Rietschel M - Search Results

1

DAOA/G72 predicts the progression of prodromal syndromes to first episode psychosis.

Mössner R, Schuhmacher A, Wagner M, Quednow BB, Frommann I, Kühn KU, Schwab SG, Rietschel M, Falkai P, Wölwer W, Ruhrmann S, Bechdolf A, Gaebel W, Klosterkötter J, Maier W. Mössner R, et al. Among authors: rietschel m. Eur Arch Psychiatry Clin Neurosci. 2010 Apr;260(3):209-15. doi: 10.1007/s00406-009-0044-y. Epub 2009 Sep 10. Eur Arch Psychiatry Clin Neurosci. 2010. PMID: 19763662 Free PMC article.

2

[Genetic association in psychiatric diseases. Concepts and findings].

Propping P, Nöthen MM, Körner J, Rietschel M, Maier W. Propping P, et al. Among authors: rietschel m. Nervenarzt. 1994 Nov;65(11):725-40. Nervenarzt. 1994. PMID: 7816149 Review. German. No abstract available.

3

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

4

Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases.

Rietschel M, Nöthen MM, Albus M, Maier W, Minges J, Bondy B, Körner J, Hemmer S, Fimmers R, Möller HJ, Wildenauer D, Propping P. Rietschel M, et al. Schizophr Res. 1996 May;20(1-2):181-6. doi: 10.1016/0920-9964(95)00074-7. Schizophr Res. 1996. PMID: 8794508

5

The human serotonin 7 (5-HT7) receptor gene: genomic organization and systematic mutation screening in schizophrenia and bipolar affective disorder.

Erdmann J, Nöthen MM, Shimron-Abarbanell D, Rietschel M, Albus M, Borrmann M, Maier W, Franzek E, Körner J, Weigelt B, Fimmers R, Propping P. Erdmann J, et al. Among authors: rietschel m. Mol Psychiatry. 1996 Nov;1(5):392-7. Mol Psychiatry. 1996. PMID: 9154233

6

Investigation of complement C4B deficiency in schizophrenia.

Schroers R, Nöthen MM, Rietschel M, Albus M, Maier W, Schwab S, Wildenauer D, Fimmers R, Propping P, Dewald G. Schroers R, et al. Among authors: rietschel m. Hum Hered. 1997 Sep-Oct;47(5):279-82. doi: 10.1159/000154424. Hum Hered. 1997. PMID: 9358016

7

Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies.

Deckert J, Nöthen MM, Albus M, Franzek E, Rietschel M, Ren H, Stiles GL, Knapp M, Weigelt B, Maier W, Beckmann H, Propping P. Deckert J, et al. Among authors: rietschel m. Am J Med Genet. 1998 Feb 7;81(1):18-23. doi: 10.1002/(sici)1096-8628(19980207)81:1<18::aid-ajmg4>3.0.co;2-j. Am J Med Genet. 1998. PMID: 9514582

8

Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis.

Schwab SG, Hallmayer J, Albus M, Lerer B, Hanses C, Kanyas K, Segman R, Borrman M, Dreikorn B, Lichtermann D, Rietschel M, Trixler M, Maier W, Wildenauer DB. Schwab SG, et al. Among authors: rietschel m. Am J Med Genet. 1998 Jul 10;81(4):302-7. Am J Med Genet. 1998. PMID: 9674975

9

Analysis of a polymorphism in the tuberous sclerosis (TSC2) gene does not predispose to schizophrenia.

Przkora R, Falkai P, von Deimling A, Wiestler OD, Albus M, Rietschel M, Maier W, Bayer TA. Przkora R, et al. Among authors: rietschel m. Eur Arch Psychiatry Clin Neurosci. 1998;248(6):314-5. doi: 10.1007/s004060050056. Eur Arch Psychiatry Clin Neurosci. 1998. PMID: 9928911 Clinical Trial.

10

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

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