Dr Bianca Haase

B19 - R.M.C. Gunn Building
The University of Sydney

Selected grants

2012

  • Diabetes in cats: Investigating the genetic predisposition of Burmese cats; Haase B; Constance H. Aird Diabetes Bequest/Faculty of Veterinary Science Bequest.

2011

  • Osteochondrodysplasia in Cats; Haase B, Wade C, Malik (Krochmalik) R, Lyons L; Morris Animal Foundation (USA)/Research Support.
  • Bodyweight: investigation of genetic aspects in an experimental cat population; Haase B, Wade C, Wichert B, Bjornvad C; Morris Animal Foundation (USA)/Cat Health Network.
  • Osteochondrodysplasia in Cats; Haase B, Wade C, Lyons L, Malik (Krochmalik) R; Morris Animal Foundation (USA)/Cat Health Network.

Selected publications

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Journals

  • Petersen, J., Mickelson, J., Rendahl, A., Haase, B., Wade, C. (2013). Genome-wids Analysis Reveals Selection for Important Traits in Domestic Horse Breeds. PLoS Genetics, 9(1), e1003211.
  • Haring, T., Haase, B., Zini, E., Hartnack, S., Uebelhart, D., Gaudenz, D., Wichert, B. (2013). Overweight and impaired insulin sensitivity present in growing cats. Journal of Animal Physiology and Animal Nutrition.
  • Signer-Hasler, H., Flury, C., Haase, B., Burger, D., Simianer, H., Leeb, T., Rieder, S. (2012). A Genome-Wide Association Study Reveals Loci Influencing Height and Other Conformation Traits in Horses. PLoS One, 7(5), e37282.
  • Gabreski, N., Haase, B., Armstrong, C., Distl, O., Brooks, S. (2012). Investigation of allele frequencies for Lavender foal syndrome in the horse. Animal Genetics, 43, 646-646.
  • Hauswirth, R., Haase, B., Blatter, M., Brooks, S., Burger, D., Drogemuller, C., Gerber, V., Henke, D., Janda, J., Jude, R., Matthews, J., Wilkinson-White, L., et al (2012). Mutations in MITF and PAX3 cause " Splashed White" and Other white Spotting Phenotypes in Horses. PLoS Genetics, 8(4), 1-9.
  • Bellone, R., Archer, S., Wade, C., Cuka-Lawson, C., Haase, B., Leeb, T., Forsyth, G., Sandmeyer, L., Grahn, B. (2010). Association analysis of candidate SNPs in TRPM1 with leopard complex spotting (LP ) and congenital stationary night blindness (CSNB) in horses. Animal Genetics, 41(Suppl. 2), 207-207.

Conferences

  • Willet, C., Gandolfi, B., Malik (Krochmalik), R., Lyons, L., Wade, C., Haase, B. (2012). Feline osteochondrodysplasia of Scottish Fold cats. 33rd Conference of the International Society for Animal Genetics, Brisbane: University of Queensland Press.

2013

  • Petersen, J., Mickelson, J., Rendahl, A., Haase, B., Wade, C. (2013). Genome-wids Analysis Reveals Selection for Important Traits in Domestic Horse Breeds. PLoS Genetics, 9(1), e1003211.
  • Haring, T., Haase, B., Zini, E., Hartnack, S., Uebelhart, D., Gaudenz, D., Wichert, B. (2013). Overweight and impaired insulin sensitivity present in growing cats. Journal of Animal Physiology and Animal Nutrition.

2012

  • Signer-Hasler, H., Flury, C., Haase, B., Burger, D., Simianer, H., Leeb, T., Rieder, S. (2012). A Genome-Wide Association Study Reveals Loci Influencing Height and Other Conformation Traits in Horses. PLoS One, 7(5), e37282.
  • Willet, C., Gandolfi, B., Malik (Krochmalik), R., Lyons, L., Wade, C., Haase, B. (2012). Feline osteochondrodysplasia of Scottish Fold cats. 33rd Conference of the International Society for Animal Genetics, Brisbane: University of Queensland Press.
  • Gabreski, N., Haase, B., Armstrong, C., Distl, O., Brooks, S. (2012). Investigation of allele frequencies for Lavender foal syndrome in the horse. Animal Genetics, 43, 646-646.
  • Hauswirth, R., Haase, B., Blatter, M., Brooks, S., Burger, D., Drogemuller, C., Gerber, V., Henke, D., Janda, J., Jude, R., Matthews, J., Wilkinson-White, L., et al (2012). Mutations in MITF and PAX3 cause " Splashed White" and Other white Spotting Phenotypes in Horses. PLoS Genetics, 8(4), 1-9.

2010

  • Bellone, R., Archer, S., Wade, C., Cuka-Lawson, C., Haase, B., Leeb, T., Forsyth, G., Sandmeyer, L., Grahn, B. (2010). Association analysis of candidate SNPs in TRPM1 with leopard complex spotting (LP ) and congenital stationary night blindness (CSNB) in horses. Animal Genetics, 41(Suppl. 2), 207-207.

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