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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:

Central Nervous System Involvement as Outcome Measure for Clinical Trials Efficacy in Myotonic Dystrophy Type 1
Costanza Simoncini, Giulia Spadoni, Elisa Lai, et al.
Frontiers in Neurology (2020) Vol. 11
Open Access | Times Cited: 17

Showing 17 citing articles:

Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy
Thiéry De Serres‐Bérard, Marion Pierre, Mohamed Chahine, et al.
Neurobiology of Disease (2021) Vol. 160, pp. 105532-105532
Open Access | Times Cited: 16
Brain Pathogenesis and Potential Therapeutic Strategies in Myotonic Dystrophy Type 1
Jie Liu, Zhen‐Ni Guo, Xiu‐Li Yan, et al.
Frontiers in Aging Neuroscience (2021) Vol. 13
Open Access | Times Cited: 13
Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1
Masayuki Nakamori, Hiroshi Shimizu, Kotaro Ogawa, et al.
Brain Communications (2022) Vol. 4, Iss. 3
Open Access | Times Cited: 9
Cognitive impairment, neuroimaging abnormalities, and their correlations in myotonic dystrophy: a comprehensive review
Yanyun Wu, Qianqian Wei, Junyu Lin, et al.
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
Myotonic dystrophies: an update on clinical features, molecular mechanisms, management, and gene therapy
M. Rimoldi, Sabrina Lucchiari, Serena Pagliarani, et al.
Neurological Sciences (2024)
Open Access | Times Cited: 1
Longitudinal Changes in Neuropsychological Functioning in Japanese Patients with Myotonic Dystrophy Type 1: A Five Year Follow-Up Study
Haruo Fujino, Shugo Suwazono, Yukihiko Ueda, et al.
Journal of Neuromuscular Diseases (2023) Vol. 10, Iss. 6, pp. 1083-1092
Open Access | Times Cited: 3
Cognitive, neuropsychological and emotional-behavioural functioning in a sample of children with myotonic dystrophy type 1
Federica Ricci, Martina Vacchetti, Chiara Brusa, et al.
European Journal of Paediatric Neurology (2022) Vol. 39, pp. 59-64
Closed Access | Times Cited: 5
Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1)
Salvatore Rossi, Gabriella Silvestri
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 3, pp. 2204-2204
Open Access | Times Cited: 2
A validated WAIS-IV short-form to estimate intellectual functioning in myotonic dystrophy type 1
Joana Garmendia, Garazi Labayru, Jone Aliri, et al.
Neuromuscular Disorders (2022) Vol. 32, Iss. 9, pp. 749-753
Open Access | Times Cited: 3
Automatic Text-Mining Approach to Identify Molecular Target Candidates Associated with Metabolic Processes for Myotonic Dystrophy Type 1
Dhvani H. Kuntawala, Filipa Martins, Rui Vitorino, et al.
International Journal of Environmental Research and Public Health (2023) Vol. 20, Iss. 3, pp. 2283-2283
Open Access | Times Cited: 1
Clinical characteristics of different forms of myotonic dystrophy type 1
E. K. Erokhina, Е. А. Melnik, D. Vlodavets
Russian Journal of Child Neurology (2023) Vol. 18, Iss. 1, pp. 22-37
Open Access | Times Cited: 1
Editorial: Sleep disorders in neuromuscular diseases: treatable conditions: the evolving scenario of sleep in neuromuscular disorders
C. Angelini, Gabriele Siciliano, Carl F. Ansevin
Frontiers in Neurology (2024) Vol. 15
Open Access
Speech and language abnormalities in myotonic dystrophy: An overview
Sakhaa Hanoun, Yuyao Sun, Farzad Ebrahimi, et al.
Journal of Clinical Neuroscience (2021) Vol. 96, pp. 212-220
Closed Access | Times Cited: 3
Shedding light on motor premanifest myotonic dystrophy type 1: A molecular, muscular and central nervous system follow‐up study
Joana Garmendia, Garazi Labayru, Miren Zulaica, et al.
European Journal of Neurology (2022) Vol. 30, Iss. 1, pp. 215-223
Open Access | Times Cited: 2
Rest-activity disturbances and light exposure in myotonic dystrophy type 1 patients with apathy: An exploratory study using actigraphy
Luc Laberge, Alexandre Maltais, Olivier Turcotte, et al.
Journal of Affective Disorders Reports (2023) Vol. 14, pp. 100637-100637
Open Access
Differences in diffusion tensor imaging parameters of brain white matter tracts between patients with myotonic dystrophy type 1 and type 2 — a retrospective single-centre study
Edyta Maj, Tomasz Wolak, Joanna De Meulder, et al.
Neurologia i Neurochirurgia Polska (2023) Vol. 57, Iss. 5, pp. 430-437
Open Access
Myotonic Dystrophy Type 1: A Comprehensive Literary Review
Aditya Tripathi, Alex Miliken
Journal of Student Research (2023) Vol. 12, Iss. 4
Open Access
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