Fischer C - Search Results

1

Investigation of SHANK3 in schizophrenia.

de Sena Cortabitarte A, Degenhardt F, Strohmaier J, Lang M, Weiss B, Roeth R, Giegling I, Heilmann-Heimbach S, Hofmann A, Rujescu D, Fischer C, Rietschel M, Nöthen MM, Rappold GA, Berkel S. de Sena Cortabitarte A, et al. Among authors: fischer c. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun;174(4):390-398. doi: 10.1002/ajmg.b.32528. Epub 2017 Mar 28. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28371232

2

A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders.

de Sena Cortabitarte A, Berkel S, Cristian FB, Fischer C, Rappold GA. de Sena Cortabitarte A, et al. Among authors: fischer c. J Neurodev Disord. 2018 Apr 17;10(1):15. doi: 10.1186/s11689-018-9233-1. J Neurodev Disord. 2018. PMID: 29665782 Free PMC article.

3

Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.

Niesler B, Weiss B, Fischer C, Nöthen MM, Propping P, Bondy B, Rietschel M, Maier W, Albus M, Franzek E, Rappold GA. Niesler B, et al. Among authors: fischer c. Pharmacogenetics. 2001 Feb;11(1):21-7. doi: 10.1097/00008571-200102000-00003. Pharmacogenetics. 2001. PMID: 11207027

4

The human SHOX mutation database.

Niesler B, Fischer C, Rappold GA. Niesler B, et al. Among authors: fischer c. Hum Mutat. 2002 Nov;20(5):338-41. doi: 10.1002/humu.10125. Hum Mutat. 2002. PMID: 12402330

5

Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder.

Niesler B, Flohr T, Nöthen MM, Fischer C, Rietschel M, Franzek E, Albus M, Propping P, Rappold GA. Niesler B, et al. Among authors: fischer c. Pharmacogenetics. 2001 Aug;11(6):471-5. doi: 10.1097/00008571-200108000-00002. Pharmacogenetics. 2001. PMID: 11505217

6

Double crossover in the human Xp/Yp pseudoautosomal region and its bearing on interference.

Rappold GA, Klink A, Weiss B, Fischer C. Rappold GA, et al. Among authors: fischer c. Hum Mol Genet. 1994 Aug;3(8):1337-40. doi: 10.1093/hmg/3.8.1337. Hum Mol Genet. 1994. PMID: 7987311

7

The human pseudoautosomal regions: a review for genetic epidemiologists.

Flaquer A, Rappold GA, Wienker TF, Fischer C. Flaquer A, et al. Among authors: fischer c. Eur J Hum Genet. 2008 Jul;16(7):771-9. doi: 10.1038/ejhg.2008.63. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398439 Review.

8

Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients.

Frank B, Niesler B, Bondy B, Späth M, Pongratz DE, Ackenheil M, Fischer C, Rappold G. Frank B, et al. Among authors: fischer c. Clin Rheumatol. 2004 Aug;23(4):338-44. doi: 10.1007/s10067-004-0927-2. Epub 2004 May 7. Clin Rheumatol. 2004. PMID: 15293096

9

Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomere.

Henke A, Fischer C, Rappold GA. Henke A, et al. Among authors: fischer c. Genomics. 1993 Dec;18(3):478-85. doi: 10.1016/s0888-7543(11)80003-0. Genomics. 1993. PMID: 8307556

10

The novel human SHOX allelic variant database.

Niesler B, Röth R, Wilke S, Fujimura F, Fischer C, Rappold G. Niesler B, et al. Among authors: fischer c. Hum Mutat. 2007 Oct;28(10):933-8. doi: 10.1002/humu.20542. Hum Mutat. 2007. PMID: 17726696

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