Cichon S - Search Results

1

CLCN2 variants in idiopathic generalized epilepsy.

Kleefuss-Lie A, Friedl W, Cichon S, Haug K, Warnstedt M, Alekov A, Sander T, Ramirez A, Poser B, Maljevic S, Hebeisen S, Kubisch C, Rebstock J, Horvath S, Hallmann K, Dullinger JS, Rau B, Haverkamp F, Beyenburg S, Schulz H, Janz D, Giese B, Müller-Newen G, Propping P, Elger CE, Fahlke C, Lerche H. Kleefuss-Lie A, et al. Among authors: cichon s. Nat Genet. 2009 Sep;41(9):954-5. doi: 10.1038/ng0909-954. Nat Genet. 2009. PMID: 19710712 No abstract available.

2

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. Among authors: cichon s. Am J Med Genet. 2002 Jan 8;114(1):46-50. doi: 10.1002/ajmg.1624. Am J Med Genet. 2002. PMID: 11840505

3

Human metabotropic glutamate receptor 2 gene (GRM2): chromosomal sublocalization (3p21.1-p21.2) and genomic organization.

Martí SB, Cichon S, Propping P, Nöthen M. Martí SB, et al. Among authors: cichon s. Am J Med Genet. 2002 Jan 8;114(1):12-4. doi: 10.1002/ajmg.1622. Am J Med Genet. 2002. PMID: 11840499

4

Association study of 20 genetic variants at the (D)-amino acid oxidase gene in schizophrenia.

Suliman H, Schumacher J, Becker T, Cichon S, Schulze TG, Propping P, Rietschel M, Nöthen MM, Jamra RA. Suliman H, et al. Among authors: cichon s. Psychiatr Genet. 2010 Apr;20(2):82-3. doi: 10.1097/YPG.0b013e3283351244. Psychiatr Genet. 2010. PMID: 20145586 No abstract available.

5

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: cichon s. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994

6

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. Hum Mol Genet. 1994 Jan;3(1):209. doi: 10.1093/hmg/3.1.209. Hum Mol Genet. 1994. PMID: 8162032 No abstract available.

7

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.

Levy-Nissenbaum E, Betz RC, Frydman M, Simon M, Lahat H, Bakhan T, Goldman B, Bygum A, Pierick M, Hillmer AM, Jonca N, Toribio J, Kruse R, Dewald G, Cichon S, Kubisch C, Guerrin M, Serre G, Nöthen MM, Pras E. Levy-Nissenbaum E, et al. Among authors: cichon s. Nat Genet. 2003 Jun;34(2):151-3. doi: 10.1038/ng1163. Nat Genet. 2003. PMID: 12754508

8

Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder.

Abou Jamra R, Gobina CM, Becker T, Georgi A, Schulze TG, Schmael C, Cichon S, Propping P, Rietschel M, Nöthen MM, Schumacher J. Abou Jamra R, et al. Among authors: cichon s. Psychiatr Genet. 2008 Aug;18(4):199-203. doi: 10.1097/YPG.0b013e3283050a83. Psychiatr Genet. 2008. PMID: 18628682

9

Lack of imprinting of the human dopamine D4 receptor (DRD4) gene.

Cichon S, Nöthen MM, Wolf HK, Propping P. Cichon S, et al. Am J Med Genet. 1996 Apr 9;67(2):229-31. doi: 10.1002/(SICI)1096-8628(19960409)67:2<229::AID-AJMG17>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723054

10

Pharmacogenetics of schizophrenia.

Cichon S, Nöthen MM, Rietschel M, Propping P. Cichon S, et al. Am J Med Genet. 2000 Spring;97(1):98-106. doi: 10.1002/(sici)1096-8628(200021)97:1<98::aid-ajmg12>3.0.co;2-w. Am J Med Genet. 2000. PMID: 10813809 Review.

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