Nöthen MM - Search Results

1

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

Ludwig KU, Roeske D, Herms S, Schumacher J, Warnke A, Plume E, Neuhoff N, Bruder J, Remschmidt H, Schulte-Körne G, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: nothen mm. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):503-511. doi: 10.1002/ajmg.b.31007. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19591125

2

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: nothen mm. Psychiatr Genet. 1994 Fall;4(3):167-75. doi: 10.1097/00041444-199400430-00007. Psychiatr Genet. 1994. PMID: 7719703

3

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.

Nöthen MM, Cichon S, Hemmer S, Hebebrand J, Remschmidt H, Lehmkuhl G, Poustka F, Schmidt M, Catalano M, Fimmers R, et al. Nöthen MM, et al. Hum Mol Genet. 1994 Dec;3(12):2207-12. doi: 10.1093/hmg/3.12.2207. Hum Mol Genet. 1994. PMID: 7881421

4

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: nothen mm. 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

5

Evidence for linkage of spelling disability to chromosome 15.

Schulte-Körne G, Grimm T, Nöthen MM, Müller-Myhsok B, Cichon S, Vogt IR, Propping P, Remschmidt H. Schulte-Körne G, et al. Among authors: nothen mm. Am J Hum Genet. 1998 Jul;63(1):279-82. doi: 10.1086/301919. Am J Hum Genet. 1998. PMID: 9634517 Free PMC article. No abstract available.

6

Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.

Stöber G, Hebebrand J, Cichon S, Brüss M, Bönisch H, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Propping P, Nöthen MM. Stöber G, et al. Among authors: nothen mm. Am J Med Genet. 1999 Apr 16;88(2):158-63. doi: 10.1002/(sici)1096-8628(19990416)88:2<158::aid-ajmg12>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10206236

7

Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.

Nöthen MM, Schulte-Körne G, Grimm T, Cichon S, Vogt IR, Müller-Myhsok B, Propping P, Remschmidt H. Nöthen MM, et al. Eur Child Adolesc Psychiatry. 1999;8 Suppl 3:56-9. doi: 10.1007/pl00010696. Eur Child Adolesc Psychiatry. 1999. PMID: 10638372

8

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

9

Lack of association between a functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene and tardive dyskinesia in schizophrenia.

Schulze TG, Schumacher J, Müller DJ, Krauss H, Alfter D, Maroldt A, Ahle G, Maroldt AO, Novo y Fernández A, Weber T, Held T, Propping P, Maier W, Nöthen MM, Rietschel M. Schulze TG, et al. Among authors: nothen mm. Am J Med Genet. 2001 Aug 8;105(6):498-501. doi: 10.1002/ajmg.1472. Am J Med Genet. 2001. PMID: 11496364

10

Metabotropic glutamate receptor 3 (GRM3) gene variation is not associated with schizophrenia or bipolar affective disorder in the German population.

Martí SB, Cichon S, Propping P, Nöthen M. Martí SB, et al. Am J Med Genet. 2002 Jan 8;114(1):46-50. doi: 10.1002/ajmg.1624. Am J Med Genet. 2002. PMID: 11840505

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