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 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. [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, 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]
  • 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, 394-406.
  • 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.
  • 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.
  • 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, 315-317.
  • 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]
  • Welle, M., Philipp, U., Refenacht, S., Roosje, P., Scharfenstein, M., Schultz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., Haase, B., et al (2009). MLPH Genotype - Melanin Phenotype Correlation in Dilute Dogs. Journal of Heredity: an international journal of genomic and evolutionary diversity, 100(Suppl. 1), S75-S79.
  • Morina, R., Knorr, C., Haase, B., Leeb, T., Seuberlich, T., Zurbriggen, A., Brem, G., Schutz, E., Brenig, B. (2009). 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.
  • 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, 623-629.
  • 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.
  • 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.
  • 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. [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, 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]

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, 394-406.
  • 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.
  • 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.
  • 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, 315-317.

2009

  • 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]
  • Welle, M., Philipp, U., Refenacht, S., Roosje, P., Scharfenstein, M., Schultz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., Haase, B., et al (2009). MLPH Genotype - Melanin Phenotype Correlation in Dilute Dogs. Journal of Heredity: an international journal of genomic and evolutionary diversity, 100(Suppl. 1), S75-S79.
  • Morina, R., Knorr, C., Haase, B., Leeb, T., Seuberlich, T., Zurbriggen, A., Brem, G., Schutz, E., Brenig, B. (2009). 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.
  • 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, 623-629.

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.
  • 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.
  • 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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