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Last Name

Hyunjoo Lee, MD, PhD

TitleAssistant Professor
InstitutionBoston University School of Medicine
DepartmentOphthalmology
DivisionGeneral Ophthalmology
Address850 Harrison Ave
Boston MA 02118
Phone(617) 414-4020
 Self-Described Keywords
  • cornea
  • cataract
  • refractive surgery
  • molecular biology
 Publications
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Lee HJ, Munir WM. Eventual Endothelial Failure After Initial Corneal Clearing After a Detached Endothelial Graft in Fuchs Dystrophy. Cornea. 2017 Feb; 36(2):241-243. PMID: 28060074.
    View in: PubMed
  2. Bryant T, Lee HJ. To the Editor. Cornea. 2017 Jan 04. PMID: 28098660.
    View in: PubMed
  3. Lee HJ, Colby KA. A review of the clinical and genetic aspects of aniridia. Semin Ophthalmol. 2013 Sep-Nov; 28(5-6):306-12. PMID: 24138039.
    View in: PubMed
  4. Hamill CE, Bozorg S, Peggy Chang HY, Lee H, Sayegh RR, Shukla AN, Chodosh J. Corneal alkali burns: a review of the literature and proposed protocol for evaluation and treatment. Int Ophthalmol Clin. 2013; 53(4):185-94. PMID: 24088945.
    View in: PubMed
  5. Lee HJ, Pazin DE, Kahlon RS, Correa SM, Albrecht KH. Novel markers of early ovarian pre-granulosa cells are expressed in an Sry-like pattern. Dev Dyn. 2009 Apr; 238(4):812-25. PMID: 19301398.
    View in: PubMed
  6. Thiagalingam S, Cheng KH, Lee HJ, Mineva N, Thiagalingam A, Ponte JF. Histone deacetylases: unique players in shaping the epigenetic histone code. Ann N Y Acad Sci. 2003 Mar; 983:84-100. PMID: 12724214.
    View in: PubMed
  7. Thiagalingam S, Foy RL, Cheng KH, Lee HJ, Thiagalingam A, Ponte JF. Loss of heterozygosity as a predictor to map tumor suppressor genes in cancer: molecular basis of its occurrence. Curr Opin Oncol. 2002 Jan; 14(1):65-72. PMID: 11790983.
    View in: PubMed
  8. Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet. 2000 Apr; 24(4):349-54. PMID: 10742096.
    View in: PubMed
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