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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:

Andrographolide reduces cognitive impairment in young and mature AβPPswe/PS-1 mice
Felipe Serrano, Cheril Tapia‐Rojas, Francisco J. Carvajal, et al.
Molecular Neurodegeneration (2014) Vol. 9, Iss. 1
Open Access | Times Cited: 104

Showing 1-25 of 104 citing articles:

Overview of pharmacological activities of Andrographis paniculata and its major compound andrographolide
Yan Dai, Shaoru Chen, Ling Chai, et al.
Critical Reviews in Food Science and Nutrition (2018) Vol. 59, Iss. sup1, pp. S17-S29
Closed Access | Times Cited: 242
WNT Signaling in Disease
NG Li, Prameet Kaur, Nawat Bunnag, et al.
Cells (2019) Vol. 8, Iss. 8, pp. 826-826
Open Access | Times Cited: 197
Epigenetic editing of the Dlg4/PSD95 gene improves cognition in aged and Alzheimer’s disease mice
Fernando J. Bustos, Estíbaliz Ampuero, Nur Jury, et al.
Brain (2017) Vol. 140, Iss. 12, pp. 3252-3268
Open Access | Times Cited: 164
Is there a future for andrographolide to be an anti-inflammatory drug? Deciphering its major mechanisms of action
W.S. Daniel Tan, Wupeng Liao, Shuo Zhou, et al.
Biochemical Pharmacology (2017) Vol. 139, pp. 71-81
Closed Access | Times Cited: 154
Solid lipid nanoparticles for delivery of andrographolide across the blood-brain barrier: in vitro and in vivo evaluation
Giulia Graverini, Vieri Piazzini, Elisa Landucci, et al.
Colloids and Surfaces B Biointerfaces (2017) Vol. 161, pp. 302-313
Closed Access | Times Cited: 130
Role of Wnt Signaling in Adult Hippocampal Neurogenesis in Health and Disease
Sebastián B. Arredondo, Daniela Valenzuela-Bezanilla, Muriel D. Mardones, et al.
Frontiers in Cell and Developmental Biology (2020) Vol. 8
Open Access | Times Cited: 119
Loss of canonical Wnt signaling is involved in the pathogenesis of Alzheimer's disease
NibaldoC Inestrosa, Cheril Tapia‐Rojas
Neural Regeneration Research (2018) Vol. 13, Iss. 10, pp. 1705-1705
Open Access | Times Cited: 116
Role of Wnt Signaling in Central Nervous System Injury
Catherine Lambert, Pedro Cisternas, Nibaldo C. Inestrosa
Molecular Neurobiology (2015) Vol. 53, Iss. 4, pp. 2297-2311
Closed Access | Times Cited: 108
A review for the neuroprotective effects of andrographolide in the central nervous system
Jiashu Lu, Yao‐Ying Ma, Jingjing Wu, et al.
Biomedicine & Pharmacotherapy (2019) Vol. 117, pp. 109078-109078
Open Access | Times Cited: 107
Andrographolide alleviates Parkinsonism in MPTP‐PD mice via targeting mitochondrial fission mediated by dynamin‐related protein 1
Ji Geng, Wen Liu, Jian Gao, et al.
British Journal of Pharmacology (2019) Vol. 176, Iss. 23, pp. 4574-4591
Open Access | Times Cited: 99
Natural products as a potential modulator of microglial polarization in neurodegenerative diseases
Xin Jin, Mingyan Liu, Dongfang Zhang, et al.
Pharmacological Research (2019) Vol. 145, pp. 104253-104253
Closed Access | Times Cited: 92
Wnt Signaling in the Central Nervous System: New Insights in Health and Disease
Carolina A. Oliva, Carla Montecinos-Oliva, Nibaldo C. Inestrosa
Progress in molecular biology and translational science (2018), pp. 81-130
Closed Access | Times Cited: 84
Traditional Chinese Medicine: Role in Reducing β-Amyloid, Apoptosis, Autophagy, Neuroinflammation, Oxidative Stress, and Mitochondrial Dysfunction of Alzheimer’s Disease
Shiyu Chen, Yue Gao, Jiayi Sun, et al.
Frontiers in Pharmacology (2020) Vol. 11
Open Access | Times Cited: 83
Primary cilia and ciliary signaling pathways in aging and age-related brain disorders
Rong Ma, Naseer A. Kutchy, Liang Chen, et al.
Neurobiology of Disease (2021) Vol. 163, pp. 105607-105607
Open Access | Times Cited: 75
Andrographolide, a natural anti-inflammatory agent: An Update
Xiaohong Li, Weichen Yuan, Jibiao Wu, et al.
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 56
The dual face of microglia (M1/M2) as a potential target in the protective effect of nutraceuticals against neurodegenerative diseases
Samar F. Darwish, Abdullah M. M. Elbadry, Amir S. Elbokhomy, et al.
Frontiers in Aging (2023) Vol. 4
Open Access | Times Cited: 28
Impact of micronutrients and nutraceuticals on cognitive function and performance in Alzheimer's disease
Lorenza Guarnieri, Francesca Bosco, Antonio Leo, et al.
Ageing Research Reviews (2024) Vol. 95, pp. 102210-102210
Open Access | Times Cited: 13
Wnt signaling loss accelerates the appearance of neuropathological hallmarks of Alzheimer's disease in J20‐APP transgenic and wild‐type mice
Cheril Tapia‐Rojas, Nibaldo C. Inestrosa
Journal of Neurochemistry (2017) Vol. 144, Iss. 4, pp. 443-465
Open Access | Times Cited: 75
Andrographolide recovers cognitive impairment in a natural model of Alzheimer's disease (Octodon degus)
Daniela S. Rivera, Carolina B. Lindsay, Juan F. Codocedo, et al.
Neurobiology of Aging (2016) Vol. 46, pp. 204-220
Closed Access | Times Cited: 74
Pathogenicity of Lupus Anti–Ribosomal P Antibodies: Role of Cross‐Reacting Neuronal Surface P Antigen in Glutamatergic Transmission and Plasticity in a Mouse Model
Fabián Segovia‐Miranda, Felipe Serrano, Agnieszka Dyrda, et al.
Arthritis & Rheumatology (2015) Vol. 67, Iss. 6, pp. 1598-1610
Closed Access | Times Cited: 73
Discovery of a Potent Dual Inhibitor of Acetylcholinesterase and Butyrylcholinesterase with Antioxidant Activity that Alleviates Alzheimer-like Pathology in Old APP/PS1 Mice
Elisabet Viayna, Nicolas Coquelle, Monika Cieslikiewicz‐Bouet, et al.
Journal of Medicinal Chemistry (2020) Vol. 64, Iss. 1, pp. 812-839
Open Access | Times Cited: 68
Stealth and Cationic Nanoliposomes as Drug Delivery Systems to Increase Andrographolide BBB Permeability
Vieri Piazzini, Elisa Landucci, Giulia Graverini, et al.
Pharmaceutics (2018) Vol. 10, Iss. 3, pp. 128-128
Open Access | Times Cited: 65
Beneficial effects of anAndrographis paniculataextract and andrographolide on cognitive functions in streptozotocin-induced diabetic rats
Ajit Kumar Thakur, Geeta Rai, Shyam Sunder Chatterjee, et al.
Pharmaceutical Biology (2016) Vol. 54, Iss. 9, pp. 1528-1538
Open Access | Times Cited: 63
Andrographolide Activates Keap1/Nrf2/ARE/HO-1 Pathway in HT22 Cells and Suppresses Microglial Activation by Aβ42through Nrf2-Related Inflammatory Response
Ji Yeon Seo, Euisun Pyo, Jin‐Pyo An, et al.
Mediators of Inflammation (2017) Vol. 2017, pp. 1-12
Open Access | Times Cited: 62
A network-based analysis of key pharmacological pathways of Andrographis paniculata acting on Alzheimer's disease and experimental validation
Lili Gu, Jiaqi Lü, Qin Li, et al.
Journal of Ethnopharmacology (2019) Vol. 251, pp. 112488-112488
Closed Access | Times Cited: 60
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