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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:

“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

Showing 1-25 of 119 citing articles:

Genetics of Parkinson's Disease
Christine Klein, Ana Westenberger
Cold Spring Harbor Perspectives in Medicine (2012) Vol. 2, Iss. 1, pp. a008888-a008888
Open Access | Times Cited: 1234
The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy
Gregor K. Wenning, Iva Stanković, Luca Vignatelli, et al.
Movement Disorders (2022) Vol. 37, Iss. 6, pp. 1131-1148
Open Access | Times Cited: 460
The expanding universe of disorders of the basal ganglia
José Á. Obeso, María Rodríguez‐Oroz, María Stamelou, et al.
The Lancet (2014) Vol. 384, Iss. 9942, pp. 523-531
Closed Access | Times Cited: 207
Movement disorders with neuronal antibodies: syndromic approach, genetic parallels and pathophysiology
Bettina Balint, Angela Vincent, Hans‐Michael Meinck, et al.
Brain (2017) Vol. 141, Iss. 1, pp. 13-36
Open Access | Times Cited: 175
Multiple System Atrophy: An Oligodendroglioneural Synucleinopathy1
K. A. Jellinger
Journal of Alzheimer s Disease (2017) Vol. 62, Iss. 3, pp. 1141-1179
Open Access | Times Cited: 172
Genetics of Parkinson disease
Aloysius Domingo, Christine Klein
Handbook of clinical neurology (2018), pp. 211-227
Closed Access | Times Cited: 128
Parkinsonism, movement disorders and genetics in frontotemporal dementia
José Fidel Baizabal‐Carvallo, Joseph Jankovic
Nature Reviews Neurology (2016) Vol. 12, Iss. 3, pp. 175-185
Closed Access | Times Cited: 108
A critique of the second consensus criteria for multiple system atrophy
Iva Stanković, Niall Quinn, Luca Vignatelli, et al.
Movement Disorders (2019) Vol. 34, Iss. 7, pp. 975-984
Open Access | Times Cited: 86
Multiple System Atrophy: Recent Developments and Future Perspectives
Wassilios G. Meissner, Pierre‐Olivier Fernagut, Benjamin Dehay, et al.
Movement Disorders (2019) Vol. 34, Iss. 11, pp. 1629-1642
Closed Access | Times Cited: 83
Understanding the Multiple Role of Mitochondria in Parkinson’s Disease and Related Disorders: Lesson From Genetics and Protein–Interaction Network
Valentina Nicoletti, Giovanni Palermo, Eleonora Del Prete, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 57
Parkinsonian syndrome in familial frontotemporal dementia
Joanna Siuda, Shinsuke Fujioka, Zbigniew K. Wszołek
Parkinsonism & Related Disorders (2014) Vol. 20, Iss. 9, pp. 957-964
Open Access | Times Cited: 88
Classification of advanced stages of Parkinson’s disease: translation into stratified treatments
Rejko Krüger, Jochen Klucken, Daniel Weiß, et al.
Journal of Neural Transmission (2017) Vol. 124, Iss. 8, pp. 1015-1027
Open Access | Times Cited: 83
Genetics of Progressive Supranuclear Palsy
Sun Young Im, Young Eun Kim, Yun Joong Kim
Journal of Movement Disorders (2015) Vol. 8, Iss. 3, pp. 122-129
Open Access | Times Cited: 73
Default mode network links to visual hallucinations: A comparison between Parkinson's disease and multiple system atrophy
Raffaella Franciotti, Stefano Delli Pizzi, Bernardo Perfetti, et al.
Movement Disorders (2015) Vol. 30, Iss. 9, pp. 1237-1247
Closed Access | Times Cited: 72
Atypical parkinsonian syndromes: a general neurologist's perspective
Angela Deutschländer, Owen A. Ross, Dennis W. Dickson, et al.
European Journal of Neurology (2017) Vol. 25, Iss. 1, pp. 41-58
Open Access | Times Cited: 61
Genetics of Progressive Supranuclear Palsy: A Review
Yafei Wen, Yafang Zhou, Bin Jiao, et al.
Journal of Parkinson s Disease (2020) Vol. 11, Iss. 1, pp. 93-105
Open Access | Times Cited: 49
Genotype–Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review
Christina Wittke, Sonja Petkovic, Valerija Dobričić, et al.
Movement Disorders (2021) Vol. 36, Iss. 7, pp. 1499-1510
Open Access | Times Cited: 35
X‐Linked Levodopa‐Responsive Parkinsonism‐Epilepsy Syndrome: A Novel PGK1 Mutation and Literature Review
Thiago Gonçalves Guimarães, Jacy Bezerra Parmera, Matheus Augusto Araújo Castro, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 5, pp. 556-566
Closed Access | Times Cited: 5
Should genetic testing for SCAs be included in the diagnostic workup for MSA?
Han‐Joon Kim, Beom S. Jeon, Jung Hwan Shin, et al.
Neurology (2014) Vol. 83, Iss. 19, pp. 1733-1738
Closed Access | Times Cited: 46
Current Limitations in the Treatment of Parkinson’s and Alzheimer’s Diseases: State-of-the-Art and Future Perspective of Polymeric Carriers
Chiara Tonda‐Turo, Nicola Origlia, Clara Mattu, et al.
Current Medicinal Chemistry (2018) Vol. 25, Iss. 41, pp. 5755-5771
Closed Access | Times Cited: 46
Patterns of gray matter atrophy in atypical parkinsonism syndromes: a VBM meta‐analysis
Fang Yu, Daniel S. Barron, Bundhit Tantiwongkosi, et al.
Brain and Behavior (2015) Vol. 5, Iss. 6
Open Access | Times Cited: 45
Differential Diagnosis of Rare Subtypes of Progressive Supranuclear Palsy and PSP-Like Syndromes—Infrequent Manifestations of the Most Common Form of Atypical Parkinsonism
Patrycja Krzosek, Natalia Madetko‐Alster, Anna Migda, et al.
Frontiers in Aging Neuroscience (2022) Vol. 14
Open Access | Times Cited: 22
New insights from a multi-ethnic Asian progressive supranuclear palsy cohort
Shen‐Yang Lim, Alfand Marl F. Dy Closas, Ai Huey Tan, et al.
Parkinsonism & Related Disorders (2023) Vol. 108, pp. 105296-105296
Closed Access | Times Cited: 12
The genetic basis of multiple system atrophy
Fan Shuen Tseng, Joel Qi Xuan Foo, Aaron Shengting, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 12
Progressive Supranuclear Palsy
Christian R. Baumann
Cambridge University Press eBooks (2025), pp. 380-389
Closed Access
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