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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:

Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease
Paul J. Hop, Dongbing Lai, Pamela Keagle, et al.
Nature Genetics (2024) Vol. 56, Iss. 7, pp. 1371-1376
Open Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

A STING–CASM–GABARAP pathway activates LRRK2 at lysosomes
Amanda Bentley‐DeSousa, Agnes Roczniak-Ferguson, Shawn M. Ferguson
The Journal of Cell Biology (2025) Vol. 224, Iss. 2
Open Access | Times Cited: 2
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinic
Shen‐Yang Lim, Ai Huey Tan, Azlina Ahmad, et al.
The Lancet Neurology (2024)
Closed Access | Times Cited: 8
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson’s disease
Thomas P Spargo, Chloe F. Sands, Isabella R. Juan, et al.
Cell Reports (2025), pp. 115355-115355
Open Access | Times Cited: 1
LRRK2 in Parkinson's disease: upstream regulation and therapeutic targeting
Yulan Xiong, Jianzhong Yu
Trends in Molecular Medicine (2024) Vol. 30, Iss. 10, pp. 982-996
Closed Access | Times Cited: 7
Editorial on: Confirmation of RAB32 Ser71Arg involvement in Parkinson's disease
Emil K. Gustavsson
Movement Disorders (2025) Vol. 40, Iss. 1, pp. 5-6
Closed Access
LRRK2, lysosome damage, and Parkinson's disease
Amanda Bentley‐DeSousa, D.J. Clegg, Shawn M. Ferguson
Current Opinion in Cell Biology (2025) Vol. 93, pp. 102482-102482
Open Access
18F-FDG PET findings in Parkinson's disease associated to RAB 32 S71R variant
Francesco Cavallieri, Alessandro Fraternali, Annachiara Arnone, et al.
Parkinsonism & Related Disorders (2025) Vol. 134, pp. 107343-107343
Closed Access
Accumulation of Damaging Lipids in the Arf1‐Ablated Neurons Promotes Neurodegeneration through Releasing mtDNA and Activating Inflammatory Pathways in Microglia
Xu Li, Shuhan Jin, Danke Wang, et al.
Advanced Science (2025)
Open Access
Identification of Ser71Arg mutation in RAB32 gene in familial Parkinson’s disease from Southern Italy
Monica Gagliardi, Radha Procopio, Grazia Annesi, et al.
npj Parkinson s Disease (2025) Vol. 11, Iss. 1
Open Access
A STING-CASM-GABARAP Pathway Activates LRRK2 at Lysosomes
Amanda Bentley‐DeSousa, Agnes Roczniak-Ferguson, Shawn M. Ferguson
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 9
RAB32 Variants in a German Parkinson's Disease Cohort
Carolin Gabbert, Cholpon Shambetova, Christoph Much, et al.
Movement Disorders (2024)
Closed Access | Times Cited: 3
Haploinsufficiency ofITSN1is associated with Parkinson’s disease
Thomas P Spargo, Chloe F. Sands, Isabella R. Juan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Confirmation of RAB32 Ser71Arg Involvement in Parkinson's Disease
Guillaume Cogan, Christelle Tesson, Christine Brefel‐Courbon, et al.
Movement Disorders (2024) Vol. 40, Iss. 1, pp. 174-175
Open Access | Times Cited: 2
Genetic and Epidemiological Insights into RAB32‐Linked Parkinson's Disease
Mandy Radefeldt, Sabrina Lemke, Kridsadakorn Chaichoompu, et al.
Movement Disorders (2024)
Open Access | Times Cited: 2
Parkinson’s disease-associated shifts between DNA methylation and DNA hydroxymethylation in human brain
Juliana Choza, Mahek Virani, Nathan C. Kuhn, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Parkinson’s families project: a UK-wide study of early onset and familial Parkinson’s disease
Clodagh Towns, Zih‐Hua Fang, Manuela Tan, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 1
Microglia: roles and genetic risk in Parkinson’s disease
A. Trainor, Debra S. MacDonald, Jay Penney
Frontiers in Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
Soma-centered control of synaptic autophagy by Rab39-regulated anterograde trafficking of Atg9
Ayse Kilic, Dirk Vandekerkhove, Sabine Kuenen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Genetic evidence for a link between frontotemporal dementia and Parkinson’s disease: the case of RAB32 Ser71Arg
Andrea Panzavolta, Francesco Cavallieri, Franco Valzania, et al.
Journal of Neurology (2024) Vol. 272, Iss. 1
Closed Access | Times Cited: 1
The RAB32 p.Ser71Arg Variant in Parkinsonisms: Insights from a Large Italian Cohort
Luca Magistrelli, Marta Benedetta Brumana, Valeria Rimoldi, et al.
Movement Disorders (2024)
Open Access | Times Cited: 1
RAB32 variant is associated with PD susceptibility
Heather Wood
Nature Reviews Neurology (2024) Vol. 20, Iss. 8, pp. 456-456
Closed Access
Knockout of the LRRK2-counteracting RAB phosphatase PPM1H disrupts axonal autophagy and exacerbates alpha-synuclein aggregation
Michel Fricke, Anna Mechel, Björn Twellsieck, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
RAB32 Variants in a Chinese Parkinson's Disease Cohort
Shichan Wang, Ruwei Ou, Jingxuan Huang, et al.
Movement Disorders (2024)
Open Access
Ancestry-specific gene expression in peripheral monocytes mediates risk of neurodegenerative disease
Aaron Z. Wagen, Regina H. Reynolds, Jia Nee Foo, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
A rare variant in the UQCRC1 gene, p.(Gly405Val) in three Austrian Parkinson's Patients
Christof Brücke, Thomas Brücke, Walter Pirker, et al.
Parkinsonism & Related Disorders (2024), pp. 107250-107250
Open Access
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