Dr Alexander Drew

Senior Research Fellow
ANZAC Research Institute


Map

Selected publications

Download citations: PDF RTF Endnote

Journals

  • Drew, A., Cutrupi, A., Brewer, M., Nicholson, G., Kennerson, M. (2016). A 1.35A�Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2. Human Genetics, 135(11), 1269-1278. [More Information]
  • Albulym, O., Kennerson, M., Harms, M., Drew, A., Siddell, A., Auer-Grumbach, M., Pestronk, A., Connolly, A., Baloh, R., Zuchner, S., Reddel, S., Nicholson, G. (2016). MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs. Annals of Neurology, 79(3), 419-427. [More Information]
  • Tey, S., Ahmad-Annuar, A., Drew, A., Shahrizaila, N., Nicholson, G., Kennerson, M. (2016). Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies. Clinical Genetics, 90(2), 127-133. [More Information]
  • Perez-Siles, G., Ly, C., Grant, A., Drew, A., Yiu, E., Ryan, M., Chuang, D., Tso, S., Nicholson, G., Kennerson, M. (2016). Pathogenic mechanisms underlying x-linked charcot-marie-tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation. Neurobiology of Disease, 94, 237-244. [More Information]
  • Drew, A., Blair, I., Nicholson, G. (2011). Molecular Genetics and Mechanisms of Disease in Distal Hereditary Motor Neuropathies: Insights Directing Future Genetic Studies. Current Molecular Medicine, 11(8), 650-665. [More Information]

2016

  • Drew, A., Cutrupi, A., Brewer, M., Nicholson, G., Kennerson, M. (2016). A 1.35A�Mb DNA fragment is inserted into the DHMN1 locus on chromosome 7q34-q36.2. Human Genetics, 135(11), 1269-1278. [More Information]
  • Albulym, O., Kennerson, M., Harms, M., Drew, A., Siddell, A., Auer-Grumbach, M., Pestronk, A., Connolly, A., Baloh, R., Zuchner, S., Reddel, S., Nicholson, G. (2016). MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs. Annals of Neurology, 79(3), 419-427. [More Information]
  • Tey, S., Ahmad-Annuar, A., Drew, A., Shahrizaila, N., Nicholson, G., Kennerson, M. (2016). Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies. Clinical Genetics, 90(2), 127-133. [More Information]
  • Perez-Siles, G., Ly, C., Grant, A., Drew, A., Yiu, E., Ryan, M., Chuang, D., Tso, S., Nicholson, G., Kennerson, M. (2016). Pathogenic mechanisms underlying x-linked charcot-marie-tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation. Neurobiology of Disease, 94, 237-244. [More Information]

2011

  • Drew, A., Blair, I., Nicholson, G. (2011). Molecular Genetics and Mechanisms of Disease in Distal Hereditary Motor Neuropathies: Insights Directing Future Genetic Studies. Current Molecular Medicine, 11(8), 650-665. [More Information]

To update your profile click here. For support on your academic profile contact .