Dr Bianca Waud

DVM, PhD

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

Telephone +61 (02) 8627 0277

Teaching and supervision

  • Senior Lecturer in Veterinary Systems Biology
  • DVM Year 1 Coordinator

Current research students

Project title Research student
Interplay between haplotype and topological domain structure in the canine genome Bobbie CANSDALE
Advances in Felid Genetics and Genomics Georgie SAMAHA

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

  • 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, Malik R, Lyons L; Morris Animal Foundation (USA)/Research Support.
  • 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

  • Gandolfi, B., Alamri, S., Darby, W., Adhikari, B., Lattimer, J., Malik, R., Wade, C., Lyons, L., Cheng, J., Bateman, J., Haase, B., et al (2016). A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats. Osteoarthritis and Cartilage, 24(8), 1441-1450. [More Information]
  • Haase, B., Mazrier, H., Wade, C. (2016). Digging for known genetic mutations underlying inherited bone and cartilage characteristics and disorders in the dog and cat. Veterinary and Comparative Orthopaedics and Traumatology, 29(4), 269-276. [More Information]
  • Haase, B., Mazrier, H., Wade, C. (2016). Digging for known genetic mutations underlying inherited bone and cartilage characteristics and disorders in the dog and cat. Veterinary and Comparative Orthopaedics and Traumatology, 29, 269-276. [More Information]
  • Bertolini, F., Gandolfi, B., Soo Kim, E., Lyons, L., Haase, B., Rothschild, M. (2016). Evidence of selection signatures that shape the Persian cat breed. Mammalian Genome, 27(3-4), 144-155. [More Information]
  • Cheng, S., Wigney, D., Haase, B., Wade, C. (2016). Inheritance of chronic superficial keratitis in Australian Greyhounds. Animal Genetics. [More Information]
  • Finn, J., Haase, B., Willet, C., Van Rooy, D., Chew, T., Wade, C., Hamilton (Ellis), N., Velie, B. (2016). The relationship between coat colour phenotype and equine behaviour: A pilot study. Applied Animal Behaviour Science, 174, 66-69. [More Information]
  • Fenn, D., Raudsepp, T., Cothran, E., Hamilton (Ellis), N., Haase, B. (2016). Validation of a candidate causative mutation for white spotting in donkeys. Animal Genetics. [More Information]
  • Fenn, D., Raudsepp, T., Cothran, E., Hamilton (Ellis), N., Haase, B. (2016). Validation of a candidate causative mutation for white spotting in donkeys. Animal Genetics, , 1-1. [More Information]
  • Haase, B., Jagannathan, V., Reider, S., Leeb, T. (2015). A novel KIT variant in an Icelandic horse with white-spotted coat colour. Animal Genetics, 46(4), 466-466. [More Information]
  • Willet, C., Makara, M., Reppas, G., Tsoukalas, G., Malik, R., Haase, B., Wade, C. (2015). Canine Disorder Mirrors Human Disease: Exonic Deletion in HES7 Causes Autosomal Recessive Spondylocostal Dysostosis in Miniature Schnauzer Dogs. PloS One, 10(2), 1-13. [More Information]
  • Willet, C., Haase, B., Charleston, M., Wade, C. (2015). Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker. Bioinformatics, 31(4), 599-601. [More Information]
  • Arnott, E., Peek, L., Early, J., Pan, A., Haase, B., Chew, T., McGreevy, P., Wade, C. (2015). Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. Canine Genetics and Epidemiology, 2, 1-6. [More Information]
  • Haase, B., Rieder, S., Leeb, T. (2015). Two variants in the KIT gene as candidate causive mutations for a dominant white and white spotting phenotype in the donkey. Animal Genetics, 46(3), 321-324. [More Information]
  • Shelton, G., Rider, B., Child, G., Tzannes, S., Guo, L., Moghadaszadeh, B., Troiano, E., Haase, B., Wade, C., Beggs, A. (2015). X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene. Skeletal Muscle, 5(1), 1-12. [More Information]
  • 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]
  • 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), 1-6. [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, 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, 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, 1-12. [More Information]
  • Welle, M., Philipp, U., Refenacht, S., Roosje, P., Scharfenstein, M., Schultz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., et al (2009). MLPH Genotype - Melanin Phenotype Correlation in Dilute Dogs. Journal of Heredity, 2(38), 15883-15888. [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]
  • Danilowicz, 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

  • Gandolfi, B., Alamri, S., Darby, B., Lattimer, J., Malik, R., Wade, C., Lyons, L., Cheng, J., Bateman, J., McIntyre, P., Haase, B., et al (2016). A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats. Society for Molecular Biology and Evolution (SMBE) and Genetics Society of Australia (GSA), N/A: N/A.
  • Finn, J., Haase, B., Willet, C., Van Rooy, D., Chew, T., Wade, C., Hamilton (Ellis), N., Velie, B. (2016). The relationship between coat colour phenotype and equine behaviour: a pilot studu. Society for Molecular Biology and Evolution (SMBE) and Genetics Society of Australia (GSA), N/A: N/A.
  • 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.

2016

  • Gandolfi, B., Alamri, S., Darby, W., Adhikari, B., Lattimer, J., Malik, R., Wade, C., Lyons, L., Cheng, J., Bateman, J., Haase, B., et al (2016). A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats. Osteoarthritis and Cartilage, 24(8), 1441-1450. [More Information]
  • Gandolfi, B., Alamri, S., Darby, B., Lattimer, J., Malik, R., Wade, C., Lyons, L., Cheng, J., Bateman, J., McIntyre, P., Haase, B., et al (2016). A dominant TRPV4 variant underlies osteochondrodysplasia in Scottish fold cats. Society for Molecular Biology and Evolution (SMBE) and Genetics Society of Australia (GSA), N/A: N/A.
  • Haase, B., Mazrier, H., Wade, C. (2016). Digging for known genetic mutations underlying inherited bone and cartilage characteristics and disorders in the dog and cat. Veterinary and Comparative Orthopaedics and Traumatology, 29(4), 269-276. [More Information]
  • Haase, B., Mazrier, H., Wade, C. (2016). Digging for known genetic mutations underlying inherited bone and cartilage characteristics and disorders in the dog and cat. Veterinary and Comparative Orthopaedics and Traumatology, 29, 269-276. [More Information]
  • Bertolini, F., Gandolfi, B., Soo Kim, E., Lyons, L., Haase, B., Rothschild, M. (2016). Evidence of selection signatures that shape the Persian cat breed. Mammalian Genome, 27(3-4), 144-155. [More Information]
  • Cheng, S., Wigney, D., Haase, B., Wade, C. (2016). Inheritance of chronic superficial keratitis in Australian Greyhounds. Animal Genetics. [More Information]
  • Finn, J., Haase, B., Willet, C., Van Rooy, D., Chew, T., Wade, C., Hamilton (Ellis), N., Velie, B. (2016). The relationship between coat colour phenotype and equine behaviour: a pilot studu. Society for Molecular Biology and Evolution (SMBE) and Genetics Society of Australia (GSA), N/A: N/A.
  • Finn, J., Haase, B., Willet, C., Van Rooy, D., Chew, T., Wade, C., Hamilton (Ellis), N., Velie, B. (2016). The relationship between coat colour phenotype and equine behaviour: A pilot study. Applied Animal Behaviour Science, 174, 66-69. [More Information]
  • Fenn, D., Raudsepp, T., Cothran, E., Hamilton (Ellis), N., Haase, B. (2016). Validation of a candidate causative mutation for white spotting in donkeys. Animal Genetics. [More Information]
  • Fenn, D., Raudsepp, T., Cothran, E., Hamilton (Ellis), N., Haase, B. (2016). Validation of a candidate causative mutation for white spotting in donkeys. Animal Genetics, , 1-1. [More Information]

2015

  • Haase, B., Jagannathan, V., Reider, S., Leeb, T. (2015). A novel KIT variant in an Icelandic horse with white-spotted coat colour. Animal Genetics, 46(4), 466-466. [More Information]
  • Willet, C., Makara, M., Reppas, G., Tsoukalas, G., Malik, R., Haase, B., Wade, C. (2015). Canine Disorder Mirrors Human Disease: Exonic Deletion in HES7 Causes Autosomal Recessive Spondylocostal Dysostosis in Miniature Schnauzer Dogs. PloS One, 10(2), 1-13. [More Information]
  • Willet, C., Haase, B., Charleston, M., Wade, C. (2015). Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker. Bioinformatics, 31(4), 599-601. [More Information]
  • Arnott, E., Peek, L., Early, J., Pan, A., Haase, B., Chew, T., McGreevy, P., Wade, C. (2015). Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. Canine Genetics and Epidemiology, 2, 1-6. [More Information]
  • Haase, B., Rieder, S., Leeb, T. (2015). Two variants in the KIT gene as candidate causive mutations for a dominant white and white spotting phenotype in the donkey. Animal Genetics, 46(3), 321-324. [More Information]
  • Shelton, G., Rider, B., Child, G., Tzannes, S., Guo, L., Moghadaszadeh, B., Troiano, E., Haase, B., Wade, C., Beggs, A. (2015). X-linked myotubular myopathy in Rottweiler dogs is caused by a missense mutation in Exon 11 of the MTM1 gene. Skeletal Muscle, 5(1), 1-12. [More Information]

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]

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), 1-6. [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, 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, 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, 1-12. [More Information]
  • Welle, M., Philipp, U., Refenacht, S., Roosje, P., Scharfenstein, M., Schultz, E., Brenig, B., Linek, M., Mecklenburg, L., Grest, P., et al (2009). MLPH Genotype - Melanin Phenotype Correlation in Dilute Dogs. Journal of Heredity, 2(38), 15883-15888. [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]
  • Danilowicz, 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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