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:
Cell signaling pathways in autosomal-dominant leukodystrophy (ADLD): the intriguing role of the astrocytes
Stefano Ratti, Isabella Rusciano, Sara Mongiorgi, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2781-2795
Open Access | Times Cited: 15
Stefano Ratti, Isabella Rusciano, Sara Mongiorgi, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 6, pp. 2781-2795
Open Access | Times Cited: 15
Showing 15 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
Nuclear Phospholipids and Signaling: An Update of the Story
Irene Casalin, Eleonora Ceneri, Stefano Ratti, et al.
Cells (2024) Vol. 13, Iss. 8, pp. 713-713
Open Access | Times Cited: 4
Irene Casalin, Eleonora Ceneri, Stefano Ratti, et al.
Cells (2024) Vol. 13, Iss. 8, pp. 713-713
Open Access | Times Cited: 4
An oligodendrocyte silencer element underlies the pathogenic impact of lamin B1 structural variants
Bruce Nmezi, Guillermo Rodríguez Bey, Talia DeFrancesco Oranburg, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Bruce Nmezi, Guillermo Rodríguez Bey, Talia DeFrancesco Oranburg, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
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
Location-dependent role of phospholipase C signaling in the brain: Physiology and pathology
Isabella Rusciano, Maria Vittoria Marvi, Eric Owusu Obeng, et al.
Advances in Biological Regulation (2020) Vol. 79, pp. 100771-100771
Closed Access | Times Cited: 20
Isabella Rusciano, Maria Vittoria Marvi, Eric Owusu Obeng, et al.
Advances in Biological Regulation (2020) Vol. 79, pp. 100771-100771
Closed Access | Times Cited: 20
Emerging cellular themes in leukodystrophies
Joseph C. Nowacki, Ashley M. Fields, Meng‐meng Fu
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 12
Joseph C. Nowacki, Ashley M. Fields, Meng‐meng Fu
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 12
What Is the Role of Nuclear Envelope Proteins in Neurologic Disorders?
Eduardo E. Benarroch
Neurology (2024) Vol. 102, Iss. 5
Closed Access | Times Cited: 2
Eduardo E. Benarroch
Neurology (2024) Vol. 102, Iss. 5
Closed Access | Times Cited: 2
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
Nuclear Phospholipids and Signaling: An Update of the Story
Irene Casalin, Eleonora Ceneri, Stefano Ratti, et al.
(2024)
Open Access | Times Cited: 1
Irene Casalin, Eleonora Ceneri, Stefano Ratti, et al.
(2024)
Open Access | Times Cited: 1
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
Disorders with prominent posterior fossa involvement
Xavier Ayrignac
Handbook of clinical neurology (2024), pp. 317-332
Closed Access
Xavier Ayrignac
Handbook of clinical neurology (2024), pp. 317-332
Closed Access
A retrospective review of LMNB1-related autosomal dominant leukodystrophy
Judit Perez Ortiz, Karthik Muthusamy, W. Oliver Tobin, et al.
Journal of Rare Diseases (2024) Vol. 3, Iss. 1
Open Access
Judit Perez Ortiz, Karthik Muthusamy, W. Oliver Tobin, et al.
Journal of Rare Diseases (2024) Vol. 3, Iss. 1
Open Access
Impact of Nuclear Peripheral Chromatin Lamin LMNB1 Gene in the Proliferation and Migration of Glioma Cells
Xiang-Cheng Shi, Ting Zhang, Cheng Li, et al.
Neurochemical Research (2024) Vol. 50, Iss. 1
Closed Access
Xiang-Cheng Shi, Ting Zhang, Cheng Li, et al.
Neurochemical Research (2024) Vol. 50, Iss. 1
Closed Access
