Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

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

Showing 1-25 of 180 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
Parkinson’s Disease: Biomarkers, Treatment, and Risk Factors
Fatemeh Nouri Emamzadeh, Andrei Surguchov
Frontiers in Neuroscience (2018) Vol. 12
Open Access | Times Cited: 470
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
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
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 Sac1 Domain of SYNJ 1 Identified Mutated in a Family with Early‐Onset Progressive P arkinsonism with Generalized Seizures
Catharine E. Krebs, Siamak Karkheiran, James Powell, et al.
Human Mutation (2013) Vol. 34, Iss. 9, pp. 1200-1207
Open Access | Times Cited: 313
Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism
Marialuisa Quadri, Mingyan Fang, Marina Picillo, et al.
Human Mutation (2013) Vol. 34, Iss. 9, pp. 1208-1215
Closed Access | Times Cited: 289
Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson’s Disease
Maria Nguyen, Yvette C. Wong, Daniel Ysselstein, et al.
Trends in Neurosciences (2018) Vol. 42, Iss. 2, pp. 140-149
Open Access | Times Cited: 270
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
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
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
Parkinson Sac Domain Mutation in Synaptojanin 1 Impairs Clathrin Uncoating at Synapses and Triggers Dystrophic Changes in Dopaminergic Axons
Mian Cao, Yumei Wu, Ghazaleh Ashrafi, et al.
Neuron (2017) Vol. 93, Iss. 4, pp. 882-896.e5
Open Access | Times Cited: 174
Autophagic and endo-lysosomal dysfunction in neurodegenerative disease
Bilal R. Malik, Daniel C. Maddison, Gaynor A. Smith, et al.
Molecular Brain (2019) Vol. 12, Iss. 1
Open Access | Times Cited: 157
Monogenic Parkinson’s Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing
Fangzhi Jia, Avi Fellner, Kishore R. Kumar
Genes (2022) Vol. 13, Iss. 3, pp. 471-471
Open Access | Times Cited: 91
DNAJC6Mutations Associated With Early‐Onset Parkinson's Disease
Simone Olgiati, Marialuisa Quadri, Mingyan Fang, et al.
Annals of Neurology (2015) Vol. 79, Iss. 2, pp. 244-256
Closed Access | Times Cited: 171
Impaired intracellular trafficking defines early Parkinson's disease
Benjamin H.M. Hunn, Stephanie J. Cragg, J. Paul Bolam, et al.
Trends in Neurosciences (2015) Vol. 38, Iss. 3, pp. 178-188
Open Access | Times Cited: 169
An updated review of Parkinson's disease genetics and clinicopathological correlations
Mariana Ferreira, João Massano
Acta Neurologica Scandinavica (2016) Vol. 135, Iss. 3, pp. 273-284
Open Access | Times Cited: 162
The genetic architecture of mitochondrial dysfunction in Parkinson’s disease
Simone B. Larsen, Zoé Hanss, Rejko Krüger
Cell and Tissue Research (2018) Vol. 373, Iss. 1, pp. 21-37
Open Access | Times Cited: 159
LRRK2 phosphorylation of auxilin mediates synaptic defects in dopaminergic neurons from patients with Parkinson’s disease
Maria Nguyen, Dimitri Krainc
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 21, pp. 5576-5581
Open Access | Times Cited: 134
LRRK2 Pathways Leading to Neurodegeneration
Mark Cookson
Current Neurology and Neuroscience Reports (2015) Vol. 15, Iss. 7
Open Access | Times Cited: 133
The Role of Co-chaperones in Synaptic Proteostasis and Neurodegenerative Disease
Erica L. Gorenberg, Sreeganga S. Chandra
Frontiers in Neuroscience (2017) Vol. 11
Open Access | Times Cited: 130
Genetics of Parkinson disease
Aloysius Domingo, Christine Klein
Handbook of clinical neurology (2018), pp. 211-227
Closed Access | Times Cited: 128
Parkinson Disease from Mendelian Forms to Genetic Susceptibility: New Molecular Insights into the Neurodegeneration Process
Amin Karimi-Moghadam, Saeid Charsouei, Benjamin Bell, et al.
Cellular and Molecular Neurobiology (2018) Vol. 38, Iss. 6, pp. 1153-1178
Open Access | Times Cited: 124
Role of the endolysosomal system in Parkinson’s disease
D. J. Vidyadhara, John E. Lee, Sreeganga S. Chandra
Journal of Neurochemistry (2019) Vol. 150, Iss. 5, pp. 487-506
Open Access | Times Cited: 124
Page 1 - Next Page

Scroll to top