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:
Lamin B1 Accumulation’s Effects on Autosomal Dominant Leukodystrophy (ADLD): Induction of Reactivity in the Astrocytes
Stefano Ratti, Isabella Rusciano, Sara Mongiorgi, et al.
Cells (2021) Vol. 10, Iss. 10, pp. 2566-2566
Open Access | Times Cited: 7
Stefano Ratti, Isabella Rusciano, Sara Mongiorgi, et al.
Cells (2021) Vol. 10, Iss. 10, pp. 2566-2566
Open Access | Times Cited: 7
Showing 7 citing articles:
The wide and growing range of lamin B-related diseases: from laminopathies to cancer
Camilla Evangelisti, Isabella Rusciano, Sara Mongiorgi, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 2
Open Access | Times Cited: 55
Camilla Evangelisti, Isabella Rusciano, Sara Mongiorgi, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 2
Open Access | Times Cited: 55
Blood-brain barrier biomarkers
Juan F. Zapata-Acevedo, Alejandra Mantilla-Galindo, Karina Vargas-Sánchez, et al.
Advances in clinical chemistry (2024), pp. 1-88
Closed Access | Times Cited: 9
Juan F. Zapata-Acevedo, Alejandra Mantilla-Galindo, Karina Vargas-Sánchez, et al.
Advances in clinical chemistry (2024), pp. 1-88
Closed Access | Times Cited: 9
Case report: LMNB1 duplication-mediated autosomal dominant adult leukodystrophy in a Chinese family and literature review of Chinese patients
Yumeng Jiang, Lu Han, Yaqi Li, et al.
Frontiers in Neuroscience (2025) Vol. 19
Open Access
Yumeng Jiang, Lu Han, Yaqi Li, et al.
Frontiers in Neuroscience (2025) Vol. 19
Open Access
Understanding the Ultra-Rare Disease Autosomal Dominant Leukodystrophy: an Updated Review on Morpho-Functional Alterations Found in Experimental Models
Irene Neri, Giulia Ramazzotti, Sara Mongiorgi, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 11, pp. 6362-6372
Open Access | Times Cited: 8
Irene Neri, Giulia Ramazzotti, Sara Mongiorgi, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 11, pp. 6362-6372
Open Access | Times Cited: 8
Lamin B1 as a key modulator of the developing and aging brain
Foteini‐Dionysia Koufi, Irene Neri, Giulia Ramazzotti, et al.
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 7
Foteini‐Dionysia Koufi, Irene Neri, Giulia Ramazzotti, et al.
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 7
Structural Variants at the LMNB1 Locus: Deciphering Pathomechanisms in Autosomal Dominant Adult‐Onset Demyelinating Leukodystrophy
Paola Dimartino, Mariia Zadorozhna, Verónica Yumiceba, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 855-870
Open Access | Times Cited: 2
Paola Dimartino, Mariia Zadorozhna, Verónica Yumiceba, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 855-870
Open Access | Times Cited: 2
[Research advances in the clinical genetics of leukodystrophy in children].
Zhe-Lan Huang, Wenhao Zhou
PubMed (2022) Vol. 24, Iss. 6, pp. 711-716
Closed Access
Zhe-Lan Huang, Wenhao Zhou
PubMed (2022) Vol. 24, Iss. 6, pp. 711-716
Closed Access
