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Brenig, Bertram; Steingräber, Lilith; Shan, Shuwen; Xu, Fangzheng; Hirschfeld, Marc; Andag, Reiner; Spengeler, M; Dietschi, Elisabeth; Mischke, Reinhard; Leeb, Tosso (2019). Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter. Haematologica - the hematology journal, 104(11), pp. 2307-2313. Ferrata-Storti Foundation 10.3324/haematol.2018.215426
Awasthi, Nivedita; Drögemüller, Cord; Jagannathan, Vidhya; Keller, Irene; Wüthrich, Daniel; Bruggmann, Rémy; Beck, Julia; Schütz, Ekkehard; Brenig, Bertram; Demmel, Steffi; Moser, Simon; Signer-Hasler, Heidi; Pieńkowska-Schelling, Aldona; Schelling, Claude; Sande Melon, Marcos; Rongen, Ronald; Rieder, Stefan; Kelsh, Robert N.; Mercader Huber, Nadia and Leeb, Tosso (2017). A structural variant in the 5’-flanking region of the TWIST2 gene affects melanocyte development in belted cattle. PLoS ONE, 12(6), e0180170. Public Library of Science 10.1371/journal.pone.0180170
Menzi, Fiona; Keller, Irene; Reber, Irene; Beck, Julia; Brenig, Bertram; Schütz, Ekkehard; Leeb, Tosso; Drögemüller, Cord (2016). Genomic amplification of the caprine EDNRA locus might lead to a dose dependent loss of pigmentation. Scientific Reports, 6, p. 28438. Nature Publishing Group 10.1038/srep28438
Schütz, Ekkehard; Brenig, Bertram; Scharfenstein, Melanie; Drögemüller, Cord; Leeb, Tosso (2013). Osteogenesis imperfecta in dachshunds. Veterinary record, 172(12), p. 319. British Veterinary Association 10.1136/vr.f1823
Schütz, Ekkehard; Drögemüller, Cord; Leeb, Tosso; Scharfenstein, Melanie; Brenig, Bertram (2012). Osteogenesis imperfecta beim Dackel. Kleintierpraxis, 57(2), pp. 57-62. Schaper
Drögemüller, Cord; Giese, Alexander; Martins-Wess, Flávia; Wiedemann, Sabine; Andersson, Leif; Brenig, Bertram; Fries, Ruedi; Leeb, Tosso (2006). The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence. Mammalian genome, 17(1), pp. 58-66. New York, N.Y.: Springer-Verlag 10.1007/s00335-005-0104-1
