Cited In for PMID: 21880868

Year	Number of Results
2011	3
2012	5
2013	9
2014	10
2015	7
2016	8
2017	8
2018	3
2019	4
2020	5
2021	7
2022	2
2023	3
2024	0

1

Mitochondrial DNA polymerase gamma mutations: an ever expanding molecular and clinical spectrum.

Tang S, Wang J, Lee NC, Milone M, Halberg MC, Schmitt ES, Craigen WJ, Zhang W, Wong LJ. Tang S, et al. J Med Genet. 2011 Oct;48(10):669-81. doi: 10.1136/jmedgenet-2011-100222. Epub 2011 Aug 31. J Med Genet. 2011. PMID: 21880868

2

C17orf80 binds the mitochondrial genome to promote its replication.

Wu H, Zhang W, Xu F, Peng K, Liu X, Ding W, Ma Q, Cheng H, Wang X. Wu H, et al. J Cell Biol. 2023 Oct 2;222(10):e202302037. doi: 10.1083/jcb.202302037. Epub 2023 Sep 7. J Cell Biol. 2023. PMID: 37676315 Free PMC article.

3

DNA polymerase gamma variants and hepatotoxicity during maintenance therapy of childhood acute lymphoblastic leukemia: is there a causal relationship?

Harju T, Hurme-Niiranen A, Suo-Palosaari M, Nygaard Nielsen S, Hinttala R, Schmiegelow K, Uusimaa J, Harila A, Niinimäki R. Harju T, et al. Pharmacogenomics J. 2023 Sep;23(5):105-111. doi: 10.1038/s41397-023-00303-0. Epub 2023 May 3. Pharmacogenomics J. 2023. PMID: 37138020 Free PMC article.

4

AIMedGraph: a comprehensive multi-relational knowledge graph for precision medicine.

Quan X, Cai W, Xi C, Wang C, Yan L. Quan X, et al. Database (Oxford). 2023 Feb 28;2023:baad006. doi: 10.1093/database/baad006. Database (Oxford). 2023. PMID: 36856726 Free PMC article.

5

Host genetic susceptibility underlying SARS-CoV-2-associated Multisystem Inflammatory Syndrome in Brazilian Children.

Santos-Rebouças CB, Piergiorge RM, Dos Santos Ferreira C, Seixas Zeitel R, Gerber AL, Rodrigues MCF, Guimarães APC, Silva RM, Fonseca AR, Souza RC, de Souza ATAM, Rossi ÁD, Porto LCMS, Cardoso CC, de Vasconcelos ATR. Santos-Rebouças CB, et al. Mol Med. 2022 Dec 12;28(1):153. doi: 10.1186/s10020-022-00583-5. Mol Med. 2022. PMID: 36510129 Free PMC article.

6

Molecular Genetics Overview of Primary Mitochondrial Myopathies.

Arena IG, Pugliese A, Volta S, Toscano A, Musumeci O. Arena IG, et al. J Clin Med. 2022 Jan 26;11(3):632. doi: 10.3390/jcm11030632. J Clin Med. 2022. PMID: 35160083 Free PMC article. Review.

7

Disease Modeling of Mitochondrial Cardiomyopathy Using Patient-Specific Induced Pluripotent Stem Cells.

Tokuyama T, Ahmed RE, Chanthra N, Anzai T, Uosaki H. Tokuyama T, et al. Biology (Basel). 2021 Sep 29;10(10):981. doi: 10.3390/biology10100981. Biology (Basel). 2021. PMID: 34681080 Free PMC article. Review.

8

Polymerase Gamma Mitochondrial DNA Depletion Syndrome Initially Presenting as Disproportionate Respiratory Distress in a Moderately Premature Neonate: A Case Report.

Franklin AD, Chaudhari BP, Koboldt DC, Machut KZ. Franklin AD, et al. Front Genet. 2021 Jun 14;12:664278. doi: 10.3389/fgene.2021.664278. eCollection 2021. Front Genet. 2021. PMID: 34194468 Free PMC article.

9

Novel biallelic mutations in POLG gene: large deletion and missense variant associated with PEO.

Lin Y, Du J, Wang W, Ren H, Zhao D, Liu F, Lin P, Ji K, Zhao Y, Yan C. Lin Y, et al. Neurol Sci. 2021 Oct;42(10):4271-4280. doi: 10.1007/s10072-021-05380-2. Epub 2021 Jun 29. Neurol Sci. 2021. PMID: 34189666

10

PPFIA4 mutation: A second hit in POLG related disease?

Sourbron J, Jansen K, Aerts N, Lagae L. Sourbron J, et al. Epilepsy Behav Rep. 2021 May 7;16:100455. doi: 10.1016/j.ebr.2021.100455. eCollection 2021. Epilepsy Behav Rep. 2021. PMID: 34095804 Free PMC article.

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