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Selected Publications

  1. Harrison L, Broome C, Hightower A, Hoppe C, et al:  A daycare based study of efficacy of Haemophilus type b polysaccharine vaccine.  JAMA 1988; 120(10):1413-1418.
  2. Harrison L, Broome C, Hoppe C, et al: Haemophilus influenza type b polysaccharide vaccine: an efficacy study.  Pediatrics 1989; 84(2):155-61.
  3. Hoppe C, Styles L, Vichinsky E.  The Natural History of Sickle Cell Disease.  Current Opinion in Pediatrics 1998; 10:49-52.
  4. Hoppe C, Vichinsky E, Lewis B, Foote D, Styles L.  Hydroxyurea and sodium phenylbutyrate therapy in thalassemia intermedia.  American Journal of Hematology 1999; 62:221-227
  5. Hoppe C, Vichinsky E, Quirolo K, VanWarmerdan J, Allen K, Styles L.  The safety and efficacy of hydroxyurea in 2 to 5 year old children with sickle cell disease.  Journal of Pediatric Hematology/Oncology 2000; 22(4):330-334.
  6. Styles L, Hoppe C, Klitz W, Vichinsky E, Lubin B, Trachtenberg E.  Evidence for HLA-related susceptibility for stroke in children with sickle cell disease.  Blood 2000; 95(11):3562-3567.
  7. Hoppe C, Cheng S, Grow M, Silbergleit A, et al.  A novel multilocus genotyping assay to identify genetic predictors of stroke in sickle cell anemia.  British Journal of Haematology 2001; 114(3):718-720.
  8. Hoppe C, Walters M.  Bone marrow transplantation in sickle cell anemia.  Current Opinion in Oncology 2001; 13(2):85-89.
  9. Hoppe C, Klitz W, Noble J, Vigil L, Vichinsky E, Styles L.  Distinct HLA associations by stroke subtype in children with sickle cell anemia.  Blood 2003; 101(7):2865-2869.
  10. Hoppe C, Matsunaga A.  “Pediatric Thrombosis” in Pediatric Clinics of North America 2002, W.B. Saunders Co.; 49: 1257-1283.
  11. Hoppe C, Klitz W, Cheng S, Apple R, Steiner L, Robles R, et al.  Gene interactions and stroke risk in children with sickle cell anemia.  Blood 2004; 103(6): 2391-2396.
  12. Hoppe C.  Defining stroke risk in children with sickle cell anemia.  British Journal of Haematology 2005; 128(6):751-66.
  13. Hoppe C.  Computers or clinicians for complex disease risk assessment?  European Journal of Human Genetics, accepted for publication.


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