Williams, Kelly L.
Macquarie University
3 papers on CoChatORCID 0000-0001-6319-9473
Most cited papers
- Verified
TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
Sreedharan, J., Blair, I. P., Tripathi, V. B., Hu, X., Vance, C., Rogelj, B., Ackerley, S., Durnall, J. C., Williams, K. L., Buratti, E., et al. (2008) · Science
Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders
Cited by 2,630
- Verified
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen, W., van der Spek, R. A. A., Bakker, M. K., van Vugt, J. J. F. A., Hop, P. J., Zwamborn, R. A. J., de Klein, N., Westra, H.-J., Bakker, O. B., Deelen, P., et al. (2021) · Nature Genetics
Amyotrophic Lateral Sclerosis ResearchGenetic Associations and Epidemiology
Cited by 542
- Verified
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders
study, T. A. I. B. A. L., Nabais, M. F., Initiative, T. A. D. N., Laws, S. M., Lin, T., Vallerga, C. L., Armstrong, N. J., Blair, I. P., Kwok, J. B., Mather, K. A., et al. (2021) · Genome Biology
Epigenetics and DNA MethylationDementia and Cognitive Impairment Research
Cited by 99
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