Hyunjoo Jean Lee, MD, PhD

Assistant Professor, Ophthalmology

Hyunjoo Lee
(617) 414-4020
85 E. Concord Street

Education

  • Boston University School of Medicine, MD
  • Boston University School of Medicine, PhD
  • University of California, Berkeley, BA

Publications

  • Published on 3/1/2017

    Bryant T, Lee HJ. To the Editor. Cornea. 2017 03; 36(3):e6-e7. PMID: 28098660.

    Read at: PubMed
  • Published on 3/1/2017

    Lee HJ, Munir WM. Reply. Cornea. 2017 Mar; 36(3):e10-e11. PMID: 28141744.

    Read at: PubMed
  • Published on 2/1/2017

    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.

    Read at: PubMed
  • Published on 9/1/2013

    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.

    Read at: PubMed
  • Published on 1/1/2013

    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.

    Read at: PubMed
  • Published on 4/1/2009

    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.

    Read at: PubMed
  • Published on 3/1/2003

    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.

    Read at: PubMed
  • Published on 1/1/2002

    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.

    Read at: PubMed
  • Published on 4/1/2000

    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.

    Read at: PubMed

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