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Page 1
Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder.
Lerer B, Macciardi F, Segman RH, Adolfsson R, Blackwood D, Blairy S, Del Favero J, Dikeos DG, Kaneva R, Lilli R, Massat I, Milanova V, Muir W, Noethen M, Oruc L, Petrova T, Papadimitriou GN, Rietschel M, Serretti A, Souery D, Van Gestel S, Van Broeckhoven C, Mendlewicz J. Lerer B, et al. Among authors: macciardi f. Mol Psychiatry. 2001 Sep;6(5):579-85. doi: 10.1038/sj.mp.4000883. Mol Psychiatry. 2001. PMID: 11526472
A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorder.
Massat I, Souery D, Lipp O, Blairy S, Papadimitriou G, Dikeos D, Ackenheil M, Fuchshuber S, Hilger C, Kaneva R, Milanova V, Verheyen G, Raeymaekers P, Staner L, Oruc L, Jakovljevic M, Serretti A, Macciardi F, Van Broeckhoven C, Mendlewicz J. Massat I, et al. Among authors: macciardi f. Am J Med Genet. 2000 Apr 3;96(2):136-40. Am J Med Genet. 2000. PMID: 10893484
Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European Multicenter Association Study of affective disorders.
Massat I, Souery D, Del-Favero J, Van Gestel S, Serretti A, Macciardi F, Smeraldi E, Kaneva R, Adolfsson R, Nylander PO, Blackwood D, Muir W, Papadimitriou GN, Dikeos D, Oruc L, Segman RH, Ivezic S, Aschauer H, Ackenheil M, Fuchshuber S, Dam H, Jakovljevic M, Peltonen L, Hilger C, Hentges F, Staner L, Milanova V, Jazin E, Lerer B, Van Broeckhoven C, Mendlewicz J. Massat I, et al. Among authors: macciardi f. Am J Med Genet. 2002 Mar 8;114(2):177-85. Am J Med Genet. 2002. PMID: 11857579
Angiotensin converting enzyme gene insertion/deletion polymorphism: case-control association studies in schizophrenia, major affective disorder, and tardive dyskinesia and a family-based association study in schizophrenia.
Segman RH, Shapira Y, Modai I, Hamdan A, Zislin J, Heresco-Levy U, Kanyas K, Hirschmann S, Karni O, Finkel B, Schlafman M, Lerner A, Shapira B, Macciardi F, Lerer B. Segman RH, et al. Among authors: macciardi f. Am J Med Genet. 2002 Apr 8;114(3):310-4. doi: 10.1002/ajmg.10255. Am J Med Genet. 2002. PMID: 11920854
Pharmacogenetics of tardive dyskinesia: combined analysis of 780 patients supports association with dopamine D3 receptor gene Ser9Gly polymorphism.
Lerer B, Segman RH, Fangerau H, Daly AK, Basile VS, Cavallaro R, Aschauer HN, McCreadie RG, Ohlraun S, Ferrier N, Masellis M, Verga M, Scharfetter J, Rietschel M, Lovlie R, Levy UH, Meltzer HY, Kennedy JL, Steen VM, Macciardi F. Lerer B, et al. Among authors: macciardi f. Neuropsychopharmacology. 2002 Jul;27(1):105-19. doi: 10.1016/S0893-133X(02)00293-2. Neuropsychopharmacology. 2002. PMID: 12062911
Combined analysis of 635 patients confirms an age-related association of the serotonin 2A receptor gene with tardive dyskinesia and specificity for the non-orofacial subtype.
Lerer B, Segman RH, Tan EC, Basile VS, Cavallaro R, Aschauer HN, Strous R, Chong SA, Heresco-Levy U, Verga M, Scharfetter J, Meltzer HY, Kennedy JL, Macciardi F. Lerer B, et al. Among authors: macciardi f. Int J Neuropsychopharmacol. 2005 Sep;8(3):411-25. doi: 10.1017/S1461145705005389. Epub 2005 Apr 28. Int J Neuropsychopharmacol. 2005. PMID: 15857569 Free article.
249 results