Hemmer S - Search Results

1

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. Among authors: hemmer s. Hum Mol Genet. 1994 Dec;3(12):2207-12. doi: 10.1093/hmg/3.12.2207. Hum Mol Genet. 1994. PMID: 7881421

2

Human complement component C8. Molecular basis of the beta-chain polymorphism.

Dewald G, Hemmer S, Nöthen MM. Dewald G, et al. Among authors: hemmer s. FEBS Lett. 1994 Mar 7;340(3):211-5. doi: 10.1016/0014-5793(94)80140-1. FEBS Lett. 1994. PMID: 8131848 Free article.

3

Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial cases.

Rietschel M, Nöthen MM, Albus M, Maier W, Minges J, Bondy B, Körner J, Hemmer S, Fimmers R, Möller HJ, Wildenauer D, Propping P. Rietschel M, et al. Among authors: hemmer s. Schizophr Res. 1996 May;20(1-2):181-6. doi: 10.1016/0920-9964(95)00074-7. Schizophr Res. 1996. PMID: 8794508

4

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: hemmer s. Ann Hum Genet. 1996 Jul;60(4):281-91. doi: 10.1111/j.1469-1809.1996.tb01192.x. Ann Hum Genet. 1996. PMID: 8865989

5

A gene for universal congenital alopecia maps to chromosome 8p21-22.

Nöthen MM, Cichon S, Vogt IR, Hemmer S, Kruse R, Knapp M, Höller T, Faiyaz ul Haque M, Haque S, Propping P, Ahmad M, Rietschel M. Nöthen MM, et al. Among authors: hemmer s. Am J Hum Genet. 1998 Feb;62(2):386-90. doi: 10.1086/301717. Am J Hum Genet. 1998. PMID: 9463324 Free PMC article.

6

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: hemmer s. Mol Psychiatry. 1999 Jan;4(1):76-84. doi: 10.1038/sj.mp.4000454. Mol Psychiatry. 1999. PMID: 10089014

7

A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.

Cichon S, Schumacher J, Müller DJ, Hürter M, Windemuth C, Strauch K, Hemmer S, Schulze TG, Schmidt-Wolf G, Albus M, Borrmann-Hassenbach M, Franzek E, Lanczik M, Fritze J, Kreiner R, Reuner U, Weigelt B, Minges J, Lichtermann D, Lerer B, Kanyas K, Baur MP, Wienker TF, Maier W, Rietschel M, Propping P, Nöthen MM. Cichon S, et al. Among authors: hemmer s. Hum Mol Genet. 2001 Dec 1;10(25):2933-44. doi: 10.1093/hmg/10.25.2933. Hum Mol Genet. 2001. PMID: 11741836

8

No association between length of the (CAG)n repeat of the Huntington's disease gene and Tourette's syndrome.

Hebebrand J, Nöthen MM, Klug B, Wettke-Schäfer R, Camps A, Lisch S, Hemmer S, von Gontard A, Poustka F, Lehmkuhl G, et al. Hebebrand J, et al. Among authors: hemmer s. Biol Psychiatry. 1995 Feb 1;37(3):209-11. doi: 10.1016/0006-3223(94)00214-n. Biol Psychiatry. 1995. PMID: 7727632 No abstract available.

9

DNA copy number losses at 1p32-pter in monozygotic twins concordant for breast cancer.

el-Rifai W, Tarmo L, Hemmer S, Försti A, Pedersen N, Lichtenstein P, Ahlbom A, Söderberg M, Knuutila S, Hemminki K. el-Rifai W, et al. Among authors: hemmer s. Cancer Genet Cytogenet. 1999 Jul 15;112(2):169-72. doi: 10.1016/s0165-4608(98)00274-x. Cancer Genet Cytogenet. 1999. PMID: 10686947

10

DNA copy number changes in thyroid carcinoma.

Hemmer S, Wasenius VM, Knuutila S, Franssila K, Joensuu H. Hemmer S, et al. Am J Pathol. 1999 May;154(5):1539-47. doi: 10.1016/S0002-9440(10)65407-7. Am J Pathol. 1999. PMID: 10329606 Free PMC article.

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