| 1982 |
BS-Medical Technology
National Taiwan University, Taipei, Taiwan |
| 1987 |
Microbiology and Immunology
University of Oklahoma, Health Sciences Center
Oklahoma City OK
Thesis Title: A molecuar epidemiologic analysis of the type A streptococcal exotoxin
gene (speA) among clinical Streptococcus pyogenes strains.
Advisor: Joseph J Ferretti PhD |
| 1990 |
PhD-Microbiology and Immunology
University of Oklahoma, Health Sciences Center
Oklahoma City OK
Dissertation Title: Molecular characterization of new speA gene-containing
bacteriophages and epidemiologic analysis of erythrogenic toxin genes among clinical group
A streptococcal strains.
Advisor: Joseph J Ferretti PhD |
 |
| 1978-1982 |
Undergraduate Student, Medical Technology
National Taiwan University, Taipei, Taiwan |
| 1982-1984 |
Second Lieutenat, Army, Taiwan |
| 1984-1990 |
Graduate Student, Microbiology and Immunology
University of Oklahoma, Health Sciences Center
Oklahoma City OK |
| 1990-1991 |
Postdoctoral Fellow, Microbiology and
Immunology
University of Oklahoma, Health Sciences Center
Oklahoma City OK |
| 1992-1995 |
Postdoctoral Fellow, University of
Washington Neurology Seattle WA |
| 1995-1997 |
Postdoctoral Fellow
University of Washington School of Medicine
Department of Medicine
Division of Gerontology and Geriatric Medicine |
Kukull WA, Schellenberg GD, Bowen JD, McCormick WC, Yu CE, Teri L, Thompson JD, O'Meara
EA, Larson EB. Apolipoportein E in Alzheimer's disease risk and case
detection: A case-control study. J Clin Epidemiol 49:1143-1148, 1996.
Oshima J, Yu CE, Puissan C, Klein G, Jabkowski J, Balci S, Miki T, Nakura J, Ogihara T,
Ells J, Smith MAC, Melagno MI, Fraccaro M, Scappatici S, Matthews J, Ouais S, Jarzebowicz
A, Schellenberg GD, Martin GM. Homozygous and compound heterzygous mutations at the
Werner locus. Hum Mol Genet 5:1909-1913, 1996.
Yu CE, Oshima J, Wijsman EM, Piussan C, Matthews S, Martin GM, Schellenberg GD.
Mutations in in the consensus helicase domains of the Werner's syndrome gene. Am J
Hum Genet 60:3309-341, 1997.
Schellenberg GD, Miki T, Yu CE, Nakura J. Werner syndrome. Chapter 164.
In: Metabolic & Molecular Bases of Inherited Disease DB-ROM
(Scriver CR, et al, ed. McGraw Hill, New York NY, 1997.
Sharma V, Poorkaj P, Hisama F, Bonnycastle L, Yu CE, Massa H, Trask B, Clancy KP,
Patterson D, Weissman SM, Schellenberg GD. An expression map from human chromosome
14q24.3. Genomics 47:314-318, 1997.
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