Erdmann J - Search Results

1

Dinucleotide repeat polymorphism at the D18S99 locus.

Erdmann J, Nöthen MM. Erdmann J, et al. 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.

2

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1).

Cichon S, Nöthen MM, Erdmann J, Propping P. Cichon S, et al. Among authors: erdmann j. Hum Mol Genet. 1994 Jan;3(1):209. doi: 10.1093/hmg/3.1.209. Hum Mol Genet. 1994. PMID: 8162032 No abstract available.

3

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome).

Nöthen MM, Eggermann T, Erdmann J, Eiben B, Hofmann D, Propping P, Schwanitz G. Nöthen MM, et al. Among authors: erdmann j. Hum Genet. 1993 Oct;92(4):347-9. doi: 10.1007/BF01247332. Hum Genet. 1993. PMID: 8225314

4

Dinucleotide repeat polymorphism at the D18S365 locus.

Abels S, Erdmann J, Nöthen MM. Abels S, et al. Among authors: erdmann j. 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.

5

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

6

Lack of association between dopamine D1 and D2 receptor genes and bipolar affective disorder.

Nöthen MM, Erdmann J, Körner J, Lanczik M, Fritze J, Fimmers R, Grandy DK, O'Dowd B, Propping P. Nöthen MM, et al. Among authors: erdmann j. Am J Psychiatry. 1992 Feb;149(2):199-201. doi: 10.1176/ajp.149.2.199. Am J Psychiatry. 1992. PMID: 1346486

7

Lack of genetically determined structural variants of the human serotonin-1E (5-HT1E) receptor protein points to its evolutionary conservation.

Shimron-Abarbanell D, Nöthen MM, Erdmann J, Propping P. Shimron-Abarbanell D, et al. Among authors: erdmann j. Brain Res Mol Brain Res. 1995 Apr;29(2):387-90. doi: 10.1016/0169-328x(95)00003-b. Brain Res Mol Brain Res. 1995. PMID: 7609628

8

Identification of genetic variation in the human serotonin 1D beta receptor gene.

Nöthen MM, Erdmann J, Shimron-Abarbanell D, Propping P. Nöthen MM, et al. Among authors: erdmann j. Biochem Biophys Res Commun. 1994 Dec 15;205(2):1194-200. doi: 10.1006/bbrc.1994.2792. Biochem Biophys Res Commun. 1994. PMID: 7802650

9

The use of microsatellites in zygosity diagnosis of twins.

Erdmann J, Nöthen MM, Stratmann M, Fimmers R, Franzek E, Propping P. Erdmann J, et al. Acta Genet Med Gemellol (Roma). 1993;42(1):45-51. doi: 10.1017/s0515283600042281. Acta Genet Med Gemellol (Roma). 1993. PMID: 8191861

10

Pseudoautosomal marker DXYS20 and manic depression.

Nöthen MM, Cichon S, Erdmann J, Körner J, Rietschel M, Rappold GA, Fritze J, Propping P. Nöthen MM, et al. Among authors: erdmann j. Am J Hum Genet. 1993 Apr;52(4):841-2. Am J Hum Genet. 1993. PMID: 8460649 Free PMC article. No abstract available.

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