Sex differences in Alzheimer's disease and other dementias

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

Clinical epidemiology of Alzheimer’s disease: assessing sex and gender differences

Mielke, M., Vemuri, P., & Rocca, W. (2014) · Clinical Epidemiology · doi:10.2147/clep.s37929 · Cited by 1,021 · see citing works

Evolving Knowledge of Sex Differences in Brain Structure, Function, and Chemistry

Cosgrove, K. P., Mazure, C. M., & Staley, J. K. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.03.001 · Cited by 996 · see citing works

Sex modifies the <i>APOE</i> ‐related risk of developing Alzheimer disease

Altmann, A., Tian, L., Henderson, V. W., Greicius, M. D., & Alzheimer's Disease Neuroimaging Initiative Investigators (2014) · Annals of Neurology · doi:10.1002/ana.24135 · Cited by 891 · see citing works

Twenty years and still counting: including women as participants and studying sex and gender in biomedical research

Mazure, C. M., & Jones, D. P. (2015) · BMC Women s Health · doi:10.1186/s12905-015-0251-9 · Cited by 310 · see citing works

Analysis of the MIRIAD Data Shows Sex Differences in Hippocampal Atrophy Progression

Ardekani, B. A., Convit, A., & Bachman, A. H. (2016) · Journal of Alzheimer's Disease · doi:10.3233/jad-150780 · Cited by 141 · see citing works

Gender differences in risk factors for transition from mild cognitive impairment to Alzheimer’s disease: A CREDOS study

Kim, S., Kim, M. J., Kim, S., Kang, H. S., Lim, S. W., Myung, W., Lee, Y., Hong, C. H., Choi, S. H., Na, D. L., et al. (2015) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2015.07.002 · Cited by 127 · see citing works

Impact of Gender Differences on the Outcome of Alzheimer’s Disease

Sinforiani, E., Citterio, A., Zucchella, C., Bono, G., Corbetta, S., Merlo, P., & Mauri, M. F. (2010) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000318842 · Cited by 118 · see citing works

Sex and ESR1 genotype may influence the response to treatment with donepezil and rivastigmine in patients with Alzheimer's disease

Scacchi, R., Gambina, G., Broggio, E., & Corbo, R. M. (2014) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.4043 · Cited by 58 · see citing works

Sex Differences in Neuropsychiatric Symptoms of Alzheimer’s Disease: The Modifying Effect of Apolipoprotein Eε4 Status

Xing, Y., Tang, Y., & Jia, J. (2015) · Behavioural Neurology · doi:10.1155/2015/275256 · Cited by 38 · see citing works

Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer’s disease

Fang, E. F., Hou, Y., Palikaras, K., Adriaanse, B. A., Kerr, J. S., Yang, B., Lautrup, S., Hasan-Olive, M. M., Caponio, D., Dan, X., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0332-9 · Cited by 1,740 · see citing works

The Major Risk Factors for Alzheimer’s Disease: Age, Sex, and Genes Modulate the Microglia Response to Aβ Plaques

Sala Frigerio, C., Wolfs, L., Fattorelli, N., Thrupp, N., Voytyuk, I., Schmidt, I., Mancuso, R., Chen, W.-T., Woodbury, M. E., Srivastava, G., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.099 · Cited by 926 · see citing works

Sex Differences in the Adult Human Brain: Evidence from 5216 UK Biobank Participants

Ritchie, S. J., Cox, S. R., Shen, X., Lombardo, M. V., Reus, L. M., Alloza, C., Harris, M. A., Alderson, H. L., Hunter, S., Neilson, E., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy109 · Cited by 855 · see citing works

History and progress of hypotheses and clinical trials for Alzheimer’s disease

Liu, P.-P., Xie, Y., Meng, X.-Y., & Kang, J.-S. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0063-8 · Cited by 723 · see citing works

Sex differences in biological aging with a focus on human studies

Hägg, S., & Jylhävä, J. (2021) · eLife · doi:10.7554/elife.63425 · Cited by 442 · see citing works

Evidence-based prevention of Alzheimer's disease: systematic review and meta-analysis of 243 observational prospective studies and 153 randomised controlled trials

Yu, J.-T., Xu, W., Tan, C.-C., Andrieu, S., Suckling, J., Evangelou, E., Pan, A., Zhang, C., Jia, J., Feng, L., et al. (2020) · Journal of Neurology, Neurosurgery &amp; Psychiatry · doi:10.1136/jnnp-2019-321913 · Cited by 482 · see citing works

Elevated TREM2 Gene Dosage Reprograms Microglia Responsivity and Ameliorates Pathological Phenotypes in Alzheimer’s Disease Models

Lee, C. Y. D., Daggett, A., Gu, X., Jiang, L.-L., Langfelder, P., Li, X., Wang, N., Zhao, Y., Park, C. S., Cooper, Y., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.02.002 · Cited by 396 · see citing works

Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium

Kong, X.-Z., Mathias, S., Guadalupe, T., Glahn, D., Franke, B., Crivello, F., Tzourio-mazoyer, N., Fisher, S., Thompson, P., & Francks, C. (2018) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1718418115 · Cited by 392 · see citing works

Traumatic brain injury: sex, gender and intersecting vulnerabilities

Mollayeva, T., Mollayeva, S., & Colantonio, A. (2018) · Nature Reviews Neurology · doi:10.1038/s41582-018-0091-y · Cited by 336 · see citing works

The relevance of gender in Parkinson’s disease: a review

Picillo, M., Nicoletti, A. S. Q., Fetoni, V., Garavaglia, B., Barone, P., & Pellecchia, M. T. (2017) · Journal of Neurology · doi:10.1007/s00415-016-8384-9 · Cited by 261 · see citing works

Subjective Cognitive Decline: Level of Risk for Future Dementia and Mild Cognitive Impairment, a Meta-Analysis of Longitudinal Studies

Pike, K. E., Cavuoto, M. G., Li, L. Y., Wright, B. J., & Kinsella, G. (2021) · Neuropsychology Review · doi:10.1007/s11065-021-09522-3 · Cited by 269 · see citing works

The Role of Sex and Sex Hormones in Neurodegenerative Diseases

Vegeto, E., Villa, A. M., Torre, S. D., Crippa, V., Rusmini, P., Cristofani, R., Galbiati, M., Maggi, A. C., & Poletti, A. (2019) · Endocrine Reviews · doi:10.1210/endrev/bnz005 · Cited by 231 · see citing works

Deep learning encodes robust discriminative neuroimaging representations to outperform standard machine learning

Abrol, A., Fu, Z., Salman, M. S., Silva, R. F., Du, Y., Plis, S., & Calhoun, V. D. (2021) · Nature Communications · doi:10.1038/s41467-020-20655-6 · Cited by 221 · see citing works

The Application of Unsupervised Clustering Methods to Alzheimer’s Disease

Alashwal, H., Halaby, M. E., Crouse, J. J., ABDALLA, A. S., & Moustafa, A. A. (2019) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2019.00031 · Cited by 220 · see citing works

Alzheimer’s Risk Factors Age, APOE Genotype, and Sex Drive Distinct Molecular Pathways

Zhao, N., Ren, Y., Yamazaki, Y., Qiao, W., Li, F., Felton, L. M., Mahmoudiandehkordi, S., Kueider-Paisley, A., Sonoustoun, B., Arnold, M., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.02.034 · Cited by 225 · see citing works

Sex differences in the human brain: a roadmap for more careful analysis and interpretation of a biological reality

DeCasien, A. R., Guma, E., Liu, S., & Raznahan, A. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00448-w · Cited by 149 · see citing works

Aluminum and Alzheimer’s Disease

Colomina, M. T., & Peris‐Sampedro, F. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-60189-2_9 · Cited by 146 · see citing works

Sex differences in the response to oxidative and proteolytic stress

Tower, J., Pomatto, L. C. D., & Davies, K. J. A. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101488 · Cited by 143 · see citing works

The enigma and implications of brain hemispheric asymmetry in neurodegenerative diseases

Lubben, N., Ensink, E., Coetzee, G. A., & Labrie, V. (2021) · Brain Communications · doi:10.1093/braincomms/fcab211 · Cited by 132 · see citing works

Behavioural and Psychological Symptoms of Dementia: Correlates and Impact on Caregiver Distress

Mukherjee, A., Biswas, A., Roy, A., Biswas, S., Gangopadhyay, G., & Das, S. K. (2017) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000481568 · Cited by 129 · see citing works

Molecular and cellular pathophysiology of preclinical Alzheimer’s disease

Mufson, E. J., Ikonomović, M. D., Counts, S., Perez, S. E., Malek‐Ahmadi, M. H., Scheff, S. W., & Ginsberg, S. D. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.05.030 · Cited by 129 · see citing works

A quantitative meta-analysis of olfactory dysfunction in mild cognitive impairment

Roalf, D. R., Moberg, M. J., Turetsky, B. I., Brennan, L., Kabadi, S., Wolk, D. A., & Moberg, P. J. (2016) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2016-314638 · Cited by 124 · see citing works

Altered microRNAs related to synaptic function as potential plasma biomarkers for Alzheimer’s disease

Siedlecki‐Wullich, D., Català-Solsona, J., Fábregas, C., Hernández, I., Clarimón, J., Lleó, A., Boada, M., Saura, C. A., Rodrı́guez-Álvarez, J., & Miñano-Molina, A. J. (2019) · Alzheimer s Research & Therapy · doi:10.1186/s13195-019-0501-4 · Cited by 117 · see citing works

Microglial microRNAs mediate sex-specific responses to tau pathology

Kodama, L., Guzman, E., Etchegaray, J. I., Li, Y., Sayed, F. A., Zhou, L., Zhou, Y., Zhan, L., Le, D., Udeochu, J. C., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-019-0560-7 · Cited by 109 · see citing works

Sex-specific genetic predictors of Alzheimer’s disease biomarkers

(ADNI), A. D. N. I., Deming, Y., The Alzheimer Disease Genetics Consortium (ADGC), Dumitrescu, L., Barnes, L. L., Thambisetty, M., Kunkle, B., Gifford, K. A., Bush, W. S., Chibnik, L. B., et al. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1881-4 · Cited by 110 · see citing works

Sexual Dimorphism in the 3xTg-AD Mouse Model and Its Impact on Pre-Clinical Research

Dennison, J. L., Ricciardi, N. R., Lohse, I., Volmar, C., & Wahlestedt, C. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201014 · Cited by 100 · see citing works

Stress and Health in Nursing Students

Alvarez, H. A. O., Provencio‐Vasquez, E., Slavich, G. M., Laurent, J. G. C., Browning, M. H. E. M., McKee-Lopez, G., Robbins, L. K., & Spengler, J. D. (2019) · Nursing Research · doi:10.1097/nnr.0000000000000383 · Cited by 98 · see citing works

The association of depression with subsequent dementia diagnosis: A Swedish nationwide cohort study from 1964 to 2016

Holmquist, S., Nordström, A., & Nordström, P. (2020) · PLoS Medicine · doi:10.1371/journal.pmed.1003016 · Cited by 97 · see citing works

Sex differences in the genetic predictors of Alzheimer’s pathology

Dumitrescu, L., Barnes, L. L., Thambisetty, M., Beecham, G., Kunkle, B., Bush, W. S., Gifford, K. A., Chibnik, L. B., Mukherjee, S., De Jager, P. L., et al. (2019) · Brain · doi:10.1093/brain/awz206 · Cited by 93 · see citing works

Health and care service utilisation and cost over the life-span: a descriptive analysis of population data

Kalseth, J., & Halvorsen, T. (2020) · BMC Health Services Research · doi:10.1186/s12913-020-05295-2 · Cited by 97 · see citing works

Sex and gender differences in the treatment of Alzheimer’s disease: A systematic review of randomized controlled trials

Canevelli, M., Quarata, F., Remiddi, F., Lucchini, F., Lacorte, E., Vanacore, N., Bruno, G., & Cesari, M. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.11.035 · Cited by 88 · see citing works

Anti-inflammatory and cognitive effects of interferon-β1a (IFNβ1a) in a rat model of Alzheimer’s disease

Mudò, G., Frinchi, M., Nuzzo, D., Scaduto, P., Plescia, F., Massenti, M. F., Carlo, M. D., Cannizzaro, C., Cassata, G., Cicero, L. L., et al. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1417-4 · Cited by 82 · see citing works

OViTAD: Optimized Vision Transformer to Predict Various Stages of Alzheimer’s Disease Using Resting-State fMRI and Structural MRI Data

Sarraf, S., Sarraf, A., DeSouza, D. D., Anderson, J. A. E., Kabia, M., & The Alzheimer's Disease Neuroimagin, A. D. N. I. (2023) · Brain Sciences · doi:10.3390/brainsci13020260 · Cited by 85 · see citing works

Identification of age- and gender-associated long noncoding RNAs in the human brain with Alzheimer's disease

Cao, M., Li, H., Zhao, J., Cui, J., & Hu, G. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.05.023 · Cited by 80 · see citing works

Human microglia maturation is underpinned by specific gene regulatory networks

Han, C. Z., Li, R. Z., Hansen, E. A., Trescott, S., Fixsen, B. R., Nguyen, C. T., Mora, C., Spann, N. J., Bennett, H. R., Poirion, O., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.07.016 · Cited by 76 · see citing works

Sex differences in the development of mild cognitive impairment and probable Alzheimer’s disease as predicted by hippocampal volume or white matter hyperintensities

Burke, S. L., Hu, T., Fava, N. M., Li, T., Rodriguez, M. J., Schuldiner, K. L., Burgess, A., & Laird, A. R. (2018) · Journal of Women & Aging · doi:10.1080/08952841.2018.1419476 · Cited by 74 · see citing works

Association of Apolipoprotein E ɛ4, Educational Level, and Sex With Tau Deposition and Tau-Mediated Metabolic Dysfunction in Older Adults

Ramanan, V. K., Castillo, A. M., Knopman, D. S., Graff‐Radford, J., Lowe, V. J., Petersen, R. C., Jack, C. R., Mielke, M. M., & Vemuri, P. (2019) · JAMA Network Open · doi:10.1001/jamanetworkopen.2019.13909 · Cited by 71 · see citing works

Breath-based non-invasive diagnosis of Alzheimer’s disease: a pilot study

Tiele, A., Wicaksono, A. N., Daulton, E., Ifeachor, E., Eyre, V., Clarke, S., Timings, L., Pearson, S., Covington, J. A., & Li, X. (2019) · Journal of Breath Research · doi:10.1088/1752-7163/ab6016 · Cited by 73 · see citing works

Neuroprotective and neurotoxic outcomes of androgens and estrogens in an oxidative stress environment

Duong, P., Tenkorang, M. A. A., Trieu, J., McCuiston, C., Rybalchenko, N., & Cunningham, R. L. (2020) · Biology of Sex Differences · doi:10.1186/s13293-020-0283-1 · Cited by 74 · see citing works

Mechanistic insight into female predominance in Alzheimer’s disease based on aberrant protein S-nitrosylation of C3

Yang, H., Oh, C.-K., Amal, H., Wishnok, J. S., Lewis, S., Schahrer, E., Trudler, D., Nakamura, T., Tannenbaum, S. R., & Lipton, S. A. (2022) · Science Advances · doi:10.1126/sciadv.ade0764 · Cited by 70 · see citing works

Neuroimmune contributions to Alzheimer’s disease: a focus on human data

Haage, V., & De Jager, P. L. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01637-0 · Cited by 74 · see citing works

Sex-dependent autosomal effects on clinical progression of Alzheimer’s disease

Fan, C. C., Banks, S. J., Thompson, W. K., Chen, C., McEvoy, L. K., Tan, C. H., Kukull, W. A., Bennett, D. A. A., Farrer, L. A., Mayeux, R. P., et al. (2020) · Brain · doi:10.1093/brain/awaa164 · Cited by 69 · see citing works

Impact of Conventional Stroke Risk Factors on Stroke in Women

Madsen, T. E., Howard, V. J., Jiménez, M. C., Rexrode, K. M., Acelajado, M. C., Kleindorfer, D., & Chaturvedi, S. (2018) · Stroke · doi:10.1161/strokeaha.117.018418 · Cited by 72 · see citing works

Potential of Caffeine in Alzheimer’s Disease—A Review of Experimental Studies

Londzin, P., Zamora, M., Kąkol, B., Taborek, A., & Folwarczna, J. (2021) · Nutrients · doi:10.3390/nu13020537 · Cited by 71 · see citing works

Female specific risk factors for the development of Alzheimer’s disease neuropathology and cognitive impairment: Call for a precision medicine approach

Udeh-Momoh, C., & Watermeyer, T. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101459 · Cited by 67 · see citing works

ApoA-I deficiency increases cortical amyloid deposition, cerebral amyloid angiopathy, cortical and hippocampal astrogliosis, and amyloid-associated astrocyte reactivity in APP/PS1 mice

Button, E. B., Boyce, G. K., Wilkinson, A., Stukas, S. K., Hayat, A., Fan, J., Wadsworth, B. J., Robert, J., Martens, K. M., & Wellington, C. L. (2019) · Alzheimer s Research & Therapy · doi:10.1186/s13195-019-0497-9 · Cited by 71 · see citing works

Sex and gender in health research: updating policy to reflect evidence

Wainer, Z., Carcel, C., Hickey, M., Schiebinger, L. L., Schmiede, A., McKenzie, B. L., Jenkins, C. R., Webster, J. L., Woodward, M., Hehir, A., et al. (2019) · The Medical Journal of Australia · doi:10.5694/mja2.50426 · Cited by 67 · see citing works

Sex Differences in Healthspan Predict Lifespan in the 3xTg-AD Mouse Model of Alzheimer’s Disease

Kane, A. E., Shin, S., Wong, A. A., Fertan, E., Faustova, N. S., Howlett, S. E., & Brown, R. E. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00172 · Cited by 65 · see citing works

Roles of Progesterone, Testosterone and Their Nuclear Receptors in Central Nervous System Myelination and Remyelination

Ghoumari, A. M., Abi‐Ghanem, C., Asbelaoui, N., Schumacher, M., & Hussain, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093163 · Cited by 64 · see citing works

Decomposition of gender differences in cognitive functioning: National Survey of the Japanese elderly

Okamoto, S., Kobayashi, E., Murayama, H., Liang, J., Fukaya, T., & Shinkai, S. (2021) · BMC Geriatrics · doi:10.1186/s12877-020-01990-1 · Cited by 63 · see citing works

Towards an understanding of women’s brain aging: the immunology of pregnancy and menopause

Barth, C., & de Lange, A. G. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100850 · Cited by 59 · see citing works

Social class and the risk of dementia: A systematic review and meta-analysis of the prospective longitudinal studies

Bodryzlova, Y., Kim, A., Michaud, X., André, C., Bélanger, E., & Moullec, G. (2022) · Scandinavian Journal of Public Health · doi:10.1177/14034948221110019 · Cited by 61 · see citing works

The end game: respecting major sources of population diversity

Kopál, J., Uddin, L. Q., & Bzdok, D. (2023) · Nature Methods · doi:10.1038/s41592-023-01812-3 · Cited by 60 · see citing works

Precision medicine and drug development in Alzheimer’s disease: the importance of sexual dimorphism and patient stratification

Hampel, H., Vergallo, A., Giorgi, F. S., Kim, S. H., Depypere, H., Graziani, M., Saidi, A., Nisticò, R., & Lista, S. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2018.06.001 · Cited by 68 · see citing works

Downregulation of 14-3-3 Proteins in Alzheimer’s Disease

Gu, Q., Cuevas, E., Raymick, J. B., Kanungo, J., & Sarkar, S. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01754-y · Cited by 58 · see citing works

A clinical dose of angiotensin-converting enzyme (ACE) inhibitor and heterozygous ACE deletion exacerbate Alzheimer's disease pathology in mice

Liu, S., Ando, F., Fujita, Y., Liu, J., Maeda, T., Shen, X.-F., Kikuchi, K., Matsumoto, A., Yokomori, M., Tanabe-Fujimura, C., et al. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006420 · Cited by 48 · see citing works

Impact of impaired cerebral blood flow autoregulation on cognitive impairment

Wang, S., Tang, C., Liu, Y., Border, J. J., Roman, R. J., & Fan, F. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.1077302 · Cited by 52 · see citing works

Characterization of Music and Photograph Evoked Autobiographical Memories in People with Alzheimer’s Disease

Baird, A., Brancatisano, O., Gelding, R. W., & Thompson, W. F. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-180627 · Cited by 54 · see citing works

Parity and the risk of incident dementia: a COSMIC study

Bae, J. B., Lipnicki, D. M., Han, J. W., Sachdev, P. S., Kim, T. H., Kwak, K. P., Kim, B., Kim, S. G., Kim, J. L., Moon, S. W., et al. (2020) · Epidemiology and Psychiatric Sciences · doi:10.1017/s2045796020000876 · Cited by 54 · see citing works

Prevalence of Dementia and Cognitive Impairment No Dementia in a Large and Diverse Nationally Representative Sample: The ELSI-Brazil Study

Bertola, L., Suemoto, C. K., Aliberti, M. J. R., Gonçalves, N. G., Pinho, P. J. D. M. R., Costa, E., Lima‐Costa, M. F., & Ferri, C. P. (2023) · The Journals of Gerontology Series A · doi:10.1093/gerona/glad025 · Cited by 53 · see citing works

Neuroinflammation

Mukhara, D., Oh, U., & Neigh, G. N. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64123-6.00017-5 · Cited by 58 · see citing works

Exploring sex differences: insights into gene expression, neuroanatomy, neurochemistry, cognition, and pathology

Lafta, M. S., Mwinyi, J., Affatato, O., Rukh, G., Dang, J., Andersson, G., & Schiöth, H. B. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1340108 · Cited by 62 · see citing works

Sex differences in the genetic architecture of Alzheimer’s disease

Dumitrescu, L., Mayeda, E. R., Sharman, K., Moore, A. M., & Hohman, T. J. (2019) · Current Genetic Medicine Reports · doi:10.1007/s40142-019-0157-1 · Cited by 48 · see citing works

Longitudinal amyloid and tau PET imaging in Alzheimer's disease: A systematic review of methodologies and factors affecting quantification

Bollack, A., Pemberton, H., Collij, L. E., Markiewicz, P. J., Cash, D. M., Farrar, G., & Barkhof, F. (2023) · Alzheimer s & Dementia · doi:10.1002/alz.13158 · Cited by 49 · see citing works

Reconsidering repurposing: long-term metformin treatment impairs cognition in Alzheimer’s model mice

Cho, S. Y., Kim, E. W., Park, S. J., Phillips, B. U., Jeong, J., Kim, H., Heath, C. J., Kim, D., Jang, Y., López‐Cruz, L., et al. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02755-9 · Cited by 49 · see citing works

Cognitive Activity and Onset Age of Incident Alzheimer Disease Dementia

Wilson, R. S., Wang, T., Yu, L., Grodstein, F., Bennett, D. A., & Boyle, P. A. (2021) · Neurology · doi:10.1212/wnl.0000000000012388 · Cited by 47 · see citing works

ATG5 (autophagy related 5) in microglia controls hippocampal neurogenesis in Alzheimer disease

Tang, X., Walter, E., Wohleb, E., Fan, Y.-B., & Wang, C.-R. (2023) · Autophagy · doi:10.1080/15548627.2023.2277634 · Cited by 44 · see citing works

Prediction of Alzheimer’s Disease-Associated Genes by Integration of GWAS Summary Data and Expression Data

Hao, S., Wang, R., Zhang, Y., & Zhan, H. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2018.00653 · Cited by 47 · see citing works

Amyloid-β PET—Correlation with cerebrospinal fluid biomarkers and prediction of Alzheimer´s disease diagnosis in a memory clinic

Müller, E. G., Edwin, T. H., Stokke, C., Navelsaker, S. S., Babovic, A., Bogdanović, N., Knapskog, A., & Revheim, M. E. (2019) · PLoS ONE · doi:10.1371/journal.pone.0221365 · Cited by 47 · see citing works

Spinal muscular atrophy: Broad disease spectrum and sex-specific phenotypes

Singh, N. N., Hoffman, S., Reddi, P. P., & Singh, R. N. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.166063 · Cited by 47 · see citing works

ESR1 dysfunction triggers neuroinflammation as a critical upstream causative factor of the Alzheimer’s disease process

Liu, J., Yuan, S., Niu, X., Kelleher, R., & Sheridan, H. (2022) · Aging · doi:10.18632/aging.204359 · Cited by 46 · see citing works

Wildfire Smoke Exposure and Incident Dementia

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Sex differences in dementia: on the potentially mediating effects of educational attainment and experiences of psychological distress

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