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The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia.
Håvik B, Le Hellard S, Rietschel M, Lybæk H, Djurovic S, Mattheisen M, Mühleisen TW, Degenhardt F, Priebe L, Maier W, Breuer R, Schulze TG, Agartz I, Melle I, Hansen T, Bramham CR, Nöthen MM, Stevens B, Werge T, Andreassen OA, Cichon S, Steen VM. Håvik B, et al. Among authors: rietschel m. Biol Psychiatry. 2011 Jul 1;70(1):35-42. doi: 10.1016/j.biopsych.2011.01.030. Epub 2011 Mar 24. Biol Psychiatry. 2011. PMID: 21439553
Association and linkage studies in bipolar affective disorder.
Lanczik M, Nöthen M, Körner J, Rietschel M, Erdmann J, Stratmann M, Cichon S, Lichtermann D, Maier W, Propping P, et al. Lanczik M, et al. Among authors: rietschel m. Clin Neuropharmacol. 1992;15 Suppl 1 Pt A:580A-581A. doi: 10.1097/00002826-199201001-00301. Clin Neuropharmacol. 1992. PMID: 1498960 No abstract available.
Tyrosine hydroxylase gene and manic-depressive illness.
Rietschel M, Nöthen MM, Maier W, Albus M, Franzek E, Propping P. Rietschel M, et al. Lancet. 1995 May 27;345(8961):1368. doi: 10.1016/s0140-6736(95)92566-x. Lancet. 1995. PMID: 7752774 No abstract available.
Dopamine D2 receptor molecular variant and schizophrenia.
Nöthen MM, Wildenauer D, Cichon S, Albus M, Maier W, Minges J, Lichtermann D, Bondy B, Rietschel M, Körner J, et al. Nöthen MM, et al. Among authors: rietschel m. Lancet. 1994 May 21;343(8908):1301-2. doi: 10.1016/s0140-6736(94)92194-6. Lancet. 1994. PMID: 7910313 No abstract available.
Mutation in the beta amyloid precursor protein gene and schizophrenia.
Nöthen MM, Erdmann J, Propping P, Lanczik M, Rietschel M, Körner J, Maier W, Albus M, Ertl MA, Wildenauer DB. Nöthen MM, et al. Among authors: rietschel m. Biol Psychiatry. 1993 Oct 1;34(7):502. doi: 10.1016/0006-3223(93)90244-8. Biol Psychiatry. 1993. PMID: 8268336 No abstract available.
CNTF and psychiatric disorders.
Nöthen MM, Cichon S, Eggermann K, Propping P, Knapp M, Maier W, Rietschel M. Nöthen MM, et al. Among authors: rietschel m. Nat Genet. 1996 Jun;13(2):142-3; author reply 144. doi: 10.1038/ng0696-142b. Nat Genet. 1996. PMID: 8640216 No abstract available.
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia.
Erdmann J, Shimron-Abarbanell D, Rietschel M, Albus M, Maier W, Körner J, Bondy B, Chen K, Shih JC, Knapp M, Propping P, Nöthen MM. Erdmann J, et al. Among authors: rietschel m. Hum Genet. 1996 May;97(5):614-9. doi: 10.1007/BF02281871. Hum Genet. 1996. PMID: 8655141
916 results