PUBLICATIONS (1996- )
Psychiatric Genetics: Affective and Other Disorders
Kotler, M., Cohen, H., Segman, R., Gritsenko, I., Nemanov, L., Lerer, B., Kramer, I., Zer-Zion, M., Kletz, I., Ebstein, R.P.: Excess dopamine D4 (DRD4) exon III seven repeat allele in opioid dependent subjects. Molecular Psychiatry 2: 251-254, 1997.
Ebstein RP, Segman R, Benjamin J, Osher Y, Nemanov L, Belmaker RH: 5-HT2c receptor polymorphism associated with the human personality trait of reward dependence: Interaction with dopamine D4 receptor and dopamine D3 receptor polymorphisms. American Journal of Medical Genetics 74: 65-72. 1997.
Knowles, J.A., Rao, P.A., Cox-Matise, T., Loth, J.E., de Jesus, G.M., Levine, L., Das, K., Penchaszadeh, G.K., Alexander, J.R., Lerer, B., Endicott, J., Ott, J., Gilliam, T.C., Baron, M.: No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. American Journal of Human Genetics 62: 916-924, 1998.
Aita, V.M., Liu, J., Knowles, J.A., Terwilliger, J.D., Baltazar, R., Grunn, A., Loth, J.E., Kanyas, K., Lerer, B., Endicott, J., Wang, Z., Penchaszadeh, G., Gilliam, T.C., Baron, M.: A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. American Journal of Human Genetics 64: 210-217, 1999.
Souery, D., Lipp, O., Mahieu, B., Serretti, A., Cavallini, C., Ackenheil, M., Adolfsson, R., Aschauer, H., Blackwood, D., Dam, H., de Bruyn, A., Demartelaer, V., Dikeos, D., Fuchshuber, S., Heiden, M., Jablensky, A., Kessing, L., Lerer, B., Macedo, A., Mellerup, T., Milanova, V., Muir, W., Nylander, P.O., Oruc, L., Papadimitriou, G.N., Pekkarinen, P., Peltonen, L., Pinto de Azevedo, M.H., Pull, C., Shapira, B., Smeraldi, E., Staner, L., Stefanis, C., Verga, M., Verheyen, G., Macciardi, F., Van Broeckhaven, C., Mendlewicz, J.: European collaborative project on affective disorders: Interactions between genetic and psychosocial vulnerability factors. Psychiatric Genetics 8:197-205, 1998
Souery, D., Lipp, O., Mahieu, B., Serretti, A., Rivelli, S.K., Cavallini, C., Ackenheil, M., Adolfsson, R., Aschauer, H., Blackwood, D., Dam, Dikeos, D., Fuchshuber, S., Heiden, M., Jablensky, A., Jakoveljevic, M., Kessing, L., Lerer, B., Mellerup, T., Milanova, V., Muir, W., Nylander, P.O., Oruc, L., Papadimitriou, G.N., Pekkarinen, P., Peltonen, L., Pull, C., Raeymaekers, P., Shapira, B., Smeraldi, E., Staner, L., Stefanis, C., Verga, M., Verheyen, G., Macciardi, F., Van Broeckhoven, C., Mendlewicz, J.: Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in bipolar affective disorder: A multicenter association study. American Journal of Medical Genetics (Neuropsychiatric Genetics) 88:527-532, 1999.
Segman, R.H., Lerer, B.: Genetic factors in the etiology of bipolar disorder. In: Soares, J., Gershon, S. (Eds) Basic Mechanisms and Therapeutic Applications of Bipolar Disorder. Marcel Dekker, New York, 2000
Frisch, A., Michaelovsky, E., Rokach, R., Amir, I., Hermesh, H., Laor, N., Fuchs, C., Zohar, J., Lerer, B., Buniak, S.F., Landa, S., Poyurovsky, M., Shapira, B., Weizman, R.: Association between obsessive compulsive disorder and polymorphisms of genes encoding components of the serotonergic and dopaminergic pathways. European Neuropsychopharmacology. 10:205-9, 2000
|