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916 results

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Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples.
Treutlein J, Kissling C, Frank J, Wiemann S, Dong L, Depner M, Saam C, Lascorz J, Soyka M, Preuss UW, Rujescu D, Skowronek MH, Rietschel M, Spanagel R, Heinz A, Laucht M, Mann K, Schumann G. Treutlein J, et al. Among authors: rietschel m. Mol Psychiatry. 2006 Jun;11(6):594-602. doi: 10.1038/sj.mp.4001813. Mol Psychiatry. 2006. PMID: 16550213
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios.
Wittekindt O, Schwab SG, Burgert E, Knapp M, Albus M, Lerer B, Hallmayer J, Rietschel M, Segman R, Borrmann M, Lichtermann D, Crocq MA, Maier W, Morris-Rosendahl DJ, Wildenauer DB. Wittekindt O, et al. Among authors: rietschel m. Mol Psychiatry. 1999 May;4(3):267-70. doi: 10.1038/sj.mp.4000495. Mol Psychiatry. 1999. PMID: 10395217
Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.
Schwab SG, Knapp M, Mondabon S, Hallmayer J, Borrmann-Hassenbach M, Albus M, Lerer B, Rietschel M, Trixler M, Maier W, Wildenauer DB. Schwab SG, et al. Among authors: rietschel m. Am J Hum Genet. 2003 Jan;72(1):185-90. doi: 10.1086/345463. Epub 2002 Dec 9. Am J Hum Genet. 2003. PMID: 12474144 Free PMC article.
Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study.
Massat I, Souery D, Del-Favero J, Nothen M, Blackwood D, Muir W, Kaneva R, Serretti A, Lorenzi C, Rietschel M, Milanova V, Papadimitriou GN, Dikeos D, Van Broekhoven C, Mendlewicz J. Massat I, et al. Among authors: rietschel m. Mol Psychiatry. 2005 Jun;10(6):598-605. doi: 10.1038/sj.mp.4001615. Mol Psychiatry. 2005. PMID: 15583702 Clinical Trial.
Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.
Schulze TG, Ohlraun S, Czerski PM, Schumacher J, Kassem L, Deschner M, Gross M, Tullius M, Heidmann V, Kovalenko S, Jamra RA, Becker T, Leszczynska-Rodziewicz A, Hauser J, Illig T, Klopp N, Wellek S, Cichon S, Henn FA, McMahon FJ, Maier W, Propping P, Nöthen MM, Rietschel M. Schulze TG, et al. Among authors: rietschel m. Am J Psychiatry. 2005 Nov;162(11):2101-8. doi: 10.1176/appi.ajp.162.11.2101. Am J Psychiatry. 2005. PMID: 16263850
No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder.
Brüggemann D, Sobanski E, Alm B, Schubert T, Schmalzried H, Philipsen A, Breen G, Becker T, Georgi A, Skowronek MH, Schulze TG, Treutlein J, Rietschel M. Brüggemann D, et al. Among authors: rietschel m. Psychiatr Genet. 2007 Apr;17(2):121. doi: 10.1097/YPG.0b013e32801231d4. Psychiatr Genet. 2007. PMID: 17413453 No abstract available.
916 results