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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:

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell, et al.
The American Journal of Human Genetics (2011) Vol. 89, Iss. 3, pp. 398-406
Open Access | Times Cited: 278

Showing 1-25 of 278 citing articles:

Parkinson's disease
Lorraine V. Kalia, Anthony E. Lang
The Lancet (2015) Vol. 386, Iss. 9996, pp. 896-912
Closed Access | Times Cited: 4852
Signals from the lysosome: a control centre for cellular clearance and energy metabolism
Carmine Settembre, Alessandro Fraldi, Diego L. Medina, et al.
Nature Reviews Molecular Cell Biology (2013) Vol. 14, Iss. 5, pp. 283-296
Open Access | Times Cited: 1516
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: 1235
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database
Christina M. Lill, Johannes T. Roehr, Matthew B. McQueen, et al.
PLoS Genetics (2012) Vol. 8, Iss. 3, pp. e1002548-e1002548
Open Access | Times Cited: 528
Parkinson’s Disease: Biomarkers, Treatment, and Risk Factors
Fatemeh Nouri Emamzadeh, Andrei Surguchov
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 472
The genetics of Parkinson disease
Hao Deng, Peng Wang, Joseph Jankovic
Ageing Research Reviews (2017) Vol. 42, pp. 72-85
Closed Access | Times Cited: 466
Parkinson Disease Subtypes
Mary Ann Thenganatt, Joseph Jankovic
JAMA Neurology (2014) Vol. 71, Iss. 4, pp. 499-499
Closed Access | Times Cited: 462
Advances in the genetics of Parkinson disease
Joanne Trinh, Matthew J. Farrer
Nature Reviews Neurology (2013) Vol. 9, Iss. 8, pp. 445-454
Closed Access | Times Cited: 443
Parkinson’s Disease: Etiology, Neuropathology, and Pathogenesis
Antonina Kouli, Kelli Torsney, Wei‐Li Kuan
Codon Publications eBooks (2018), pp. 3-26
Open Access | Times Cited: 360
Alpha-synuclein structure and Parkinson’s disease – lessons and emerging principles
Richard M. Meade, David P. Fairlie, Jody M. Mason
Molecular Neurodegeneration (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 349
The genetics of Parkinson's disease: Progress and therapeutic implications
Andrew Singleton, Matthew J. Farrer, Vincenzo Bonifati
Movement Disorders (2013) Vol. 28, Iss. 1, pp. 14-23
Open Access | Times Cited: 331
Genetics of Parkinson's disease
Christina M. Lill
Molecular and Cellular Probes (2016) Vol. 30, Iss. 6, pp. 386-396
Closed Access | Times Cited: 321
The genetics and neuropathology of Parkinson’s disease
Henry Houlden, Andrew Singleton
Acta Neuropathologica (2012) Vol. 124, Iss. 3, pp. 325-338
Open Access | Times Cited: 303
Dementia with Lewy bodies: an update and outlook
Tiago F. Outeiro, David J. Koss, Daniel Erskine, et al.
Molecular Neurodegeneration (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 298
DNAJC13 mutations in Parkinson disease
Carles Vilariño‐Güell, Alex Rajput, Austen J. Milnerwood, et al.
Human Molecular Genetics (2013) Vol. 23, Iss. 7, pp. 1794-1801
Open Access | Times Cited: 293
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
Integrating Pathways of Parkinson's Disease in a Molecular Interaction Map
Kazuhiro Fujita, Marek Ostaszewski, Yukiko Matsuoka, et al.
Molecular Neurobiology (2013) Vol. 49, Iss. 1, pp. 88-102
Open Access | Times Cited: 265
Ribosomal Protein s15 Phosphorylation Mediates LRRK2 Neurodegeneration in Parkinson’s Disease
Ian Martin, Jungwoo Wren Kim, Byoung Dae Lee, et al.
Cell (2014) Vol. 157, Iss. 2, pp. 472-485
Open Access | Times Cited: 256
The genetic background of Parkinson's disease: current progress and future prospects
Kallirhoe Kalinderi, Sevasti Bostantjopoulou, Liana Fidani
Acta Neurologica Scandinavica (2016) Vol. 134, Iss. 5, pp. 314-326
Open Access | Times Cited: 255
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
Progress in unraveling the genetic etiology of Parkinson disease in a genomic era
Aline Verstraeten, Jessie Theuns, Christine Van Broeckhoven
Trends in Genetics (2015) Vol. 31, Iss. 3, pp. 140-149
Closed Access | Times Cited: 212
Translation deregulation in human disease
Soroush Tahmasebi, Arkady Khoutorsky, Michael B. Mathews, et al.
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 12, pp. 791-807
Open Access | Times Cited: 210
Genetics of Parkinson's disease – state of the art, 2013
Vincenzo Bonifati
Parkinsonism & Related Disorders (2013) Vol. 20, pp. S23-S28
Closed Access | Times Cited: 204
Signaling pathways in Parkinson’s disease: molecular mechanisms and therapeutic interventions
Dong-Chen Xu, Yong Chen, Yang Xu, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 202
PINK1 and Parkin Control Localized Translation of Respiratory Chain Component mRNAs on Mitochondria Outer Membrane
Stephan Gehrke, Zhihao Wu, Michael Klinkenberg, et al.
Cell Metabolism (2015) Vol. 21, Iss. 1, pp. 95-108
Open Access | Times Cited: 200
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