OpenAlex Citation Counts

OpenAlex Citations Logo

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:

A role of gut–microbiota–brain axis via subdiaphragmatic vagus nerve in depression-like phenotypes in Chrna7 knock-out mice
Yong Yang, Akifumi Eguchi, Xiayun Wan, et al.
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2022) Vol. 120, pp. 110652-110652
Open Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

Emerging role of the host microbiome in neuropsychiatric disorders: overview and future directions
Kenji Hashimoto
Molecular Psychiatry (2023) Vol. 28, Iss. 9, pp. 3625-3637
Open Access | Times Cited: 51

Gut microbiota-derived short-chain fatty acids and depression: deep insight into biological mechanisms and potential applications
Junzhe Cheng, Hongkun Hu, Yumeng Ju, et al.
General Psychiatry (2024) Vol. 37, Iss. 1, pp. e101374-e101374
Open Access | Times Cited: 34

The communication mechanism of the gut-brain axis and its effect on central nervous system diseases: A systematic review
Shengwen Lu, Qiqi Zhao, Yu Guan, et al.
Biomedicine & Pharmacotherapy (2024) Vol. 178, pp. 117207-117207
Closed Access | Times Cited: 21

The gut-brain axis and cognitive control: A role for the vagus nerve
Léa Décarie-Spain, Anna Hayes, Logan Tierno Lauer, et al.
Seminars in Cell and Developmental Biology (2023) Vol. 156, pp. 201-209
Closed Access | Times Cited: 36

Short-Chain Fatty Acids in the Microbiota–Gut–Brain Axis: Role in Neurodegenerative Disorders and Viral Infections
Atreye Majumdar, Indira Priya Siva Venkatesh, Anirban Basu
ACS Chemical Neuroscience (2023) Vol. 14, Iss. 6, pp. 1045-1062
Closed Access | Times Cited: 33

Neuroinflammation through the vagus nerve-dependent gut–microbiota–brain axis in treatment-resistant depression
Kenji Hashimoto
Progress in brain research (2023), pp. 61-77
Closed Access | Times Cited: 31

Gut microbiota: A magical multifunctional target regulated by medicine food homology species
Wei‐Fang Zuo, Qiwen Pang, Lai-Ping Yao, et al.
Journal of Advanced Research (2023) Vol. 52, pp. 151-170
Open Access | Times Cited: 28

Polygonum sibiricum polysaccharides exert the antidepressant‐like effects in chronic unpredictable mild stress‐induced depressive mice by modulating microbiota‐gut‐brain axis
Yingyu Zhang, Yuan Sun, Yupei Liu, et al.
Phytotherapy Research (2023) Vol. 37, Iss. 8, pp. 3408-3423
Closed Access | Times Cited: 23

Transcutaneous vagus nerve stimulation: a new strategy for Alzheimer’s disease intervention through the brain-gut-microbiota axis?
Long Yan, Hong Li, Yulin Qian, et al.
Frontiers in Aging Neuroscience (2024) Vol. 16
Open Access | Times Cited: 12

Depression-like phenotypes in mice following common bile duct ligation: Insights into the gut–liver–brain axis via the vagus nerve
Yong Yang, Akifumi Eguchi, Chisato Mori, et al.
Neurobiology of Disease (2024) Vol. 192, pp. 106433-106433
Open Access | Times Cited: 11

The vagus nerve: An old but new player in brain–body communication
Li Ma, Hanbing Wang, Kenji Hashimoto
Brain Behavior and Immunity (2024)
Open Access | Times Cited: 9

Key role of the gut–microbiota–brain axis via the subdiaphragmatic vagus nerve in demyelination of the cuprizone-treated mouse brain
Xingming Wang, Akifumi Eguchi, Yong Yang, et al.
Neurobiology of Disease (2022) Vol. 176, pp. 105951-105951
Open Access | Times Cited: 35

Role of oxidative phosphorylation in the antidepressant effects of arketamine via the vagus nerve-dependent spleen-brain axis
Lijia Chang, Wei Yan, Youge Qu, et al.
Neurobiology of Disease (2024) Vol. 199, pp. 106573-106573
Open Access | Times Cited: 7

Impact of broad-spectrum antibiotics on the gut–microbiota–spleen–brain axis
Xiayun Wan, Akifumi Eguchi, Akemi Sakamoto, et al.
Brain Behavior & Immunity - Health (2022) Vol. 27, pp. 100573-100573
Open Access | Times Cited: 24

Depression-like phenotypes in mice with hepatic ischemia/reperfusion injury: A role of gut–microbiota–liver–brain axis via vagus nerve
Yong Yang, Akifumi Eguchi, Xiayun Wan, et al.
Journal of Affective Disorders (2023) Vol. 345, pp. 157-167
Closed Access | Times Cited: 15

Impact of Gut Microbiota on the Peripheral Nervous System in Physiological, Regenerative and Pathological Conditions
Sonia Calabrò, Svenja Kankowski, Matilde Cescon, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8061-8061
Open Access | Times Cited: 14

Pick fecal microbiota transplantation to enhance therapy for major depressive disorder
Yiming Meng, Jing Sun, Guirong Zhang
Progress in Neuro-Psychopharmacology and Biological Psychiatry (2023) Vol. 128, pp. 110860-110860
Closed Access | Times Cited: 14

Interactions Between Antidepressants and Intestinal Microbiota
Feiyu Xu, Qinglian Xie, Weihong Kuang, et al.
Neurotherapeutics (2023) Vol. 20, Iss. 2, pp. 359-371
Closed Access | Times Cited: 13

Deciphering the gut microbiota's (Coprococcus and Subdoligranulum) impact on depression: Network pharmacology and molecular dynamics simulation
Sarvesh Sabarathinam
Pharmacology Biochemistry and Behavior (2024) Vol. 241, pp. 173805-173805
Closed Access | Times Cited: 5

Vagus nerve stimulation and gut microbiota interactions: a novel therapeutic avenue for neuropsychiatric disorders
Navid Faraji, Bahareh Payami, Negar Ebadpour, et al.
Neuroscience & Biobehavioral Reviews (2024), pp. 105990-105990
Open Access | Times Cited: 5

Page 1 - Next Page

Scroll to top