Rietschel M - Search Results

1

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.

Rietschel M, Mattheisen M, Degenhardt F; Genetic Risk and Outcome in Psychosis (GROUP Investigators); Mühleisen TW, Kirsch P, Esslinger C, Herms S, Demontis D, Steffens M, Strohmaier J, Haenisch B, Breuer R, Czerski PM, Giegling I, Strengman E, Schmael C, Mors O, Mortensen PB, Hougaard DM, Ørntoft T, Kapelski P, Priebe L, Basmanav FF, Forstner AJ, Hoffman P, Meier S, Nikitopoulos J, Moebus S, Alexander M, Mössner R, Wichmann H-, Schreiber S, Rivandeneira F, Hofman A, Uitterlinden AG, Wienker TF, Schumacher J, Hauser J, Maier W, Cantor RM, Erk S, Schulze TG; SGENE-plus Consortium; Craddock N, Owen MJ, O'Donovan MC, Børglum AD, Rujescu D, Walter H, Meyer-Lindenberg A, Nöthen NM, Ophoff RA, Cichon S. Rietschel M, et al. Mol Psychiatry. 2012 Sep;17(9):906-17. doi: 10.1038/mp.2011.80. Epub 2011 Jul 12. Mol Psychiatry. 2012. PMID: 21747397

2

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.

3

Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls.

Körner J, Rietschel M, Hunt N, Castle D, Gill M, Nöthen MM, Craddock N, Daniels J, Owen M, Fimmers R, et al. Körner J, et al. Among authors: rietschel m. Psychiatr Genet. 1994 Fall;4(3):167-75. doi: 10.1097/00041444-199400430-00007. Psychiatr Genet. 1994. PMID: 7719703

4

[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.

5

Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression.

Cichon S, Nöthen MM, Rietschel M, Körner J, Propping P. Cichon S, et al. Among authors: rietschel m. Biol Psychiatry. 1994 Dec 15;36(12):850-3. doi: 10.1016/0006-3223(94)90597-5. Biol Psychiatry. 1994. PMID: 7893850 Clinical Trial. No abstract available.

6

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder.

Rietschel M, Nöthen MM, Lannfelt L, Sokoloff P, Schwartz JC, Lanczik M, Fritze J, Cichon S, Fimmers R, Körner J, et al. Rietschel M, et al. Psychiatry Res. 1993 Mar;46(3):253-9. doi: 10.1016/0165-1781(93)90093-v. Psychiatry Res. 1993. PMID: 8493294

7

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

8

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

9

Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.

Cichon S, Nöthen MM, Stöber G, Schroers R, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Wildenauer D, Fimmers R, Propping P. Cichon S, et al. Among authors: rietschel m. Am J Med Genet. 1996 Jul 26;67(4):424-8. doi: 10.1002/(SICI)1096-8628(19960726)67:4<424::AID-AJMG21>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8837716

10

Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia.

Deckert J, Nöthen MM, Rietschel M, Wildenauer D, Bondy B, Ertl MA, Knapp M, Schofield PR, Albus M, Maier W, Propping P. Deckert J, et al. Among authors: rietschel m. J Neural Transm (Vienna). 1996;103(12):1447-55. doi: 10.1007/BF01271259. J Neural Transm (Vienna). 1996. PMID: 9029412 Clinical Trial.

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