Nöthen MM - Search Results

1

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.

Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, Hoffmann P. Ludwig KU, et al. Among authors: nothen mm. Psychiatr Genet. 2008 Dec;18(6):310-2. doi: 10.1097/YPG.0b013e3283063a78. Psychiatr Genet. 2008. PMID: 19018237 Free PMC article.

2

Dinucleotide repeat polymorphism at the human CD59 locus.

Nöthen MM, Dewald G. Nöthen MM, et al. Clin Genet. 1995 Mar;47(3):165-6. doi: 10.1111/j.1399-0004.1995.tb03952.x. Clin Genet. 1995. PMID: 7543386 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: nothen mm. Psychiatr Genet. 1994 Fall;4(3):167-75. doi: 10.1097/00041444-199400430-00007. Psychiatr Genet. 1994. PMID: 7719703

4

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

5

Dinucleotide repeat polymorphism at the D18S365 locus.

Abels S, Erdmann J, Nöthen MM. Abels S, et al. Among authors: nothen mm. Hum Mol Genet. 1993 Oct;2(10):1747. doi: 10.1093/hmg/2.10.1747-a. Hum Mol Genet. 1993. PMID: 8268941 No abstract available.

6

Dinucleotide repeat polymorphism at the D18S99 locus.

Erdmann J, Nöthen MM. Erdmann J, et al. Among authors: nothen mm. Hum Mol Genet. 1993 Jan;2(1):91. doi: 10.1093/hmg/2.1.91-a. Hum Mol Genet. 1993. PMID: 8490634 No abstract available.

7

Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor gene.

Cichon S, Nöthen MM, Catalano M, Di Bella D, Maier W, Lichtermann D, Minges J, Albus M, Borrmann M, Franzek E, et al. Cichon S, et al. Among authors: nothen mm. Psychiatr Genet. 1995 Fall;5(3):97-103. doi: 10.1097/00041444-199505030-00001. Psychiatr Genet. 1995. PMID: 8746407

8

Apolipoprotein E genotype distribution in schizophrenia.

Zhu S, Nöthen MM, Uhlhaas S, Rietschel M, Körner J, Lanczik M, Fimmers R, Propping P. Zhu S, et al. Among authors: nothen mm. Psychiatr Genet. 1996 Summer;6(2):75-9. doi: 10.1097/00041444-199622000-00007. Psychiatr Genet. 1996. PMID: 8840393

9

The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.

Dewald G, Cichon S, Bryant SP, Hemmer S, Nöthen MM, Spurr NK. Dewald G, et al. Among authors: nothen mm. Ann Hum Genet. 1996 Jul;60(4):281-91. doi: 10.1111/j.1469-1809.1996.tb01192.x. Ann Hum Genet. 1996. PMID: 8865989

10

5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity.

Hinney A, Ziegler A, Nöthen MM, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: nothen mm. Lancet. 1997 Nov 1;350(9087):1324-5. doi: 10.1016/S0140-6736(05)62485-3. Lancet. 1997. PMID: 9357428 No abstract available.

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