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:

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

Showing 8 citing articles:

Atypical Presentation of an LMNB1 Duplication Involving the Silencer Region
Jia Dong James Wang, Tamara N. Kimball, Savvina Prapiadou, et al.
Neurology Genetics (2025) Vol. 11, Iss. 3
Closed Access

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

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

Gene and Cellular Therapies for Leukodystrophies
Fatima Aerts‐Kaya, Niek P. van Til
Pharmaceutics (2023) Vol. 15, Iss. 11, pp. 2522-2522
Open Access | Times Cited: 5

SUN5 interacts with nuclear membrane LaminB1 and cytoskeletal GTPase Septin12 mediating the sperm head-and-tail junction
Yunfei Zhang, Gang Liu, Lihua Huang, et al.
Molecular Human Reproduction (2024) Vol. 30, Iss. 7
Closed Access | Times Cited: 1

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

Genetic Heterogeneity in Four Probands Reveals HGSNAT, KDM6B, LMNA and WFS1 Related Neurodevelopmental Disorders
Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B. Williams, et al.
Biomedicines (2024) Vol. 12, Iss. 12, pp. 2736-2736
Open Access

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