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Journal Abstract Search

192 related items for PubMed ID: 37191617

  • 1. Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia.
    Yang E, Yu J, Liu X, Chu H, Li L.
    Invest Ophthalmol Vis Sci; 2023 May 01; 64(5):10. PubMed ID: 37191617
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  • 7. X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia.
    Xiao X, Li S, Jia X, Guo X, Zhang Q.
    Mol Vis; 2016 May 01; 22():1257-1266. PubMed ID: 27829781
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  • 10. Trio-based whole-exome sequencing reveals mutations in early-onset high myopia.
    Ye L, Guo YM, Cai YX, Wei J, Huang J, Bi J, Chen D, Li FF, Huang XF.
    BMJ Open Ophthalmol; 2024 May 24; 9(1):. PubMed ID: 38789272
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  • 11. Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance.
    Wang Y, Xiao X, Li X, Yi Z, Jiang Y, Zhang F, Zhou L, Li S, Jia X, Sun W, Wang P, Zhang Q.
    Br J Ophthalmol; 2023 Oct 24; 107(10):1545-1553. PubMed ID: 36180177
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  • 12. Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.
    Jin ZB, Wu J, Huang XF, Feng CY, Cai XB, Mao JY, Xiang L, Wu KC, Xiao X, Kloss BA, Li Z, Liu Z, Huang S, Shen M, Cheng FF, Cheng XW, Zheng ZL, Chen X, Zhuang W, Zhang Q, Young TL, Xie T, Lu F, Qu J.
    Proc Natl Acad Sci U S A; 2017 Apr 18; 114(16):4219-4224. PubMed ID: 28373534
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  • 14. Mutation screening of 17 candidate genes in a cohort of 67 probands with early-onset high myopia.
    Liu F, Wang J, Xing Y, Li T.
    Ophthalmic Physiol Opt; 2020 May 18; 40(3):271-280. PubMed ID: 32215939
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  • 16. De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia.
    Huang X, Rui X, Zhang S, Qi X, Rong W, Sheng X.
    BMC Med Genomics; 2023 Apr 21; 16(1):84. PubMed ID: 37085840
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  • 18. Novel TRPM1 mutations in two Chinese families with early-onset high myopia, with or without complete congenital stationary night blindness.
    Zhou L, Li T, Xing YQ, Li Y, Wu QS, Zhang MJ.
    Int J Ophthalmol; 2016 Apr 21; 9(10):1396-1402. PubMed ID: 27803854
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  • 19. Variants in HNRNPH1 are associated with high myopia in humans and ocular coloboma in zebrafish.
    Ouyang J, Li S, Sun W, Xiao X, Wang Y, Jiang Y, Zhang Q.
    Clin Genet; 2022 Nov 21; 102(5):424-433. PubMed ID: 35989590
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  • 20. Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes.
    Sun W, Huang L, Xu Y, Xiao X, Li S, Jia X, Gao B, Wang P, Guo X, Zhang Q.
    Invest Ophthalmol Vis Sci; 2015 Dec 21; 56(13):8365-72. PubMed ID: 26747767
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