
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Locus coeruleus integrity is related to tau burden and memory loss in autosomal-dominant Alzheimer's disease
Martin J. Dahl, Mara Mather, Markus Werkle‐Bergner, et al.
Neurobiology of Aging (2021) Vol. 112, pp. 39-54
Open Access | Times Cited: 91
Martin J. Dahl, Mara Mather, Markus Werkle‐Bergner, et al.
Neurobiology of Aging (2021) Vol. 112, pp. 39-54
Open Access | Times Cited: 91
Showing 1-25 of 91 citing articles:
A phase II study repurposing atomoxetine for neuroprotection in mild cognitive impairment
Allan I. Levey, Deqiang Qiu, Liping Zhao, et al.
Brain (2021) Vol. 145, Iss. 6, pp. 1924-1938
Open Access | Times Cited: 66
Allan I. Levey, Deqiang Qiu, Liping Zhao, et al.
Brain (2021) Vol. 145, Iss. 6, pp. 1924-1938
Open Access | Times Cited: 66
Priorities for research on neuromodulatory subcortical systems in Alzheimer's disease: Position paper from the NSS PIA of ISTAART
Alexander J. Ehrenberg, Michael A. Kelberman, Kathy Liu, et al.
Alzheimer s & Dementia (2023) Vol. 19, Iss. 5, pp. 2182-2196
Open Access | Times Cited: 34
Alexander J. Ehrenberg, Michael A. Kelberman, Kathy Liu, et al.
Alzheimer s & Dementia (2023) Vol. 19, Iss. 5, pp. 2182-2196
Open Access | Times Cited: 34
Noradrenergic and cholinergic systems take centre stage in neuropsychiatric diseases of ageing
Isabella F. Orlando, James M. Shine, Trevor W. Robbins, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 149, pp. 105167-105167
Open Access | Times Cited: 33
Isabella F. Orlando, James M. Shine, Trevor W. Robbins, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 149, pp. 105167-105167
Open Access | Times Cited: 33
The integrity of dopaminergic and noradrenergic brain regions is associated with different aspects of late-life memory performance
Martin J. Dahl, Shelby L. Bachman, Shubir Dutt, et al.
Nature Aging (2023) Vol. 3, Iss. 9, pp. 1128-1143
Open Access | Times Cited: 31
Martin J. Dahl, Shelby L. Bachman, Shubir Dutt, et al.
Nature Aging (2023) Vol. 3, Iss. 9, pp. 1128-1143
Open Access | Times Cited: 31
Spatiotemporal patterns of locus coeruleus integrity predict cortical tau and cognition
Elisenda Bueichekú, Ibai Díez, Chan Mi Kim, et al.
Nature Aging (2024) Vol. 4, Iss. 5, pp. 625-637
Open Access | Times Cited: 14
Elisenda Bueichekú, Ibai Díez, Chan Mi Kim, et al.
Nature Aging (2024) Vol. 4, Iss. 5, pp. 625-637
Open Access | Times Cited: 14
Microstructural integrity of the locus coeruleus and its tracts reflect noradrenergic degeneration in Alzheimer’s disease and Parkinson’s disease
Chen‐Pei Lin, Irene Frigerio, John G. J. M. Bol, et al.
Translational Neurodegeneration (2024) Vol. 13, Iss. 1
Open Access | Times Cited: 10
Chen‐Pei Lin, Irene Frigerio, John G. J. M. Bol, et al.
Translational Neurodegeneration (2024) Vol. 13, Iss. 1
Open Access | Times Cited: 10
Noradrenaline in the aging brain: Promoting cognitive reserve or accelerating Alzheimer's disease?
Mara Mather
Seminars in Cell and Developmental Biology (2021) Vol. 116, pp. 108-124
Open Access | Times Cited: 46
Mara Mather
Seminars in Cell and Developmental Biology (2021) Vol. 116, pp. 108-124
Open Access | Times Cited: 46
Evidence for a modulating effect of transcutaneous auricular vagus nerve stimulation (taVNS) on salivary alpha-amylase as indirect noradrenergic marker: A pooled mega-analysis
Manon Giraudier, Carlos Ventura‐Bort, Andreas M. Burger, et al.
Brain stimulation (2022) Vol. 15, Iss. 6, pp. 1378-1388
Open Access | Times Cited: 32
Manon Giraudier, Carlos Ventura‐Bort, Andreas M. Burger, et al.
Brain stimulation (2022) Vol. 15, Iss. 6, pp. 1378-1388
Open Access | Times Cited: 32
Declining locus coeruleus–dopaminergic and noradrenergic modulation of long-term memory in aging and Alzheimer’s disease
Martin J. Dahl, Agnieszka Kulesza, Markus Werkle‐Bergner, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 153, pp. 105358-105358
Open Access | Times Cited: 21
Martin J. Dahl, Agnieszka Kulesza, Markus Werkle‐Bergner, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 153, pp. 105358-105358
Open Access | Times Cited: 21
Ultra-high field imaging, plasma markers and autopsy data uncover a specific rostral locus coeruleus vulnerability to hyperphosphorylated tau
Maxime Van Egroo, Joost M. Riphagen, Nicholas J. Ashton, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 6, pp. 2412-2422
Open Access | Times Cited: 20
Maxime Van Egroo, Joost M. Riphagen, Nicholas J. Ashton, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 6, pp. 2412-2422
Open Access | Times Cited: 20
Noradrenaline in Alzheimer’s Disease: A New Potential Therapeutic Target
Irene L. Gutiérrez, Cinzia Dello Russo, Fabiana Novellino, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 11, pp. 6143-6143
Open Access | Times Cited: 26
Irene L. Gutiérrez, Cinzia Dello Russo, Fabiana Novellino, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 11, pp. 6143-6143
Open Access | Times Cited: 26
State-of-the-art imaging of neuromodulatory subcortical systems in aging and Alzheimer’s disease: Challenges and opportunities
Nina Engels, Elouise A. Koops, Prokopis C. Prokopiou, et al.
Neuroscience & Biobehavioral Reviews (2022) Vol. 144, pp. 104998-104998
Open Access | Times Cited: 25
Nina Engels, Elouise A. Koops, Prokopis C. Prokopiou, et al.
Neuroscience & Biobehavioral Reviews (2022) Vol. 144, pp. 104998-104998
Open Access | Times Cited: 25
It is the locus coeruleus! Or… is it?: a proposition for analyses and reporting standards for structural and functional magnetic resonance imaging of the noradrenergic locus coeruleus
Yeo‐Jin Yi, Falk Lüsebrink, Mareike Ludwig, et al.
Neurobiology of Aging (2023) Vol. 129, pp. 137-148
Open Access | Times Cited: 15
Yeo‐Jin Yi, Falk Lüsebrink, Mareike Ludwig, et al.
Neurobiology of Aging (2023) Vol. 129, pp. 137-148
Open Access | Times Cited: 15
Daily heart rate variability biofeedback training decreases locus coeruleus MRI contrast in younger adults in a randomized clinical trial
Shelby L. Bachman, Steve W. Cole, Hyun Joo Yoo, et al.
International Journal of Psychophysiology (2023) Vol. 193, pp. 112241-112241
Open Access | Times Cited: 15
Shelby L. Bachman, Steve W. Cole, Hyun Joo Yoo, et al.
International Journal of Psychophysiology (2023) Vol. 193, pp. 112241-112241
Open Access | Times Cited: 15
Age-related differences in the functional topography of the locus coeruleus and their implications for cognitive and affective functions
Dániel Veréb, Mite Mijalkov, Anna Canal‐Garcia, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 13
Dániel Veréb, Mite Mijalkov, Anna Canal‐Garcia, et al.
eLife (2023) Vol. 12
Open Access | Times Cited: 13
Fully automated segmentation of the locus coeruleus: application to assess the effects of age, sex and education
Robin de Florès, T. K. Blanchard, Emilie Foyard, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Robin de Florès, T. K. Blanchard, Emilie Foyard, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Regenerating Locus Coeruleus‐Norepinephrine (LC ‐NE ) Function: A Novel Approach for Neurodegenerative Diseases
Ya-Na Yang, Yunlong Tao
Cell Proliferation (2025)
Open Access
Ya-Na Yang, Yunlong Tao
Cell Proliferation (2025)
Open Access
Locus coeruleus tau validates and informs high-resolution MRI in aging and at earliest Alzheimer’s pathology stages
Alexander T. Hary, Sarabjit Chadha, Nathaniel D. Mercaldo, et al.
Acta Neuropathologica Communications (2025) Vol. 13, Iss. 1
Open Access
Alexander T. Hary, Sarabjit Chadha, Nathaniel D. Mercaldo, et al.
Acta Neuropathologica Communications (2025) Vol. 13, Iss. 1
Open Access
Examining the Role of the Noradrenergic Locus Coeruleus for Predicting Attention and Brain Maintenance in Healthy Old Age and Disease: An MRI Structural Study for the Alzheimer’s Disease Neuroimaging Initiative
Emanuele R. G. Plini, Erik O’Hanlon, Rory Boyle, et al.
Cells (2021) Vol. 10, Iss. 7, pp. 1829-1829
Open Access | Times Cited: 32
Emanuele R. G. Plini, Erik O’Hanlon, Rory Boyle, et al.
Cells (2021) Vol. 10, Iss. 7, pp. 1829-1829
Open Access | Times Cited: 32
Testing locus coeruleus-norepinephrine accounts of working memory, attention control, and fluid intelligence
Matthew K. Robison, Kathryn J. Ralph, Dawn M. Gondoli, et al.
Cognitive Affective & Behavioral Neuroscience (2023) Vol. 23, Iss. 4, pp. 1014-1058
Open Access | Times Cited: 11
Matthew K. Robison, Kathryn J. Ralph, Dawn M. Gondoli, et al.
Cognitive Affective & Behavioral Neuroscience (2023) Vol. 23, Iss. 4, pp. 1014-1058
Open Access | Times Cited: 11
Noradrenergic alterations in Parkinson’s disease: a combined 11C-yohimbine PET/neuromelanin MRI study
Chloé Laurencin, Sophie Lancelot, Sarah Brosse, et al.
Brain (2023) Vol. 147, Iss. 4, pp. 1377-1388
Open Access | Times Cited: 11
Chloé Laurencin, Sophie Lancelot, Sarah Brosse, et al.
Brain (2023) Vol. 147, Iss. 4, pp. 1377-1388
Open Access | Times Cited: 11
Locus Coeruleus-Norepinephrine System: Spheres of Influence and Contribution to the Development of Neurodegenerative Diseases
Vladimir N. Nikolenko, Irina Dmitriyevna Borminskaya, Arina T. Nikitina, et al.
Frontiers in Bioscience-Landmark (2024) Vol. 29, Iss. 3
Open Access | Times Cited: 4
Vladimir N. Nikolenko, Irina Dmitriyevna Borminskaya, Arina T. Nikitina, et al.
Frontiers in Bioscience-Landmark (2024) Vol. 29, Iss. 3
Open Access | Times Cited: 4
Locus coeruleus integrity and neuropsychiatric symptoms in a cohort of early‐ and late‐onset Alzheimer's disease
Neus Falgàs, Marta Peña‐González, Andrea Val‐Guardiola, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 9, pp. 6351-6364
Open Access | Times Cited: 4
Neus Falgàs, Marta Peña‐González, Andrea Val‐Guardiola, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 9, pp. 6351-6364
Open Access | Times Cited: 4
Monoaminergic neurotransmitters are bimodal effectors of tau aggregation
Xinmin Chang, Andy K.-S. Tse, Marina Fayzullina, et al.
Science Advances (2025) Vol. 11, Iss. 5
Open Access
Xinmin Chang, Andy K.-S. Tse, Marina Fayzullina, et al.
Science Advances (2025) Vol. 11, Iss. 5
Open Access
Noradrenaline and Acetylcholine shape Functional Connectivity organization of NREM substages: an empirical and simulation study
Fernando Lehue, Carlos Coronel‐Oliveros, Vicente Medel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Fernando Lehue, Carlos Coronel‐Oliveros, Vicente Medel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access