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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:

Mutant Huntingtin Protein Interaction Map Implicates Dysregulation of Multiple Cellular Pathways in Neurodegeneration of Huntington’s Disease
Sonia Podvin, Sara Brin Rosenthal, William Poon, et al.
Journal of Huntington s Disease (2022) Vol. 11, Iss. 3, pp. 243-267
Open Access | Times Cited: 19

Showing 19 citing articles:

Huntington’s Disease: Complex Pathogenesis and Therapeutic Strategies
Huichun Tong, Tianqi Yang, Shuying Xu, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 7, pp. 3845-3845
Open Access | Times Cited: 22
Parthanatos: Mechanisms, modulation, and therapeutic prospects in neurodegenerative disease and stroke
Yang Liu, Lauren Guttman, Valina L. Dawson, et al.
Biochemical Pharmacology (2024) Vol. 228, pp. 116174-116174
Closed Access | Times Cited: 16
14-3-3 proteins—a moonlight protein complex with therapeutic potential in neurological disorder: in-depth review with Alzheimer’s disease
Gholamareza Abdi, Mukul Jain, Nil Patil, et al.
Frontiers in Molecular Biosciences (2024) Vol. 11
Open Access | Times Cited: 9
Advances in Stem Cell Therapy for Huntington’s Disease: A Comprehensive Literature Review
Siddharth Shah, Hadeel M. Mansour, Brandon Lucke‐Wold
Cells (2025) Vol. 14, Iss. 1, pp. 42-42
Open Access | Times Cited: 1
Apoptosis Genes as a Key to Identification of Inverse Comorbidity of Huntington’s Disease and Cancer
E. Yu. Bragina, Д. Е. Гомбоева, Olga Saik, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 11, pp. 9385-9385
Open Access | Times Cited: 12
CAG repeat expansion in the Huntington’s disease gene shapes linear and circular RNAs biogenesis
Dilara Ayyildiz, Guendalina Bergonzoni, Alan Monziani, et al.
PLoS Genetics (2023) Vol. 19, Iss. 10, pp. e1010988-e1010988
Open Access | Times Cited: 12
What Is the Function and Relevance of 14-3-3 Proteins in Neurologic Disease?
Eduardo E. Benarroch
Neurology (2025) Vol. 104, Iss. 5
Closed Access
Progressive alterations in polysomal architecture and activation of ribosome stalling relief factors in a mouse model of Huntington's disease
Eva Martin-Solana, Irene Díaz‐López, Yamina Mohamedi, et al.
Neurobiology of Disease (2024) Vol. 195, pp. 106488-106488
Open Access | Times Cited: 3
Insights into AlphaFold’s breakthrough in neurodegenerative diseases
Hira Mubeen, Ammara Masood, Asma Zafar, et al.
Irish Journal of Medical Science (1971 -) (2024)
Closed Access | Times Cited: 2
Unraveling the Molecular Jam: How Crowding Shapes Protein Aggregation in Neurodegenerative Disorders
Shashi Prakash Patel, Tejas Nikam, Bhargavi Sreepathi, et al.
ACS Chemical Biology (2024) Vol. 19, Iss. 10, pp. 2118-2130
Closed Access | Times Cited: 2
Saccharomyces cerevisiae as a research tool for RNA‐mediated human disease
Stephanie Gastelum, Allison F. Michael, Timothy A. Bolger
Wiley Interdisciplinary Reviews - RNA (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 6
Mutant-Huntingtin Molecular Pathways Elucidate New Targets for Drug Repurposing
V.S. Makeeva, Nadezhda S. Dyrkheeva, Olga I. Lavrik, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 16798-16798
Open Access | Times Cited: 5
Huntingtin loss-of-function contributes to transcriptional deregulation in Huntington's disease
Kozłowska Emilia, Ciołak Agata, Adamek Grażyna, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Increased FAN1 expression by mRNA-LNP attenuates CAG repeat expansion in Huntington patients’ iPSC-derived astrocytes
Yung‐Chih Cheng, Gosia Nocula-Lugowska, Julita A Ramirez, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Proteostasis function and dysfunction in Huntington's disease
Juliana Abramovich, Korbin Kleczko, Vincent B. Masto, et al.
Elsevier eBooks (2024), pp. 205-227
Closed Access
Developmental and physiological impacts of pathogenic human huntingtin protein in the nervous system
Tadros A. Hana, Veronika G. Mousa, Alice Lin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Identification of pivotal genes and pathways in Chorea-acanthocytosis using comprehensive bioinformatic analysis
Ravinder Sharma, Kiran Yadav, Leeza Monga, et al.
PLoS ONE (2024) Vol. 19, Iss. 9, pp. e0309594-e0309594
Open Access
Developmental and physiological impacts of pathogenic human huntingtin protein in the nervous system
Tadros A. Hana, Veronika G. Mousa, Alice Lin, et al.
Neurobiology of Disease (2024) Vol. 203, pp. 106732-106732
Open Access
Evolutionary, Protein–Protein Interaction (PPI), and Domain–Domain Analyses in Huntington’s Disease
Sai Gopala Swamy Gadde, K. Pravallika, K. Srinivas
Lecture notes in electrical engineering (2023), pp. 11-23
Closed Access
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