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Robert Williamson's selected work
Non-invasive in vivo hyperspectral imaging of the retina for potential biomarker use in Al..
Effect of APOE Genotype on Amyloid Deposition, Brain Volume, and Memory in Cognitively Nor..
Displaying the 5 most recent projects by Robert Williamson.
Displaying the 52 most recent scholarly works by Robert Williamson.
If Human Brain Organoids Are the Answer to Understanding Dementia, What Are the Questions?
Lezanne Ooi, Mirella Dottori, Anthony L Cook, Martin Engel, Vini Gautam, Alexandra Grubman, Damian Hernandez, Anna E King, Simon Maksour, Helena Targa Dias Anastacio, Rachelle Balez, Alice Pebay, Colin Pouton, Michael Valenzuela, Anthony White, Robert Williamson
Journal article | 2020 | The Neuroscientist
Because our beliefs regarding our individuality, autonomy, and personhood are intimately bound up with our brains, there is a publ..
Non-invasive in vivo hyperspectral imaging of the retina for potential biomarker use in Alzheimer's disease
Xavier Hadoux, Flora Hui, Jeremiah KH Lim, Colin L Masters, Alice Pebay, Sophie Chevalier, Jason Ha, Samantha Loi, Christopher J Fowler, Christopher Rowe, Victor L Villemagne, Edward N Taylor, Christopher Fluke, Jean-Paul Soucy, Frederic Lesage, Jean-Philippe Sylvestre, Pedro Rosa-Neto, Sulantha Mathotaarachchi, Serge Gauthier, Ziad S Nasreddine, et al.
Journal article | 2019 | NATURE COMMUNICATIONS
Effect of APOE Genotype on Amyloid Deposition, Brain Volume, and Memory in Cognitively Normal Older Individuals
Yen Ying Lim, Robert Williamson, Simon M Laws, Victor L Villemagne, Pierrick Bourgeat, Christopher Fowler, Stephanie Rainey-Smith, Olivier Salvado, Ralph N Martins, Christopher C Rowe, Colin L Masters, Paul Maruff
Journal article | 2017 | Journal of Alzheimer's Disease
BACKGROUND: The association between the apolipoprotein E (APOE) ɛ4 allele and high risk of developing Alzheimer's disease (AD) dem..
Generation of Induced Pluripotent Stem Cell Lines from Friedreich Ataxia Patients
Jun Liu, Paul J Verma, Marguerite V Evans-Galea, Martin B Delatycki, Anna Michalska, Jessie Leung, Duncan Crombie, Joseph P Sarsero, Robert Williamson, Mirella Dottori, Alice Pebay
Journal article | 2011 | Stem Cell Reviews and Reports
Stimulation of Activin A/Nodal signaling is insufficient to induce definitive endoderm formation of cord blood-derived unrestricted somatic stem cells
Caitlin E Filby, Robert Williamson, Peter van Kooy, Alice Pebay, Mirella Dottori, Ngaire J Elwood, Faten Zaibak
Journal article | 2011 | Stem Cell Research & Therapy
"You're One of Us Now": Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP)
Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki
Journal article | 2008 | American Journal of Medical Genetics
Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis
MB Delatycki, KJ Allen, AE Nisselle, V Collins, S Metcalfe, D du Sart, J Halliday, MA Aitken, I Macciocca, V Hill, A Wakefield, A Ritchie, AA Gason, AJ Nicoll, LW Powell, R Williamson
Journal article | 2005 | The Lancet
Transgene copy number-dependent rescue of murine beta-globin knockout mice carrying a 183 kb human beta-globin BAC genomic fragment
J Vadolas, H Wardan, M Bosmans, F Zaibak, D Jamsai, L Voullaire, R Williamson, PA Ioannou
Journal article | 2005 | Biochimica et Biophysica Acta-Gene Structure & Expression
Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis
AE Nisselle, MB Delatycki, V Collins, S Metcalfe, MA Aitken, D du Sart, J Halliday, I Macciocca, A Wakefield, V Hill, A Gason, B Warner, V Calabro, R Williamson, KJ Allen
Journal article | 2004 | Clinical Genetics
Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype
MG de Silva, K Elliott, HH Dahl, E Fitzpatrick, S Wilcox, M Delatycki, R Williamson, D Efron, M Lynch, S Forrest
Journal article | 2003 | Journal of Medical Genetics
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness
HHM Dahl, K Saunders, TM Kelly, AH Osborn, S Wilcox, B Cone-Wesson, JL Wunderlich, D Du Sart, M Kamarinos, RJM Gardner, S Dennehy, R Williamson, N Vallance, P Mutton
Journal article | 2001 | Medical Journal of Australia
Honours, Awards and Fellowships
FRCPA - Fellow of the Royal College of Pathologists, Australia
FAA - Fellow of the Australian Academy of Science
Paediatrics Royal Children'S Hospital
Royal College of Physicians of London
Doctor of Philosophy
University of London
Honorary Doctor of Medicine
Institution not known