Dr Bianca Haase

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

In the media

Genetics Behind Horses' Face and Leg Markings Studied,Bianca was recently interviewed for the American horse magazine "The Horse "to read the full story http://www.thehorse.com/articles/32985/genetics-behind-horses-face-and-leg-markings-studied

Selected grants

2013

  • Genetic investigation of diabetes in Burmese cats; Haase B, Beatty J; Feline Health Research Fund (FHRF)/Research Grant.
  • Genetic investigation of diabetes in Burmese cats; Beatty J, Haase B; Australian Companion Animal Health Foundation/Research Support.

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

  • Haase, B., Signer-Hasler, H., Binns, M., Obexer-Ruff, G., Hauswirth, R., Bellone, R., Burger, D., Rieder, S., Wade, C., Leeb, T. (2013). Accumulating Mutations in Series of Haplotypes at the KIT and MITF Loci are Major Determinants of White Markings in Franches-Montagnes Horses. PLoS One, 8(9), e75071 pg 1-10.
  • Haase, B., Blatter, M., Gerber, V., Poncet, P., Leeb, T., Rieder, S., Henke, D., Janett, F., Burger, D. (2013). Clinical evaluation of the new coat colour macchiato in a male Franches-Montagnes horse [Klinische und genetische Befunde bei einem männlichen Freiberger mit der neuen Fellfarbe Macchiato]. Schweizer Archiv fuer Tierheilkunde, 155(4), 229-232. [More Information]
  • Bellone, R., Holl, H., Setalura, V., Devi, S., Maddodi, N., Haase, B., Archer, S., Sandmeyer, L., Ludwig, A., Foerster, D., et al (2013). Evidence for a Retroviral Insertion in TRPM1 as the cause of congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse. PLoS One, 8(10), 1-14. [More Information]
  • Petersen, J., Mickelson, J., Cothran, E., Andersson, L., Axelsson, J., Bailey, E., Bannasch, D., Binns, M., Borges, A., Brama, P., Haase, B., Wade, C., et al (2013). Genetic Diversity in the Modern Horse Illustrated from Genome-Wide SNP Data. PLoS One, 8(1), 1-15.
  • Petersen, J., Mickelson, J., Rendahl, A., Valberg, S., Andersson, L., Axelsson, J., Bailey, E., Bannasch, D., Binns, M., Borges, A., Haase, B., Wade, C., et al (2013). Genome-Wide Analysis Reveals Selection for Important Traits in Domestic Horse Breeds. PLoS Genetics, 9(1), 1-17. [More Information]
  • Hauswirth, R., Jude, R., Haase, B., Bellone, R., Archer, S., Holl, H., Brooks, S., Tozaki, T., Penedo, M., Rieder, S., et al (2013). Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes. Animal Genetics, 44(6), 763-765. [More Information]
  • 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, 97(5), 813-819. [More Information]
  • 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. [More Information]
  • 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. [More Information]
  • 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., Haase, B., Hamilton, N., Tammen, I., Wade, C. (2013). USE OF NEW SEQUENCING TECHNOLOGIES FOR MUTATION DETECTION. 10th Dorothy Russell Havemeyer Foundation International Equine Genome Mapping Workshop, Not Knwon.
  • 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

  • Haase, B., Signer-Hasler, H., Binns, M., Obexer-Ruff, G., Hauswirth, R., Bellone, R., Burger, D., Rieder, S., Wade, C., Leeb, T. (2013). Accumulating Mutations in Series of Haplotypes at the KIT and MITF Loci are Major Determinants of White Markings in Franches-Montagnes Horses. PLoS One, 8(9), e75071 pg 1-10.
  • Haase, B., Blatter, M., Gerber, V., Poncet, P., Leeb, T., Rieder, S., Henke, D., Janett, F., Burger, D. (2013). Clinical evaluation of the new coat colour macchiato in a male Franches-Montagnes horse [Klinische und genetische Befunde bei einem männlichen Freiberger mit der neuen Fellfarbe Macchiato]. Schweizer Archiv fuer Tierheilkunde, 155(4), 229-232. [More Information]
  • Bellone, R., Holl, H., Setalura, V., Devi, S., Maddodi, N., Haase, B., Archer, S., Sandmeyer, L., Ludwig, A., Foerster, D., et al (2013). Evidence for a Retroviral Insertion in TRPM1 as the cause of congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse. PLoS One, 8(10), 1-14. [More Information]
  • Petersen, J., Mickelson, J., Cothran, E., Andersson, L., Axelsson, J., Bailey, E., Bannasch, D., Binns, M., Borges, A., Brama, P., Haase, B., Wade, C., et al (2013). Genetic Diversity in the Modern Horse Illustrated from Genome-Wide SNP Data. PLoS One, 8(1), 1-15.
  • Petersen, J., Mickelson, J., Rendahl, A., Valberg, S., Andersson, L., Axelsson, J., Bailey, E., Bannasch, D., Binns, M., Borges, A., Haase, B., Wade, C., et al (2013). Genome-Wide Analysis Reveals Selection for Important Traits in Domestic Horse Breeds. PLoS Genetics, 9(1), 1-17. [More Information]
  • Hauswirth, R., Jude, R., Haase, B., Bellone, R., Archer, S., Holl, H., Brooks, S., Tozaki, T., Penedo, M., Rieder, S., et al (2013). Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes. Animal Genetics, 44(6), 763-765. [More Information]
  • 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, 97(5), 813-819. [More Information]
  • Willet, C., Haase, B., Hamilton, N., Tammen, I., Wade, C. (2013). USE OF NEW SEQUENCING TECHNOLOGIES FOR MUTATION DETECTION. 10th Dorothy Russell Havemeyer Foundation International Equine Genome Mapping Workshop, Not Knwon.

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. [More Information]
  • 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. [More Information]

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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