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:

Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function
Vanessa A. Morais, Patrik Verstreken, Anne Roethig, et al.
EMBO Molecular Medicine (2009) Vol. 1, Iss. 2, pp. 99-111
Open Access | Times Cited: 402

Showing 1-25 of 402 citing articles:

The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson’s Disease
Alicia M. Pickrell, Richard J. Youle
Neuron (2015) Vol. 85, Iss. 2, pp. 257-273
Open Access | Times Cited: 1876

The Role of Oxidative Stress in Parkinson's Disease
Vera Dias, Eunsung Junn, M. Maral Mouradian
Journal of Parkinson s Disease (2013) Vol. 3, Iss. 4, pp. 461-491
Open Access | Times Cited: 1473

Mitochondria, oxidative stress and neurodegeneration
Antonio Federico, Elena Cardaioli, Paola Da Pozzo, et al.
Journal of the Neurological Sciences (2012) Vol. 322, Iss. 1-2, pp. 254-262
Closed Access | Times Cited: 729

Drosophila Parkin requires PINK1 for mitochondrial translocation and ubiquitinates Mitofusin
Elena Ziviani, Ran Tao, Alexander J. Whitworth
Proceedings of the National Academy of Sciences (2010) Vol. 107, Iss. 11, pp. 5018-5023
Open Access | Times Cited: 699

Mitochondrial dysfunction in Parkinson's disease
Konstanze F. Winklhofer, Christian Haass
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2009) Vol. 1802, Iss. 1, pp. 29-44
Open Access | Times Cited: 662

Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences
Nicole Exner, A. Kathrin Lutz, Christian Haass, et al.
The EMBO Journal (2012) Vol. 31, Iss. 14, pp. 3038-3062
Open Access | Times Cited: 567

Oxidative stress in the aging substantia nigra and the etiology of Parkinson's disease
Benjamin G. Trist, Dominic J. Hare, Kay L. Double
Aging Cell (2019) Vol. 18, Iss. 6
Open Access | Times Cited: 567

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

PINK1 deficiency impairs mitochondrial homeostasis and promotes lung fibrosis
Marta Bueno, Yen‐Chun Lai, Yair Romero, et al.
Journal of Clinical Investigation (2014) Vol. 125, Iss. 2, pp. 521-538
Open Access | Times Cited: 527

Mitochondria at the neuronal presynapse in health and disease
Michael J. Devine, Josef T. Kittler
Nature reviews. Neuroscience (2018) Vol. 19, Iss. 2, pp. 63-80
Open Access | Times Cited: 511

Mitochondrial dysfunction and mitophagy in Parkinson's: from familial to sporadic disease
Brent J. Ryan, Selim Hoek, Edward A. Fon, et al.
Trends in Biochemical Sciences (2015) Vol. 40, Iss. 4, pp. 200-210
Open Access | Times Cited: 489

Inhibition of mitochondrial fusion by α-synuclein is rescued by PINK1, Parkin and DJ-1
Frits Kamp, Nicole Exner, A. Kathrin Lutz, et al.
The EMBO Journal (2010) Vol. 29, Iss. 20, pp. 3571-3589
Open Access | Times Cited: 449

The PINK1–Parkin pathway promotes both mitophagy and selective respiratory chain turnover in vivo
Evelyn S. Vincow, Gennifer E. Merrihew, Ruth E. Thomas, et al.
Proceedings of the National Academy of Sciences (2013) Vol. 110, Iss. 16, pp. 6400-6405
Open Access | Times Cited: 434

Oxidative stress and cellular pathologies in Parkinson’s disease
Lesly Puspita, Sun Young Chung, Jae‐Won Shim
Molecular Brain (2017) Vol. 10, Iss. 1
Open Access | Times Cited: 413

Mitochondria and Neuroplasticity
Aiwu Cheng, Yan Hou, Mark P. Mattson
ASN NEURO (2010) Vol. 2, Iss. 5, pp. AN20100019-AN20100019
Open Access | Times Cited: 389

Loss of Parkin or PINK1 Function Increases Drp1-dependent Mitochondrial Fragmentation
A. Kathrin Lutz, Nicole Exner, Mareike E. Fett, et al.
Journal of Biological Chemistry (2009) Vol. 284, Iss. 34, pp. 22938-22951
Open Access | Times Cited: 366

Parkin and PINK1: much more than mitophagy
Leslie A. Scarffe, Daniel A. Stevens, Valina L. Dawson, et al.
Trends in Neurosciences (2014) Vol. 37, Iss. 6, pp. 315-324
Open Access | Times Cited: 349

Vitamin K 2 Is a Mitochondrial Electron Carrier That Rescues Pink1 Deficiency
Melissa Vos, Giovanni Esposito, Janaka N. Edirisinghe, et al.
Science (2012) Vol. 336, Iss. 6086, pp. 1306-1310
Open Access | Times Cited: 336

Roles of long noncoding RNAs in brain development, functional diversification and neurodegenerative diseases
Ping Wu, Xialin Zuo, Houliang Deng, et al.
Brain Research Bulletin (2013) Vol. 97, pp. 69-80
Closed Access | Times Cited: 336

Dynamin-related protein 1 and mitochondrial fragmentation in neurodegenerative diseases
P. Hemachandra Reddy, T. P. Reddy, Maria Mańczak, et al.
Brain Research Reviews (2010) Vol. 67, Iss. 1-2, pp. 103-118
Open Access | Times Cited: 334

PINK1 Loss-of-Function Mutations Affect Mitochondrial Complex I Activity via NdufA10 Ubiquinone Uncoupling
Vanessa A. Morais, Dominik Haddad, Katleen Craessaerts, et al.
Science (2014) Vol. 344, Iss. 6180, pp. 203-207
Closed Access | Times Cited: 324

Molecular Mechanisms of Disease-Causing Missense Mutations
Shannon Stefl, Hafumi Nishi, Marharyta Petukh, et al.
Journal of Molecular Biology (2013) Vol. 425, Iss. 21, pp. 3919-3936
Open Access | Times Cited: 296

Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli
Veronica Costa, Marta Giacomello, Roman Hudec, et al.
EMBO Molecular Medicine (2010) Vol. 2, Iss. 12, pp. 490-503
Open Access | Times Cited: 265

Non-coding RNAs with essential roles in neurodegenerative disorders
Evgenia Salta, Bart De Strooper
The Lancet Neurology (2012) Vol. 11, Iss. 2, pp. 189-200
Closed Access | Times Cited: 238

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