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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:

Copy number variability in Parkinson’s disease: assembling the puzzle through a systems biology approach
Valentina La Cognata, Giovanna Morello, Velia D’Agata, et al.
Human Genetics (2016) Vol. 136, Iss. 1, pp. 13-37
Open Access | Times Cited: 58

Showing 1-25 of 58 citing articles:

3D brain Organoids derived from pluripotent stem cells: promising experimental models for brain development and neurodegenerative disorders
Chun‐Ting Lee, Raphael M. Bendriem, Wells W. Wu, et al.
Journal of Biomedical Science (2017) Vol. 24, Iss. 1
Open Access | Times Cited: 155
Human tyrosine hydroxylase in Parkinson’s disease and in related disorders
Toshiharu Nagatsu, Akira Nakashima, Hiroshi Ichinose, et al.
Journal of Neural Transmission (2018) Vol. 126, Iss. 4, pp. 397-409
Closed Access | Times Cited: 153
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures
Vincenzo A. Gennarino, Elizabeth E. Palmer, Laura M. McDonell, et al.
Cell (2018) Vol. 172, Iss. 5, pp. 924-936.e11
Open Access | Times Cited: 120
Dysregulated miRNAs as Biomarkers and Therapeutical Targets in Neurodegenerative Diseases
Giulia Gentile, Giovanna Morello, Valentina La Cognata, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 5, pp. 770-770
Open Access | Times Cited: 46
Neurogenetic disorders across the lifespan: from aberrant development to degeneration
Richard A. Hickman, Sarah A. O’Shea, Mark F. Mehler, et al.
Nature Reviews Neurology (2022) Vol. 18, Iss. 2, pp. 117-124
Open Access | Times Cited: 34
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
Eric Yu, Uladzislau Rudakou, Lynne Krohn, et al.
Movement Disorders (2020) Vol. 36, Iss. 1, pp. 178-187
Open Access | Times Cited: 45
Single-cell transcriptomics of human iPSC differentiation dynamics reveal a core molecular network of Parkinson’s disease
Gabriela Novak, Dimitrios Kyriakis, Kamil Grzyb, et al.
Communications Biology (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 23
Paying attention: the neurocognition of archery, Middle Stone Age bow hunting, and the shaping of the sapient mind
Marlize Lombard
Phenomenology and the Cognitive Sciences (2024)
Open Access | Times Cited: 5
Omics Data and Their Integrative Analysis to Support Stratified Medicine in Neurodegenerative Diseases
Valentina La Cognata, Giovanna Morello, Sebastiano Cavallaro
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4820-4820
Open Access | Times Cited: 29
iPSCs: A Preclinical Drug Research Tool for Neurological Disorders
Gabriele Bonaventura, Rosario Iemmolo, Giuseppe Antonino Attaguile, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4596-4596
Open Access | Times Cited: 28
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease
Chaodong Wang, Hankui Liu, Xuying Li, et al.
npj Parkinson s Disease (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 4
Mosaicism in Short Tandem Repeat Disorders: A Clinical Perspective
Rose M. Doss, Susana Lopez-Ignacio, Anna Dischler, et al.
Genes (2025) Vol. 16, Iss. 2, pp. 216-216
Open Access
The Evolution of Cognitive Abilities in Marine Animals: Insights from Cognition Gene Polymorphism in Coelacanths and Lungfish
Zhizhou Zhang, Shuaiyu Zhang, Yongdong Xu
Research Square (Research Square) (2025)
Closed Access
Chronic Systemic Inflammation Exacerbates Neurotoxicity in a Parkinson’s Disease Model
Perla Ugalde‐Muñiz, Ingrid Fetter-Pruneda, Luz Navarro, et al.
Oxidative Medicine and Cellular Longevity (2020) Vol. 2020, pp. 1-19
Open Access | Times Cited: 28
Catecholamines and Parkinson’s disease: tyrosine hydroxylase (TH) over tetrahydrobiopterin (BH4) and GTP cyclohydrolase I (GCH1) to cytokines, neuromelanin, and gene therapy: a historical overview
Toshiharu Nagatsu
Journal of Neural Transmission (2023) Vol. 131, Iss. 6, pp. 617-630
Closed Access | Times Cited: 10
Cross-examining candidate genes implicated in multiple system atrophy
Jared S. Katzeff, Katherine Phan, Sivaraman Purushothuman, et al.
Acta Neuropathologica Communications (2019) Vol. 7, Iss. 1
Open Access | Times Cited: 26
Genetic Risk Profiling in Parkinson’s Disease and Utilizing Genetics to Gain Insight into Disease-Related Biological Pathways
Ashley Hall, Sara Bandrés‐Ciga, Mónica Díez-Fairén, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 19, pp. 7332-7332
Open Access | Times Cited: 26
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
The contribution of CNVs to the most common aging-related neurodegenerative diseases
Giulia Gentile, Valentina La Cognata, Sebastiano Cavallaro
Aging Clinical and Experimental Research (2020) Vol. 33, Iss. 5, pp. 1187-1195
Closed Access | Times Cited: 23
Proteomic Profiling of the Substantia Nigra to Identify Determinants of Lewy Body Pathology and Dopaminergic Neuronal Loss
Vladislav Petyuk, Lei Yu, Heather Olson, et al.
Journal of Proteome Research (2021) Vol. 20, Iss. 5, pp. 2266-2282
Open Access | Times Cited: 17
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
Elucidating distinct molecular signatures of Lewy body dementias
Joshua Harvey, Ehsan Pishva, Leonidas Chouliaras, et al.
Neurobiology of Disease (2023) Vol. 188, pp. 106337-106337
Open Access | Times Cited: 6
Genetic landscape of Parkinson’s disease and related diseases in Luxembourg
Zied Landoulsi, Sinthuja Pachchek, Dheeraj Reddy Bobbili, et al.
Frontiers in Aging Neuroscience (2023) Vol. 15
Open Access | Times Cited: 6
Levodopa-responsive dystonia caused by biallelic PRKN exon inversion invisible to exome sequencing
Hagar Mor‐Shaked, Emuna Paz‐Ebstein, Adily Basal, et al.
Brain Communications (2021) Vol. 3, Iss. 3
Open Access | Times Cited: 13
Association of Helicobacter pylori treatment with Parkinsonism and related disorders: A systematic review and meta-analysis
Fusheng Bai, Xinming Li
Life Sciences (2021) Vol. 281, pp. 119767-119767
Closed Access | Times Cited: 12
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