elderly Women

Crooks, V. C., Lubben, J., Petitti, D. B., Little, D., & Chiu, V. (2008) · American Journal of Public Health · doi:10.2105/ajph.2007.115923 · Cited by 390 · see citing works

Early and late life cognitive activity and cognitive systems in old age

WILSON, R. S., BARNES, L. L., KRUEGER, K. R., HOGANSON, G., BIENIAS, J. L., & BENNETT, D. A. (2005) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617705050459 · Cited by 355 · see citing works

Effect of social networks on 10 year survival in very old Australians: the Australian longitudinal study of aging

Giles, L. C., Glonek, G. F. V., Luszcz, M. A., & Andrews, G. R. (2005) · Journal of Epidemiology & Community Health · doi:10.1136/jech.2004.025429 · Cited by 324 · see citing works

Mild cognitive impairment

Boyle, P. A., Wilson, R. S., Aggarwal, N. T., Tang, Y., & Bennett, D. A. (2006) · Neurology · doi:10.1212/01.wnl.0000228244.10416.20 · Cited by 314 · see citing works

Diffusion tensor imaging and aging—A review.

Moseley, M. (2002) · NMR in Biomedicine · doi:10.1002/nbm.785 · Cited by 302 · see citing works

Longitudinal course and neuropathologic outcomes in original vs revised MCI and in pre-MCI

Storandt, M., Grant, E., Miller, J. P., & Morris, J. C. (2006) · Neurology · doi:10.1212/01.wnl.0000228231.26111.6e · Cited by 285 · see citing works

Apolipoprotein E ε4 allele, AD pathology, and the clinical expression of Alzheimer’s disease

Bennett, D. A., Wilson, R. S., Schneider, J. A., Evans, D. A., Aggarwal, N. T., Arnold, S. E., Cochran, E. J., Berry-Kravis, E., & Bienias, J. L. (2003) · Neurology · doi:10.1212/01.wnl.0000042478.08543.f7 · Cited by 282 · see citing works

Diabetes is related to cerebral infarction but not to AD pathology in older persons

Arvanitakis, Z., Schneider, J. A., Wilson, R. S., Li, Y., Arnold, S. E., Wang, Z., & Bennett, D. A. (2006) · Neurology · doi:10.1212/01.wnl.0000247053.45483.4e · Cited by 280 · see citing works

Longitudinal MRI atrophy biomarkers: Relationship to conversion in the ADNI cohort

Risacher, S. L., Shen, L., West, J. D., Kim, S., McDonald, B. C., Beckett, L. A., Harvey, D. J., Jack, C. R., Weiner, M. W., & Saykin, A. J. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.04.029 · Cited by 276 · see citing works

Diffusion tensor imaging in mild cognitive impairment and Alzheimerʼs disease: a review

Chua, T. C., Wen, W., Slavin, M. J., & Sachdev, P. S. (2008) · Current Opinion in Neurology · doi:10.1097/wco.0b013e3282f4594b · Cited by 273 · see citing works

Subcortical infarcts, Alzheimer's disease pathology, and memory function in older persons

Schneider, J. A., Boyle, P. A., Arvanitakis, Z., Bienias, J. L., & Bennett, D. A. (2007) · Annals of Neurology · doi:10.1002/ana.21142 · Cited by 264 · see citing works

SOCIAL NETWORKS AND INFLAMMATORY MARKERS IN THE FRAMINGHAM HEART STUDY

LOUCKS, E. B., SULLIVAN, L. M., D’AGOSTINO Sr, R. B., LARSON, M. G., BERKMAN, L. F., & BENJAMIN, E. J. (2006) · Journal of Biosocial Science · doi:10.1017/s0021932005001203 · Cited by 247 · see citing works

Statin therapy is associated with reduced neuropathologic changes of Alzheimer disease

Li, G., Larson, E. B., Sonnen, J. A., Shofer, J. B., Petrie, E. C., Schantz, A. M., Peskind, E. R., Raskind, M. A., Breitner, J. C. S., & Montine, T. J. (2007) · Neurology · doi:10.1212/01.wnl.0000277657.95487.1c · Cited by 237 · see citing works

AD lesions and infarcts in demented and non‐demented Japanese‐American men

Petrovitch, H., Ross, G. W., Steinhorn, S. C., Abbott, R. D., Markesbery, W., Davis, D., Nelson, J., Hardman, J., Masaki, K., Vogt, M. R., et al. (2005) · Annals of Neurology · doi:10.1002/ana.20318 · Cited by 230 · see citing works

Different Patterns of Cerebral Injury in Dementia With or Without Diabetes

Sonnen, J. A. (2009) · Archives of Neurology · doi:10.1001/archneurol.2008.579 · Cited by 223 · see citing works

Effect of infarcts on dementia in the Baltimore longitudinal study of aging

Troncoso, J. C., Zonderman, A. B., Resnick, S. M., Crain, B., Pletnikova, O., & O'Brien, R. J. (2008) · Annals of Neurology · doi:10.1002/ana.21413 · Cited by 219 · see citing works

What Aspects of Social Network Are Protective for Dementia? Not the Quantity But the Quality of Social Interactions Is Protective Up to 15 Years Later

Amieva, H., Stoykova, R., Matharan, F., Helmer, C., Antonucci, T. C., & Dartigues, J. (2010) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3181f5e121 · Cited by 217 · see citing works

Hippocampal disconnection contributes to memory dysfunction in individuals at risk for Alzheimer’s disease

Stoub, T. R., deToledo‐Morrell, L., Stebbins, G. T., Leurgans, S. E., Bennett, D. A., & Shah, R. C. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603414103 · Cited by 200 · see citing works

Statins, incident Alzheimer disease, change in cognitive function, and neuropathology

Arvanitakis, Z., Schneider, J. A., Wilson, R. S., Bienias, J. L., Kelly, J. F., Evans, D. A., & Bennett, D. A. (2008) · Neurology · doi:10.1212/01.wnl.0000288181.00826.63 · Cited by 199 · see citing works

MRI predictors of risk of incident Alzheimer disease

Stoub, T. R., Bulgakova, M., Leurgans, S. E., Bennett, D. A., Fleischman, D. A., Turner, D. A., & deToledo‐Morrell, L. (2005) · Neurology · doi:10.1212/01.wnl.0000160089.43264.1a · Cited by 188 · see citing works

Type 2 Diabetes Is Negatively Associated With Alzheimer's Disease Neuropathology

Beeri, M. S., Silverman, J. M., Davis, K. L., Marin, D. B., Grossman, H. T., Schmeidler, J., Purohit, D. P., Perl, D. P., Davidson, M. H., Mohs, R. C., et al. (2005) · The Journals of Gerontology Series A · doi:10.1093/gerona/60.4.471 · Cited by 187 · see citing works

Volumetric MRI vs clinical predictors of Alzheimer disease in mild cognitive impairment

Fleisher, A., Sun, S., Taylor, C., Ward, C., Gamst, A. C., Petersen, R. C., Jack, C. R., Aisen, P. S. S., & Thal, L. J. (2008) · Neurology · doi:10.1212/01.wnl.0000287091.57376.65 · Cited by 177 · see citing works

Role of the neuropathology of Alzheimer disease in dementia in the oldest-old

Haroutunian, V., Schnaider-Beeri, M., Schmeidler, J., Wysocki, M., Purohit, D. P., Perl, D. P., Libow, L. S., Lesser, G. T., Maroukian, M., & Grossman, H. T. (2008) · Archives of Neurology · doi:10.1001/archneur.65.9.1211 · Cited by 154 · see citing works

Synaptic proteins, neuropathology and cognitive status in the oldest-old

Head, E., Corrada, M. M., Kahle-Wrobleski, K., Kim, R. C., Sarsoza, F., Goodus, M., & Kawas, C. H. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.10.001 · Cited by 145 · see citing works

Mild cognitive impairment in different functional domains and incident Alzheimer's disease

Aggarwal, N. T. (2005) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2004.053561 · Cited by 138 · see citing works

Loneliness and cognition in older people: The Dublin Healthy Ageing study

O’Luanaigh, C., O'Connell, H. P., Chin, A., Hamilton, F., Coen, R. F., Walsh, C., Walsh, J. B., Caokley, D., Cunningham, C. J., & LAWLOR, B. A. (2011) · Aging & Mental Health · doi:10.1080/13607863.2011.628977 · Cited by 127 · see citing works

Cognitive reserve, presynaptic proteins, and dementia in the elderly

Honer, W. G., Barr, A. M., Sawada, K., Thornton, A. E., Morris, M. C., Leurgans, S. E., Schneider, J. A., & Bennett, D. A. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.38 · Cited by 100 · see citing works

A diffusion tensor MRI study of patients with MCI and AD with a 2-year clinical follow-up

Scola, E., Bozzali, M., Agosta, F., Magnani, G., Franceschi, M., Sormani, M. P., Cercignani, M., Pagani, E., Falautano, M., Filippi, M., et al. (2010) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.2009.189639 · Cited by 98 · see citing works

Neuropathologic intermediate phenotypes enhance association to Alzheimer susceptibility alleles

Bennett, D. A., De Jager, P. L., Leurgans, S. E., & Schneider, J. A. (2009) · Neurology · doi:10.1212/wnl.0b013e3181a2e87d · Cited by 93 · see citing works

Social Networks and Incident Stroke Among Women With Suspected Myocardial Ischemia

Rutledge, T. R., Linke, S., Olson, M. B., Francis, J., Johnson, B. D., Bittner, V., York, K. M., McClure, C., Kelsey, S. F., Reís, S. E., et al. (2008) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3181656e09 · Cited by 76 · see citing works

Age, Alzheimer's disease and dementia in the Baltimore Longitudinal Study of Ageing

Dolan, D., Troncoso, J., Resnick, S. M., Crain, B. J., Zonderman, A. B., & O'Brien, R. J. (2010) · Brain · doi:10.1093/brain/awq141 · Cited by 70 · see citing works

Changes in parahippocampal white matter integrity in amnestic mild cognitive impairment: A diffusion tensor imaging study

Rogalski, E., Murphy, C. M., deToledo-Morrell, L., Shah, R. C., Moseley, M. E., Bammer, R., & Stebbins, G. T. (2009) · Behavioural Neurology · doi:10.3233/ben-2009-0235 · Cited by 59 · see citing works

Changes in Parahippocampal White Matter Integrity in Amnestic Mild Cognitive Impairment: A Diffusion Tensor Imaging Study

Rogalski, E. J., Murphy, C. M., deToledo‐Morrell, L., Shah, R. C., Moseley, M. E., Bammer, R., & Stebbins, G. T. (2009) · Behavioural Neurology · doi:10.1155/2009/408037 · Cited by 58 · see citing works

Linking Hippocampal Structure and Function to Memory Performance in an Aging Population

Reitz, C., Brickman, A. M., Brown, T. R., Manly, J. J., DeCarli, C. S., Small, S. A., & Mayeux, R. P. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.214 · Cited by 54 · see citing works

Impact of social network on cognitive performances and age-related cognitive decline across a 20-year follow-up

Stoykova, R., Matharan, F., Dartigues, J.-F., & Amieva, H. (2011) · International Psychogeriatrics · doi:10.1017/s1041610211001165 · Cited by 53 · see citing works

Loneliness and vascular biomarkers: the Dublin Healthy Ageing Study

O’Luanaigh, C., O'Connell, H. P., Chin, A., Hamilton, F., Coen, R. F., Walsh, C., Walsh, J. B., Coakley, D., Molloy, A. M., Scott, J. M., et al. (2011) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.2695 · Cited by 45 · see citing works

Atrophy and dysfunction of parahippocampal white matter in mild Alzheimer's disease

Wang, C., Stebbins, G. T., Medina, D. A., Shah, R. C., Bammer, R., Moseley, M. E., & deToledo‐Morrell, L. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.01.020 · Cited by 31 · see citing works

Blood Pressure and Lower Limb Function in Older Persons

Shah, R. C., Wilson, R. S., Bienias, J. L., Arvanitakis, Z., Evans, D. A., & Bennett, D. A. A. (2006) · The Journals of Gerontology Series A · doi:10.1093/gerona/61.8.839 · Cited by 20 · see citing works

Defeating Alzheimer's disease and other dementias: a priority for European science and society

Winblad, B., Amouyel, P., Andrieu, S., Ballard, C., Brayne, C., Brodaty, H., Cedazo-Minguez, A., Dubois, B., Edvardsson, D., Feldman, H., et al. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)00062-4 · Cited by 1,676 · see citing works

Diagnosis and Management of Dementia: Review

Arvanitakis, Z., Shah, R. C., & Bennett, D. A. (2019) · JAMA · doi:10.1001/jama.2019.4782 · Cited by 1,451 · see citing works

Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci

De Jager, P. L., Srivastava, G., Lunnon, K., Burgess, J., Schalkwyk, L. C., Yu, L., Eaton, M. L., Keenan, B. T., Ernst, J., McCabe, C., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3786 · Cited by 956 · see citing works

Contribution of cerebrovascular disease in autopsy confirmed neurodegenerative disease cases in the National Alzheimer’s Coordinating Centre

Toledo, J. B., Arnold, S. E., Raible, K., Brettschneider, J., Xie, S. X., Grossman, M., Monsell, S. E., Kukull, W. A., & Trojanowski, J. Q. (2013) · Brain · doi:10.1093/brain/awt188 · Cited by 849 · see citing works

Impact of multiple pathologies on the threshold for clinically overt dementia

Kapasi, A., DeCarli, C., & Schneider, J. A. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1717-7 · Cited by 739 · see citing works

The overlap between vascular disease and Alzheimer’s disease - lessons from pathology

Attems, J., & Jellinger, K. A. (2014) · BMC Medicine · doi:10.1186/s12916-014-0206-2 · Cited by 739 · see citing works

Target risk factors for dementia prevention: a systematic review and Delphi consensus study on the evidence from observational studies: Major risk factors for dementia prevention

Deckers, K., van Boxtel, M. P. J., Schiepers, O. J. G., de Vugt, M., Muñoz Sánchez, J. L., Anstey, K. J., Brayne, C., Dartigues, J.-F., Engedal, K., Kivipelto, M., et al. (2015) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.4245 · Cited by 534 · see citing works

Epigenetic age of the pre-frontal cortex is associated with neuritic plaques, amyloid load, and Alzheimer’s disease related cognitive functioning

Levine, M. E., Lu, A. T., Bennett, D. A., & Horvath, S. (2015) · Aging · doi:10.18632/aging.100864 · Cited by 455 · see citing works

TDP-43 stage, mixed pathologies, and clinical Alzheimer’s-type dementia

James, B. D., Wilson, R. S., Boyle, P. A., Trojanowski, J. Q., Bennett, D. A., & Schneider, J. A. (2016) · Brain · doi:10.1093/brain/aww224 · Cited by 407 · see citing works

Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer’s disease susceptibility

Raj, T., Li, Y. I., Wong, G., Humphrey, J., Wang, M., Ramdhani, S., Wang, Y.-C., Ng, B., Gupta, I., Haroutunian, V., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0238-1 · Cited by 430 · see citing works

Neuropathology of Alzheimer's Disease

Trejo‐Lopez, J. A., Yachnis, A. T., & Prokop, S. (2021) · Neurotherapeutics · doi:10.1007/s13311-021-01146-y · Cited by 398 · see citing works

Untangling Genetic Risk for Alzheimer’s Disease

Pimenova, A. A., Raj, T., & Goate, A. M. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.05.014 · Cited by 223 · see citing works

Clinical and multimodal biomarker correlates of ADNI neuropathological findings

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Brain and blood metabolome for Alzheimer's dementia: findings from a targeted metabolomics analysis

Huo, Z., Yu, L., Yang, J., Zhu, Y., Bennett, D. A., & Zhao, J. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.10.014 · Cited by 154 · see citing works

Multiple comorbid neuropathologies in the setting of Alzheimer's disease neuropathology and implications for drug development

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Single-Cell RNA Sequencing: Unraveling the Brain One Cell at a Time

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NMNAT2:HSP90 Complex Mediates Proteostasis in Proteinopathies

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Clinical and imaging features of mixed Alzheimer and vascular pathologies

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Can we prevent Alzheimer's disease? Secondary “prevention” trials in Alzheimer's disease

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The prevalence, correlation, and co-occurrence of neuropathology in old age: harmonisation of 12 measures across six community-based autopsy studies of dementia

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Association of White Matter Rarefaction, Arteriolosclerosis, and Tau With Dementia in Chronic Traumatic Encephalopathy

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The Epidemiology of Olfactory Disorders

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ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology

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RNA-Seq investigations of human post-mortem trigeminal ganglia

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Extra-virgin olive oil for potential prevention of Alzheimer disease

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Brain tocopherols related to Alzheimer's disease neuropathology in humans

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Cerebral amyloid angiopathy interacts with neuritic amyloid plaques to promote tau and cognitive decline

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Alzheimer’s Disease and ncRNAs

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Influenza Vaccination Reduces Dementia Risk in Chronic Kidney Disease Patients: A Population-Based Cohort Study

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Watershed microinfarct pathology and cognition in older persons

Kapasi, A., Leurgans, S. E., James, B. D., Boyle, P. A., Arvanitakis, Z., Nag, S., Bennett, D. A., Buchman, A. S., & Schneider, J. A. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.05.027 · Cited by 48 · see citing works

The epigenome in Alzheimer’s disease: current state and approaches for a new path to gene discovery and understanding disease mechanism

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Entorhinal Cortex: Antemortem Cortical Thickness and Postmortem Neurofibrillary Tangles and Amyloid Pathology

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Entorhinal Cortex Thickness across the Human Lifespan

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Post-mortem brain analyses of the Lothian Birth Cohort 1936: extending lifetime cognitive and brain phenotyping to the level of the synapse

Henstridge, C. M., Jackson, R. J., Kim, J. M., Herrmann, A. G., Wright, A. K., Harris, S. E., Bastin, M. E., Starr, J. M., Wardlaw, J. M., Gillingwater, T. H., et al. (2015) · Acta Neuropathologica Communications · doi:10.1186/s40478-015-0232-0 · Cited by 40 · see citing works

In vivo hippocampal subfield shape related to TDP-43, amyloid beta, and tau pathologies

Hanko, V., Apple, A. C., Alpert, K. I., Warren, K., Schneider, J. A., Arfanakis, K., Bennett, D. A., & Wang, L. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.10.013 · Cited by 41 · see citing works

TREM2 gene expression associations with Alzheimer’s disease neuropathology are region-specific: implications for cortical versus subcortical microglia

Winfree, R. L., Seto, M., Dumitrescu, L. C., Menon, V., Jager, P. L. D., Wang, Y., Schneider, J. A., Bennett, D. A., Jefferson, A. L., & Hohman, T. J. (2023) · Acta Neuropathologica · doi:10.1007/s00401-023-02564-2 · Cited by 38 · see citing works

Presynaptic proteins complexin-I and complexin-II differentially influence cognitive function in early and late stages of Alzheimer’s disease

Ramos‐Miguel, A., Sawada, K., Jones, A. A., Thornton, A. E., Barr, A. M., Leurgans, S. E., Schneider, J. A., Bennett, D. A., & Honer, W. G. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1647-9 · Cited by 39 · see citing works

Cell type-specific histone acetylation profiling of Alzheimer’s disease subjects and integration with genetics

Ramamurthy, E., Welch, G., Cheng, J., Yuan, Y., Gunsalus, L. M., Bennett, D. A., Tsai, L., & Pfenning, A. R. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.948456 · Cited by 39 · see citing works

Blood pressure variability, dementia, and role of antihypertensive medications in older adults

Mahinrad, S., Bennett, D. A., Sorond, F. A., & Gorelick, P. B. (2023) · Alzheimer's & Dementia · doi:10.1002/alz.12935 · Cited by 32 · see citing works

Trends in the incidence of dementia: design and methods in the Alzheimer Cohorts Consortium

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Insights into the pathological basis of dementia from population‐based neuropathology studies

Wharton, S. B., Simpson, J. E., Ince, P. G., Richardson, C. D., Merrick, R. L., Matthews, F. E., Brayne, C., & CFAS (2023) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12923 · Cited by 24 · see citing works

I GF2R circular RNA hsa_circ_0131235 expression in the middle temporal cortex is associated with AD pathology

Bigarré, I. M., Trombetta, B. A., Guo, Y., Arnold, S. E., & Carlyle, B. C. (2021) · Brain and Behavior · doi:10.1002/brb3.2048 · Cited by 26 · see citing works

Pathologic and clinical correlates of region-specific brain GFAP in Alzheimer’s disease

Phillips, J., Winfree, R. L., Seto, M., Schneider, J. A., Bennett, D. A., Dumitrescu, L. C., & Hohman, T. J. (2024) · Acta Neuropathologica · doi:10.1007/s00401-024-02828-5 · Cited by 23 · see citing works

Social Cognition Deficits: Current Position and Future Directions for Neuropsychological Interventions in Cerebrovascular Disease

Njomboro, P. (2017) · Behavioural Neurology · doi:10.1155/2017/2627487 · Cited by 22 · see citing works

Integration of transcriptome-wide association study with neuronal dysfunction assays provides functional genomics evidence for Parkinson’s disease genes

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Ex-vivo quantitative susceptibility mapping of human brain hemispheres

Evia, A. M., Kotrotsou, A., Tamhane, A. A., Dawe, R. J., Kapasi, A., Leurgans, S. E., Schneider, J. A., Bennett, D. A., & Arfanakis, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188395 · Cited by 19 · see citing works

Parahippocampal white matter volume predicts Alzheimer's disease risk in cognitively normal old adults

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Rate of brain aging and APOE ε4 are synergistic risk factors for Alzheimer’s disease

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Association between hippocampal microglia, AD and LATE‐NC, and cognitive decline in older adults

Kapasi, A., Yu, L., Leurgans, S. E., Agrawal, S., Boyle, P. A., Bennett, D. A., & Schneider, J. A. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.13780 · Cited by 15 · see citing works

Longitudinal cognitive performance of Alzheimer's disease neuropathological subtypes

Uretsky, M., Gibbons, L. E., Mukherjee, S., Trittschuh, E. H., Fardo, D. W., Boyle, P. A., Keene, C. D., Saykin, A. J., Crane, P. K., Schneider, J. A., et al. (2021) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1002/trc2.12201 · Cited by 15 · see citing works

In-vivo neuronal dysfunction by Aβ and tau overlaps with brain-wide inflammatory mechanisms in Alzheimer’s disease

Sanchez-Rodriguez, L. M., Khan, A. F., Adewale, Q., Bezgin, G., Therriault, J., Arias, J. F., Servaes, S., Rahmouni, N., Tissot, C., Stevenson, J., et al. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1383163 · Cited by 15 · see citing works

A ‘Comprehensive Visual Rating Scale’ for predicting progression to dementia in patients with mild cognitive impairment

Jang, J., Park, J. H., Kim, S., Park, Y. H., Pyun, J., Lim, J., Kim, Y., Youn, Y. C., Kim, S., & Initiative, T. A. D. N. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201852 · Cited by 10 · see citing works

Cell type-specific histone acetylation profiling of Alzheimer’s Disease subjects and integration with geneticsPreprint

Ramamurthy, E., Welch, G., Cheng, J., Yuan, Y., Gunsalus, L. M., Bennett, D. A., Tsai, L., & Pfenning, A. R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.26.010330 · Cited by 10 · see citing works

Understanding Alzheimer disease

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Elevated protease-activated receptor 4 (PAR4) gene expression in Alzheimer’s disease predicts cognitive decline

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Latin American Delphi Consensus on Vascular Cognitive Impairment: Definitions, Clinical Features, Pathophysiology, Prevention and Treatment

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Resilienz gegenüber psychischen Störungen im Alter

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Risk of Dementia in Patients Who Underwent Surgery under Neuraxial Anesthesia: A Nationwide Cohort Study

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The role of lifestyle factors in primary prevention of dementia

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Accelerometer-Measured Physical Activity Data Sets (Global Physical Activity Data Set Catalogue) That Include Markers of Cardiometabolic Health: Systematic Scoping Review

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Depressive symptoms and cognitive function in the U.S. POINTER study

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Prävention im Alter – Was ist gesichert?

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Paradigmenwechsel in der Demenzforschung

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rtPA in acute stroke patients with history of cognitive impairment

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Transcriptomic signatures of Aβ- and tau-induced neuronal dysfunction reveal inflammatory processes at the core of Alzheimer’s disease pathophysiologyPreprint

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Alzheimer’s disease syndrome – Recognizing the complexity of dementia

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Predictive analytics in Alzheimer’s disease: pioneering memory projection

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Optimisation et évaluation de la perfusion cérébrale par technique de marquage de spin dans la Maladie d'Alzheimer à début précoce

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A Multi-Omics Study of Cognitive Resilience to Alzheimer’s Disease

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Overview and Findings from the Religious Orders Study

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Religious Orders Study and Rush Memory and Aging Project

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Postmortem Indices Linking Risk Factors to Cognition

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Cognition and Neuropathology in Aging: Multidimensional Perspectives from the Rush Religious Orders Study and Rush Memory and Aging Project

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Overview and Findings from the Rush Memory and Aging Project

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