Cited by

• Increased risk of hearing loss associated with MT-RNR1 gene mutations: a real-world investigation among Han Taiwanese Population.

  Chen HK, Hsieh YW, Hsu HY, Liu TY, Zhang YT, Lin CD, Tsai FJ. Chen HK, et al. BMC Med Genomics. 2024 Jun 5;17(1):155. doi: 10.1186/s12920-024-01921-8. BMC Med Genomics. 2024. PMID: 38840095 Free PMC article.
• The Role of Mitochondrial DNA Variation in Drug Response: A Systematic Review.

  Jones SW, Ball AL, Chadwick AE, Alfirevic A. Jones SW, et al. Front Genet. 2021 Aug 17;12:698825. doi: 10.3389/fgene.2021.698825. eCollection 2021. Front Genet. 2021. PMID: 34484295 Free PMC article.
• A Novel Approach for the Identification of Pharmacogenetic Variants in MT-RNR1 through Next-Generation Sequencing Off-Target Data.

  Lanillos J, Santos M, Carcajona M, Roldan-Romero JM, Martinez AM, Calsina B, Monteagudo M, Leandro-García LJ, Montero-Conde C, Cascón A, Maietta P, Alvarez S, Robledo M, Rodriguez-Antona C. Lanillos J, et al. J Clin Med. 2020 Jul 2;9(7):2082. doi: 10.3390/jcm9072082. J Clin Med. 2020. PMID: 32630724 Free PMC article.
• CZ CELLxGENE Discover: a single-cell data platform for scalable exploration, analysis and modeling of aggregated data.

  CZI Cell Science Program; Abdulla S, Aevermann B, Assis P, Badajoz S, Bell SM, Bezzi E, Cakir B, Chaffer J, Chambers S, Cherry JM, Chi T, Chien J, Dorman L, Garcia-Nieto P, Gloria N, Hastie M, Hegeman D, Hilton J, Huang T, Infeld A, Istrate AM, Jelic I, Katsuya K, Kim YJ, Liang K, Lin M, Lombardo M, Marshall B, Martin B, McDade F, Megill C, Patel N, Predeus A, Raymor B, Robatmili B, Rogers D, Rutherford E, Sadgat D, Shin A, Small C, Smith T, Sridharan P, Tarashansky A, Tavares N, Thomas H, Tolopko A, Urisko M, Yan J, Yeretssian G, Zamanian J, Mani A, Cool J, Carr A. CZI Cell Science Program, et al. Nucleic Acids Res. 2025 Jan 6;53(D1):D886-D900. doi: 10.1093/nar/gkae1142. Nucleic Acids Res. 2025. PMID: 39607691 Free PMC article.
• The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.

  Igumnova V, Veidemane L, Vīksna A, Capligina V, Zole E, Ranka R. Igumnova V, et al. J Hum Genet. 2019 Mar;64(3):199-206. doi: 10.1038/s10038-018-0544-6. Epub 2018 Dec 6. J Hum Genet. 2019. PMID: 30523288