Dr Purvi Kakadiya

Selected publications and creative works (Research Outputs)

  • Sandhöfer N, Metzeler, K. H., Kakadia, P. M., Pasalic, Z., Hiddemann, W., Neusser, M., ... Spiekermann, K. (2017). A Fluorescence in Situ Hybridization-Based Screen Allows Rapid Detection of Adverse Cytogenetic Alterations in Patients with Acute Myeloid Leukemia. Genes, chromosomes & cancer10.1002/gcc.22466
    Other University of Auckland co-authors: Stefan Bohlander
  • Kakadia, P. M., Schmidmaier, R., Völkl A, Schneider, I., Huk, N., Schneider, S., ... Spiekermann, K. (2016). An ETV6-ABL1 fusion in a patient with chronic myeloproliferative neoplasm: Initial response to Imatinib followed by rapid transformation into ALL. Leukemia research reports, 6, 50-54. 10.1016/j.lrr.2016.09.002
    Other University of Auckland co-authors: Stefan Bohlander
  • Garbes, L., Kim, K., Rieß A, Hoyer-Kuhn, H., Beleggia, F., Bevot, A., ... Savarirayan, R. (2015). Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta. American Journal of Human Genetics, 96 (3), 432-439. 10.1016/j.ajhg.2015.01.002
    Other University of Auckland co-authors: Stefan Bohlander
  • Garbes, L., Kim, K., Rieß A, Hoyer-Kuhn, H., Beleggia, F., Bevot, A., ... Savarirayan, R. (2015). Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta. American journal of human genetics, 96 (3), 432-439. 10.1016/j.ajhg.2015.01.002
    Other University of Auckland co-authors: Stefan Bohlander
  • Sandhoefer, N., Metzeler, K., Kakadia, P., Huk, N., Konstandin, N., Dufour, A., ... Bohlander, S. (2015). A Fluorescence in-Situ Hybridization-Based Screen Allows Rapid Detection of Adverse Cytogenetics in Patients (PTS) with Acute Myeloid Leukemia (AML). ANNALS OF HEMATOLOGY, 94, S86-S87.
    Other University of Auckland co-authors: Stefan Bohlander
  • Köhnke T, Sauter, D., Ringel, K., Hoster, E., Laubender, R. P., Hubmann, M., ... Dufour, A. (2015). Early assessment of minimal residual disease in AML by flow cytometry during aplasia identifies patients at increased risk of relapse. Leukemia, 29 (2), 377-386. 10.1038/leu.2014.186
    Other University of Auckland co-authors: Stefan Bohlander
  • Garbes, L., Kim, K., Riess, A., Hoyer-Kuhn, H., Beleggia, F., Bevot, A., ... Savarirayan, R. (2015). Mutations in SEC24D Cause a Syndromic Form of Osteogenesis Imperfecta with Craniofacial Dysplasia.. MOLECULAR BIOLOGY OF THE CELL. (pp. 1).
    Other University of Auckland co-authors: Stefan Bohlander
  • Bohlander, S. K., & Kakadia, P. M. (2015). DNA Repair and Chromosomal Translocations. (pp. 1-37). 10.1007/978-3-319-20291-4_1
    Other University of Auckland co-authors: Stefan Bohlander