Cichon S - Search Results

1

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.

Yousaf A, Waltes R, Haslinger D, Klauck SM, Duketis E, Sachse M, Voran A, Biscaldi M, Schulte-Rüther M, Cichon S, Nöthen M, Ackermann J, Koch I, Freitag CM, Chiocchetti AG. Yousaf A, et al. Among authors: cichon s. Transl Psychiatry. 2020 Jul 5;10(1):215. doi: 10.1038/s41398-020-00906-2. Transl Psychiatry. 2020. PMID: 32624584 Free PMC article.

2

Single-strand conformation analysis (SSCA) of the dopamine D1 receptor gene (DRD1) reveals no significant mutation in patients with schizophrenia and manic depression.

Cichon S, Nöthen MM, Rietschel M, Körner J, Propping P. Cichon S, et al. Biol Psychiatry. 1994 Dec 15;36(12):850-3. doi: 10.1016/0006-3223(94)90597-5. Biol Psychiatry. 1994. PMID: 7893850 Clinical Trial. No abstract available.

3

Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.

Dewald G, Nöthen MM, Cichon S. Dewald G, et al. Among authors: cichon s. Biochem Biophys Res Commun. 1993 Jul 15;194(1):458-64. doi: 10.1006/bbrc.1993.1841. Biochem Biophys Res Commun. 1993. PMID: 8101442

4

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.

5

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D3 receptor protein: no role in the genetic predisposition to bipolar affective disorder.

Rietschel M, Nöthen MM, Lannfelt L, Sokoloff P, Schwartz JC, Lanczik M, Fritze J, Cichon S, Fimmers R, Körner J, et al. Rietschel M, et al. Among authors: cichon s. Psychiatry Res. 1993 Mar;46(3):253-9. doi: 10.1016/0165-1781(93)90093-v. Psychiatry Res. 1993. PMID: 8493294

6

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

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. Psychiatr Genet. 1995 Fall;5(3):97-103. doi: 10.1097/00041444-199505030-00001. Psychiatr Genet. 1995. PMID: 8746407

8

Systematic screening for mutations in the 5'-regulatory region of the human dopamine D1 receptor (DRD1) gene in patients with schizophrenia and bipolar affective disorder.

Cichon S, Nöthen MM, Stöber G, Schroers R, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Wildenauer D, Fimmers R, Propping P. Cichon S, et al. Am J Med Genet. 1996 Jul 26;67(4):424-8. doi: 10.1002/(SICI)1096-8628(19960726)67:4<424::AID-AJMG21>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8837716

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: cichon 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

10

Assignment of the human serotonin 4 receptor gene (HTR4) to the long arm of chromosome 5 (5q31-q33).

Cichon S, Kesper K, Propping P, Nöthen MM. Cichon S, et al. Mol Membr Biol. 1998 Apr-Jun;15(2):75-8. doi: 10.3109/09687689809027521. Mol Membr Biol. 1998. PMID: 9724925

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