Albus M - Search Results

1

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: albus m. Mol Psychiatry. 1996 Nov;1(5):392-7. Mol Psychiatry. 1996. PMID: 9154233

2

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients.

Frank B, Niesler B, Nöthen MM, Neidt H, Propping P, Bondy B, Rietschel M, Maier W, Albus M, Rappold G. Frank B, et al. Among authors: albus m. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):1-5. doi: 10.1002/ajmg.b.30070. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389765

3

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: albus m. J Neural Transm (Vienna). 1996;103(12):1447-55. doi: 10.1007/BF01271259. J Neural Transm (Vienna). 1996. PMID: 9029412 Clinical Trial.

4

Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis.

Schwab SG, Eckstein GN, Hallmayer J, Lerer B, Albus M, Borrmann M, Lichtermann D, Ertl MA, Maier W, Wildenauer DB. Schwab SG, et al. Among authors: albus m. Mol Psychiatry. 1997 Mar;2(2):156-60. doi: 10.1038/sj.mp.4000263. Mol Psychiatry. 1997. PMID: 9106241

5

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: albus 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

6

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: albus 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.

7

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.

Nöthen MM, Cichon S, Rohleder H, Hemmer S, Franzek E, Fritze J, Albus M, Borrmann-Hassenbach M, Kreiner R, Weigelt B, Minges J, Lichtermann D, Maier W, Craddock N, Fimmers R, Höller T, Baur MP, Rietschel M, Propping P. Nöthen MM, et al. Among authors: albus m. Mol Psychiatry. 1999 Jan;4(1):76-84. doi: 10.1038/sj.mp.4000454. Mol Psychiatry. 1999. PMID: 10089014

8

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1).

Grünhage F, Schulze TG, Müller DJ, Lanczik M, Franzek E, Albus M, Borrmann-Hassenbach M, Knapp M, Cichon S, Maier W, Rietschel M, Propping P, Nöthen MM. Grünhage F, et al. Among authors: albus m. Mol Psychiatry. 2000 May;5(3):275-82. doi: 10.1038/sj.mp.4000711. Mol Psychiatry. 2000. PMID: 10889530

9

Investigation of the human serotonin 6 [5-HT6] receptor gene in bipolar affective disorder and schizophrenia.

Vogt IR, Shimron-Abarbanell D, Neidt H, Erdmann J, Cichon S, Schulze TG, Müller DJ, Maier W, Albus M, Borrmann-Hassenbach M, Knapp M, Rietschel M, Propping P, Nöthen MM. Vogt IR, et al. Among authors: albus m. Am J Med Genet. 2000 Apr 3;96(2):217-21. Am J Med Genet. 2000. PMID: 10893499

10

Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls.

Rietschel M, Schorr A, Albus M, Franzek E, Kreiner R, Held T, Knapp M, Müller DJ, Schulze TG, Propping P, Maier W, Nöthen MM. Rietschel M, et al. Among authors: albus m. Am J Med Genet. 2000 Jun 12;96(3):310-1. doi: 10.1002/1096-8628(20000612)96:3<310::aid-ajmg15>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10898906

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

182 results

Search Page