Knapp M - Search Results

1

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: knapp m. Mol Psychiatry. 2000 May;5(3):275-82. doi: 10.1038/sj.mp.4000711. Mol Psychiatry. 2000. PMID: 10889530

2

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: knapp m. Hum Genet. 1996 May;97(5):614-9. doi: 10.1007/BF02281871. Hum Genet. 1996. PMID: 8655141

3

Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.

Shimron-Abarbanell D, Harms H, Erdmann J, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Sander T, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: knapp m. Am J Med Genet. 1996 Apr 9;67(2):225-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<225::AID-AJMG16>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723053

4

Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.

Stöber G, Nöthen MM, Pörzgen P, Brüss M, Bönisch H, Knapp M, Beckmann H, Propping P. Stöber G, et al. Among authors: knapp m. Am J Med Genet. 1996 Nov 22;67(6):523-32. doi: 10.1002/(SICI)1096-8628(19961122)67:6<523::AID-AJMG3>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8950409

5

Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated region.

Shimron-Abarbanell D, Erdmann J, Vogt IR, Bryant SP, Spurr NK, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: knapp m. Biochem Biophys Res Commun. 1997 Apr 7;233(1):6-9. doi: 10.1006/bbrc.1997.6390. Biochem Biophys Res Commun. 1997. PMID: 9144385

6

Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease.

Deckert J, Nöthen MM, Franke P, Delmo C, Fritze J, Knapp M, Maier W, Beckmann H, Propping P. Deckert J, et al. Among authors: knapp m. Mol Psychiatry. 1998 Jan;3(1):81-5. doi: 10.1038/sj.mp.4000345. Mol Psychiatry. 1998. PMID: 9491818

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: knapp 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

Serotonin transporter gene and schizophrenia: evidence for association/linkage disequilibrium in families with affected siblings.

Hranilovic D, Schwab SG, Jernej B, Knapp M, Lerer B, Albus M, Rietschel M, Kanyas K, Borrmann M, Lichtermann D, Maier W, Wildenauer DB. Hranilovic D, et al. Among authors: knapp m. Mol Psychiatry. 2000 Jan;5(1):91-5. doi: 10.1038/sj.mp.4000599. Mol Psychiatry. 2000. PMID: 10673774

9

DRD4 exon III VNTR polymorphism-susceptibility factor for heroin dependence? Results of a case-control and a family-based association approach.

Franke P, Nöthen MM, Wang T, Knapp M, Lichtermann D, Neidt H, Sander T, Propping P, Maier W. Franke P, et al. Among authors: knapp m. Mol Psychiatry. 2000 Jan;5(1):101-4. doi: 10.1038/sj.mp.4000583. Mol Psychiatry. 2000. PMID: 10673776

10

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: knapp m. Am J Med Genet. 2000 Apr 3;96(2):217-21. Am J Med Genet. 2000. PMID: 10893499

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