PubMed (OMIM) for id: 10352

Year	Number of Results
1998	1
2005	1
2017	3
2018	1
2019	2
2020	1
2021	1
2022	2
2024	0

1

A relatively common hypomorphic variant in WARS2 causes monogenic disease.

Ilinca A, Kafantari E, Puschmann A. Ilinca A, et al. Parkinsonism Relat Disord. 2022 Jan;94:129-131. doi: 10.1016/j.parkreldis.2022.01.012. Epub 2022 Jan 19. Parkinsonism Relat Disord. 2022. PMID: 35074316 No abstract available.

2

WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia.

Skorvanek M, Rektorova I, Mandemakers W, Wagner M, Steinfeld R, Orec L, Han V, Pavelekova P, Lackova A, Kulcsarova K, Ostrozovicova M, Gdovinova Z, Plecko B, Brunet T, Berutti R, Kuipers DJS, Boumeester V, Havrankova P, Tijssen MAJ, Kaiyrzhanov R, Rizig M, Houlden H, Winkelmann J, Bonifati V, Zech M, Jech R. Skorvanek M, et al. Parkinsonism Relat Disord. 2022 Jan;94:54-61. doi: 10.1016/j.parkreldis.2021.11.030. Epub 2021 Dec 2. Parkinsonism Relat Disord. 2022. PMID: 34890876

3

Mutation of the WARS2 Gene as the Cause of a Severe Hyperkinetic Movement Disorder.

Hübers A, Huppertz HJ, Wortmann SB, Kassubek J. Hübers A, et al. Mov Disord Clin Pract. 2019 Nov 7;7(1):88-90. doi: 10.1002/mdc3.12855. eCollection 2020 Jan. Mov Disord Clin Pract. 2019. PMID: 31970218 Free PMC article. No abstract available.

4

Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy.

Maffezzini C, Laine I, Dallabona C, Clemente P, Calvo-Garrido J, Wibom R, Naess K, Barbaro M, Falk A, Donnini C, Freyer C, Wredenberg A, Wedell A. Maffezzini C, et al. Mol Genet Genomic Med. 2019 Jun;7(6):e654. doi: 10.1002/mgg3.654. Epub 2019 Mar 28. Mol Genet Genomic Med. 2019. PMID: 30920170 Free PMC article.

5

Biallelic mutations in mitochondrial tryptophanyl-tRNA synthetase cause Levodopa-responsive infantile-onset Parkinsonism.

Burke EA, Frucht SJ, Thompson K, Wolfe LA, Yokoyama T, Bertoni M, Huang Y, Sincan M, Adams DR, Taylor RW, Gahl WA, Toro C, Malicdan MCV. Burke EA, et al. Clin Genet. 2018 Mar;93(3):712-718. doi: 10.1111/cge.13172. Epub 2018 Feb 5. Clin Genet. 2018. PMID: 29120065 Free PMC article.

6

Biallelic variants in WARS2 encoding mitochondrial tryptophanyl-tRNA synthase in six individuals with mitochondrial encephalopathy.

Wortmann SB, Timal S, Venselaar H, Wintjes LT, Kopajtich R, Feichtinger RG, Onnekink C, Mühlmeister M, Brandt U, Smeitink JA, Veltman JA, Sperl W, Lefeber D, Pruijn G, Stojanovic V, Freisinger P, V Spronsen F, Derks TG, Veenstra-Knol HE, Mayr JA, Rötig A, Tarnopolsky M, Prokisch H, Rodenburg RJ. Wortmann SB, et al. Hum Mutat. 2017 Dec;38(12):1786-1795. doi: 10.1002/humu.23340. Epub 2017 Oct 6. Hum Mutat. 2017. PMID: 28905505

7

Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy.

Theisen BE, Rumyantseva A, Cohen JS, Alcaraz WA, Shinde DN, Tang S, Srivastava S, Pevsner J, Trifunovic A, Fatemi A. Theisen BE, et al. Am J Med Genet A. 2017 Sep;173(9):2505-2510. doi: 10.1002/ajmg.a.38339. Epub 2017 Jun 26. Am J Med Genet A. 2017. PMID: 28650581

8

Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability.

Musante L, Püttmann L, Kahrizi K, Garshasbi M, Hu H, Stehr H, Lipkowitz B, Otto S, Jensen LR, Tzschach A, Jamali P, Wienker T, Najmabadi H, Ropers HH, Kuss AW. Musante L, et al. Hum Mutat. 2017 Jun;38(6):621-636. doi: 10.1002/humu.23205. Epub 2017 Mar 23. Hum Mutat. 2017. PMID: 28236339

9

Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS.

Bonnefond L, Fender A, Rudinger-Thirion J, Giegé R, Florentz C, Sissler M. Bonnefond L, et al. Biochemistry. 2005 Mar 29;44(12):4805-16. doi: 10.1021/bi047527z. Biochemistry. 2005. PMID: 15779907

10

Assignment of the human mitochondrial tryptophanyl-tRNA synthetase (WARS2) to 1p13.3-->p13.1 by radiation hybrid mapping.

Martinez-Dominguez MT, Justesen J, Kruse TA, Hansen LL. Martinez-Dominguez MT, et al. Cytogenet Cell Genet. 1998;83(3-4):249-50. doi: 10.1159/000015196. Cytogenet Cell Genet. 1998. PMID: 10072595 No abstract available.

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