Dr Bianca Haase

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

In the media

Selected grants

2015

  • Genomics of Deafness in the Dalmatian; Wade C, Haase B; American Kennel Club Canine Health Foundation/Research Support.

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 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 R; Morris Animal Foundation (USA)/Cat Health Network.

Selected publications

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Journals

  • Willet, C., Haase, B. (2014). An updated felCat5 SNP manifest for the illumina Feline 63k SNP genotyping array. Animal Genetics, 45(5), 614-615. [More Information]
  • Willet, C., Haase, B. (2014). An updated felCat5 SNP manifest manifest for the illumina Feline 63k SNP genotyping array. Animal Genetics, 45(4), 614-615.
  • Welle, M., Philipp, U., Refenacht, S., Roosje, P., Scharfenstein, M., Schultz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., et al (2014). Peroxide defect formation in zirconate perovskites. Journal of Heredity: an international journal of genomic and evolutionary diversity, 2(38), 15883-15888. [More Information]
  • 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), 1-10. [More Information]
  • 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 mannlichen 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., Archer, S., Sandmeyer, L., Ludwig, A., Foerster, D., Pruvost, M., Haase, B., 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. [More Information]
  • 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]
  • Blatter, M., Haase, B., Gerber, V., Poncet, P., Leeb, T., Rieder, S., Henke, D., Janett, F., Burger, D. (2013). Klinische und genetische Befunde bei einem mannlichen Freiberger mit der neuen Fellfarbe Macchato. Schweizer Archiv fuer Tierheilkunde, 155(4), 229-232.
  • 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(5), 650-650. [More Information]
  • 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]
  • Hasler, H., Flury, C., Menet, S., Haase, B., Leeb, T., Simianer, H., Poncet, P., Rieder, S. (2011). Genetic diversity in an indigenous horse breed - implications for mating strategies and the control of future inbreeding. Journal of Animal Breeding and Genetics (Print), 128(5), 394-406. [More Information]
  • Haring, T., Wichert, B., Dolf, G., Haase, B. (2011). Segregation Analysis of Overweight Body Condition in an Experimental Cat Population. Journal of Heredity: an international journal of genomic and evolutionary diversity, 102, S28-S31. [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. [More Information]
  • Schmitz, A., Demmel, S., Peters, L., Leeb, T., Mevissen, M., Haase, B. (2010). Comparative human-horse sequence analysis of the CYP3A subfamily gene cluster. Animal Genetics, 41(Suppl. 2), 72-79. [More Information]
  • Haase, B., Rieder, S., Tozaki, T., Hasegawa, T., Penedo, M., Jude, R., Leeb, T. (2010). Five Novel KIT mutations in horses with white coat colour phenotypes. Animal Genetics, 42, 337-339.
  • Haase, B., Obexer-Ruff, G., Dolf, G., Rieder, S., Burger, D., Poncet, P., Gerber, V., Howard, J., Leeb, T. (2010). Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation. The Veterinary Journal, 184(3), 315-317. [More Information]
  • Morina, R., Knorr, C., Haase, B., Leeb, T., Seuberlich, T., Zurbriggen, A., Brem, G., Schutz, E., Brenig, B. (2010). Molecular analysis of carbohydrate N- acetylgalactosamine 4-0 sulfotransferase 8 (CHST8) as a candidate gene for bovine spongiform encephalopathy susceptibility. Animal Genetics, 41, 85-88. [More Information]
  • Drögemüller, C., Becker, D., Brunner, A., Haase, B., Kircher, P., Seeliger, F., Fehr, M., Baumann, U., Lindblad-Toh, K., Leeb, T. (2009). A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta. PLoS Genetics, 5(7), 1-9. [More Information]
  • Tester, S., Juillerat, V., Doherr, M., Haase, B., Polak, M., Ehrensperger, F., Leeb, T., Zurbriggen, A., Seuberlich, T. (2009). Biochemical typing of pathological prion protein in aging cattle with BSE. Virology Journal, 6, 64. [More Information]
  • Haase, B., Brooks, S., Tozaki, T., Burger, D., Poncet, P., Rieder, S., Hasegawa, T., Penedo, M., Leeb, T. (2009). Seven novelKIT mutations in horses with white coat colour phenotypes. Animal Genetics, 40(5), 623-629. [More Information]
  • Haase, B., Jude, R., Brooks, S., Leeb, T. (2008). An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds. Animal Genetics, 39, 306-309. [More Information]
  • Daniłowicz, E., Akouchekian, M., Drogemuller, C., Haase, B., Kuiper, H., Distl, O., Leeb, T. (2008). Molecular Characterization and SNP Development for the Porcine Il6 and Il10 Genes. Animal Biotechnology, 19(3), 159-165. [More Information]
  • Reinshagen, C., Keller, K., Haase, B., Leeb, T., Naim, H., Zimmer, K. (2008). Mosaic Pattern of Sucrase Isomaltase Deficiency in Two Brothers. Pediatric Research: international journal of human developmental biology, 63(1), 79-83. [More Information]

Conferences

  • Willet, C., Haase, B., Hamilton (Ellis), 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, 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.

2014

  • Willet, C., Haase, B. (2014). An updated felCat5 SNP manifest for the illumina Feline 63k SNP genotyping array. Animal Genetics, 45(5), 614-615. [More Information]
  • Willet, C., Haase, B. (2014). An updated felCat5 SNP manifest manifest for the illumina Feline 63k SNP genotyping array. Animal Genetics, 45(4), 614-615.
  • Welle, M., Philipp, U., Refenacht, S., Roosje, P., Scharfenstein, M., Schultz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., et al (2014). Peroxide defect formation in zirconate perovskites. Journal of Heredity: an international journal of genomic and evolutionary diversity, 2(38), 15883-15888. [More Information]

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), 1-10. [More Information]
  • 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 mannlichen 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., Archer, S., Sandmeyer, L., Ludwig, A., Foerster, D., Pruvost, M., Haase, B., 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. [More Information]
  • 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]
  • Blatter, M., Haase, B., Gerber, V., Poncet, P., Leeb, T., Rieder, S., Henke, D., Janett, F., Burger, D. (2013). Klinische und genetische Befunde bei einem mannlichen Freiberger mit der neuen Fellfarbe Macchato. Schweizer Archiv fuer Tierheilkunde, 155(4), 229-232.
  • 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 (Ellis), 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, 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(5), 650-650. [More Information]
  • 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]

2011

  • Hasler, H., Flury, C., Menet, S., Haase, B., Leeb, T., Simianer, H., Poncet, P., Rieder, S. (2011). Genetic diversity in an indigenous horse breed - implications for mating strategies and the control of future inbreeding. Journal of Animal Breeding and Genetics (Print), 128(5), 394-406. [More Information]
  • Haring, T., Wichert, B., Dolf, G., Haase, B. (2011). Segregation Analysis of Overweight Body Condition in an Experimental Cat Population. Journal of Heredity: an international journal of genomic and evolutionary diversity, 102, S28-S31. [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. [More Information]
  • Schmitz, A., Demmel, S., Peters, L., Leeb, T., Mevissen, M., Haase, B. (2010). Comparative human-horse sequence analysis of the CYP3A subfamily gene cluster. Animal Genetics, 41(Suppl. 2), 72-79. [More Information]
  • Haase, B., Rieder, S., Tozaki, T., Hasegawa, T., Penedo, M., Jude, R., Leeb, T. (2010). Five Novel KIT mutations in horses with white coat colour phenotypes. Animal Genetics, 42, 337-339.
  • Haase, B., Obexer-Ruff, G., Dolf, G., Rieder, S., Burger, D., Poncet, P., Gerber, V., Howard, J., Leeb, T. (2010). Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation. The Veterinary Journal, 184(3), 315-317. [More Information]
  • Morina, R., Knorr, C., Haase, B., Leeb, T., Seuberlich, T., Zurbriggen, A., Brem, G., Schutz, E., Brenig, B. (2010). Molecular analysis of carbohydrate N- acetylgalactosamine 4-0 sulfotransferase 8 (CHST8) as a candidate gene for bovine spongiform encephalopathy susceptibility. Animal Genetics, 41, 85-88. [More Information]

2009

  • Drögemüller, C., Becker, D., Brunner, A., Haase, B., Kircher, P., Seeliger, F., Fehr, M., Baumann, U., Lindblad-Toh, K., Leeb, T. (2009). A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta. PLoS Genetics, 5(7), 1-9. [More Information]
  • Tester, S., Juillerat, V., Doherr, M., Haase, B., Polak, M., Ehrensperger, F., Leeb, T., Zurbriggen, A., Seuberlich, T. (2009). Biochemical typing of pathological prion protein in aging cattle with BSE. Virology Journal, 6, 64. [More Information]
  • Haase, B., Brooks, S., Tozaki, T., Burger, D., Poncet, P., Rieder, S., Hasegawa, T., Penedo, M., Leeb, T. (2009). Seven novelKIT mutations in horses with white coat colour phenotypes. Animal Genetics, 40(5), 623-629. [More Information]

2008

  • Haase, B., Jude, R., Brooks, S., Leeb, T. (2008). An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds. Animal Genetics, 39, 306-309. [More Information]
  • Daniłowicz, E., Akouchekian, M., Drogemuller, C., Haase, B., Kuiper, H., Distl, O., Leeb, T. (2008). Molecular Characterization and SNP Development for the Porcine Il6 and Il10 Genes. Animal Biotechnology, 19(3), 159-165. [More Information]
  • Reinshagen, C., Keller, K., Haase, B., Leeb, T., Naim, H., Zimmer, K. (2008). Mosaic Pattern of Sucrase Isomaltase Deficiency in Two Brothers. Pediatric Research: international journal of human developmental biology, 63(1), 79-83. [More Information]

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