Articles dans des revues avec comité de lecture (224)
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Verheyen, G. R., Villafuerte, S. M., Del-Favero, J., Souery, D., Mendlewicz, J., Van Broeckhoven, C., & Raeymaekers, P. (1999). Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder. European journal of human genetics, 7(4), 427-434. doi:10.1038/sj.ejhg.5200318200.
Dikeos, D., Papadimitriou, G., Avramopoulos, D., Karadima, G., Daskalopoulou, E., Souery, D., Mendlewicz, J., Vassilopoulos, D., & Stefanis, C. N. (1999). Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder. Psychiatric genetics, 9(4), 189-195.202.
Souery, D., Lipp, O., Mendlewicz, J., Amsterdam, J., De Montigny, C., Lecrubier, Y., Montgomery, S., Racagni, G., & Zohar, J. (1999). Treatment resistant depression: Methodological overview and operational criteria. European neuropsychopharmacology, 9(1-2), 83-91. doi:10.1016/S0924-977X(98)00004-2203.
Blairy, S., Souery, D., Lipp, O., Verheyen, G. R., Raeymaekers, P., Serretti, A., Macciardi, F., Van Broeckhoven, C., & Mendlewicz, J. (1998). Association between social adjustment and candidate genes polymorphism in remitted bipolar and unipolar patients. American journal of medical genetics. Part B, Neuropsychiatric genetics, 81(6), 522.204.
Villafuerte, S. M., Verheyen, G. R., Del-Favero, J., Souery, D., Mendlewicz, J., Raeymaekers, P., & Van Broeckhoven, C. (1998). Manic depressive disorder and chromosome 18. American journal of medical genetics. Part B, Neuropsychiatric genetics, 81(6), 475-476.205.
Verheyen, G. R., Oruč, L., Souery, D., Claes, S., Aalbregtse, M., Cassiman, J.-J., Mendlewicz, J., Ivezić, S. Š., Van Broeckhoven, C., & Raeymaekers, P. (1998). Genetic analysis of the 12Q candidate region for bipolar disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, 81(6), 540-541.206.
Souery, D., Lipp, O., Rivelli, S. S., Cavallini, M. C., Raeymaekers, P., Verheyen, G. R., Macciardi, F., Van Broeckhoven, C., & Mendlewicz, J. (1998). Tyrosine hydroxylase polymorphism and phenotypic heterogeneity in unipolar affective disorder: A european multicenter association study. American journal of medical genetics. Part B, Neuropsychiatric genetics, 81(6), 511.207.
Staner, L., Hilger, C., Hentges, F., Monreal, J., Hoffmann, A., Couturier, M., Le Bon, O., Stefos, G., Souery, D., & Mendlewicz, J. (1998). Association between novelty-seeking and the dopamine D3 receptor gene in bipolar patients: A preliminary report. American journal of medical genetics, 81(2), 192-194. doi:10.1002/(SICI)1096-8628(19980328)81:2<192::AID-AJMG12>3.0.CO;2-C209.
Souery, D., Mahieu, B. A., Delcoigne, B., De Maertelaer, V., Pull, C., Staner, L., Mendlewicz, J., et al. (1998). European Collaborative Project on Affective Disorders: Interactions between genetic and psychosocial vulnerability factors. Psychiatric genetics, 8(4), 197-205.