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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:

Clinical spectrum of Kufor‐Rakeb syndrome in the Chilean kindred with ATP13A2 mutations
María Isabel Behrens, Norbert Brüggemann, Pedro Chaná, et al.
Movement Disorders (2010) Vol. 25, Iss. 12, pp. 1929-1937
Closed Access | Times Cited: 103

Showing 1-25 of 103 citing articles:

“Manganese-induced neurotoxicity: a review of its behavioral consequences and neuroprotective strategies”
Tanara V. Peres, Maria Rosa Chitolina Schetinger, Pan Chen, et al.
BMC Pharmacology and Toxicology (2016) Vol. 17, Iss. 1
Open Access | Times Cited: 325
Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature
Susanne A. Schneider, Roy N. Alcalay
Movement Disorders (2017) Vol. 32, Iss. 11, pp. 1504-1523
Open Access | Times Cited: 274
Manganese homeostasis in the nervous system
Pan Chen, Sudipta Chakraborty, Somshuvra Mukhopadhyay, et al.
Journal of Neurochemistry (2015) Vol. 134, Iss. 4, pp. 601-610
Open Access | Times Cited: 248
Monogenic Parkinson's disease and parkinsonism: Clinical phenotypes and frequencies of known mutations
Andreas Puschmann
Parkinsonism & Related Disorders (2013) Vol. 19, Iss. 4, pp. 407-415
Open Access | Times Cited: 232
The genetic landscape of Parkinson's disease
Ariane Lunati, Suzanne Lesage, Alexis Brice
Revue Neurologique (2018) Vol. 174, Iss. 9, pp. 628-643
Open Access | Times Cited: 189
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update
Lara M. Lange, Paulina González-Latapí, Rajasumi Rajalingam, et al.
Movement Disorders (2022) Vol. 37, Iss. 5, pp. 905-935
Open Access | Times Cited: 87
Neuroimaging Features of Neurodegeneration with Brain Iron Accumulation
Michael C. Kruer, Nathalie Boddaert, Susanne A. Schneider, et al.
American Journal of Neuroradiology (2011) Vol. 33, Iss. 3, pp. 407-414
Open Access | Times Cited: 208
Manganese and the Brain
Karin Tuschl, Philippa B. Mills, Peter T. Clayton
International review of neurobiology (2013), pp. 277-312
Closed Access | Times Cited: 191
DNAJC6 is responsible for juvenile parkinsonism with phenotypic variability
Çiğdem Köroğlu, Leyla Baysal-Kıraç, Murat Çetinkaya, et al.
Parkinsonism & Related Disorders (2012) Vol. 19, Iss. 3, pp. 320-324
Closed Access | Times Cited: 180
Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations
Susanne A. Schneider, John Hardy, Kailash P. Bhatia
Movement Disorders (2011) Vol. 27, Iss. 1, pp. 42-53
Closed Access | Times Cited: 172
Genetics and Epigenetics of Parkinson's Disease
Fabio Coppedè
The Scientific World JOURNAL (2012) Vol. 2012, pp. 1-12
Open Access | Times Cited: 169
PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity
David Ramonet, Agata Podhajska, Klodjan Stafa, et al.
Human Molecular Genetics (2011) Vol. 21, Iss. 8, pp. 1725-1743
Open Access | Times Cited: 156
The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms
Jin‐Sung Park, Nicholas Blair, Carolyn M. Sue
Movement Disorders (2015) Vol. 30, Iss. 6, pp. 770-779
Closed Access | Times Cited: 154
Loss-of-function mutations in theATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)
Alejandro Estrada‐Cuzcano, Shaun Martin, Teodora Chamova, et al.
Brain (2016) Vol. 140, Iss. 2, pp. 287-305
Open Access | Times Cited: 148
Regulation of Intracellular Manganese Homeostasis by Kufor-Rakeb Syndrome-associated ATP13A2 Protein
Jieqiong Tan, Tongmei Zhang, Li Jiang, et al.
Journal of Biological Chemistry (2011) Vol. 286, Iss. 34, pp. 29654-29662
Open Access | Times Cited: 141
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits
Patrick J. Schultheis, Sheila M. Fleming, Amy K. Clippinger, et al.
Human Molecular Genetics (2013) Vol. 22, Iss. 10, pp. 2067-2082
Open Access | Times Cited: 133
A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers
Fabiana H.G. Farias, Rong Zeng, Gary S. Johnson, et al.
Neurobiology of Disease (2011) Vol. 42, Iss. 3, pp. 468-474
Closed Access | Times Cited: 124
Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA)
Susanne A. Schneider, Petr Dušek, John Hardy, et al.
Current Neuropharmacology (2013) Vol. 11, Iss. 1, pp. 59-79
Open Access | Times Cited: 121
“Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy—A diagnostic guide
María Stamelou, Niall Quinn, Kailash P. Bhatia
Movement Disorders (2013) Vol. 28, Iss. 9, pp. 1184-1199
Closed Access | Times Cited: 119
Eye Movements in Parkinson’s Disease and Inherited Parkinsonian Syndromes
Elena Pretegiani, Lance M. Optican
Frontiers in Neurology (2017) Vol. 8
Open Access | Times Cited: 101
Juvenile parkinsonism: Differential diagnosis, genetics, and treatment
Nicki Niemann, Joseph Jankovic
Parkinsonism & Related Disorders (2019) Vol. 67, pp. 74-89
Closed Access | Times Cited: 95
ATP13A2 facilitates HDAC6 recruitment to lysosome to promote autophagosome–lysosome fusion
Ruoxi Wang, Jieqiong Tan, Tingting Chen, et al.
The Journal of Cell Biology (2018) Vol. 218, Iss. 1, pp. 267-284
Open Access | Times Cited: 89
Implications of DNA Methylation in Parkinson’s Disease
Ernesto G. Miranda-Morales, Karin Meier, Ada Agustina Sandoval-Carrillo, et al.
Frontiers in Molecular Neuroscience (2017) Vol. 10
Open Access | Times Cited: 88
DNA Methylation: A Promising Approach in Management of Alzheimer’s Disease and Other Neurodegenerative Disorders
Gagandeep Kaur, Suraj Singh S. Rathod, Mohammed M. Ghoneim, et al.
Biology (2022) Vol. 11, Iss. 1, pp. 90-90
Open Access | Times Cited: 53
Pathogenic effects of novel mutations in the P‐type ATPase ATP13A2 ( PARK9 ) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism
Jin‐Sung Park, Prachi Mehta, Antony A. Cooper, et al.
Human Mutation (2011) Vol. 32, Iss. 8, pp. 956-964
Open Access | Times Cited: 113
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