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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:

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
Rita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Acta Neuropathologica (2019) Vol. 137, Iss. 6, pp. 901-918
Open Access | Times Cited: 43

Showing 1-25 of 43 citing articles:

The third generation sequencing: the advanced approach to genetic diseases
Tiantian Xiao, Wenhao Zhou
Translational Pediatrics (2020) Vol. 9, Iss. 2, pp. 163-173
Open Access | Times Cited: 113
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Cyril Pottier, Yingxue Ren, Ralph B. Perkerson, et al.
Acta Neuropathologica (2019) Vol. 137, Iss. 6, pp. 879-899
Open Access | Times Cited: 101
The impact of rare genetic variants on Alzheimer disease
Lara De Deyn, Kristel Sleegers
Nature Reviews Neurology (2025)
Closed Access | Times Cited: 1
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: 56
Limiting RyR2 Open Time Prevents Alzheimer’s Disease-Related Neuronal Hyperactivity and Memory Loss but Not β-Amyloid Accumulation
Jinjing Yao, Bo Sun, Ádám Institóris, et al.
Cell Reports (2020) Vol. 32, Iss. 12, pp. 108169-108169
Open Access | Times Cited: 50
Challenge accepted: uncovering the role of rare genetic variants in Alzheimer’s disease
Marzieh Khani, Elizabeth Gibbons, José Brás, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 33
Bioinformatics Analysis of Next Generation Sequencing Data Identifies Molecular Biomarkers Associated With Type 2 Diabetes Mellitus
Varun Alur, Varshita Raju, Basavaraj Vastrad, et al.
Clinical Medicine Insights Endocrinology and Diabetes (2023) Vol. 16
Open Access | Times Cited: 17
Activity-dependent isomerization of Kv4.2 by Pin1 regulates cognitive flexibility
Jia–Hua Hu, Cole Malloy, G. Travis Tabor, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 35
Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases
Federica Perrone, Rita Cacace, Julie van der Zee, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 27
Uncovering Essential Tremor Genetics: The Promise of Long-Read Sequencing
Luca Marsili, Kevin R. Duque, Rachel L. Bode, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 22
Increased burden of rare protein‐truncating variants in constrained, brain‐specific and synaptic genes in extremely impulsively violent males with antisocial personality disorder
Dita Mušálková, Anna Přistoupilová, Ivana Jedličková, et al.
Genes Brain & Behavior (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 4
The genetic landscape of early‐onset Alzheimer's disease in China
Wei Qin, Fangyu Li, Wenying Liu, et al.
Alzheimer s & Dementia (2025)
Open Access
The role of DPP6 dysregulation in neuropathology: from synaptic regulation to disease mechanisms
Xuanyan Ding, Jean de Dieu Habimana, Zhiyuan Li
Frontiers in Cellular Neuroscience (2025) Vol. 19
Open Access
Retinal ganglion cells adapt to ionic stress in experimental glaucoma
Andrew M. Boal, Nolan R. McGrady, Joseph M. Holden, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 9
Insights into the changes in the proteome of Alzheimer disease elucidated by a meta-analysis
Hazal Haytural, Rui Benfeitas, Sophia Schedin‐Weiss, et al.
Scientific Data (2021) Vol. 8, Iss. 1
Open Access | Times Cited: 20
Mutated Toll-like receptor 9 increases Alzheimer’s disease risk by compromising innate immunity protection
Rita Cacace, Lujia Zhou, Elisabeth Hendrickx Van de Craen, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 12, pp. 5380-5389
Open Access | Times Cited: 8
Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study
Zhen Zhang, Xuena Yang, Yumeng Jia, et al.
Nutrients (2021) Vol. 13, Iss. 10, pp. 3343-3343
Open Access | Times Cited: 20
GWAS Identifies DPP6 as Risk Gene of Cognitive Decline in Parkinson’s Disease
Chunyu Li, Yanbing Hou, Ruwei Ou, et al.
The Journals of Gerontology Series A (2024) Vol. 79, Iss. 8
Open Access | Times Cited: 2
Survey of organ‐derived small extracellular vesicles and particles (sEVPs) to identify selective protein markers in mouse serum
Kotb Abdelmohsen, Allison B. Herman, Angelica E. Carr, et al.
Journal of Extracellular Biology (2023) Vol. 2, Iss. 8
Open Access | Times Cited: 6
A Systematic Bioinformatics Workflow With Meta-Analytics Identified Potential Pathogenic Factors of Alzheimer’s Disease
Sze Chung Yuen, Hongmei Zhu, Siu-wai Leung
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 15
Neuronal Roles of the Multifunctional Protein Dipeptidyl Peptidase-like 6 (DPP6)
Cole Malloy, Maisie Ahern, Lin Lin, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 16, pp. 9184-9184
Open Access | Times Cited: 9
Neuronal Differentiation of Induced Pluripotent Stem Cells from Schizophrenia Patients in Two-Dimensional and in Three-Dimensional Cultures Reveals Increased Expression of the Kv4.2 Subunit DPP6 That Contributes to Decreased Neuronal Activity
Maximilian Naujock, Anna Speidel, Sandra E. Fischer, et al.
Stem Cells and Development (2020) Vol. 29, Iss. 24, pp. 1577-1587
Closed Access | Times Cited: 14
Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer’s Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene
Luisa Benussi, Antonio Longobardi, Cemile Koçoğlu, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13633-13633
Open Access | Times Cited: 12
Investigation of the role of matrix metalloproteinases in the genetic etiology of Alzheimer's disease
Julie Hoogmartens, Elisabeth Hens, Sebastiaan Engelborghs, et al.
Neurobiology of Aging (2021) Vol. 104, pp. 105.e1-105.e6
Open Access | Times Cited: 11
Clinical application of whole genome sequencing in young onset dementia: challenges and opportunities
Aamira Huq, Bryony A. Thompson, Ingrid Winship
Expert Review of Molecular Diagnostics (2024) Vol. 24, Iss. 8, pp. 659-675
Closed Access | Times Cited: 1
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