Michael Chao Chen

Title(s)Hs Clinical Instructor, Urology
SchoolMedicine
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC. Invest Ophthalmol Vis Sci. 2010 Aug; 51(8):4006-12. Aldave AJ, Rosenwasser GO, Yellore VS, Papp JC, Sobel EM, Pham MN, Chen MC, Dandekar S, Sripracha R, Rayner SA, Sassani JW, Gorin MB. PMID: 20357198; PMCID: PMC2910638.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    2. Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval. Cornea. 2009 Aug; 28(7):801-7. Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel E, Papp J. PMID: 19574904; PMCID: PMC2714875.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    3. Classic lattice corneal dystrophy associated with monoclonal gammopathy after exclusion of a TGFBI mutation. Cornea. 2009 Jan; 28(1):97-8. Kamal KM, Rayner SA, Chen MC, Aldave AJ. PMID: 19092416; PMCID: PMC2784604.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    4. Corneal biomechanical measurements before and after laser in situ keratomileusis. J Cataract Refract Surg. 2008 Nov; 34(11):1886-91. Chen MC, Lee N, Bourla N, Hamilton DR. PMID: 19006734.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    5. Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy. Mol Vis. 2007 Sep 24; 13:1777-82. Yellore VS, Khan MA, Bourla N, Rayner SA, Chen MC, Sonmez B, Momi RS, Sampat KM, Gorin MB, Aldave AJ. PMID: 17960116.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    6. An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation. Ophthalmic Genet. 2007 Sep; 28(3):169-74. Yellore VS, Sonmez B, Chen MC, Rayner SA, Thonar EJ, Aldave AJ. PMID: 17896316.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
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