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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:

Coding mutations in NUS1 contribute to Parkinson’s disease
Jifeng Guo, Lu Zhang, Kai Li, et al.
Proceedings of the National Academy of Sciences (2018) Vol. 115, Iss. 45, pp. 11567-11572
Open Access | Times Cited: 83

Showing 1-25 of 83 citing articles:

Genetics of Parkinson's disease: An introspection of its journey towards precision medicine
Sara Bandrés‐Ciga, Mónica Díez-Fairén, Jonggeol Jeff Kim, et al.
Neurobiology of Disease (2020) Vol. 137, pp. 104782-104782
Open Access | Times Cited: 310
The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population
Yuwen Zhao, Lixia Qin, Hongxu Pan, et al.
Brain (2020) Vol. 143, Iss. 7, pp. 2220-2234
Open Access | Times Cited: 139
Genetics of Parkinson's disease
Ajith Cherian, K. P. Divya
Acta Neurologica Belgica (2020) Vol. 120, Iss. 6, pp. 1297-1305
Closed Access | Times Cited: 81
Nucleocytoplasmic transport defects in neurodegeneration — Cause or consequence?
Saskia Hutten, Dorothee Dormann
Seminars in Cell and Developmental Biology (2019) Vol. 99, pp. 151-162
Closed Access | Times Cited: 76
Progressive myoclonus epilepsies—Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes
Carolina Courage, Karen Oliver, Eon Joo Park, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 4, pp. 722-738
Open Access | Times Cited: 65
Parkinson's disease – genetic cause
Ajith Cherian, Divya K.P, Asish Vijayaraghavan
Current Opinion in Neurology (2023) Vol. 36, Iss. 4, pp. 292-301
Closed Access | Times Cited: 33
Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans
Guihu Zhao, Kuokuo Li, Bin Li, et al.
Nucleic Acids Research (2019)
Open Access | Times Cited: 63
Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's Disease
Yaqin Xiang, Qian Xu, Qiying Sun, et al.
Frontiers in Neurology (2019) Vol. 10
Open Access | Times Cited: 48
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study
Hongxu Pan, Yuwen Zhao, Junpu Mei, et al.
Translational Neurodegeneration (2020) Vol. 9, Iss. 1
Open Access | Times Cited: 45
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
Genetic analysis of N6-methyladenosine modification genes in Parkinson's disease
Lixia Qin, Shishi Min, Shu Li, et al.
Neurobiology of Aging (2020) Vol. 93, pp. 143.e9-143.e13
Closed Access | Times Cited: 42
'Fly-ing' from rare to common neurodegenerative disease mechanisms
Mengqi Ma, Matthew J. Moulton, Shenzhao Lu, et al.
Trends in Genetics (2022) Vol. 38, Iss. 9, pp. 972-984
Open Access | Times Cited: 23
The Chinese Parkinson's Disease Registry (CPDR): Study Design and Baseline Patient Characteristics
Xiaoxia Zhou, Zhenhua Liu, Xiaoting Zhou, et al.
Movement Disorders (2022) Vol. 37, Iss. 7, pp. 1335-1345
Closed Access | Times Cited: 23
The role of de novo mutations in adult-onset neurodegenerative disorders
Gaël Nicolas, Joris A. Veltman
Acta Neuropathologica (2018) Vol. 137, Iss. 2, pp. 183-207
Open Access | Times Cited: 44
Structural elucidation of the cis -prenyltransferase NgBR/DHDDS complex reveals insights in regulation of protein glycosylation
Ban H. Edani, Kariona A. Grabińska, Rong Zhang, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 34, pp. 20794-20802
Open Access | Times Cited: 38
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
Lysosomal cholesterol accumulation contributes to the movement phenotypes associated with NUS1 haploinsufficiency
Seok‐Ho Yu, Tong Wang, Kali Wiggins, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 7, pp. 1305-1314
Open Access | Times Cited: 30
Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson’s disease
Yangjie Zhou, Yige Wang, Juan Wan, et al.
npj Parkinson s Disease (2023) Vol. 9, Iss. 1
Open Access | Times Cited: 12
Loss of NgBR causes neuronal damage through decreasing KAT7-mediated RFX1 acetylation and FGF1 expression
Yuwei Hu, Yanni Ma, Lele Liu, et al.
Cellular and Molecular Life Sciences (2025) Vol. 82, Iss. 1
Open Access
Identification of a novel homozygous SLC13A5 nonstop mutation in a Chinese family with epileptic encephalopathy and developmental delay
Hua He, Lijuan Long, Manling Tang, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Genetic study of the NUS1 gene variants in Han Chinese patients with Parkinson’s disease
Cui Gao, Lamei Yuan, Wen Zheng, et al.
Ageing and Neurodegenerative Diseases (2025)
Open Access
Structural basis of heterotetrameric assembly and disease mutations in the human cis-prenyltransferase complex
Michal Lisnyansky, Pavla Vaňková, Adva Yeheskel, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 29
Gene4PD: A Comprehensive Genetic Database of Parkinson’s Disease
Bin Li, Guihu Zhao, Qiao Zhou, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 24
De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus
Serena Galosi, Ban H. Edani, Simone Martinelli, et al.
Brain (2021) Vol. 145, Iss. 1, pp. 208-223
Open Access | Times Cited: 24
Cocoa Extract Provides Protection against 6-OHDA Toxicity in SH-SY5Y Dopaminergic Neurons by Targeting PERK
Vincenzo Vestuto, Giuseppina Amodio, Giacomo Pepe, et al.
Biomedicines (2022) Vol. 10, Iss. 8, pp. 2009-2009
Open Access | Times Cited: 16
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