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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:

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

Showing 1-25 of 27 citing articles:

Roles of aminoacyl-tRNA synthetases in immune regulation and immune diseases
Anzheng Nie, Bao Sun, Zhihui Fu, et al.
Cell Death and Disease (2019) Vol. 10, Iss. 12
Open Access | Times Cited: 91
RNA Polymerase III Subunit Mutations in Genetic Diseases
Elisabeth Lata, Karine Choquet, Francis Sagliocco, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 49
Homozygous EPRS1 missense variant causing hypomyelinating leukodystrophy-15 alters variant-distal mRNA m6A site accessibility
Debjit Khan, Iyappan Ramachandiran, K.I. Vasu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Proteomic Profiling of Kars Knockout Zebrafish Larvae
Jingjing Wang, Yu Xiao, Ying Wang, et al.
(2025)
Closed Access
Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search
Hideki Mutai, Fuyuki Miya, Kiyomitsu Nara, et al.
Human Genetics (2025)
Closed Access
Proteomic profiling of kars knockout zebrafish larvae
Jingjing Wang, Yu Xiao, Ying Wang, et al.
Gene (2025), pp. 149377-149377
Closed Access
Setting the Stage for Treatment of Aminoacyl‐tRNA Synthetase (ARS)1‐Deficiencies: Phenotypic Characterization and a Review of Treatment Effects
Eva M. M. Hoytema van Konijnenburg, Joline Rohof, Gautam Kok, et al.
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Oligodendrocyte differentiation alters tRNA modifications and codon optimality-mediated mRNA decay
Sophie Martin, Kevin Allan, Otis Pinkard, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 17
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish
Sheng‐Jia Lin, Barbara Vona, Patrícia Gonçalves Barbalho, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 10, pp. 1933-1943
Open Access | Times Cited: 23
Phenotypic diversity of brain MRI patterns in mitochondrial aminoacyl-tRNA synthetase mutations
Charles‐Joris Roux, Giulia Barcia, Manuel Schiff, et al.
Molecular Genetics and Metabolism (2021) Vol. 133, Iss. 2, pp. 222-229
Open Access | Times Cited: 19
Expansion of the phenotypic spectrum of KARS1‐related disorders to include arthrogryposis multiplex congenita and summary of experiences with lysine supplementation
Taylor A. Bejma, Willa S. Beidler, Elizabeth VanSickle, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 11
Open Access | Times Cited: 2
KARS Mutations Impair Brain Myelination by Inducing Oligodendrocyte Deficiency: One Potential Mechanism and Improvement by Melatonin
Lijia Yu, Zhilin Chen, Xiao-Long Zhou, et al.
Journal of Pineal Research (2024) Vol. 76, Iss. 5
Open Access | Times Cited: 2
The tRNA‐associated dysregulation in immune responses and immune diseases
Chunsheng Zhu, Bao Sun, Anzheng Nie, et al.
Acta Physiologica (2019) Vol. 228, Iss. 2
Closed Access | Times Cited: 16
Bi‐allelic KARS1 pathogenic variants affecting functions of cytosolic and mitochondrial isoforms are associated with a progressive and multisystem disease
Gerarda Cappuccio, Camilla Ceccatelli Berti, Enrico Baruffini, et al.
Human Mutation (2021) Vol. 42, Iss. 6, pp. 745-761
Open Access | Times Cited: 14
Recessive aminoacyl-tRNA synthetase disorders: lessons learned from in vivo disease models
Elizabeth Kalotay, Matthias Klugmann, Gary D. Housley, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 5
Antibody Deficiency in Patients with Biallelic KARS1 Mutations
Francesco Saettini, Fabiola Guerra, Grazia Fazio, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 8, pp. 2115-2125
Closed Access | Times Cited: 4
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
Motor Neuron Diseases and Central Nervous System Tractopathies: Clinical-Radiologic Correlation and Diagnostic Approach
Amit Desai, Amit Agarwal, Alaa S. Mohamed, et al.
Radiographics (2024) Vol. 45, Iss. 1
Closed Access | Times Cited: 1
Ketogenic Diet for KARS-Related Mitochondrial Dysfunction and Progressive Leukodystrophy
Yuka Murofushi, Itaru Hayakawa, Yuichi Abe, et al.
Neuropediatrics (2021) Vol. 53, Iss. 01, pp. 065-068
Closed Access | Times Cited: 7
A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever
Jean‐Marie Ravel, Natacha Dreumont, Pauline Mosca, et al.
Human Mutation (2021) Vol. 42, Iss. 12, pp. 1576-1583
Open Access | Times Cited: 7
Progressive Early-Onset Leukodystrophy Related to Biallelic Variants in the KARS Gene: The First Case Described in Latin America
Carolina Vargas, Jorge A. Rojas, Iván Aivasovsky, et al.
Genes (2020) Vol. 11, Iss. 12, pp. 1437-1437
Open Access | Times Cited: 6
Leopard-like retinopathy and severe early-onset portal hypertension expand the phenotype of KARS1-related syndrome: a case report
Francesca Peluso, Viviana Palazzo, Giuseppe Indolfi, et al.
BMC Medical Genomics (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 5
Amino-acyl tRNA synthetases associated with leukodystrophy
Marc Engelen, Marjo S. van der Knaap, Nicole I. Wolf
Handbook of clinical neurology (2024), pp. 253-261
Closed Access
Co‐Translational Deposition of N6‐Acetyl‐L‐Lysine in Nascent Proteins Contributes to the Acetylome in Mammalian Cells
Dingyuan Guo, Nan Li, Xiaoyan Zhang, et al.
Advanced Science (2024)
Open Access
Defects in aminoacyl-tRNA synthetase cause partial B and T cell immunodeficiency
Ju A Shim, Yuna Jo, Hyun‐Ju Hwang, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 2
Open Access | Times Cited: 2
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