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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:

Role of autophagy in G2019S‐LRRK2‐associated neurite shortening in differentiated SH‐SY5Y cells
Edward D. Plowey, Salvatore J. Cherra, Yongjian Liu, et al.
Journal of Neurochemistry (2008) Vol. 105, Iss. 3, pp. 1048-1056
Open Access | Times Cited: 491

Showing 1-25 of 491 citing articles:

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Autophagy (2016) Vol. 12, Iss. 1, pp. 1-222
Open Access | Times Cited: 5728
Guidelines for the use and interpretation of assays for monitoring autophagy
Daniel J. Klionsky, Fábio Camargo Abdalla, Hagai Abeliovich, et al.
Autophagy (2012) Vol. 8, Iss. 4, pp. 445-544
Open Access | Times Cited: 3920
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Jeffrey C. Barrett, Sarah Hansoul, Dan L. Nicolae, et al.
Nature Genetics (2008) Vol. 40, Iss. 8, pp. 955-962
Open Access | Times Cited: 2590
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Daniel J. Klionsky, Amal Kamal Abdel‐Aziz, Sara Abdelfatah, et al.
Autophagy (2021) Vol. 17, Iss. 1, pp. 1-382
Open Access | Times Cited: 1970
Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling
Jisun Lee, Samantha Giordano, Jianhua Zhang
Biochemical Journal (2011) Vol. 441, Iss. 2, pp. 523-540
Open Access | Times Cited: 1359
Autophagy in major human diseases
Daniel J. Klionsky, Giulia Petroni, Ravi K. Amaravadi, et al.
The EMBO Journal (2021) Vol. 40, Iss. 19
Open Access | Times Cited: 1064
Clinical progression in Parkinson disease and the neurobiology of axons
Hsiao‐Chun Cheng, Christina Ulane, Robert E. Burke
Annals of Neurology (2010) Vol. 67, Iss. 6, pp. 715-725
Open Access | Times Cited: 911
Loss of PINK1 Function Promotes Mitophagy through Effects on Oxidative Stress and Mitochondrial Fission
Ruben K. Dagda, Salvatore J. Cherra, Scott Kulich, et al.
Journal of Biological Chemistry (2009) Vol. 284, Iss. 20, pp. 13843-13855
Open Access | Times Cited: 899
The role of protein clearance mechanisms in organismal ageing and age-related diseases
David Vı́lchez, Isabel Sáez, Andrew Dillin
Nature Communications (2014) Vol. 5, Iss. 1
Open Access | Times Cited: 616
Interplay of LRRK2 with chaperone-mediated autophagy
Samantha J. Orenstein, Sheng‐Han Kuo, Inmaculada Tasset, et al.
Nature Neuroscience (2013) Vol. 16, Iss. 4, pp. 394-406
Open Access | Times Cited: 555
What Genetics Tells us About the Causes and Mechanisms of Parkinson's Disease
Olga Corti, Suzanne Lesage, Alexis Brice
Physiological Reviews (2011) Vol. 91, Iss. 4, pp. 1161-1218
Closed Access | Times Cited: 554
The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease
Mark Cookson
Nature reviews. Neuroscience (2010) Vol. 11, Iss. 12, pp. 791-797
Open Access | Times Cited: 523
Genetic Correction of a LRRK2 Mutation in Human iPSCs Links Parkinsonian Neurodegeneration to ERK-Dependent Changes in Gene Expression
Peter Reinhardt, Benjamin Schmid, Lena F. Burbulla, et al.
Cell stem cell (2013) Vol. 12, Iss. 3, pp. 354-367
Closed Access | Times Cited: 479
Axon degeneration in Parkinson's disease
Robert E. Burke, Karen L. O’Malley
Experimental Neurology (2012) Vol. 246, pp. 72-83
Open Access | Times Cited: 442
The Role of Autophagy in Parkinson's Disease
Melinda A. Lynch-Day, K. Mao, Kristine Wang, et al.
Cold Spring Harbor Perspectives in Medicine (2012) Vol. 2, Iss. 4, pp. a009357-a009357
Open Access | Times Cited: 434
LRRK2 regulates autophagic activity and localizes to specific membrane microdomains in a novel human genomic reporter cellular model
Javier Alegre‐Abarrategui, Helen Christian, Michele MP Lufino, et al.
Human Molecular Genetics (2009) Vol. 18, Iss. 21, pp. 4022-4034
Open Access | Times Cited: 417
Dopaminergic Neuronal Loss, Reduced Neurite Complexity and Autophagic Abnormalities in Transgenic Mice Expressing G2019S Mutant LRRK2
David Ramonet, João Paulo Lima Daher, Brian M. Lin, et al.
PLoS ONE (2011) Vol. 6, Iss. 4, pp. e18568-e18568
Open Access | Times Cited: 384
LRRK2 Is Involved in the IFN-γ Response and Host Response to Pathogens
Agnès Gardet, Yair Benita, Chun Li, et al.
The Journal of Immunology (2010) Vol. 185, Iss. 9, pp. 5577-5585
Open Access | Times Cited: 380
Ser 1292 Autophosphorylation Is an Indicator of LRRK2 Kinase Activity and Contributes to the Cellular Effects of PD Mutations
Zejuan Sheng, Shuo Zhang, Daisy Bustos, et al.
Science Translational Medicine (2012) Vol. 4, Iss. 164
Closed Access | Times Cited: 356
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, Iakov N. Rudenko, Alice Kaganovich, et al.
Proceedings of the National Academy of Sciences (2014) Vol. 111, Iss. 7, pp. 2626-2631
Open Access | Times Cited: 349
LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice
Martin C. Herzig, Carine Kolly, Elke Persohn, et al.
Human Molecular Genetics (2011) Vol. 20, Iss. 21, pp. 4209-4223
Open Access | Times Cited: 343
Regulation of autophagy by mTOR-dependent and mTOR-independent pathways: autophagy dysfunction in neurodegenerative diseases and therapeutic application of autophagy enhancers
Sovan Sarkar
Biochemical Society Transactions (2013) Vol. 41, Iss. 5, pp. 1103-1130
Closed Access | Times Cited: 342
The kinase LRRK2 is a regulator of the transcription factor NFAT that modulates the severity of inflammatory bowel disease
Zhihua Liu, Jinwoo Lee, Scott M. Krummey, et al.
Nature Immunology (2011) Vol. 12, Iss. 11, pp. 1063-1070
Open Access | Times Cited: 339
Abberant α-Synuclein Confers Toxicity to Neurons in Part through Inhibition of Chaperone-Mediated Autophagy
Maria Xilouri, Tereza Vogiatzi, Kostas Vekrellis, et al.
PLoS ONE (2009) Vol. 4, Iss. 5, pp. e5515-e5515
Open Access | Times Cited: 333
Autophagy in neurodegenerative diseases: pathogenesis and therapy
Fang Guo, Xinyao Liu, Huaibin Cai, et al.
Brain Pathology (2017) Vol. 28, Iss. 1, pp. 3-13
Open Access | Times Cited: 331
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