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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:

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 26-50 of 84 citing articles:

STING signaling in the brain: Molecular threats, signaling activities, and therapeutic challenges
Kun Yang, Zhen Tang, Cong Xing, et al.
Neuron (2023) Vol. 112, Iss. 4, pp. 539-557
Open Access | Times Cited: 13
Identification of a large homozygous VPS13C deletion in a patient with early‐onset Parkinsonism
Hossein Darvish, Paloma Bravo, Abbas Tafakhori, et al.
Movement Disorders (2018) Vol. 33, Iss. 12, pp. 1968-1970
Open Access | Times Cited: 46
Utility and implications of exome sequencing in early‐onset Parkinson's disease
Joanne Trinh, Katja Lohmann, H. Baumann, et al.
Movement Disorders (2018) Vol. 34, Iss. 1, pp. 133-137
Open Access | Times Cited: 42
Glial α‐synuclein promotes neurodegeneration characterized by a distinct transcriptional program in vivo
Abby L. Olsen, Mel Β. Feany
Glia (2019) Vol. 67, Iss. 10, pp. 1933-1957
Open Access | Times Cited: 37
New generation genetic testing entering the clinic
Sorina Gorcenco, Andreea Ilinca, Wejdan Almasoudi, et al.
Parkinsonism & Related Disorders (2020) Vol. 73, pp. 72-84
Open Access | Times Cited: 33
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson’s disease
Stefanie Smolders, Stéphanie Philtjens, David Crosiers, et al.
Acta Neuropathologica Communications (2021) Vol. 9, Iss. 1
Open Access | Times Cited: 28
The mutation spectrum of Parkinson‐disease‐related genes in early‐onset Parkinson's disease in ethnic Chinese
Yongping Chen, Shihui Yu, Guohui Zhang, et al.
European Journal of Neurology (2022) Vol. 29, Iss. 11, pp. 3218-3228
Closed Access | Times Cited: 20
Genetic Evidence for Endolysosomal Dysfunction in Parkinson’s Disease: A Critical Overview
Vidal Yahya, Alessio Di Fonzo, Edoardo Monfrini
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6338-6338
Open Access | Times Cited: 12
Neurodegenerative and Neurodevelopmental Roles for Bulk Lipid Transporters VPS13A and BLTP2
Sarah D. Neuman, Rajan Thakur, Scott J. Gratz, et al.
Movement Disorders (2025)
Open Access
STING mediates lysosomal quality control and recovery through its proton channel function and TFEB activation in lysosomal storage disorders
Zhen Tang, Cong Xing, Antonina M. Araszkiewicz, et al.
Molecular Cell (2025)
Closed Access
The bridge-like lipid transport protein VPS13C/PARK23 mediates ER–lysosome contacts following lysosome damage
X.F. Wang, Peng Xu, Amanda Bentley‐DeSousa, et al.
Nature Cell Biology (2025)
Open Access
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles
J. Nicholas Cochran, Emily McKinley, J. Nicholas Cochran, et al.
Molecular Case Studies (2019) Vol. 5, Iss. 6, pp. a003491-a003491
Open Access | Times Cited: 34
XK-Associated McLeod Syndrome: Nonhematological Manifestations and Relation to VPS13A Disease
Kevin Peikert, Andreas Hermann, Adrian Danek
Transfusion Medicine and Hemotherapy (2022) Vol. 49, Iss. 1, pp. 4-12
Open Access | Times Cited: 17
Disease relevance of rare VPS13B missense variants for neurodevelopmental Cohen syndrome
Malte Zorn, Jirko Kühnisch, Sebastian Bachmann, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 17
VPS13B is localized at the interface between Golgi cisternae and is a functional partner of FAM177A1
Berrak Uğur, Florian Schueder, Jimann Shin, et al.
The Journal of Cell Biology (2024) Vol. 223, Iss. 12
Open Access | Times Cited: 3
Yeast as a Model to Find New Drugs and Drug Targets for VPS13-Dependent Neurodegenerative Diseases
Joanna Kamińska, Piotr Soczewka, Weronika Rzepnikowska, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 9, pp. 5106-5106
Open Access | Times Cited: 15
A multicenter study of genetic testing for Parkinson’s disease in the clinical setting
Anja Kovanda, Valentino Rački, Gaber Bergant, et al.
npj Parkinson s Disease (2022) Vol. 8, Iss. 1
Open Access | Times Cited: 14
Tweek-dependent formation of ER-PM contact sites enables astrocyte phagocytic function and remodeling of neurons
Yunsik Kang, Amanda Jefferson, Amy E. Sheehan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 7
Analysis of common and rare VPS13C variants in late-onset Parkinson disease
Uladzislau Rudakou, Jennifer A. Ruskey, Lynne Krohn, et al.
Neurology Genetics (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 19
Impact of endolysosomal dysfunction upon exosomes in neurodegenerative diseases
María Izco, Estefanía Carlos, Lydia Álvarez-Erviti
Neurobiology of Disease (2022) Vol. 166, pp. 105651-105651
Open Access | Times Cited: 12
Mutation screening and burden analysis of VPS13C in Chinese patients with early-onset Parkinson's disease
Xiaojing Gu, Chunyu Li, Yongping Chen, et al.
Neurobiology of Aging (2020) Vol. 94, pp. 311.e1-311.e4
Closed Access | Times Cited: 18
Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease
Laurie Robak, Renqian Du, Bo Yuan, et al.
Neurology Genetics (2020) Vol. 6, Iss. 5
Open Access | Times Cited: 17
Genetic Testing for Parkinson Disease
Lola Cook, Jeanine Schulze, Catherine Kopil, et al.
Neurology Clinical Practice (2020) Vol. 11, Iss. 1, pp. 69-77
Open Access | Times Cited: 16
Genome‐Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India
Prashanth Lingappa Kukkle, Thenral S. Geetha, Ruchi Chaudhary, et al.
Advanced Biology (2022) Vol. 6, Iss. 11
Closed Access | Times Cited: 10
VPS13C-associated Parkinson's disease: Two novel cases and review of the literature
Edoardo Monfrini, Francesca Spagnolo, Margherita Canesi, et al.
Parkinsonism & Related Disorders (2021) Vol. 94, pp. 37-39
Open Access | Times Cited: 14

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