Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

MLC1 protein: a likely link between leukodystrophies and brain channelopathies
Maria Stefania Brignone, Angela Lanciotti, Serena Camerini, et al.
Frontiers in Cellular Neuroscience (2015) Vol. 09
Open Access | Times Cited: 35

Showing 26-50 of 35 citing articles:

Emerging Concepts in Vector Development for Glial Gene Therapy: Implications for Leukodystrophies
Georg von Jonquières, Caroline Rae, Gary D. Housley
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 8
Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome
Michael S. Breen, Xuanjia Fan, Tess Levy, et al.
Human Genetics and Genomics Advances (2022) Vol. 4, Iss. 1, pp. 100145-100145
Open Access | Times Cited: 6
Megalencephalic leukoencephalopathy with subcortical cysts protein-1: A new calcium-sensitive protein functionally activated by endoplasmic reticulum calcium release and calmodulin binding in astrocytes
Maria Stefania Brignone, Angela Lanciotti, Paola Molinari, et al.
Neurobiology of Disease (2023) Vol. 190, pp. 106388-106388
Open Access | Times Cited: 3
Astroglia in Leukodystrophies
Maria Susana Jorge, Marianna Bugiani
Advances in experimental medicine and biology (2019), pp. 199-225
Closed Access | Times Cited: 8
The Mlc1 Promoter Directs Müller Cell-specific Gene Expression in the Retina
Yosuke Danjo, Youichi Shinozaki, Akiyo Natsubori, et al.
Translational Vision Science & Technology (2022) Vol. 11, Iss. 1, pp. 25-25
Open Access | Times Cited: 5
Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder
Safiah Alhazmi, Maryam Alzahrani, Reem M. Farsi, et al.
Pharmacogenomics and Personalized Medicine (2022) Vol. Volume 15, pp. 705-720
Open Access | Times Cited: 4
Metachromatic Leukodystrophy: Diagnosis and Treatment Challenges
Nayibe Tatiana Sánchez Alvarez, Paula K. Bautista‐Niño, Juanita Trejos-Suárez, et al.
Bionatura (2021) Vol. 3, Iss. 3, pp. 2083-2090
Open Access | Times Cited: 3
A case of megalencephalic leukoencephalopathy with subcortical cysts type 1 was identified with a novel compound heterozygous alteration (c.135delC; c.423+2dupT) in China
Cheng Dai, Wen‐Bin He, Juan Du, et al.
Clinical Case Reports (2017) Vol. 5, Iss. 6, pp. 961-967
Open Access | Times Cited: 2
A homozygous missense variant in the MLC1 gene underlies megalencephalic leukoencephalopathy with subcortical cysts in large kindred: Heterozygous carriers show seizure and mild motor function deterioration
Syeda Ain ul Batool, Ahmed Almatrafi, Fatima Fadhli, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 4, pp. 1075-1082
Closed Access | Times Cited: 2
Ubr1-induced selective endo-phagy/autophagy protects against the endosomal and Ca2+-induced proteostasis disease stress
Ben B. Wang, Haijin Xu, Sandra Isenmann, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
Previous Page - Page 2

Scroll to top