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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:

Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management
Mahmoud Reza Ashrafi, Ali Reza Tavasoli
Brain and Development (2017) Vol. 39, Iss. 5, pp. 369-385
Closed Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Diagnosis, prognosis, and treatment of leukodystrophies
Marjo S. van der Knaap, Raphael Schiffmann, Fanny Mochel, et al.
The Lancet Neurology (2019) Vol. 18, Iss. 10, pp. 962-972
Closed Access | Times Cited: 144
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies
Mahmoud Reza Ashrafi, Man Amanat, Masoud Garshasbi, et al.
Expert Review of Neurotherapeutics (2019) Vol. 20, Iss. 1, pp. 65-84
Closed Access | Times Cited: 69
Biallelic KARS pathogenic variants cause an early-onset progressive leukodystrophy
Masayuki Itoh, Hongmei Dai, Shin‐ichi Horike, et al.
Brain (2019) Vol. 142, Iss. 3, pp. 560-573
Open Access | Times Cited: 27
Treacher Collins syndrome mutations in Saccharomyces cerevisiae destabilize RNA polymerase I and III complex integrity
Nancy Walker‐Kopp, Ashleigh J. Jackobel, Gianno Pannafino, et al.
Human Molecular Genetics (2017) Vol. 26, Iss. 21, pp. 4290-4300
Open Access | Times Cited: 25
Glial cells in the driver seat of leukodystrophy pathogenesis
Luis Garcia, Julia Hacker, Sunetra Sase, et al.
Neurobiology of Disease (2020) Vol. 146, pp. 105087-105087
Open Access | Times Cited: 22
Affected astrocytes in the spinal cord of the leukodystrophy vanishing white matter
Prisca S. Leferink, Nicole Breeuwsma, Marianna Bugiani, et al.
Glia (2017) Vol. 66, Iss. 4, pp. 862-873
Open Access | Times Cited: 21
Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel
Bindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar, et al.
Journal of Child Neurology (2020) Vol. 35, Iss. 7, pp. 433-441
Closed Access | Times Cited: 15
Leukodystrophies in Children: Diagnosis, Care, and Treatment
Joshua L. Bonkowsky, Stephanie Keller, Jamie K. Capal, et al.
PEDIATRICS (2021) Vol. 148, Iss. 3
Open Access | Times Cited: 13
Update on leukodystrophies and developing trials
G Ceravolo, Kristina Zhelcheska, Violetta Squadrito, et al.
Journal of Neurology (2023) Vol. 271, Iss. 1, pp. 593-605
Open Access | Times Cited: 5
The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System
Mahmoud Reza Ashrafi, Zahra Rezaei, Morteza Heidari, et al.
Journal of Child Neurology (2018) Vol. 33, Iss. 4, pp. 255-259
Closed Access | Times Cited: 15
Novel mutations in the GJC2 gene associated with Pelizaeus–Merzbacher-like disease
Marta Owczarek‐Lipska, Lejla Mulahasanovic, Carolin D. Obermaier, et al.
Molecular Biology Reports (2019) Vol. 46, Iss. 4, pp. 4507-4516
Closed Access | Times Cited: 14
Overview of Neuro-Ophthalmic Findings in Leukodystrophies
C Bettinger, Simon Dulz, Yevgeniya Atiskova, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 17, pp. 5114-5114
Open Access | Times Cited: 1
Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients
Zahra Rezaei, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
Neuropediatrics (2019) Vol. 50, Iss. 02, pp. 130-134
Closed Access | Times Cited: 11
Expanded Phenotypic Definition Identifies Hundreds of Potential Causative Genes for Leukodystrophies and Leukoencephalopathies
Veronica M. Urbik, Marilyn Schmiedel, Haille E. Soderholm, et al.
Child Neurology Open (2020) Vol. 7, pp. 2329048X2093900-2329048X2093900
Open Access | Times Cited: 11
Independent occurrence of de novo HSPD1 and HIP1 variants in brothers with different neurological disorders – leukodystrophy and autism
Toshiyuki Yamamoto, Keiko Yamamoto‐Shimojima, Yuki Ueda, et al.
Human Genome Variation (2018) Vol. 5, Iss. 1
Open Access | Times Cited: 10
Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease
Alexa Derksen, Hung‐Yu Shih, Diane Forget, et al.
Human Genetics and Genomics Advances (2021) Vol. 2, Iss. 3, pp. 100034-100034
Open Access | Times Cited: 8
Leukoencephalopathy hypomyelination with brainstem and spinal cord involvement and leg spasticity caused by DARS1 mutations
Jingyi Zhu, Xiaomin Guo, Ningjing Ran, et al.
Frontiers in Genetics (2023) Vol. 13
Open Access | Times Cited: 3
Case Report: Mutation in AIMP2/P38, the Scaffold for the Multi-Trna Synthetase Complex, and Association With Progressive Neurodevelopmental Disorders
Mahta Mazaheri, Mahdie Yavari, Hadi Zare Marzouni, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 5
Spongiform leucoencephalomyelopathy in border terriers: clinical, electrophysiological and imaging features
Rodrigo Gutierrez‐Quintana, Marκ McLaughlin, Llorenç Grau‐Roma, et al.
Veterinary Record (2019) Vol. 185, Iss. 12, pp. 375-375
Open Access | Times Cited: 7
Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy
Erfan Heidari, Maryam Rasoulinezhad, Neda Pak, et al.
Mitochondrion (2021) Vol. 60, pp. 12-20
Closed Access | Times Cited: 6
Occupational Therapy Intervention in the Child with Leukodystrophy: Case Report
Rachele Simeon, Anna Berardi, Donatella Valente, et al.
Children (2023) Vol. 10, Iss. 7, pp. 1257-1257
Open Access | Times Cited: 2
Histone Acetylation Defects in Brain Precursor Cells: A Potential Pathogenic Mechanism Causing Proliferation and Differentiation Dysfunctions in Mitochondrial Aspartate-Glutamate Carrier Isoform 1 Deficiency
Eleonora Poeta, Sabrina Petralla, Giorgia Babini, et al.
Frontiers in Cellular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 4
Asociación entre la mutación homocigota c.318A>T en el exón 2 del gen EIF2B5 y la forma infantil de la leucoencefalopatía con sustancia blanca evanescente
Carmen Esmer, Gabriela Blanco Hernández, Víctor Saavedra Alanís, et al.
Boletín Médico del Hospital Infantil de México (2017) Vol. 74, Iss. 5, pp. 364-369
Open Access | Times Cited: 3
Seizure as the Early and Main Manifestation of Infantile Vanishing White Matter Disease: A Case Report
Negin Rezaei, Sedighe Nikbakht, Mahmoud Reza Ashrafi, et al.
Iranian Journal of Pediatrics (2018) Vol. 28, Iss. 2
Open Access | Times Cited: 3
Developmental Delay, Hypomyelination, and Nystagmus: Case and Approach
Luís Guilherme Ramanzini, Julia Maria Frare, T. F. Lopes, et al.
Neuro-Ophthalmology (2024) Vol. 48, Iss. 5, pp. 369-372
Closed Access
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