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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:

Dysfunction of the CNS-Heart Axis in Mouse Models of Huntington's Disease
Michał Mielcarek, Linda Inuabasi, Marie K. Bondulich, et al.
PLoS Genetics (2014) Vol. 10, Iss. 8, pp. e1004550-e1004550
Open Access | Times Cited: 88

Showing 1-25 of 88 citing articles:

Integrated genomics and proteomics define huntingtin CAG length–dependent networks in mice
Peter Langfelder, Jeffrey P. Cantle, Doxa Chatzopoulou, et al.
Nature Neuroscience (2016) Vol. 19, Iss. 4, pp. 623-633
Open Access | Times Cited: 352
The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington’s disease patients
Andreas Neueder, Christian Landles, Rhia Ghosh, et al.
Scientific Reports (2017) Vol. 7, Iss. 1
Open Access | Times Cited: 200
CRISPR/Cas9: a powerful genetic engineering tool for establishing large animal models of neurodegenerative diseases
Zhuchi Tu, Weili Yang, Sen Yan, et al.
Molecular Neurodegeneration (2015) Vol. 10, Iss. 1
Open Access | Times Cited: 116
HDAC4 as a potential therapeutic target in neurodegenerative diseases: a summary of recent achievements
Michał Mielcarek, Daniel Zielonka, Alisia Carnemolla, et al.
Frontiers in Cellular Neuroscience (2015) Vol. 9
Open Access | Times Cited: 102
Frequency of nuclear mutant huntingtin inclusion formation in neurons and glia is cell‐type‐specific
Anne H. P. Jansen, Maurik van Hal, Ilse C. op den Kelder, et al.
Glia (2016) Vol. 65, Iss. 1, pp. 50-61
Open Access | Times Cited: 102
Exogenous GDF11 induces cardiac and skeletal muscle dysfunction and wasting
Teresa A. Zimmers, Yanling Jiang, Meijing Wang, et al.
Basic Research in Cardiology (2017) Vol. 112, Iss. 4
Open Access | Times Cited: 99
Skeletal muscle pathology in Huntington's disease
Daniel Zielonka, Izabela Piotrowska, T Marcinkowski, et al.
Frontiers in Physiology (2014) Vol. 5
Open Access | Times Cited: 98
Mouse Models of Huntington’s Disease
Pamela Farshim, Gillian P. Bates
Methods in molecular biology (2018), pp. 97-120
Closed Access | Times Cited: 75
Transcriptional Signature of an Altered Purine Metabolism in the Skeletal Muscle of a Huntington's Disease Mouse Model
Michał Mielcarek, Ryszard T. Smoleński, Mark Isalan
Frontiers in Physiology (2017) Vol. 8
Open Access | Times Cited: 71
Update on Huntington's disease: Advances in care and emerging therapeutic options
Daniel Zielonka, Michał Mielcarek, G. Bernhard Landwehrmeyer
Parkinsonism & Related Disorders (2014) Vol. 21, Iss. 3, pp. 169-178
Closed Access | Times Cited: 67
Allele-Specific Reduction of the Mutant Huntingtin Allele Using Transcription Activator-Like Effectors in Human Huntington's Disease Fibroblasts
Kyle D. Fink, Peter Deng, Josh Gutierrez, et al.
Cell Transplantation (2016) Vol. 25, Iss. 4, pp. 677-686
Open Access | Times Cited: 63
Systemic manifestation and contribution of peripheral tissues to Huntington’s disease pathogenesis
Chia-Lung Chuang, Fabio Demontis
Ageing Research Reviews (2021) Vol. 69, pp. 101358-101358
Open Access | Times Cited: 43
Systemic Symptoms in Huntington's Disease: A Comprehensive Review
Raja Mehanna, Joseph Jankovic
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 5, pp. 453-464
Closed Access | Times Cited: 7
HDAC4-Myogenin Axis As an Important Marker of HD-Related Skeletal Muscle Atrophy
Michał Mielcarek, Marta Toczek, Cleo J. L. M. Smeets, et al.
PLoS Genetics (2015) Vol. 11, Iss. 3, pp. e1005021-e1005021
Open Access | Times Cited: 61
Correlations of Behavioral Deficits with Brain Pathology Assessed through Longitudinal MRI and Histopathology in the R6/1 Mouse Model of Huntington’s Disease
Ivan Rattray, Edward J. Smith, William R. Crum, et al.
PLoS ONE (2013) Vol. 8, Iss. 12, pp. e84726-e84726
Open Access | Times Cited: 55
Huntington's disease is a multi-system disorder
Michał Mielcarek
Rare Diseases (2015) Vol. 3, Iss. 1, pp. e1058464-e1058464
Open Access | Times Cited: 53
Subcellular Localization And Formation Of Huntingtin Aggregates Correlates With Symptom Onset And Progression In A Huntington’S Disease Model
Christian Landles, Rebecca E Milton, Nadira Ali, et al.
Brain Communications (2020) Vol. 2, Iss. 2
Open Access | Times Cited: 45
Mechanistic insights into connexin-mediated neuroglia crosstalk in neurodegenerative diseases
Simona Denaro, Simona D’Aprile, Nunzio Vicario, et al.
Frontiers in Cellular Neuroscience (2025) Vol. 19
Open Access
Transcriptional dysregulation in Huntington’s disease: The role of histone deacetylases
Sorabh Sharma, Rajeev Taliyan
Pharmacological Research (2015) Vol. 100, pp. 157-169
Closed Access | Times Cited: 46
Epigenetics in Neurodegenerative Diseases: The Role of Histone Deacetylases
Sorabh Sharma, K C Sarathlal, Rajeev Taliyan
CNS & Neurological Disorders - Drug Targets (2018) Vol. 18, Iss. 1, pp. 11-18
Closed Access | Times Cited: 46
Neuro-Cardio Mechanisms in Huntington’s Disease and Other Neurodegenerative Disorders
Bethan J. Critchley, Mark Isalan, Michał Mielcarek
Frontiers in Physiology (2018) Vol. 9
Open Access | Times Cited: 42
Phenotype onset in Huntington’s disease knock‐in mice is correlated with the incomplete splicing of the mutant huntingtin gene
Nicholas R. Franich, Miriam A. Hickey, Chunni Zhu, et al.
Journal of Neuroscience Research (2019) Vol. 97, Iss. 12, pp. 1590-1605
Open Access | Times Cited: 42
Progressive cardiac arrhythmias and ECG abnormalities in the Huntington’s disease BACHD mouse model
Yujie Zhu, Isaac Shamblin, Efraín Rodríguez Jiménez, et al.
Human Molecular Genetics (2019) Vol. 29, Iss. 3, pp. 369-381
Open Access | Times Cited: 41
Interrelationship between Alzheimer’s disease and cardiac dysfunction: the brain–heart continuum?
Mingjie Yang, Congye Li, Yingmei Zhang, et al.
Acta Biochimica et Biophysica Sinica (2019) Vol. 52, Iss. 1, pp. 1-8
Closed Access | Times Cited: 41
An impaired metabolism of nucleotides underpins a novel mechanism of cardiac remodeling leading to Huntington's disease related cardiomyopathy
Marta Toczek, Daniel Zielonka, Paulina Żukowska, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2016) Vol. 1862, Iss. 11, pp. 2147-2157
Open Access | Times Cited: 38
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