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Publications

  1. Böhringer S, Epplen JT, Krawczak M (2000) Genetic association studies of bronchial asthma a need for Bonferroni correction? Hum Genet, 107, 197

  2. Krawczak M, Boehringer S, Epplen JT (2001) Correcting for multiple testing in genetic association studies: the legend lives on. Hum Genet,109, 566-567

  3. Böhringer S, Epplen JT (2001) Genetische Variabilität in Populationen: Prädiktiver Indikator und Klassifikationsinstrument für die Pharmakogenomik? [Genetic diversity in populations: An instrument to classify and predict in phramacogenomics?] Med Genet, 13, 249-51

  4. Böhringer S, Gödde R, Böhringer D, Schulte T, Epplen JT (2002) A software package for drawing ideograms automatically. Online Journal of Bioninformatics, 1, 51-59

  5. Miterski B, Böhringer S, Klein W, Sindern E, Haupts M, Schimrigk S, Epplen JT (2002) Inhibitors in the NFkB cascade comprise prime candidate genes predisposing to multiple sclerosis, especially in selected combinations. Genes Immun, 3, 211-9

  6. Epplen JT, Böhringer S (2002) Microsatellites. In: Encyclopedia of the human genome, Nature Publishing Group

  7. Goedde R, Sawcer S, Böhringer S, Miterski B, Sindern E, Haupts M, Schimrigk S, Compston A, Epplen JT (2002) A genome screen for linkage disequilibrium in HLA-DRB1*15-positive Germans with multiple sclerosis based on 4666 microsatellite markers. Hum Genet, 111:270-7

  8. Böhringer D, Reinhard T, Böhringer S, Enczmann J, Godehard E, Sundmacher R. (2002) Predicting time on the waiting list for HLA matched corneal grafts. Tissue Antigens, 59:407-11

  9. Böhringer S, Hardt C, Miterski B, Steland A, Epplen JT (2003) Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data. Eur J Hum Genet, 11:573-84

  10. Schulte T, Böhringer S, Schöls L, Müller T, Fischer C, Riess O, Przuntek H, Berger K, Epplen JT, Krüger R (2003) Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease. J Neural Transm, 110:749-55

  11. Böhringer D, Reinhard T, Duquesnoy RJ, Böhringer S, Enczmann J, Lange P, Claas F, Sundmacher R (2004) Beneficial effect of matching at the HLA-A and -B amino-acid triplet level on rejection-free clear graft survival in penetrating keratoplasty. Transplantation, 15:417-21.

  12. Reinhard T, Bohringer D, Enczmann J, Kogler G, Wernet P, Bohringer S, Sundmacher R (2004) HLA class I/II matching and chronic endothelial cell loss in penetrating normal risk keratoplasty. Acta Ophthalmol Scand, 82:13-8.

  13. Zeschnigk M, Böhringer S, Price EA, Onadim Z, Mashöfer L, Lohmann D (2004) A real time PCR assay for comparative quantification of methylated alleles at the retinoblastoma locus. Nucleic Acids Res, 32:e125

  14. Teber ÖA, Gillessen-Kaesbach G, Fischer S, Böhringer S, Albrecht B, Albert A, Arslan-Kirchner M, Engel W, Haan E, Hagedorn-Greiwe M, Hammans C, Henn W, Hinkel GK, König R, Kunstmann E, Kunze J, Neumann L, Prott EC, Rauch A, Rott HD, Seidel H, Spranger S, Sprengel M, Zoll B, Lohmann DR, Wieczorek D (2004) Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation. Eur J Hum Genet in press

Book articles

  1. Böhringer S, Epplen JT (2002) Neurogenetische Volkskrankheiten - komplexe genetische Erkrankungen [Common neurological genetic disorders - complex genetic diseases] In: Neurogenetik (Riess, O and Schöls, L eds.), Kohlhammer Verlag, Stuttgart

  2. Böhringer S (2003) Descriptive Methods in Large Scale Association Studies In: Jahresschrift der Bochumer Interdiszisziplinären Gesellschaft e.V. 2002 (Muno, R ed.), ibidem, Stuttgart

Other publications

  1. Böhringer S (2000) Inexakter Mustervergleich in genetischen Datenbanken [Inexact pattern matching in genetic databases]. Master's thesis

  2. Böhringer S, Epplen JT (2000) Die Molekularbiologie und die molekulare Medizin [Molecular biology and molecular medicine]. Biologie in unserer Zeit, 30, 366-367

  3. Böhringer S (2001) Statistische Untersuchungen zu genetisch komplexen Erkrankungen: Beispiel Multiple Sklerose [Statistical analyses in genetically complex disease: example Multiple Sclerosis]. PhD thesis

  4. Böhringer S (2003) Building a diskless Linux Cluster for high performance computations from a standard Linux distribution. Online Manual (pdf, html)

  5. Böhringer S, Steland A (2003) Einsatz von Rechenclustern in der statistischen Genetik [Usage of computer clusters in statistical genetics]. RUBENS - Zeitschrift der Ruhr-Universität, 79:1


Last changed: Mon, 25 Jul 2016