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Mendlewicz, J., Souery, D., Mahieu, B., Lipp, O., Lindbald, K., Zander, C., Schalling, M., Nylander, P. O., Engström, C., Adolfsson, R., De Bruyne, A., & Van Broeckhoven, C. (1997). Expanded trinucleotide CAG repeats in families with bipolar affective disorder. Biological psychiatry, 42(12), 1115-1122. doi:10.1016/S0006-3223(97)00395-84.
Souery, D., Lipp, O., Mahieu, B., Mendelbaum, K., De Bruyne, A., De Maertelaer, V., Van Broeckhoven, C., & Mendlewicz, J. (1996). Excess tyrosine hydroxylase restriction fragment length polymorphism homozygosity in unipolar but not bipolar patients: A preliminary report. Biological psychiatry, 40(4), 305-308. doi:10.1016/0006-3223(96)00038-85.
De Bruyne, A., Souery, D., Mendelbaum, K., Mendlewicz, J., & Van Broeckhoven, C. (1996). Linkage analysis of families with bipolar illness and chromosome 18 markers. Biological psychiatry, 39(8), 679-688. doi:10.1016/0006-3223(95)00293-67.
Lindblad, K., Nylander, P. O., De Bruyne, A., Sourey, D., Zander, C., Engström, C., Holmgren, G., Hudson, T., Chotai, J., Mendlewicz, J., Van Broeckhoven, C., Schalling, M., & Adolfsson, R. (1995). Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method. Neurobiology of disease, 2(1), 55-62.8.
Mendelbaum, K., Sevy, S., Souery, D., Papadimitriou, G., De Bruyne, A., Raeymaekers, P., Van Broeckhoven, C., & Mendlewicz, J. (1995). Manic-depressive illness and linkage reanalysis in the Xq27-Xq28 region of chromosome X. Neuropsychobiology, 31(2), 58-63.9.
De Bruyne, A., Mendelbaum, K., Sandkuijl, L., Delvenne, V., Hirsch, D., Staner, L., Mendlewicz, J., & Van Broeckhoven, C. (1994). Nonlinkage of bipolar illness to tyrosine hydroxylase, tyrosinase, and D2 and D4 dopamine receptor genes on chromosome 11. The American journal of psychiatry, 151(1), 102-106. doi:10.1176/ajp.151.1.102 Communications publiées lors de congrès ou colloques nationaux et internationaux (4)
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Van Broeckhoven, C., De Bruyne, A., Raeymaekers, P., Sandkuijl, L., Mendelbaum, K., Delvenne, V., & Mendlewicz, J. (1991). Linkage analysis of families with manic depressive illness with markers from chromosome X and 11. 8th International Congress of Human Genetics (p. 362) American Journal of Human Genetics(49, 4: 6-11 octobre 1991: Washington).2.
Van Broeckhoven, C., De Bruyne, A., Raeymaekers, P., Sandkuijl, L., Raes, G., Mendelbaum, K., Delvenne, V., & Mendlewicz, J. (1991). Exclusion of tight linkage to chromosome X and 11 DNA markers in fifteen families with manic depressive illness. Second world congress on Psychiatric Genetics (p. 48) Psychiatric Genetics(2, 1: 14 - 16 août, 1991: Londres).3.
De Bruyne, A., Raeymaekers, P., Sandkuijl, L., Raes, G., Mendelbaum, K., Delvenne, V., Mendlewicz, J., & Van Broeckhoven, C. (1991). Genetic analysis of manic depressive illness with chromosome X and 11 DNA markers. European society of human genetics: Annual meeting (p. 384) Clinical Genetics(40, 5: 13 - 16 juillet, 1991: Louvain).