1. Averdunk, Luisa, Sticht, Heinrich, Surowy, Harald, Alkuraya, Fowzan S, Wieczorek, Dagmar. 2021. The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. In Journal of molecular medicine (Berlin, Germany), 99, 1755-1768. doi:10.1007/s00109-021-02124-9. https://pubmed.ncbi.nlm.nih.gov/34536092/
2. Llauradó, Arnau, Gratacòs-Viñola, Margarida, Rovira-Moreno, Eulàlia, Garcia-Arumi, Elena, Juntas-Morales, Raul. 2023. Distal hereditary motor neuropathy due to a novel YARS1 gene pathogenic variant. In Muscle & nerve, 67, E22-E24. doi:10.1002/mus.27788. https://pubmed.ncbi.nlm.nih.gov/36631979/
3. Morant, Laura, Erfurth, Maria-Luise, Jordanova, Albena. 2021. Drosophila Models for Charcot-Marie-Tooth Neuropathy Related to Aminoacyl-tRNA Synthetases. In Genes, 12, . doi:10.3390/genes12101519. https://pubmed.ncbi.nlm.nih.gov/34680913/
4. Forrest, Megan E, Meyer, Alayne P, Laureano Figueroa, Stephanie M, Antonellis, Anthony. 2022. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. In Cold Spring Harbor molecular case studies, 8, . doi:10.1101/mcs.a006246. https://pubmed.ncbi.nlm.nih.gov/36307205/
5. Morant, Laura, Petrovic-Erfurth, Maria-Luise, Jordanova, Albena. 2023. An Adapted GeneSwitch Toolkit for Comparable Cellular and Animal Models: A Proof of Concept in Modeling Charcot-Marie-Tooth Neuropathy. In International journal of molecular sciences, 24, . doi:10.3390/ijms242216138. https://pubmed.ncbi.nlm.nih.gov/38003325/