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:

Changes in Gene Expression and Neuroinflammation in the Hippocampus after Focal Brain Ischemia: Involvement in the Long-Term Cognitive and Mental Disorders
Г. Т. Шишкина, T. S. Kalinina, N. V. Gulyaeva, et al.
Biochemistry (Moscow) (2021) Vol. 86, Iss. 6, pp. 657-666
Open Access | Times Cited: 22

Showing 22 citing articles:

Gut microbiota is causally associated with poststroke cognitive impairment through lipopolysaccharide and butyrate
Huidi Wang, Mingsi Zhang, Jie Li, et al.
Journal of Neuroinflammation (2022) Vol. 19, Iss. 1
Open Access | Times Cited: 73

AdipoRon’s Impact on Alzheimer’s Disease—A Systematic Review and Meta-Analysis
Sandra Maria Barbalho, Lucas Fornari Laurindo, Bárbara de Oliveira Zanuso, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 2, pp. 484-484
Open Access | Times Cited: 1

Dual roles of interleukin-33 in cognitive function by regulating central nervous system inflammation
Xiuqin Rao, Fuzhou Hua, Lieliang Zhang, et al.
Journal of Translational Medicine (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 31

Effects of Microplastic Accumulation on Neuronal Death After Global Cerebral Ischemia
Dong Yeon Kim, Min Kyu Park, Hyun Wook Yang, et al.
Cells (2025) Vol. 14, Iss. 4, pp. 241-241
Open Access

The Impact of Cerebral Ischemia on Antioxidant Enzymes Activity and Neuronal Damage in the Hippocampus
Jafar Sadeghzadeh, Leila Hosseini, Ahmad Mobed, et al.
Cellular and Molecular Neurobiology (2023) Vol. 43, Iss. 8, pp. 3915-3928
Closed Access | Times Cited: 5

Changes in gene expression and neuroinflammation in the hippocampus of rats with poststroke cognitive impairment
Jiemei Chen, Jiena Hong, Chao Li, et al.
Experimental Biology and Medicine (2023) Vol. 248, Iss. 10, pp. 883-896
Open Access | Times Cited: 4

Genes Involved by Dexamethasone in Prevention of Long-Term Memory Impairment Caused by Lipopolysaccharide-Induced Neuroinflammation
Г. Т. Шишкина, Т. С. Калинина, Д. А. Ланшаков, et al.
Biomedicines (2023) Vol. 11, Iss. 10, pp. 2595-2595
Open Access | Times Cited: 4

Identifying the Involvement of Pro-Inflammatory Signal in Hippocampal Gene Expression Changes after Experimental Ischemia: Transcriptome-Wide Analysis
Г. Т. Шишкина, N. V. Gulyaeva, Д. А. Ланшаков, et al.
Biomedicines (2021) Vol. 9, Iss. 12, pp. 1840-1840
Open Access | Times Cited: 8

Comparative Investigation of Expression of Glutamatergic and GABAergic Genes in the Rat Hippocampus after Focal Brain Ischemia and Central LPS Administration
Tatyana S. Kalinina, Г. Т. Шишкина, Dmitriy A. Lanshakov, et al.
Biochemistry (Moscow) (2023) Vol. 88, Iss. 4, pp. 539-550
Open Access | Times Cited: 2

Resolution of Cerebral Inflammation Following Subarachnoid Hemorrhage
Victor Patsouris, Kinga G. Blecharz-Lang, Melina Nieminen-Kelhä, et al.
Neurocritical Care (2023) Vol. 39, Iss. 1, pp. 218-228
Open Access | Times Cited: 2

A study on the mnemotropic and antidepressant-like effects of the low-molecular-weight mimetic of nerve growth factor, dipeptide GK-2, in experimental ischemic stroke
P. Yu. Povarnina, Н. М. Сазонова, Д. М. Никифоров, et al.
Pharmacokinetics and Pharmacodynamics (2024), Iss. 1, pp. 14-22
Open Access

Central Responses to Peripheral Inflammation May Include Decreased Expression of Key Apoptotic Protease Caspase-3 in the Brainstem
A. V. Bannova, Г. Т. Шишкина, Н. Н. Дыгало
Journal of Evolutionary Biochemistry and Physiology (2024) Vol. 60, Iss. 3, pp. 890-897
Closed Access

Central responses to peripheral inflammation may include decreased expression of key apoptotic protease caspase-3 in brainstem
A. V. Bannova, Г. Т. Шишкина, Н. Н. Дыгало
Журнал эволюционной биохимии и физиологии (2024) Vol. 60, Iss. 3, pp. 291-298
Closed Access

Hippocampus, Spatial Memory, and Neuroimmuomodulation
Huangui Xiong, Jingdong Zhang, Jianuo Liu
NeuroImmune Pharmacology and Therapeutics (2024), pp. 317-328
Closed Access

ErbB4 processing is involved in OGD/R induced neuron injury
Aiqing Deng, Shouyan Wang, Jianxin Qin, et al.
Journal of Stroke and Cerebrovascular Diseases (2023) Vol. 32, Iss. 11, pp. 107373-107373
Open Access | Times Cited: 1

Neuroadaptive Biochemical Mechanisms of Remote Ischemic Conditioning
К. А. Баранова, Natalia N. Nalivaeva, Е. А. Рыбникова
(2023)
Open Access | Times Cited: 1

Neuroadaptive Biochemical Mechanisms of Remote Ischemic Conditioning
К. А. Баранова, Natalia N. Nalivaeva, Е. А. Рыбникова
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 17032-17032
Open Access | Times Cited: 1

Rapid Alterations of the Expression of Active Caspase-3 and Glucocorticoid Receptors in the Cells of the Striatum during Neuroinflammation
В. В. Булыгина, Г. Т. Шишкина, Д. А. Ланшаков, et al.
Neurochemical Journal (2023) Vol. 17, Iss. 3, pp. 387-393
Closed Access

Comparative investigation of glutamate and GABA gene expression in the hippocampus after focal brain ischemia and central lps administration
Т. С. Калинина, Г. Т. Шишкина, Dmitriy A. Lanshakov, et al.
Биохимия (2023) Vol. 88, Iss. 4, pp. 656-670
Closed Access

Rapid Changes in the Expression of Active Caspase-3 and Glucocorticoid Receptors in Striatum Cells Induced by Neuroinflammation
В. В. Булыгина, Г. Т. Шишкина, Д. А. Ланшаков, et al.
Нейрохимия (2023) Vol. 40, Iss. 3, pp. 265-272
Closed Access

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