Ms Kitty Lo

F07 - Carslaw Building
The University of Sydney


Teaching and supervision

Timetable

K_Lo

Selected publications

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Journals

  • Bochukova, E., Lawler, K., Croizier, S., Keogh, J., Patel, N., Strohbehn, G., Lo, K., Humphrey, J., Hokken-Koelega, A., Damen, L., et al (2018). A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome. Cell Reports, 22(13), 3401-3408. [More Information]
  • Devoy, A., Kalmar, B., Stewart, M., Park, H., Burke, B., Noy, S., Redhead, Y., Humphrey, J., Lo, K., Jaeger, J., et al (2017). Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in �FUSDelta14� knockin mice. Brain, 140(11), 2797-2805. [More Information]
  • Hensman, D., Flower, M., Lo, K., Miller, J., van Ommen, G., Hoen, P., Stone, T., Guinee, A., Langbehn, D., Jones, L., et al (2017). Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's disease. Scientific Reports, 7(March 2017), 1-12. [More Information]
  • Hensman, D., Pardinas, A., Langbehn, D., Lo, K., Leavitt, B., Roos, R., Durr, A., Mead, S., Holmans, P., Jones, L., et al (2017). Identification of genetic variants associated with Huntington�s disease progression: a genome-wide association study. The Lancet Neurology, 16(9), 701-711. [More Information]
  • Lo, K., Karampetsou, E., Boustred, C., McKay, F., Mason, S., Hill, M., Plagnol, V., Chitty, L. (2016). Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities. American Journal of Human Genetics, 98(1), 34-44. [More Information]
  • Lynch, C., Murphy, T., Ravi, V., Hobbs, G., Lo, K., Ward, C. (2016). Radio detections of southern ultracool dwarfs. Monthly Notices of the Royal Astronomical Society, 457(2), 1224-1232. [More Information]
  • Miller, J., Lo, K., Andre, R., Hensman, D., Trager, U., Stone, T., Jones, L., Holmans, P., Plagnol, V., Tabrizi, S. (2016). RNA-Seq of Huntington's Disease Patient Myeloid Cells Reveals Innate Transcriptional Dysregulation Associated With Proinflammatory Pathway Activation. Human Molecular Genetics, 25(14), 2893--2904. [More Information]
  • Farrell, S., Murphy, T., Lo, K. (2015). Autoclassification of the Variable 3XMM Sources using the Random Forest Machine Learning Algorithm. Astrophysical Journal, 813(28), 1-17. [More Information]
  • Curtis, J., Luo, Y., Zenner, H., Cuchet-Lourenco, D., Wu, C., Lo, K., Maes, M., Alisaac, A., Stebbings, E., Liu, J., et al (2015). Susceptibility to tuberculosis is associated with variants in the�ASAP1�gene encoding a regulator of dendritic cell migration. Nature Genetics, 47(5), 523-527. [More Information]
  • Lo, K., Farrell, S., Murphy, T., Gaensler, B. (2014). Automatic classification of time-variable x-ray sources. Astrophysical Journal, 786(1), 1-16. [More Information]
  • Hill, M., Wright, D., Daley, R., Lewis, C., McKay, F., Mason, S., Lench, N., Howarth, A., Boustred, C., Lo, K., et al (2014). Evaluation of noninvasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal noninvasive diagnosis (RAPID) protocol. BMC Pregnancy and Childbirth, 14(229), 1-10. [More Information]
  • Lo, K., Boustred, C., Chitty, L., Plagnol, V. (2014). RAPIDR: an analysis package for Non-invasive prenatal testing of aneuploidy. Bioinformatics, 30(20), 2965-2967. [More Information]
  • Murphy, T., Chatterjee, S., Kaplan, D., Banyer, J., Bell, M., Bignall, H., Bower, G., Cameron, R., Coward, D., Cordes, J., Curran, J., Farrell, S., Gaensler, B., Green, A., Hancock, P., Lo, K., et al (2013). VAST: An ASKAP survey for variables and slow transients. Publications of the Astronomical Society of Australia, 30(1), 1-27. [More Information]
  • Lo, K., Bray, D., Hobbs, G., Murphy, T., Gaensler, B., Melrose, D., Ravi, V., Manchester, R., Keith, M. (2012). Observations and modelling of pulsed radio emission from CU Virginis. Monthly Notices of the Royal Astronomical Society, 421(4), 3316-3324. [More Information]

Conferences

  • Lo, K., Murphy, T., Rebbapragada, U., Wagstaff, K. (2013). Online classification for time-domain astronomy. IEEE 13th International Conference on Data Mining (ICDM 2013), Piscataway: Institute of Electrical and Electronics Engineers (IEEE). [More Information]

2018

  • Bochukova, E., Lawler, K., Croizier, S., Keogh, J., Patel, N., Strohbehn, G., Lo, K., Humphrey, J., Hokken-Koelega, A., Damen, L., et al (2018). A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome. Cell Reports, 22(13), 3401-3408. [More Information]

2017

  • Devoy, A., Kalmar, B., Stewart, M., Park, H., Burke, B., Noy, S., Redhead, Y., Humphrey, J., Lo, K., Jaeger, J., et al (2017). Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in �FUSDelta14� knockin mice. Brain, 140(11), 2797-2805. [More Information]
  • Hensman, D., Flower, M., Lo, K., Miller, J., van Ommen, G., Hoen, P., Stone, T., Guinee, A., Langbehn, D., Jones, L., et al (2017). Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's disease. Scientific Reports, 7(March 2017), 1-12. [More Information]
  • Hensman, D., Pardinas, A., Langbehn, D., Lo, K., Leavitt, B., Roos, R., Durr, A., Mead, S., Holmans, P., Jones, L., et al (2017). Identification of genetic variants associated with Huntington�s disease progression: a genome-wide association study. The Lancet Neurology, 16(9), 701-711. [More Information]

2016

  • Lo, K., Karampetsou, E., Boustred, C., McKay, F., Mason, S., Hill, M., Plagnol, V., Chitty, L. (2016). Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities. American Journal of Human Genetics, 98(1), 34-44. [More Information]
  • Lynch, C., Murphy, T., Ravi, V., Hobbs, G., Lo, K., Ward, C. (2016). Radio detections of southern ultracool dwarfs. Monthly Notices of the Royal Astronomical Society, 457(2), 1224-1232. [More Information]
  • Miller, J., Lo, K., Andre, R., Hensman, D., Trager, U., Stone, T., Jones, L., Holmans, P., Plagnol, V., Tabrizi, S. (2016). RNA-Seq of Huntington's Disease Patient Myeloid Cells Reveals Innate Transcriptional Dysregulation Associated With Proinflammatory Pathway Activation. Human Molecular Genetics, 25(14), 2893--2904. [More Information]

2015

  • Farrell, S., Murphy, T., Lo, K. (2015). Autoclassification of the Variable 3XMM Sources using the Random Forest Machine Learning Algorithm. Astrophysical Journal, 813(28), 1-17. [More Information]
  • Curtis, J., Luo, Y., Zenner, H., Cuchet-Lourenco, D., Wu, C., Lo, K., Maes, M., Alisaac, A., Stebbings, E., Liu, J., et al (2015). Susceptibility to tuberculosis is associated with variants in the�ASAP1�gene encoding a regulator of dendritic cell migration. Nature Genetics, 47(5), 523-527. [More Information]

2014

  • Lo, K., Farrell, S., Murphy, T., Gaensler, B. (2014). Automatic classification of time-variable x-ray sources. Astrophysical Journal, 786(1), 1-16. [More Information]
  • Hill, M., Wright, D., Daley, R., Lewis, C., McKay, F., Mason, S., Lench, N., Howarth, A., Boustred, C., Lo, K., et al (2014). Evaluation of noninvasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal noninvasive diagnosis (RAPID) protocol. BMC Pregnancy and Childbirth, 14(229), 1-10. [More Information]
  • Lo, K., Boustred, C., Chitty, L., Plagnol, V. (2014). RAPIDR: an analysis package for Non-invasive prenatal testing of aneuploidy. Bioinformatics, 30(20), 2965-2967. [More Information]

2013

  • Lo, K., Murphy, T., Rebbapragada, U., Wagstaff, K. (2013). Online classification for time-domain astronomy. IEEE 13th International Conference on Data Mining (ICDM 2013), Piscataway: Institute of Electrical and Electronics Engineers (IEEE). [More Information]
  • Murphy, T., Chatterjee, S., Kaplan, D., Banyer, J., Bell, M., Bignall, H., Bower, G., Cameron, R., Coward, D., Cordes, J., Curran, J., Farrell, S., Gaensler, B., Green, A., Hancock, P., Lo, K., et al (2013). VAST: An ASKAP survey for variables and slow transients. Publications of the Astronomical Society of Australia, 30(1), 1-27. [More Information]

2012

  • Lo, K., Bray, D., Hobbs, G., Murphy, T., Gaensler, B., Melrose, D., Ravi, V., Manchester, R., Keith, M. (2012). Observations and modelling of pulsed radio emission from CU Virginis. Monthly Notices of the Royal Astronomical Society, 421(4), 3316-3324. [More Information]

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