OpenAlex Citation Counts

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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:

Visualizing reactive astrocyte-neuron interaction in Alzheimer’s disease using 11C-acetate and 18F-FDG
Min‐Ho Nam, Hae Young Ko, Dongwoo Kim, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 2957-2974
Open Access | Times Cited: 37

Showing 1-25 of 37 citing articles:

Neuroprotective and anti‐inflammatory effects of curcumin in Alzheimer's disease: Targeting neuroinflammation strategies
Elena Azzini, Sheila I. Peña‐Corona, Héctor Hernández‐Parra, et al.
Phytotherapy Research (2024) Vol. 38, Iss. 6, pp. 3169-3189
Closed Access | Times Cited: 27

Fully bioresorbable hybrid opto-electronic neural implant system for simultaneous electrophysiological recording and optogenetic stimulation
Myeongki Cho, Jeong-Kyu Han, Jungmin Suh, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 26

Astrocytic autophagy plasticity modulates Aβ clearance and cognitive function in Alzheimer’s disease
Suhyun Kim, Heejung Chun, Yunha Kim, et al.
Molecular Neurodegeneration (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 15

Phytomedicine for neurodegenerative diseases: The road ahead
Dev Madhubala, Aparup Patra, Mojibur R. Khan, et al.
Phytotherapy Research (2024) Vol. 38, Iss. 6, pp. 2993-3019
Closed Access | Times Cited: 10

SIRT2 and ALDH1A1 as critical enzymes for astrocytic GABA production in Alzheimer’s disease
Mridula Bhalla, Jinhyeong Joo, Daeun Kim, et al.
Molecular Neurodegeneration (2025) Vol. 20, Iss. 1
Open Access | Times Cited: 1

Relationship Between Reactive Astrocytes, by [18F]SMBT-1 Imaging, with Amyloid-Beta, Tau, Glucose Metabolism, and TSPO in Mouse Models of Alzheimer’s Disease
Yanyan Kong, Cinzia Maschio, Xuefeng Shi, et al.
Molecular Neurobiology (2024) Vol. 61, Iss. 10, pp. 8387-8401
Open Access | Times Cited: 6

Recent Update on PET/CT Radiotracers for Imaging Cerebral Glioma
Dongwoo Kim, Suk-Hyun Lee, Hee Sung Hwang, et al.
Nuclear Medicine and Molecular Imaging (2024) Vol. 58, Iss. 4, pp. 237-245
Open Access | Times Cited: 5

Identification of therapeutic targets for Alzheimer’s Disease Treatment using bioinformatics and machine learning
Zhongcong Xie, Yongli Situ, Li Deng, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access

Age-related changes of human brain metabolism
Shufang Qian, Yi Ba, Le Xue, et al.
European Journal of Nuclear Medicine and Molecular Imaging (2025)
Closed Access

Tonic excitation by astrocytic GABA causes neuropathic pain by augmenting neuronal activity and glucose metabolism
Yeon Ha Ju, Jongwook Cho, Jiyoung Park, et al.
Experimental & Molecular Medicine (2024) Vol. 56, Iss. 5, pp. 1193-1205
Open Access | Times Cited: 4

Disrupted astrocyte-neuron signaling reshapes brain activity in epilepsy and Alzheimer’s disease
Mengjie Wu, Ruonan Zhang, Peng Fu, et al.
Neuroscience (2025)
Closed Access

Astrocyte‐Specific Phenotyping of FAD4T as an Alzheimer's Disease Mouse Model
Ki Jung Kim, Jae‐Hun Lee, Jiwoon Lim, et al.
Glia (2025)
Closed Access

Neuroglia in neurodegeneration: Alzheimer, Parkinson, and Huntington disease
Dmitry Lim, Carlos Matute, Fabio Cavaliere, et al.
Handbook of clinical neurology (2025), pp. 9-44
Closed Access

A Key Mediator and Imaging Target in Alzheimer’s Disease: Unlocking the Role of Reactive Astrogliosis Through MAOB
Min‐Ho Nam, H.R. Na, C. Justin Lee, et al.
Nuclear Medicine and Molecular Imaging (2024) Vol. 58, Iss. 4, pp. 177-184
Closed Access | Times Cited: 3

Long-term LPS systemic administration leads to memory impairment and disturbance in astrocytic homeostasis
Gabriel Henrique Schirmbeck, Marina Seady, Fernanda Fróes, et al.
NeuroToxicology (2023) Vol. 99, pp. 322-331
Open Access | Times Cited: 7

Visualizing cancer-originating acetate uptake through monocarboxylate transporter 1 in reactive astrocytes in the glioblastoma tumor microenvironment
Dongwoo Kim, Hae Young Ko, Jee-In Chung, et al.
Neuro-Oncology (2023) Vol. 26, Iss. 5, pp. 843-857
Closed Access | Times Cited: 7

Imaging Neuroinflammation: Quantification of Astrocytosis in a Multitracer PET Approach
E. Rodriguez-Vieitez, Amit Kumar, Mona‐Lisa Malarte, et al.
Methods in molecular biology (2024), pp. 195-218
Closed Access | Times Cited: 2

The role and potential therapeutic targets of astrocytes in central nervous system demyelinating diseases
Rui Tan, Rui Hong, Chunxiao Sui, et al.
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 5

In vivo reactive astrocyte imaging using [18F]SMBT-1 in tauopathy and familial Alzheimer’s disease mouse models - a multitracer study
Yanyan Kong, Fang Xie, Xiuzhe Wang, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 4

Diagnostic and therapeutic potential of tonic gamma‐aminobutyric acid from reactive astrocytes in brain diseases
Wuhyun Koh, C. Justin Lee
Clinical and Translational Medicine (2024) Vol. 14, Iss. 4
Open Access | Times Cited: 1

In vivo reactive astrocyte imaging using [18F]SMBT-1 in tauopathy and familial Alzheimer's disease mouse models: A multi-tracer study
Yanyan Kong, Lei Cao, Jiao Wang, et al.
Journal of the Neurological Sciences (2024) Vol. 462, pp. 123079-123079
Open Access | Times Cited: 1

Cross-scale targeted remodeling of neurovascular and neurometabolic coupling in Alzheimer’s disease by natural self-assembled SIRT1 activator
Dongju Zhao, Fan Yang, Yining Liu, et al.
Nano Today (2024) Vol. 57, pp. 102340-102340
Closed Access | Times Cited: 1

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