cwiese@lbl.gov
(510) 486-4024 (voice)
(510) 486-6816 (fax)

Lawrence Berkeley Nat'l Laboratory, Life Sciences Division
Building 74, Room 3080
1 Cyclotron Road, MS 74R0157
Berkeley, CA 94720

Technical University, Darmstadt, Germany, M.Sc., 1990, Biochemistry
Christian-Albrechts-University, Kiel, Germany, Ph.D., 1995, Cell Biology

Moises HW, Wiese C, Yang L. Molekulargenetik der Schizophrenie. Nervenheilkunde. 1992; 11: 248-250.

Wiese C, Lannfelt L, Kristbjarnarson H, Yang L, Zoega T, Sokoloff P, Ivarsson O, Schwartz JC, Moises HW, Helgason T. No evidence of linkage between schizophrenia and D3 dopamine receptor gene locus in Icelandic pedigrees. Psychiatry Research. 1993; 46, 69-78.

Yang L, Li T, Wiese C, Lannfelt L, Sokoloff P, Schwartz JC, Liu X, Moises HW. No association between schizophrenia and homozygosity at the D3 dopamine receptor gene. American Journal of Medical Genetics. 1993; 48:83-86.

Li T, Yang L, Wiese C, Xu CT, Zeng Z, Giros B, Caron MG, Moises HW, Liu X. No association between alleles or genotypes at the dopamine transporter gene and schizophrenia. Psychiatry Research. 1994; 52:17-23.

Moises HW, Yang L, Kristbjarnarson H, Wiese C, Byerley W, Macciardi F, Arolt V, Blackwood D, Liu X, Sjgren B, Aschauer HN, Hwu HG, Jang K, Livesley WJ, Kennedy JL, Zoega T, Ivarsson O, Bui MT, Yu MH, Havsteen B, Commenges D, Weissenbach J, Schwinger E, Gottesman II, Pakstis AJ, Wetterberg L, Kidd KK, Helgason T. An international two-stage genome-wide search for schizophrenia susceptibility genes. Nature Genetics. 1995; 11:321-324.

Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study. American Journal of Medical Genetics. 1996; 67: 580-594.

Schizophrenia Collaborative Linkage Group (Chromosome 22). A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12. American Journal of Medical Genetics. 1996; 67: 40-45.

Taucher-Scholz G, Wiese C, Kraft G. Interaction of high-linear energy transfer radiation with DNA: Effects on the induction and processing of double-strand breaks. Radiation Research. 1997; 148: 504-506.

Vallada H, Curtis D, Sham P, Kunugi H., et al. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Research. 1998; 32: 115-121.

Grosovsky A, Bethel H, Parks K, Ritter L, Giver C, Gauny S, Wiese C, Kronenberg A. Genomic instability in human lymphoid cells exposed to 1 GeV/amu Fe ions. Physica Medica. 2001; 17 Suppl 1: 238-240.

Gauny S, Wiese C, Kronenberg A. Mechanisms of mutagenesis in human cells exposed to 55 MeV protons. Physica Medica. 2001; 17 Suppl 1: 235-237.

Wiese C, Gauny S, Liu W, Cherbonnel-Lasserre C, Kronenberg A. Different mechanisms of radiation-induced loss of heterozygosity in two human lymphoid cell lines from a single donor. Cancer Research. 2001; 61: 1129-1137.

Wiese C, Galande S. Elimination of reducing agent from the immunoprecipitate solubilization buffer facilitates quantitative detection of p53 antigen. BioTechniques. 2001; 30: 960-963.

Wiese C, Collins DW, Albala JS, Thompson LH, Kronenberg A, Schild D. Interactions involving the Rad51 paralogs Rad51C and XRCC3 in human cells. Nucleic Acids Research. 2002; 30: 1001-1008.

Wiese C, Pierce A, Gauny S, Jasin M, Kronenberg A. Gene conversion is strongly induced in human cells by double strand breaks and is modulated by the expression of BCL-xL. Cancer Research. 2002; 62: 1279-1283.

Fournier C, Wiese C, Taucher-Scholz G. Accumulation of the cell cycle regulators TP53 and CDKN1A (p21) in human fibroblasts after low and high-LET radiation. Radiation Research. 2004; 161: 675-684.

Wiese C, Hinz JM, Tebbs RS, Nham PB, Urbin SS, Collins DW, Thompson LH, Schild D. Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination. Nucleic Acids Research. 2006; 34: 2833-2843.

6/15/06