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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:

Multifaceted Genes in Amyotrophic Lateral Sclerosis-Frontotemporal Dementia
Ramya Ranganathan, Shaila Haque, Kayesha Coley, et al.
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

Amyotrophic lateral sclerosis: a neurodegenerative disorder poised for successful therapeutic translation
Richard J. Mead, Ning Shan, H. Joseph Reiser, et al.
Nature Reviews Drug Discovery (2022) Vol. 22, Iss. 3, pp. 185-212
Open Access | Times Cited: 269
Recent Updates on the Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
Laxmi Kirola, Ashim Mukherjee, Mousumi Mutsuddi
Molecular Neurobiology (2022) Vol. 59, Iss. 9, pp. 5673-5694
Closed Access | Times Cited: 52
Intrinsically disordered proteins and proteins with intrinsically disordered regions in neurodegenerative diseases
Orkid Coskuner‐Weber, Ozan Mirzanli, Vladimir N. Uversky
Biophysical Reviews (2022) Vol. 14, Iss. 3, pp. 679-707
Open Access | Times Cited: 46
Protein aggregation and therapeutic strategies in SOD1- and TDP-43- linked ALS
Maria Tsekrekou, Μαρία Γιαννάκου, Katerina Papanikolopoulou, et al.
Frontiers in Molecular Biosciences (2024) Vol. 11
Open Access | Times Cited: 14
Unraveling the complex interplay between genes, environment, and climate in ALS
Rosario Vasta, Ruth Chia, Bryan J. Traynor, et al.
EBioMedicine (2021) Vol. 75, pp. 103795-103795
Open Access | Times Cited: 53
Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit
Rita Sattler, Bryan J. Traynor, Janice Robertson, et al.
Neurology and Therapy (2023) Vol. 12, Iss. 6, pp. 1821-1843
Open Access | Times Cited: 22
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia
Lyndal Henden, Liam G. Fearnley, Natalie Grima, et al.
Science Advances (2023) Vol. 9, Iss. 18
Open Access | Times Cited: 20
Emerging Trends in the Field of Inflammation and Proteinopathy in ALS/FTD Spectrum Disorder
Fabiola De Marchi, Toni Franjkic, Paride Schito, et al.
Biomedicines (2023) Vol. 11, Iss. 6, pp. 1599-1599
Open Access | Times Cited: 17
Looking to the Future of the Role of Macrophages and Extracellular Vesicles in Neuroinflammation in ALS
Elisabetta Carata, Marco Muci, Simona Di Giulio, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11251-11251
Open Access | Times Cited: 17
Amplifying the Heat Shock Response Ameliorates ALS and FTD Pathology in Mouse and Human Models
Mhoriam Ahmed, Charlotte Spicer, Jasmine Harley, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 12, pp. 6896-6915
Open Access | Times Cited: 14
TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: From pathomechanisms to therapeutic strategies
Pei‐Chuan Ho, Tsung‐Chi Hsieh, Kuen‐Jer Tsai
Ageing Research Reviews (2024) Vol. 100, pp. 102441-102441
Open Access | Times Cited: 6
Amyotrophic lateral sclerosis; clinical features, differential diagnosis and pathology
Michael A. van Es
International review of neurobiology (2024), pp. 1-47
Closed Access | Times Cited: 5
Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis
Milena Janković, Ivana Novaković, Phepy G. A. Dawod, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 18, pp. 9832-9832
Open Access | Times Cited: 29
Prospects for gene replacement therapies in amyotrophic lateral sclerosis
Ilaria Giovannelli, Adrian Higginbottom, Janine Kirby, et al.
Nature Reviews Neurology (2022) Vol. 19, Iss. 1, pp. 39-52
Closed Access | Times Cited: 17
Respiratory failure as main presentation sign of MAPT-related disorder
M Favier, Maïté Formaglio, Anne Cosson, et al.
Journal of Neurology (2025) Vol. 272, Iss. 2
Closed Access
Integrative transcriptome profiling for identifying ALS potential treatment using the drug repurposing approach
Navid Kashani, Amir Sabbaghian, Fatemeh EmamiPari, et al.
Egyptian Journal of Medical Human Genetics (2025) Vol. 26, Iss. 1
Open Access
The landscape of cognitive impairment in superoxide dismutase 1-amyotrophic lateral sclerosis
Ilaria Martinelli, Elisabetta Zucchi, Cecilia Simonini, et al.
Neural Regeneration Research (2022) Vol. 18, Iss. 7, pp. 1427-1427
Open Access | Times Cited: 15
Identifying FUS amyotrophic lateral sclerosis disease signatures in patient dermal fibroblasts
Karl Kumbier, Maike Roth, Zizheng Li, et al.
Developmental Cell (2024) Vol. 59, Iss. 16, pp. 2134-2142.e6
Open Access | Times Cited: 3
Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 Variants
Eleonora Dalla Bella, Enrica Bersano, Maria Grazia Bruzzone, et al.
Neurology (2022) Vol. 99, Iss. 18
Open Access | Times Cited: 14
Transcriptomic analysis of human ALS skeletal muscle reveals a disease-specific pattern of dysregulated circRNAs
Dimitrios Tsitsipatis, Krystyna Mazan-Mamczarz, Ying Si, et al.
Aging (2022) Vol. 14, Iss. 24, pp. 9832-9859
Open Access | Times Cited: 12
An atypical ALS with PSP-like symptoms caused by ANXA11 p.D40G mutation: A case report and literature review
Xin Zhang, Juan Gao, Chunling Chi, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 7
Identification and characterization of novel ERBB4 variant associated with sporadic amyotrophic lateral sclerosis (ALS)
Younghwi Kwon, Minsung Kang, Yu‐Mi Jeon, et al.
Journal of the Neurological Sciences (2024) Vol. 457, pp. 122885-122885
Closed Access | Times Cited: 2
The integrity of the corticospinal tract and corpus callosum, and the risk of ALS: univariable and multivariable Mendelian randomization
Jieying Wu, Gan Zhang, Linjing Zhang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
CRISPR deletion of a SINE-VNTR-Alu (SVA_67) retrotransposon demonstrates its ability to differentially modulate gene expression at the MAPT locus
Alexander Fröhlich, Lauren S. Hughes, Ben Middlehurst, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 6
Loss of aly/ALYREF suppresses toxicity in both tau and TDP-43 models of neurodegeneration
Rebecca L. Kow, Aristide H. Black, Aleen D. Saxton, et al.
GeroScience (2022) Vol. 44, Iss. 2, pp. 747-761
Open Access | Times Cited: 9
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