Dr Danqing Zhu

Medicine, Concord Clinical School

Telephone 02 97679104
Fax 02 97676194

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Selected publications

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Journals

  • Ganesamoorthy, D., Bruno, D., Schoumans, J., Storey, E., Delatycki, M., Zhu, D., Wei, M., Nicholson, G., Gardner, R., Slater, H. (2009). Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15. Clinical Chemistry (Washington, DC), 55(7), 1415-1418. [More Information]
  • Vallat, J., Ouvrier, R., Pollard, J., Magdelaine, C., Zhu, D., Nicholson, G., Grew, S., Ryan, M., Funalot, B. (2008). Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations. Journal of Neuropathology and Experimental Neurology, 67(11), 1097-1102. [More Information]
  • Nicholson, G., Magdelaine, C., Zhu, D., Grew, S., Ryan, M., Sturtz, F., Vallat, J., Ouvrier, R. (2008). Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations. Neurology, 70(19), 1678-1681. [More Information]
  • Zhu, D., Kennerson, M., Walizada, G., Züchner, S., Vance, J., Nicholson, G. (2005). Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Neurology, 65(3), 496-497. [More Information]
  • Züchner, S., Noureddine, M., Kennerson, M., Verhoeven, K., Claeys, K., De Jonghe, P., Oliveira, S., Merory, J., Speer, M., Stenger, J., Walizada, G., Zhu, D., Nicholson, G., et al (2005). Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease. Nature Genetics, 37(3), 289-294. [More Information]
  • Vucic, S., Kennerson, M., Zhu, D., Miedema, E., Kok, C., Nicholson, G. (2003). CMT with pyramidal features. Neurology, 60(4), 696-699.
  • Zhu, D., Kennerson, M., Merory, J., Chrast, R., Verheijen, M., Lemke, G., Nicholson, G. (2003). Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region. Neurogenetics, 4(4), 179-183.

2009

  • Ganesamoorthy, D., Bruno, D., Schoumans, J., Storey, E., Delatycki, M., Zhu, D., Wei, M., Nicholson, G., Gardner, R., Slater, H. (2009). Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15. Clinical Chemistry (Washington, DC), 55(7), 1415-1418. [More Information]

2008

  • Vallat, J., Ouvrier, R., Pollard, J., Magdelaine, C., Zhu, D., Nicholson, G., Grew, S., Ryan, M., Funalot, B. (2008). Histopathological Findings in Hereditary Motor and Sensory Neuropathy of Axonal Type With Onset in Early Childhood Associated With Mitofusin 2 Mutations. Journal of Neuropathology and Experimental Neurology, 67(11), 1097-1102. [More Information]
  • Nicholson, G., Magdelaine, C., Zhu, D., Grew, S., Ryan, M., Sturtz, F., Vallat, J., Ouvrier, R. (2008). Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations. Neurology, 70(19), 1678-1681. [More Information]

2005

  • Zhu, D., Kennerson, M., Walizada, G., Züchner, S., Vance, J., Nicholson, G. (2005). Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Neurology, 65(3), 496-497. [More Information]
  • Züchner, S., Noureddine, M., Kennerson, M., Verhoeven, K., Claeys, K., De Jonghe, P., Oliveira, S., Merory, J., Speer, M., Stenger, J., Walizada, G., Zhu, D., Nicholson, G., et al (2005). Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease. Nature Genetics, 37(3), 289-294. [More Information]

2003

  • Vucic, S., Kennerson, M., Zhu, D., Miedema, E., Kok, C., Nicholson, G. (2003). CMT with pyramidal features. Neurology, 60(4), 696-699.
  • Zhu, D., Kennerson, M., Merory, J., Chrast, R., Verheijen, M., Lemke, G., Nicholson, G. (2003). Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region. Neurogenetics, 4(4), 179-183.

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