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:

Diagnostic exome sequencing in early‐onset Parkinson's disease confirms VPS13C as a rare cause of autosomal‐recessive Parkinson's disease
Barbara Schormair, David Kemlink, Brit Mollenhauer, et al.
Clinical Genetics (2017) Vol. 93, Iss. 3, pp. 603-612
Open Access | Times Cited: 84

Showing 1-25 of 84 citing articles:

Genetic predispositions of Parkinson’s disease revealed in patient-derived brain cells
Jenne Tran, Helena Targa Dias Anastacio, Cédric Bardy
npj Parkinson s Disease (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 143
VPS13D bridges the ER to mitochondria and peroxisomes via Miro
Andrés Guillén-Samander, Marianna Leonzino, Michael G. Hanna, et al.
The Journal of Cell Biology (2021) Vol. 220, Iss. 5
Open Access | Times Cited: 135
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
A novel superfamily of bridge-like lipid transfer proteins
Sarah D. Neuman, Tim P. Levine, Arash Bashirullah
Trends in Cell Biology (2022) Vol. 32, Iss. 11, pp. 962-974
Open Access | Times Cited: 73
ER-lysosome lipid transfer protein VPS13C/PARK23 prevents aberrant mtDNA-dependent STING signaling
William Hancock‐Cerutti, Zheng Wu, Peng Xu, et al.
The Journal of Cell Biology (2022) Vol. 221, Iss. 7
Open Access | Times Cited: 69
RBG Motif Bridge-Like Lipid Transport Proteins: Structure, Functions, and Open Questions
Michael G. Hanna, Andrés Guillén-Samander, Pietro De Camilli
Annual Review of Cell and Developmental Biology (2023) Vol. 39, Iss. 1, pp. 409-434
Open Access | Times Cited: 48
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study
Ana Westenberger, Volha Skrahina, Tatiana Usnich, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2652-2667
Open Access | Times Cited: 24
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
Eunju Seong, Ryan Insolera, Marija Dulović, et al.
Annals of Neurology (2018) Vol. 83, Iss. 6, pp. 1075-1088
Open Access | Times Cited: 144
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
Axonal Endoplasmic Reticulum Dynamics and Its Roles in Neurodegeneration
Zeynep Öztürk, Cahir J. O’Kane, Juan José Pérez-Moreno
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 106
Insights into VPS13 properties and function reveal a new mechanism of eukaryotic lipid transport
Marianna Leonzino, Karin M. Reinisch, Pietro De Camilli
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids (2021) Vol. 1866, Iss. 10, pp. 159003-159003
Open Access | Times Cited: 92
The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings
Volha Skrahina, Hanaa Gaber, Eva‐Juliane Vollstedt, et al.
Movement Disorders (2020) Vol. 36, Iss. 4, pp. 1005-1010
Open Access | Times Cited: 85
VPS13A, a closely associated mitochondrial protein, is required for efficient lysosomal degradation
Sandra Muñoz‐Braceras, Alba Tornero-Écija, Olivier Vincent, et al.
Disease Models & Mechanisms (2019)
Open Access | Times Cited: 77
PARK Genes Link Mitochondrial Dysfunction and Alpha-Synuclein Pathology in Sporadic Parkinson’s Disease
Wen Li, Yuhong Fu, Glenda M. Halliday, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 68
Prevalence of ten LRRK2 variants in Parkinson's disease: A comprehensive review
Christopher S. Simpson, Lisa Vinikoor-Imler, Feiby L. Nassan, et al.
Parkinsonism & Related Disorders (2022) Vol. 98, pp. 103-113
Closed Access | Times Cited: 45
Lysosome damage triggers acute formation of ER to lysosomes membrane tethers mediated by the bridge-like lipid transport protein VPS13C
Xinbo Wang, Peng Xu, Amanda Bentley‐DeSousa, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 13
VPS13C regulates phospho-Rab10-mediated lysosomal function in human dopaminergic neurons
Leonie F. Schrӧder, Wesley Peng, Ge Gao, et al.
The Journal of Cell Biology (2024) Vol. 223, Iss. 5
Open Access | Times Cited: 10
Genetic perspective on the synergistic connection between vesicular transport, lysosomal and mitochondrial pathways associated with Parkinson’s disease pathogenesis
Stefanie Smolders, Christine Van Broeckhoven
Acta Neuropathologica Communications (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 61
Role of VPS13, a protein with similarity to ATG2, in physiology and disease
Berrak Uğur, William Hancock‐Cerutti, Marianna Leonzino, et al.
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 61-68
Open Access | Times Cited: 61
Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export
Shaun Martin, Stefanie Smolders, Chris Van den Haute, et al.
Acta Neuropathologica (2020) Vol. 139, Iss. 6, pp. 1001-1024
Open Access | Times Cited: 57
Current state of knowledge in Chorea-Acanthocytosis as core Neuroacanthocytosis syndrome
Kevin Peikert, Adrian Danek, Andreas Hermann
European Journal of Medical Genetics (2017) Vol. 61, Iss. 11, pp. 699-705
Closed Access | Times Cited: 61
Whole-exome sequencing in early-onset Parkinson's disease among ethnic Chinese
Nannan Li, Ling Wang, Jinhong Zhang, et al.
Neurobiology of Aging (2020) Vol. 90, pp. 150.e5-150.e11
Closed Access | Times Cited: 42
Targeted sequencing of Parkinson’s disease loci genes highlights SYT11, FGF20 and other associations
Uladzislau Rudakou, Eric Yu, Lynne Krohn, et al.
Brain (2020) Vol. 144, Iss. 2, pp. 462-472
Open Access | Times Cited: 42
Endoplasmic Reticulum Membrane Contact Sites, Lipid Transport, and Neurodegeneration
Andrés Guillén-Samander, Pietro De Camilli
Cold Spring Harbor Perspectives in Biology (2022) Vol. 15, Iss. 4, pp. a041257-a041257
Closed Access | Times Cited: 27
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
Movement Disorders (2023) Vol. 38, Iss. 8, pp. 1384-1396
Open Access | Times Cited: 16
Page 1 - Next Page

Scroll to top