Unravelling the molecular basis of amyotrophic lateral sclerosis

Williams, Kelly (Primary Chief Investigator)

Project: Research

Status	Active
Effective start/end date	1/01/16 → …

Genetic characterisation of ATXN2 in Australian amyotrophic lateral sclerosis
Wu, S. S. L., McCann, E. P., Chan Moi Fat, S., Grima, N., Henden, L., Fearnley, L. G., Chiu, P., Williams, K. L., Rowe, D. B., Nicholson, G. A., Kiernan, M. C., Blair, I. P., Yang, S. & Fifita, J. A., Mar 2026, In: Brain Disorders. 21, p. 1-9 9 p., 100301.
Research output: Contribution to journal › Article › peer-review

Open Access
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Characterising the genetic landscape of amyotrophic lateral sclerosis: a catalogue and assessment of over 1,000 published genetic variants
McCann, E. P., Grima, N., Fifita, J. A., Chan Moi Fat, S., Lehnert, K., Henden, L., Blair, I. P. & Williams, K. L., 7 Nov 2023, In: Journal of Neuromuscular Diseases. 10, 6, p. 1127-1141 15 p.
Research output: Contribution to journal › Article › peer-review

Open Access
File
6 Link opens in a new tab Citations (Scopus)

62 Downloads (Pure)
Simultaneous isolation of high-quality RNA and DNA from postmortem human central nervous system tissues for omics studies
Grima, N., Henden, L., Watson, O., Blair, I. P. & Williams, K. L., 29 Jan 2022, In: Journal of Neuropathology and Experimental Neurology. 81, 2, p. 135-145 11 p.
Research output: Contribution to journal › Article › peer-review
7 Link opens in a new tab Citations (Scopus)