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Publikationen

  • Enriquez Schäfer, Ramon, Becker-Follmann, Johannes: „Screening for karyotypes with abberations in the gonosomes by direct quantitative fluorescent PCR“ European Patent Application 2021.
  • Becker-Follmann, J. und D. Baas (2004). PCR - Eine Methode, drei Schritte. Biospektrum 1: 86-90.
  • Immervoll T, Loesgen S, Dutsch G, Gohlke H, Herbon N, Klugbauer S, Dempfle A, Bickeboller H, Becker-Follmann, J, Rueschendorf F, Saar K, Reis A, Wichmann HE, Wjst M. (2001). Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes. Hum Mutat 18:327-36.
  • Vanita, Singh, J. R., Sarhadi, V. K., Singh, D., Reis, A., Rueschendorf, F., Becker-Follmann, J., Jung, M., and Sperling, K. (2001). A novel form of central pouchlike cataract, with sutural opacities, maps to chromosome 15q21-22. Am. J. Hum. Genet. 68: 509-514.
  • Niemann, S., Becker-Follmann, J., Nürnberg, G., Rüschendorf, F., Sieweke, N., Hügens-Penzel, M., Traupe, H., Wienker, T. F., Reis, A., and Müller, U. (2001). Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma. Am. J. Med. Gen. 98: 32-36.
  • Graw, J., Klopp, N., Löster, J., Soewarto, D., Fuchs, H., Becker-Follmann, J., Reis, A., Wolf, E. (2001). Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.
    Genetics 157: 1313-1320.
  • Becker-Follmann, J., Zschunke, F., Parwaresch, M. R., Radzun, H. J., and Scherer G. (1997). Assignment of the human monocyte/macrophage serine esterase 1 (CES1) to human chromosome 16q13-q22.1 and of its mouse homologue to the proximal esterase cluster on mouse chromosome 8. Cytogenet. Cell Genet. 58: 1997.
  • Becker-Follmann, J., Gaa, A., Bausch, E., Natt, E., Scherer, G., and von Deimling, O. (1997). High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16q.
    Mammalian Genome 8 (3): 172-177.
  • Becker-Follmann, Johannes (1994). Vergleichende Genkartierung zwischen Chromosom 16q des Menschen und Chromosom 8 der Maus. Dissertation am Institut für Anthropologie und Humangenetik der Albert-Ludwigs-Universität Freiburg i. Br.
  • Becker-Follmann, J., Gaa, A., Bausch, E., Natt, E., Scherer, G., and von Deimling, O. (1993). Refinement of a linkage group on mouse chromsome 8 conserved on human chromosome 16q. Medizinische Genetik 5 : 129.
  • Becker-Follmann, J., Zschunke, F., Parwaresch, M. R., Radzun, H., and Scherer, G. (1992). Comparative gene mapping of monocyte/macrophage serine esterase 1 (CES1) and type IV collagenase A (CLG4A) to human chromsome 16q13-q22.1 and to the esterase cluster 1 on mouse chromosome 8. Tagungsband der Gesellschaft für Humangenetik e. V., T7/191.
  • Kaupmann K, Becker-Follmann J, Scherer G, Jockusch H, Starzinski-Powitz A. (1992). The gene for the cell adhesion molecule M-cadherin maps to mouse chromosome 8 and human chromosome 16q24.1-qter and is near the E-cadherin (uvomorulin) locus in both species.
    Genomics. Oct;14 (2):488-90.
  • Becker-Follmann, J., Kaupmann, K., Vestweber, D., Jockusch, H., Starzinski-Powitz, A., and Scherer, G., (1992). Assignment of muscle cadherin (MCAD) to human chromosome 16q24-qter and mouse chromosome 8, and of placental cadherin (PCAD)-like sequences PCADL1 to 16q22.1 and PCADL2 to 16q24-qter.
    Cytogenet. Cell Genet. 60: 168.
  • Becker, Johannes (1989). Anwendung der Pulsfeld-Gelelektrophorese zur Kartierung von Genen auf Chromosom 16q des Menschen und Chromosom 8 der Maus. Diplomarbeit am Institut für Anthropologie und Humangenetik der Albert-Ludwigs-Universität Freiburg i. Br.
  • Becker, J., Himmelbauer, H., and Scherer, G. (1989). Long range mapping of loci conserved on human chromosome 16q and mouse chromosome 8. Cytogenet. Cell Genet. 51 :959.


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